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  • 1.
    Anwar, Nargis
    et al.
    Dundalk Inst Technol, Ireland.
    Armstrong, Gordon
    Univ Limerick, Ireland.
    Laffir, Fathima
    Univ Limerick, Ireland.
    Dickinson, Calum
    Univ Limerick, Ireland.
    Vagin, Mikhail
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Fysik och elektroteknik. Linköpings universitet, Institutionen för fysik, kemi och biologi. Linköpings universitet, Tekniska fakulteten.
    McCormac, Timothy
    Dundalk Inst Technol, Ireland.
    Redox switching of polyoxometalate-doped polypyrrole films in ionic liquid media2018Inngår i: Electrochimica Acta, ISSN 0013-4686, E-ISSN 1873-3859, Vol. 265, s. 254-258Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    The surface immobilization of the parent Dawson polyoxometalate (POM) as a counter-ion for the electropolymerization of polypyrrole (PPy) or as an electrode-adhered solid was utilized for voltammetric studies of the surface adhered POM in room temperature ionic liquids (RTIL). Illustrating the efficiency of intermediate stabilization, voltammetry at POM-modified electrodes in a PF6-based RTIL revealed richer redox behaviour and higher stabilization in comparison with aqueous electrolytes and with BF4-based RTIL, respectively. High stability of the POM-doped PPy towards continuous charge-discharge voltammetric redox cycles was confirmed by minor changes in film morphology observed after the cycling in RTILs. (c) 2017 Elsevier Ltd. All rights reserved.

  • 2.
    Cattelan, Mattia
    et al.
    School of Chemistry, University of Bristol, Cantocks Close, Bristol, United Kingdom.
    Vagin, Mikhail
    Linköpings universitet, Institutionen för fysik, kemi och biologi. Linköpings universitet, Institutionen för teknik och naturvetenskap, Laboratoriet för organisk elektronik. Linköpings universitet, Tekniska fakulteten.
    Fox, Neil A.
    School of Chemistry, University of Bristol, Cantocks Close, Bristol, United Kingdom.
    Ivanov, Ivan Gueorguiev
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Halvledarmaterial. Linköpings universitet, Tekniska fakulteten.
    Shtepliuk, Ivan
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Halvledarmaterial. Linköpings universitet, Tekniska fakulteten.
    Yakimova, Rositsa
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Halvledarmaterial. Linköpings universitet, Tekniska fakulteten.
    Anodization study of epitaxial graphene: insights on the oxygen evolution reaction of graphitic materials2019Inngår i: Nanotechnology, ISSN 0957-4484, E-ISSN 1361-6528, Vol. 30, nr 28, artikkel-id 285701Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    The photoemission electron microscopy and x-ray photoemission spectroscopy were utilized for the study of anodized epitaxial graphene (EG) on silicon carbide as a fundamental aspect of the oxygen evolution reaction on graphitic materials. The high-resolution analysis of surface morphology and composition quantified the material transformation during the anodization. We investigated the surface with lateral resolution amp;lt;150 nm, revealing significant transformations on the EG and the role of multilayer edges in increasing the film capacitance.

    Fulltekst tilgjengelig fra 2020-04-24 11:07
  • 3.
    Che, Canyan
    et al.
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Laboratoriet för organisk elektronik. Linköpings universitet, Tekniska fakulteten.
    Vagin, Mikhail
    Linköpings universitet, Tekniska fakulteten. Linköpings universitet, Institutionen för teknik och naturvetenskap, Laboratoriet för organisk elektronik. Linköpings universitet, Institutionen för fysik, kemi och biologi.
    Ail, Ujwala
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Laboratoriet för organisk elektronik. Linköpings universitet, Tekniska fakulteten.
    Gueskine, Viktor
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Laboratoriet för organisk elektronik. Linköpings universitet, Tekniska fakulteten.
    Phopase, Jaywant
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Laboratoriet för organisk elektronik. Linköpings universitet, Tekniska fakulteten. Linköpings universitet, Institutionen för fysik, kemi och biologi.
    Brooke, Robert
    RISE, Norrköping, Sweden.
    Gabrielsson, Roger
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Laboratoriet för organisk elektronik. Linköpings universitet, Tekniska fakulteten.
    Jonsson, Magnus P.
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Laboratoriet för organisk elektronik. Linköpings universitet, Tekniska fakulteten.
    Mak, Wing Cheung
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Sensor- och aktuatorsystem. Linköpings universitet, Tekniska fakulteten.
    Berggren, Magnus
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Laboratoriet för organisk elektronik. Linköpings universitet, Tekniska fakulteten.
    Crispin, Xavier
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Laboratoriet för organisk elektronik. Linköpings universitet, Tekniska fakulteten.
    Twinning Lignosulfonate with a Conducting Polymer via Counter-Ion Exchange for Large-Scale Electrical Storage2019Inngår i: Advanced Sustainable Systems, ISSN 2366-7486, Vol. 3, nr 9, artikkel-id 1900039Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    Abstract Lignosulfonate (LS) is a large-scale surplus product of the forest and paper industries, and has primarily been utilized as a low-cost plasticizer in making concrete for the construction industry. LS is an anionic redox-active polyelectrolyte and is a promising candidate to boost the charge capacity of the positive electrode (positrode) in redox-supercapacitors. Here, the physical-chemical investigation of how this biopolymer incorporates into the conducting polymer PEDOT matrix, of the positrode, by means of counter-ion exchange is reported. Upon successful incorporation, an optimal access to redox moieties is achieved, which provides a 63% increase of the resulting stored electrical charge by reversible redox interconversion. The effects of pH, ionic strength, and concentrations, of included components, on the polymer?polymer interactions are optimized to exploit the biopolymer-associated redox currents. Further, the explored LS-conducting polymer incorporation strategy, via aqueous synthesis, is evaluated in an up-scaling effort toward large-scale electrical energy storage technology. By using an up-scaled production protocol, integration of the biopolymer within the conducting polymer matrix by counter-ion exchange is confirmed and the PEDOT-LS synthesized through optimized strategy reaches an improved charge capacity of 44.6 mAh g?1.

  • 4.
    Che, Canyan
    et al.
    Linköpings universitet, Institutionen för teknik och naturvetenskap. Linköpings universitet, Tekniska fakulteten.
    Vagin, Mikhail
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Fysik och elektroteknik. Linköpings universitet, Institutionen för fysik, kemi och biologi. Linköpings universitet, Tekniska fakulteten.
    Wijeratne, Kosala
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Fysik och elektroteknik. Linköpings universitet, Tekniska fakulteten.
    Zhao, Dan
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Fysik och elektroteknik. Linköpings universitet, Tekniska fakulteten.
    Warczak, Magdalena
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Fysik och elektroteknik. Linköpings universitet, Tekniska fakulteten.
    Jonsson, Magnus
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Fysik och elektroteknik. Linköpings universitet, Tekniska fakulteten.
    Crispin, Xavier
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Fysik och elektroteknik. Linköpings universitet, Tekniska fakulteten.
    Conducting Polymer Electrocatalysts for Proton-Coupled Electron Transfer Reactions: Toward Organic Fuel Cells with Forest Fuels2018Inngår i: Advanced Sustainable Systems, ISSN 2366-7486, Vol. 317Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    Lignin is one of the most abundant biopolymers, constituting 25% of plants. The pulp and paper industries extract lignin in their process and today seek new applications for this by-product. Here, it is reported that the aromatic alcohols obtained from lignin depolymerization can be used as fuel in high power density electrical power sources. This study shows that the conducting polymer poly(3,4-ethylenedioxythiophene), fabricated from abundant ele-ments via low temperature synthesis, enables efficient, direct, and reversible chemical-to-electrical energy conversion of aromatic alcohols such as lignin residues in aqueous media. A material operation principle related to the rela-tively high molecular diffusion and ionic conductivity within the conducting polymer matrix, ensuring efficient uptake of protons in the course of proton-coupled electron transfers between organic molecules is proposed.

  • 5.
    Gryszel, Maciej
    et al.
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Fysik och elektroteknik. Linköpings universitet, Tekniska fakulteten.
    Markov, Aleksandr
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Fysik och elektroteknik. Linköpings universitet, Tekniska fakulteten.
    Vagin, Mikhail
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Fysik och elektroteknik. Linköpings universitet, Tekniska fakulteten.
    Glowacki, Eric
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Fysik och elektroteknik. Linköpings universitet, Tekniska fakulteten.
    Organic heterojunction photocathodes for optimized photoelectrochemical hydrogen peroxide production2018Inngår i: Journal of Materials Chemistry A, ISSN 2050-7488, Vol. 6, nr 48, s. 24709-24716Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    Solar-to-chemical conversion of sunlight into hydrogen peroxide as a chemical fuel is an emerging carbon-free sustainable energy strategy. The process is based on the reduction of dissolved oxygen to hydrogen peroxide. Only limited amounts of photoelectrode materials have been successfully explored for photoelectrochemical production of hydrogen peroxide. Herein we detail approaches to produce robust organic semiconductor photocathodes for peroxide evolution. They are based on evaporated donor-acceptor heterojunctions between phthalocyanine and tetracarboxylic perylenediimide, respectively. These small molecules form nanocrystalline films with good operational stability and high surface area. We discuss critical parameters which allow fabrication of efficient devices. These photocathodes can support continuous generation of high concentrations of peroxide with faradaic efficiency remaining at around 70%. We find that an advantage of the evaporated heterojunctions is that they can be readily vertically stacked to produce tandem cells which produce higher voltages. This feature is desirable for fabricating two-electrode photoelectrochemical cells. Overall, the photocathodes presented here have the highest performance reported to date in terms of photocurrent for peroxide production. These results offer a viable method for peroxide photosynthesis and provide a roadmap of strategies that can be used to produce photoelectrodes with even higher efficiency and productivity.

  • 6.
    Ibupoto, Zafar Hussain
    et al.
    Division of Material Science, Department of Engineering Sciences and Mathematics, Luleå University of Technology, Luleå, Sweden; Dr. M.A Kazi Institute of Chemistry University of Sindh Jamshoro, Sindh, Pakistan.
    Tahira, Aneela
    Division of Material Science, Department of Engineering Sciences and Mathematics, Luleå University of Technology, Luleå, Sweden.
    Tang, PengYi
    Catalan Institute of Nanoscience and Nanotechnology (ICN2), CSIC and BIST, Campus UAB, Bellaterra, Barcelona, Catalonia, Spain; Catalonia Institute for Energy Research (IREC), Jardins de les Dones de Negre 1, Sant Adrià del Besòs, Barcelona, Catalonia, Spain.
    Liu, Xianjie
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Ytors Fysik och Kemi. Linköpings universitet, Tekniska fakulteten.
    Morante, Joan Ramon
    Catalonia Institute for Energy Research (IREC), Jardins de les Dones de Negre 1, Sant Adrià del Besòs, Barcelona, Catalonia, Spain.
    Fahlman, Mats
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Ytors Fysik och Kemi. Linköpings universitet, Tekniska fakulteten.
    Arbiol, Jordi
    Catalan Institute of Nanoscience and Nanotechnology (ICN2), CSIC and BIST, Campus UAB, Bellaterra, Barcelona, Catalonia, Spain; ICREA, Pg. Lluís Companys 23, Barcelona, Catalonia, Spain.
    Vagin, Mikhail
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Laboratoriet för organisk elektronik. Linköpings universitet, Tekniska fakulteten.
    Vomiero, Alberto
    Division of Material Science, Department of Engineering Sciences and Mathematics, Luleå University of Technology, Luleå, Sweden.
    MoSx@NiO Composite Nanostructures: An Advanced Nonprecious Catalyst for Hydrogen Evolution Reaction in Alkaline Media2019Inngår i: Advanced Functional Materials, ISSN 1616-301X, E-ISSN 1616-3028, Vol. 29, nr 7, artikkel-id 1807562Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    The design of the earth-abundant, nonprecious, efficient, and stable electrocatalysts for efficient hydrogen evolution reaction (HER) in alkaline media is a hot research topic in the field of renewable energies. A heterostructured system composed of MoSx deposited on NiO nanostructures (MoSx@NiO) as a robust catalyst for water splitting is proposed here. NiO nanosponges are applied as cocatalyst for MoS2 in alkaline media. Both NiO and MoS2@NiO composites are prepared by a hydrothermal method. The NiO nanostructures exhibit sponge-like morphology and are completely covered by the sheet-like MoS2. The NiO and MoS2 exhibit cubic and hexagonal phases, respectively. In the MoSx@NiO composite, the HER experiment in 1 m KOH electrolyte results in a low overpotential (406 mV) to produce 10 mA cm(-2) current density. The Tafel slope for that case is 43 mV per decade, which is the lowest ever achieved for MoS2-based electrocatalyst in alkaline media. The catalyst is highly stable for at least 13 h, with no decrease in the current density. This simple, cost-effective, and environmentally friendly methodology can pave the way for exploitation of MoSx@NiO composite catalysts not only for water splitting, but also for other applications such as lithium ion batteries, and fuel cells.

  • 7.
    Imar, Shahzad
    et al.
    Dundalk Institute Technology, Ireland.
    Maccato, Chiara
    University of Padua, Italy.
    Dickinson, Calum
    University of Limerick, Ireland.
    Laffir, Fathima
    University of Limerick, Ireland.
    Vagin, Mikhail
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Kemiska och optiska sensorsystem. Linköpings universitet, Tekniska högskolan.
    McCormac, Timothy
    Dundalk Institute Technology, Ireland.
    Enhancement of Nitrite and Nitrate Electrocatalytic Reduction through the Employment of Self-Assembled Layers of Nickel- and Copper-Substituted Crown-Type Heteropolyanions2015Inngår i: Langmuir, ISSN 0743-7463, E-ISSN 1520-5827, Vol. 31, nr 8, s. 2584-2592Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    Multilayer assemblies of two crown-type type heteropolyanions (HPA), [Cu20Cl(OH)(24)(H2O)(12)(P8W48O184)](25-) and Ni-4(P8W48O148)(WO2)](28-), have been immobilized onto glassy carbon electrode surfaces via the layer-by-layer (LBL) technique employing polycathion-stabilized silver nanoparticles (AgNP) as the cationic layer within the resulting thin films characterized by electrochemical and physical methods. The redox behaviors of both HPA monitored during LBL assembly with cyclic voltammetry and impedance spectroscopy revealed significant changes by immobilization. The presence of AgNPs led to the retention of film porosity and electronic conductivity, which has been shown with impedance and voltammeric studies of film permeabilities toward reversible redox probes. The resulting films have been characterized by physical methods. Finally, the electrocatalytic performance of obtained films with respect to nitrite and nitrate electrocatalytic reduction has been comparatively studied for both catalysts. Nickel atoms trapped inside HPA exhibited a higher specific activity for reduction.

  • 8.
    Imar, Shahzad
    et al.
    Dundalk Institute Technology, Ireland.
    Yaqub, Mustansara
    Dundalk Institute Technology, Ireland.
    Maccato, Chiara
    University of Padua, Italy.
    Dickinson, Calum
    University of Limerick, Ireland.
    Laffir, Fathima
    University of Limerick, Ireland.
    Vagin, Mikhail
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Fysik och elektroteknik. Linköpings universitet, Tekniska fakulteten.
    McCormac, Timothy
    Dundalk Institute Technology, Ireland.
    Nitrate and Nitrite Electrocatalytic Reduction at Layer-by-Layer Films Composed of Dawson-type Heteropolyanions Mono-substituted with Transitional Metal Ions and Silver Nanoparticles2015Inngår i: Electrochimica Acta, ISSN 0013-4686, E-ISSN 1873-3859, Vol. 184, s. 323-330Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    A series of Dawson-type heteropolyanions (HPAs) mono-substituted with transitional metal ions ((alpha 2)- [P2W17O61FeIII](8-), (alpha 2)-[P2W17O61CuII](8-) and (alpha 2)-[P2W17O61NiII](8-)) have exhibited electrocatalytic properties towards nitrate and nitrite reduction in slightly acidic media (pH 4.5). The immobilization of these HPAs into water-processable films developed via layer-by layer assembly with polymer-stabilized silver nanoparticles led to the fabrication of the electrocatalytic interfaces for both nitrate and nitrite reduction. The LBL assembly as well as the changes in the HPA properties by immobilization has been characterized by electrochemical methods. The effects of the substituent ions, outer layers and the cationic moieties utilized for the films assembly of the developed film on the performances of nitrate electrocatalysis has been elucidated. (C) 2015 Elsevier Ltd. All rights reserved.

  • 9.
    Karimian, Najmeh
    et al.
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biosensorer och bioelektronik. Linköpings universitet, Tekniska högskolan. Ferdowsi University of Mashhad, Iran.
    Vagin, Mikhail
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Tillämpad Fysik. Linköpings universitet, Tekniska högskolan.
    Hossein Arbab Zavar, Mohammad
    Ferdowsi University of Mashhad, Iran .
    Chamsaz, Mahmoud
    Ferdowsi University of Mashhad, Iran .
    Turner, Anthony
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biosensorer och bioelektronik. Linköpings universitet, Tekniska högskolan.
    Tiwari, Ashutosh
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biosensorer och bioelektronik. Linköpings universitet, Tekniska högskolan.
    An ultrasensitive molecularly-imprinted human cardiac troponin sensor2013Inngår i: Biosensors & bioelectronics, ISSN 0956-5663, E-ISSN 1873-4235, Vol. 50, s. 492-498Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    Cardiac troponin T (TnT) is a highly sensitive cardiac biomarker for myocardial infarction. In this study, the fabrication and characterisation of a novel sensor for human TnT based on a molecularly-imprinted electrosynthesised polymer is reported. A TnT sensitive layer was prepared by electropolymerisation of o-phenylenediamine (o-PD) on a gold electrode in the presence of TnT as a template. To develop the molecularly imprinted polymer (MIP), the template molecules were removed from the modified electrode surface by washing with alkaline ethanol. Electrochemical methods were used to monitor the processes of electropolymerisation, template removal and binding. The imprinted layer was characterised by cyclic voltammetry (CV), electrochemical impedance spectroscopy (EIS) and atomic force microscopy (AFM). The incubation of the MIP-modified electrode with respect to TnT concentration resulted in a suppression of the ferro/ferricyanide redox process. Experimental conditions were optimised and a linear relationship was observed between the peak current of [Fe(CN)(6)](3-)/[Fe (CN)(6)](4-) and the concentration of TnT in buffer over the range 0.009-0.8 ng/mL, with a detection limit of 9 pg/mL. The TnT MIP sensor was shown to have a high affinity to TnT in comparison with nonimprinted polymer (NIP) electrodes in both buffer and blood serum.

  • 10.
    Khan, Ziyauddin
    et al.
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Laboratoriet för organisk elektronik. Linköpings universitet, Tekniska fakulteten.
    Vagin, Mikhail
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Laboratoriet för organisk elektronik. Linköpings universitet, Tekniska fakulteten.
    Crispin, Xavier
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Laboratoriet för organisk elektronik. Linköpings universitet, Tekniska fakulteten.
    Can Hybrid Na-Air Batteries Outperform Nonaqueous Na-O-2 Batteries?2020Inngår i: ADVANCED SCIENCE, ISSN 2198-3844, artikkel-id 1902866Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    In recent years, there has been an upsurge in the study of novel and alternative energy storage devices beyond lithium-based systems due to the exponential increase in price of lithium. Sodium (Na) metal-based batteries can be a possible alternative to lithium-based batteries due to the similar electrochemical voltage of Na and Li together with the thousand times higher natural abundance of Na compared to Li. Though two different kinds of Na-O-2 batteries have been studied specifically based on electrolytes until now, very recently, a hybrid Na-air cell has shown distinctive advantage over nonaqueous cell systems. Hybrid Na-air batteries provide a fundamental advantage due to the formation of highly soluble discharge product (sodium hydroxide) which leads to low overpotentials for charge and discharge processes, high electrical energy efficiency, and good cyclic stability. Herein, the current status and challenges associated with hybrid Na-air batteries are reported. Also, a brief description of nonaqueous Na-O-2 batteries and its close competition with hybrid Na-air batteries are provided.

  • 11.
    Mitraka, Evangelia
    et al.
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Laboratoriet för organisk elektronik. Linköpings universitet, Tekniska fakulteten.
    Gryszel, Maciej
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Laboratoriet för organisk elektronik. Linköpings universitet, Tekniska fakulteten.
    Vagin, Mikhail
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Laboratoriet för organisk elektronik. Linköpings universitet, Tekniska fakulteten.
    Jafari, Mohammad Javad
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Molekylär fysik. Linköpings universitet, Tekniska fakulteten.
    Singh, Amritpal
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Laboratoriet för organisk elektronik. Linköpings universitet, Tekniska fakulteten.
    Warczak, Magdalena
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Laboratoriet för organisk elektronik. Linköpings universitet, Tekniska fakulteten.
    Mitrakas, Manassis
    Aristotle University of Thessaloniki, Thessaloniki, Greece.
    Berggren, Magnus
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Laboratoriet för organisk elektronik. Linköpings universitet, Tekniska fakulteten.
    Ederth, Thomas
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Molekylär fysik. Linköpings universitet, Tekniska fakulteten.
    Zozoulenko, Igor
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Laboratoriet för organisk elektronik. Linköpings universitet, Tekniska fakulteten.
    Crispin, Xavier
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Laboratoriet för organisk elektronik. Linköpings universitet, Tekniska fakulteten.
    Glowacki, Eric
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Laboratoriet för organisk elektronik. Linköpings universitet, Tekniska fakulteten.
    Electrocatalytic Production of Hydrogen Peroxide with Poly(3,4-ethylenedioxythiophene) Electrodes2019Inngår i: Advanced Sustainable Systems, ISSN 2366-7486, Vol. 3, nr 2, s. 1-6, artikkel-id 1800110Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    Electrocatalysis for energy‐efficient chemical transformations is a central concept behind sustainable technologies. Numerous efforts focus on synthesizing hydrogen peroxide, a major industrial chemical and potential fuel, using simple and green methods. Electrochemical synthesis of peroxide is a promising route. Herein it is demonstrated that the conducting polymer poly(3,4‐ethylenedioxythiophene), PEDOT, is an efficient and selective heterogeneous catalyst for the direct reduction of oxygen to hydrogen peroxide. While many metallic catalysts are known to generate peroxide, they subsequently catalyze decomposition of peroxide to water. PEDOT electrodes can support continuous generation of high concentrations of peroxide with Faraday efficiency remaining close to 100%. The mechanisms of PEDOT‐catalyzed reduction of O2 to H2O2 using in situ spectroscopic techniques and theoretical calculations, which both corroborate the existence of a chemisorbed reactive intermediate on the polymer chains that kinetically favors the selective reduction reaction to H2O2, are explored. These results offer a viable method for peroxide electrosynthesis and open new possibilities for intrinsic catalytic properties of conducting polymers.

  • 12.
    Mitraka, Evangelia
    et al.
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Fysik och elektroteknik. Linköpings universitet, Tekniska fakulteten.
    Jafari, Mohammad Javad
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Molekylär fysik. Linköpings universitet, Tekniska fakulteten.
    Vagin, Mikhail
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Fysik och elektroteknik. Linköpings universitet, Tekniska fakulteten.
    Liu, Xianjie
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Ytors Fysik och Kemi. Linköpings universitet, Tekniska fakulteten.
    Fahlman, Mats
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Ytors Fysik och Kemi. Linköpings universitet, Tekniska fakulteten.
    Ederth, Thomas
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Molekylär fysik. Linköpings universitet, Tekniska fakulteten.
    Berggren, Magnus
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Fysik och elektroteknik. Linköpings universitet, Tekniska fakulteten.
    Jonsson, Magnus
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Fysik och elektroteknik. Linköpings universitet, Tekniska fakulteten.
    Crispin, Xavier
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Fysik och elektroteknik. Linköpings universitet, Tekniska fakulteten.
    Oxygen-induced doping on reduced PEDOT2017Inngår i: Journal of Materials Chemistry A, ISSN 2050-7488, Vol. 5, nr 9, s. 4404-4412Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    The conducting polymer poly(3,4-ethylenedioxythiophene) (PEDOT) has shown promise as air electrode in renewable energy technologies like metal-air batteries and fuel cells. PEDOT is based on atomic elements of high abundance and is synthesized at low temperature from solution. The mechanism of oxygen reduction reaction (ORR) over chemically polymerized PEDOT: Cl still remains controversial with eventual role of transition metal impurities. However, regardless of the mechanistic route, we here demonstrate yet another key active role of PEDOT in the ORR mechanism. Our study demonstrates the decoupling of conductivity (intrinsic property) from electrocatalysis (as an extrinsic phenomenon) yielding the evidence of doping of the polymer by oxygen during ORR. Hence, the PEDOT electrode is electrochemically reduced (undoped) in the voltage range of ORR regime, but O-2 keeps it conducting; ensuring PEDOT to act as an electrode for the ORR. The interaction of oxygen with the polymer electrode is investigated with a battery of spectroscopic techniques.

  • 13.
    Mitraka, Evangelia
    et al.
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Laboratoriet för organisk elektronik. Linköpings universitet, Tekniska fakulteten.
    Vagin, Mikhail
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Laboratoriet för organisk elektronik. Linköpings universitet, Tekniska fakulteten.
    Sjoestedt, Anna
    RISE Bioecon, Sweden.
    Berggren, Magnus
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Laboratoriet för organisk elektronik. Linköpings universitet, Tekniska fakulteten.
    Hakansson, Karl M. O.
    RISE Bioecon, Sweden.
    Jonsson, Magnus
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Laboratoriet för organisk elektronik. Linköpings universitet, Tekniska fakulteten.
    Crispin, Xavier
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Laboratoriet för organisk elektronik. Linköpings universitet, Tekniska fakulteten.
    PEDOT-Cellulose Gas Diffusion Electrodes for Disposable Fuel CellsInngår i: ADVANCED SUSTAINABLE SYSTEMS, ISSN 2366-7486, artikkel-id 1900097Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    The mass implementation of renewable energy sources is limited by the lack of energy storage solutions operating on various timescales. Electrochemical technologies such as supercapacitors and batteries cannot handle long storage time because of self-discharge issues. The combination of fuel storage technology and fuel cells is an attractive solution for long storage times. In that context, large-scale fuel cell solutions are required for massive energy storage in cities, which leads to possible concepts such as low-cost disposable fully organic membrane assemblies in fuel cells to avoid regeneration of expensive poisoned electrodes. Here, the formation of an organic gas diffusion electrode (GDE) fabricated by paper-making production, combined with in situ polymerization is demonstrated for the first time. Cellulose is used as a 3D scaffold functionalized with poly(3,4-ethylenedioxythiophene) (PEDOT) serving as both an electrical conductor and an electrocatalyst of high efficiency for the oxygen reduction reaction. The PEDOT-cellulose porous GDE is implemented in a membrane assembly and demonstrated in a H-2-O-2 fuel cell. The demonstration of low-cost material/manufacturing that is environmentally friendly is a paradigm shift in the development of fuel cells for a sustainable society.

  • 14.
    Musumeci, Chiara
    et al.
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Fysik och elektroteknik. Linköpings universitet, Tekniska fakulteten.
    Vagin, Mikhail
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Fysik och elektroteknik. Linköpings universitet, Tekniska fakulteten.
    Zeglio, Erica
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biomolekylär och Organisk Elektronik. Linköpings universitet, Tekniska fakulteten.
    Ouyang, Liangqi
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biomolekylär och Organisk Elektronik. Linköpings universitet, Tekniska fakulteten.
    Gabrielsson, Roger
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Fysik och elektroteknik. Linköpings universitet, Tekniska fakulteten.
    Inganäs, Olle
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biomolekylär och Organisk Elektronik. Linköpings universitet, Tekniska fakulteten.
    Organic electrochemical transistors from supramolecular complexes of conjugated polyelectrolyte PEDOTS2019Inngår i: Journal of Materials Chemistry C, ISSN 2050-7526, E-ISSN 2050-7534, Vol. 7, nr 10, s. 2987-2993Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    Counterion exchange strategies are used to modify the hydrophilic character of the self-doped conjugated polyelectrolyte PEDOTS. The supramolecular complexes, soluble in organic solvents, are suitable to fabricate finely performing thin active layers in organic electrochemical transistors (OECTs). We demonstrate that ionic transport in these PEDOTS based complexes, thus their performance in OECT devices, is governed by a delicate balance among degree of doping, wettability and porosity, which can be controlled by a precise tuning of the polyelectrolyte/hydrophobic counterion ratio. We also show that the device operation can be modulated by varying the composition of the aqueous electrolyte in a range compatible with biological processes, making these materials suitable candidates to be interfaced with living cells.

  • 15.
    Méhes, Gábor
    et al.
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Laboratoriet för organisk elektronik. Linköpings universitet, Tekniska fakulteten.
    Vagin, Mikhail
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Laboratoriet för organisk elektronik. Linköpings universitet, Tekniska fakulteten.
    Mulla, Yusuf
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Laboratoriet för organisk elektronik. Linköpings universitet, Tekniska fakulteten.
    Granberg, Hjalmar
    Res Inst Sweden, Sweden.
    Che, Canyan
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Laboratoriet för organisk elektronik. Linköpings universitet, Tekniska fakulteten.
    Beni, Valerio
    Res Inst Sweden, Sweden.
    Crispin, Xavier
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Laboratoriet för organisk elektronik. Linköpings universitet, Tekniska fakulteten.
    Berggren, Magnus
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Laboratoriet för organisk elektronik. Linköpings universitet, Tekniska fakulteten.
    Stavrinidou, Eleni
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Laboratoriet för organisk elektronik. Linköpings universitet, Tekniska fakulteten.
    Simon, Daniel
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Laboratoriet för organisk elektronik. Linköpings universitet, Tekniska fakulteten.
    Solar Heat-Enhanced Energy Conversion in Devices Based on Photosynthetic Membranes and PEDOT:PSS-Nanocellulose Electrodes2020Inngår i: ADVANCED SUSTAINABLE SYSTEMS, ISSN 2366-7486, artikkel-id 1900100Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    Energy harvesting from photosynthetic membranes, proteins, or bacteria through bio-photovoltaic or bio-electrochemical approaches has been proposed as a new route to clean energy. A major shortcoming of these and solar cell technologies is the underutilization of solar irradiation wavelengths in the IR region, especially those in the far IR region. Here, a biohybrid energy-harvesting device is demonstrated that exploits IR radiation, via convection and thermoelectric effects, to improve the resulting energy conversion performance. A composite of nanocellulose and the conducting polymer system poly(3,4-ethylenedioxythiophene):polystyrene sulfonate (PEDOT:PSS) is used as the anode in biohybrid cells that includes thylakoid membranes (TMs) and redox mediators (RMs) in solution. By irradiating the conducting polymer electrode by an IR light-emitting diode, a sixfold enhancement in the harvested bio-photovoltaic power is achieved, without compromising stability of operation. Investigation of the output currents reveals that IR irradiation generates convective heat transfer in the electrolyte bulk, which enhances the redox reactions of RMs at the anode by suppressing diffusion limitations. In addition, a fast-transient thermoelectric component, originating from the PEDOT:PSS-nanocellulose-electrolyte interphase, further increases the bio-photocurrent. These results pave the way for the development of energy-harvesting biohybrids that make use of heat, via IR absorption, to enhance energy conversion efficiency.

  • 16.
    Naseer, Rashda
    et al.
    Dundalk Institute Technology, Ireland .
    Sankar Mal, Sib
    Jacobs University, Bremen, Germany .
    Ibrahim, Masooma
    Jacobs University, Bremen, Germany .
    Kortz, Ulrich
    Jacobs University, Bremen, Germany .
    Armstrong, Gordon
    University of Limerick, Ireland .
    Laffir, Fathima
    University of Limerick, Ireland .
    Dickinson, Calum
    University of Limerick, Ireland .
    Vagin, Mikhail
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Kemiska och optiska sensorsystem. Linköpings universitet, Tekniska högskolan.
    McCormac, Timothy
    Dundalk Institute Technology, Ireland .
    Redox, surface and electrocatalytic properties of layer-by-layer films based upon Fe(III)-substituted crown polyoxometalate [P8W48O184Fe16(OH)(28)(H2O)(4)](20-)2014Inngår i: Electrochimica Acta, ISSN 0013-4686, E-ISSN 1873-3859, Vol. 134, s. 450-458Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    The electrocatalytic ability of the iron-substituted crown-type polyoxometalate (POM) Li4K16[P8W48O184Fe16(OH)(28)(H2O)(4)]center dot 66H(2)O center dot 2KCl (P8W48Fe16) towards the reduction of both nitrite and hydrogen peroxide reduction has been studied in both the solution and immobilized states for the POM. P8W48Fe16 was surface immobilised onto carbon electrode surfaces through employment of the layer-by-layer technique (LBL) using pentaerythritol-based Ru(II)-metallodendrimer [RuD](PF6)(8) as the cationic layer within the resulting films. The constructed multilayer films have been extensively studied by various electrochemical techniques and surface based techniques. Cyclic voltammetry and impedance spectroscopy have been utilized to monitor the construction of the LBL film after the deposition of each monolayer. The electrochemical behaviour of both a cationic and anionic redox probes at the LBL films has been undertaken to give indications as to the films porosity. The elemental composition and the surface morphology of the LBL films was conifmrde through the employment of AFM, XPS and SEM.

  • 17.
    Naseer, Rashda
    et al.
    Dundalk Institute Technology, Ireland.
    Sankar Mal, Sib
    Jacobs University of Bremen, Germany.
    Kortz, Ulrich
    Jacobs University of Bremen, Germany.
    Armstrong, Gordon
    University of Limerick, Ireland.
    Laffir, Fathima
    University of Limerick, Ireland.
    Dickinson, Calum
    University of Limerick, Ireland.
    Vagin, Mikhail
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Fysik och elektroteknik. Linköpings universitet, Tekniska fakulteten.
    McCormac, Timothy
    Dundalk Institute Technology, Ireland.
    Electrocatalysis by crown-type polyoxometalates multi-substituted by transition metal ions: Comparative study2015Inngår i: Electrochimica Acta, ISSN 0013-4686, E-ISSN 1873-3859, Vol. 176, s. 1248-1255Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    The difference in electrochemical properties of three crown-type polyoxometalates multi-substituted by Fe3+, Ni2+ or Co2+ ions and their precursor has been rationalized with respect to their electrocatalytic performances studied in solution and in the immobilized state within the layer-by-layer film formed with a positively charged pentaerythritol-based Ru(II)-metallodendrimer. The film assembly was monitored with electrochemical methods and characterized by surface analysis techniques. An influence of the terminal layer on the electrode reaction and on film porosity has been observed. The electrocatalytic performance of the compounds on nitrite reduction was assessed in solution and in the immobilized state. (C) 2015 Elsevier Ltd. All rights reserved.

  • 18.
    Pozhitkov, Alex E.
    et al.
    University of Washington, WA 98195 USA.
    Daubert, Diane
    University of Washington, WA 98195 USA.
    Brochwicz Donimirski, Ashley
    University of Washington, WA 98195 USA.
    Goodgion, Douglas
    University of Washington, WA 98195 USA.
    Vagin, Mikhail
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Fysik och elektroteknik. Linköpings universitet, Tekniska fakulteten.
    Leroux, Brian G.
    University of Washington, WA 98195 USA.
    Hunter, Colby M.
    Alabama State University, AL 36101 USA.
    Flemmig, Thomas F.
    University of Hong Kong, Peoples R China.
    Noble, Peter A.
    Alabama State University, AL 36101 USA.
    Bryers, James D.
    University of Washington, WA 98195 USA.
    Interruption of Electrical Conductivity of Titanium Dental Implants Suggests a Path Towards Elimination Of Corrosion2015Inngår i: PLoS ONE, ISSN 1932-6203, E-ISSN 1932-6203, Vol. 10, nr 10, s. e0140393-Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    Peri-implantitis is an inflammatory disease that results in the destruction of soft tissue and bone around the implant. Titanium implant corrosion has been attributed to the implant failure and cytotoxic effects to the alveolar bone. We have documented the extent of titanium release into surrounding plaque in patients with and without peri-implantitis. An in vitro model was designed to represent the actual environment of an implant in a patients mouth. The model uses actual oral microbiota from a volunteer, allows monitoring electrochemical processes generated by biofilms growing on implants and permits control of biocorrosion electrical current. As determined by next generation DNA sequencing, microbial compositions in experiments with the in vitro model were comparable with the compositions found in patients with implants. It was determined that the electrical conductivity of titanium implants was the key factor responsible for the biocorrosion process. The interruption of the biocorrosion current resulted in a 4-5 fold reduction of corrosion. We propose a new design of dental implant that combines titanium in zero oxidation state for osseointegration and strength, interlaid with a nonconductive ceramic. In addition, we propose electrotherapy for manipulation of microbial biofilms and to induce bone healing in peri-implantitis patients.

  • 19.
    Qian, Deping
    et al.
    Linköpings universitet, Tekniska fakulteten. Linköpings universitet, Institutionen för fysik, kemi och biologi, Biomolekylär och Organisk Elektronik.
    Liu, Bo
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biomolekylär och Organisk Elektronik. Linköpings universitet, Tekniska högskolan.
    Wang, Suhao
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Fysik och elektroteknik. Linköpings universitet, Tekniska fakulteten.
    Himmelberger, Scott
    Stanford University, CA 94305 USA.
    Linares, Mathieu
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Teoretisk kemi. Linköpings universitet, Tekniska fakulteten.
    Vagin, Mikhail
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Fysik och elektroteknik. Linköpings universitet, Tekniska fakulteten.
    Muller, Christian
    Chalmers, Sweden.
    Zaifei, Zaifei
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biomolekylär och Organisk Elektronik. Linköpings universitet, Tekniska fakulteten.
    Fabiano, Simone
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Fysik och elektroteknik. Linköpings universitet, Tekniska fakulteten.
    Berggren, Magnus
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Fysik och elektroteknik. Linköpings universitet, Tekniska fakulteten.
    Salleo, Alberto
    Stanford University, CA 94305 USA.
    Inganäs, Olle
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biomolekylär och Organisk Elektronik. Linköpings universitet, Tekniska fakulteten.
    Zou, Yingping
    Central S University, Peoples R China.
    Zhang, Fengling
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biomolekylär och Organisk Elektronik. Linköpings universitet, Tekniska fakulteten.
    Modulating molecular aggregation by facile heteroatom substitution of diketopyrrolopyrrole based small molecules for efficient organic solar cells2015Inngår i: Journal of Materials Chemistry A, ISSN 2050-7488, Vol. 3, nr 48, s. 24349-24357Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    In conjugated polymers and small molecules of organic solar cells, aggregation induced by intermolecular interactions governs the performance of photovoltaics. However, little attention has been paid to the connection between molecular structure and aggregation within solar cells based on soluble small molecules. Here we demonstrate modulation of intermolecular aggregation of two synthesized molecules through heteroatom substitution to develop an understanding of the role of aggregation in conjugated molecules. Molecule 1 (M1) based on 2-ethylhexyloxy-benzene substituted benzo[1,2-b:4,5-b]dithiophene (BDTP) and diketopyrrolopyrrole (DPP) displays strong aggregation in commonly used organic solvents, which is reduced in molecule 2 (M2) by facile oxygen atom substitution on the BDTP unit confirmed by absorption spectroscopy and optical microscopy, while it successfully maintains molecular planarity and favorable charge transport characteristics. Solar cells based on M2 exhibit more than double the photocurrent of devices based on M1 and yield a power conversion efficiency of 5.5%. A systematic investigation of molecular conformation, optoelectronic properties, molecular packing and crystallinity as well as film morphology reveals structure dependent aggregation responsible for the performance difference between the two conjugated molecules.

  • 20.
    Sankoh, Supannee
    et al.
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biosensorer och bioelektronik. Linköpings universitet, Tekniska fakulteten. Prince Songkla University, Thailand.
    Vagin, Mikhail
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Fysik och elektroteknik. Linköpings universitet, Tekniska fakulteten.
    Sekretareva, Alina
    Linköpings universitet, Tekniska fakulteten. Linköpings universitet, Institutionen för fysik, kemi och biologi, Biosensorer och bioelektronik. Stanford University, CA 94305 USA.
    Thavarungkul, Panote
    Prince Songkla University, Thailand.
    Kanatharana, Proespichaya
    Prince Songkla University, Thailand.
    Mak, Wing Cheung
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biosensorer och bioelektronik. Linköpings universitet, Tekniska fakulteten.
    Colloid electrochemistry of conducting polymer: towards potential-induced in-situ drug release2017Inngår i: Electrochimica Acta, ISSN 0013-4686, E-ISSN 1873-3859, Vol. 228, s. 407-412Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    Over the past decades, controlled drug delivery system remains as one of the most important area in medicine for various diseases. We have developed a new electrochemically controlled drug release system by combining colloid electrochemistry and electro-responsive microcapsules. The pulsed electrode potential modulation led to the appearance of two processes available for the time-resolved registration in colloid microenvironment: change of the electronic charge of microparticles (from 0.5 ms to 0.1 s) followed by the drug release associated with ionic equilibration (1-10 s). The dynamic electrochemical measurements allow the distinction of drug release associated With ionic relaxation and the change of electronic charge of conducting polymer colloid microparticles. The amount of released drug (methylene blue) could be controlled by modulating the applied potential. Our study demonstrated a surface-potential driven controlled drug release of dispersion of conducting polymer carrier at the electrode interfaces, while the bulk colloids dispersion away from the electrode remains as a reservoir to improve the efficiency of localized drug release. The developed new methodology creates a model platform for the investigations of surface potential-induced in-situ electrochemical drug release mechanism. (C) 2017 Elsevier Ltd. All rights reserved.

  • 21.
    Santangelo, Francesca
    et al.
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Sensor- och aktuatorsystem. Linköpings universitet, Tekniska fakulteten.
    Shtepliuk, Ivan
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Halvledarmaterial. Linköpings universitet, Tekniska fakulteten.
    Filippini, Daniel
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Sensor- och aktuatorsystem. Linköpings universitet, Tekniska fakulteten.
    Puglisi, Donatella
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Sensor- och aktuatorsystem. Linköpings universitet, Tekniska fakulteten.
    Vagin, Mikhail
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Fysik och elektroteknik. Linköpings universitet, Tekniska fakulteten.
    Yakimova, Rositsa
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Halvledarmaterial. Linköpings universitet, Tekniska fakulteten.
    Eriksson, Jens
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Sensor- och aktuatorsystem. Linköpings universitet, Tekniska fakulteten.
    Epitaxial Graphene Sensors Combined with 3D-Printed Microfluidic Chip for Heavy Metals Detection2019Inngår i: Sensors, ISSN 1424-8220, E-ISSN 1424-8220, Vol. 19, nr 10, artikkel-id 2393Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    In this work, we investigated the sensing performance of epitaxial graphene on Si-face 4H-SiC (EG/SiC) for liquid-phase detection of heavy metals (e.g., Pb and Cd), showing fast and stable response and low detection limit. The sensing platform proposed includes 3D-printed microfluidic devices, which incorporate all features required to connect and execute lab-on-chip (LOC) functions. The obtained results indicate that EG exhibits excellent sensing activity towards Pb and Cd ions. Several concentrations of Pb2+ solutions, ranging from 125 nM to 500 mu M, were analyzed showing Langmuir correlation between signal and Pb2+ concentrations, good stability, and reproducibility over time. Upon the simultaneous presence of both metals, sensor response is dominated by Pb2+ rather than Cd2+ ions. To explain the sensing mechanisms and difference in adsorption behavior of Pb2+ and Cd2+ ions on EG in water-based solutions, we performed van-der-Waals (vdW)-corrected density functional theory (DFT) calculations and non-covalent interaction (NCI) analysis, extended charge decomposition analysis (ECDA), and topological analysis. We demonstrated that Pb2+ and Cd2+ ions act as electron-acceptors, enhancing hole conductivity of EG, due to charge transfer from graphene to metal ions, and Pb2+ ions have preferential ability to binding with graphene over cadmium. Electrochemical measurements confirmed the conductometric results, which additionally indicate that EG is more sensitive to lead than to cadmium.

  • 22.
    Sekretareva, Alina
    et al.
    Linköpings universitet, Institutionen för fysik, kemi och biologi. Linköpings universitet, Tekniska fakulteten. Stanford University, CA 94305 USA.
    Vagin, Mikhail
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Fysik och elektroteknik. Linköpings universitet, Tekniska fakulteten.
    Turner, Anthony
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biosensorer och bioelektronik. Linköpings universitet, Tekniska fakulteten.
    Eriksson, Mats
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Kemiska och optiska sensorsystem. Linköpings universitet, Tekniska fakulteten.
    Correspondence on "Can Nanoimpacts Detect Single-Enzyme Activity? Theoretical Considerations and an Experimental Study of Catalase Impacts"2017Inngår i: ACS Catalysis, ISSN 2155-5435, E-ISSN 2155-5435, Vol. 7, nr 5, s. 3591-3593Artikkel i tidsskrift (Annet vitenskapelig)
    Abstract [en]

    n/a

  • 23.
    Sekretareva, Alina
    et al.
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Kemiska och optiska sensorsystem. Linköpings universitet, Tekniska fakulteten.
    Vagin, Mikhail
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Fysik och elektroteknik. Linköpings universitet, Tekniska fakulteten.
    Volkov, Anton V.
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Fysik och elektroteknik. Linköpings universitet, Tekniska fakulteten.
    Zozoulenko, Igor V.
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Fysik och elektroteknik. Linköpings universitet, Tekniska fakulteten.
    Turner, Anthony
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biosensorer och bioelektronik. Linköpings universitet, Tekniska fakulteten.
    Eriksson, Mats
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Kemiska och optiska sensorsystem. Linköpings universitet, Tekniska fakulteten.
    Screen printed microband array based biosensor for water monitoring2015Inngår i: The Frumkin Symposium, 2015Konferansepaper (Fagfellevurdert)
  • 24.
    Sekretareva, Alina
    et al.
    Linköpings universitet, Institutionen för fysik, kemi och biologi. Linköpings universitet, Tekniska fakulteten. Uppsala Univ, Sweden.
    Vagin, Mikhail
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Fysik och elektroteknik. Linköpings universitet, Tekniska fakulteten.
    Volkov, Anton
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Laboratoriet för organisk elektronik. Linköpings universitet, Tekniska fakulteten.
    Zozoulenko, Igor
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Laboratoriet för organisk elektronik. Linköpings universitet, Tekniska fakulteten.
    Eriksson, Mats
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Sensor- och aktuatorsystem. Linköpings universitet, Tekniska fakulteten.
    Evaluation of the Electrochemically Active Surface Area of Microelectrodes by Capacitive and Faradaic Currents2019Inngår i: CHEMELECTROCHEM, ISSN 2196-0216, Vol. 6, nr 17, s. 4411-4417Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    Two experimental methods to estimate the electrochemically active surface area (EASA) of microelectrodes are investigated. One method is based on electrocapacitive measurements and depends significantly on the surface roughness as well as on other parameters. The other method is based on faradaic current measurements and depends on the geometric surface area. The experimental results are supplemented with numerical modeling of electrodes with different surface roughness. A systematic study reveals a strong influence of the scale and arrangement of the surface roughness, the measurement potential and the electrolyte concentration on the EASA of microelectrodes estimated from the electrocapacitive measurements. The results show that electrocapacitive measurements should not be used to estimate the faradaic EASA of microelectrodes with a non-negligible surface roughness.

    Fulltekst tilgjengelig fra 2020-07-21 13:29
  • 25.
    Sekretareva, Alina
    et al.
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Kemiska och optiska sensorsystem. Linköpings universitet, Tekniska fakulteten.
    Vagin, Mikhail Yu
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Fysik och elektroteknik. Linköpings universitet, Tekniska fakulteten.
    Volkov, Anton V.
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Fysik och elektroteknik. Linköpings universitet, Tekniska fakulteten.
    Zozoulenko, Igor V.
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Fysik och elektroteknik. Linköpings universitet, Tekniska fakulteten.
    Turner, Anthony P.F.
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biosensorer och bioelektronik. Linköpings universitet, Tekniska fakulteten.
    Eriksson, Mats.
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Kemiska och optiska sensorsystem. Linköpings universitet, Tekniska fakulteten.
    Total phenol analysis of water using a laccase-based microsensor array2015Inngår i: Program of the XXIII International Symposium on Bioelectrochemistry and Bioenergetics of the Bioelectrochemical Society. 14-18 June, 2015. Malmö, Sweden, Lausanne: Bioelectrochemical Society , 2015, s. 155-155Konferansepaper (Annet vitenskapelig)
    Abstract [en]

    The monitoring of phenolic compounds in raw waters and wastewaters is of great importance for environmental control. Use of biosensors for rapid, specific and simple detection of phenolic compounds is a promising approach. A number of biosensors have been developed for phenol detection. A general drawback of previously reported biosensors is their insufficient detection limits for phenols in water samples. One way to improve the detection limit is by the use of microelectrodes.

    Microband design of the microelectrodes combines convergent mass transport due to the microscale width and high output currents due to the macroscopic length. Among the various techniques available for microband electrode fabrication, we have chosen screen-printing which is a cost-effective production method.

    In this study, we report on the development of a laccase-based microscale biosensor operating under a convergent diffusion regime. Screen-printing followed by simple cutting was utilized for the fabrication of graphite microbands as a platform for further covalent immobilization of laccase. Numerical simulations, utilizing the finite element method with periodic boundary conditions, were used for modeling the voltammetric response of the developed microband electrodes. Anodization followed by covalent immobilization was used for the electrode modification with laccase. Direct and mediated laccase bioelectrocatalytic oxidation of phenols was studied on macro- and microscale graphite electrodes. Significant enhancement of the analytical performance was achieved by the establishment of convergent diffusion in the microscale sensor. Finally, the developed microsensor was utilized to monitor phenolic compounds in real waste water.

  • 26.
    Sekretaryova, Alina
    et al.
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Kemiska och optiska sensorsystem. Linköpings universitet, Tekniska högskolan.
    Beni, Valerio
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biosensorer och bioelektronik. Linköpings universitet, Tekniska högskolan.
    Eriksson, Mats
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Kemiska och optiska sensorsystem. Linköpings universitet, Tekniska högskolan.
    Karyakin, Arkady A.
    Moscow MV Lomonosov State University, Russia.
    Turner, Anthony
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biosensorer och bioelektronik. Linköpings universitet, Tekniska högskolan.
    Vagin, Mikhail
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Kemiska och optiska sensorsystem. Linköpings universitet, Tekniska högskolan.
    Cholesterol Self-Powered Biosensor2014Inngår i: Analytical Chemistry, ISSN 0003-2700, E-ISSN 1520-6882, Vol. 86, nr 19, s. 9540-9547Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    Monitoring the cholesterol level is of great importance, especially for people with high risk of developing heart disease. Here we report on reagentless cholesterol detection in human plasma with a novel single-enzyme, membrane-free, self-powered biosensor, in which both cathodic and anodic bioelectrocatalytic reactions are powered by the same substrate. Cholesterol oxidase was immobilized in a sol-gel matrix on both the cathode and the anode. Hydrogen peroxide, a product of the enzymatic conversion of cholesterol, was electrocatalytically reduced, by the use of Prussian blue, at the cathode. In parallel, cholesterol oxidation catalyzed by mediated cholesterol oxidase occurred at the anode. The analytical performance was assessed for both electrode systems separately. The combination of the two electrodes, formed on high surface-area carbon cloth electrodes, resulted in a self-powered biosensor with enhanced sensitivity (26.0 mA M-1 cm(-2)), compared to either of the two individual electrodes, and a dynamic range up to 4.1 mM cholesterol. Reagentless cholesterol detection with both electrochemical systems and with the self-powered biosensor was performed and the results were compared with the standard method of colorimetric cholesterol quantification.

  • 27.
    Sekretaryova, Alina
    et al.
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biosensorer och bioelektronik. Linköpings universitet, Tekniska högskolan.
    Beni, Valerio
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biosensorer och bioelektronik. Linköpings universitet, Tekniska högskolan.
    Eriksson, Mats
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Kemiska och optiska sensorsystem. Linköpings universitet, Tekniska högskolan.
    Turner, Anthony
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biosensorer och bioelektronik. Linköpings universitet, Tekniska högskolan.
    Vagin, Mikhail Y
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Kemiska och optiska sensorsystem. Linköpings universitet, Tekniska högskolan.
    A highly sensitive and self-powered cholesterol biosensor2014Inngår i: 24th Anniversary World Congress on Biosensors – Biosensors 2014, Elsevier, 2014Konferansepaper (Annet vitenskapelig)
    Abstract [en]

    Blood cholesterol is a very important parameter for the assessment of atherosclerosis and other lipid disorders. The total cholesterol concentration in human blood should be less than 5.17 mM. Concentrations in the range 5.17 – 6.18 mM are considered borderline high risk and levels above 6.21 mM, high risk. Cholesterol determination with high accuracy is therefore necessary in order to differentiate these levels for medical screening or diagnosis. Several attempts to develop highly sensitive cholesterol biosensors have been described, but, to the best of our knowledge, this is the first report of a self-powered cholesterol biosensor, i.e. a device delivering the analytical information from the current output of the energy of the biocatalytic conversion of cholesterol, without any external power source. This is particularly relevant to the development of inexpensive screening devices based on printed electronics.

     

    We present two complementary bioelectrocatalytic platforms suitable for the fabrication of a self-powered biosensor. Both are based on cholesterol oxidase (ChOx) immobilisation in a sol-gel matrix, as illustrated in Fig. 1 [1]. Mediated biocatalytic cholesterol oxidation [2] was used as the anodic reaction and electrocatalytic reduction of hydrogen peroxide on Prussian Blue (PB) as the cathodic reaction. Due to a synergistic effect in the self-powered cholesterol biosensor, the analytical parameters of the overall device exceeded those of the individual component half-cells, yielding a sensitivity of 0.19 A M-1 cm-2 and a dynamic range that embraces the free cholesterol concentrations found in human blood.

     

    Thus, we have demonstrated the novel concept of highly sensitive cholesterol determination using the first self-powered cholesterol biosensor. This configuration is particularly promising for incorporation in emerging plastic- and paper-based analytical instruments for decentralised diagnostics and mobile health.

     

  • 28.
    Sekretaryova, Alina N
    et al.
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biosensorer och bioelektronik. Linköpings universitet, Tekniska högskolan.
    Beni, Valerio
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biosensorer och bioelektronik. Linköpings universitet, Tekniska högskolan.
    Eriksson, Mats
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Kemiska och optiska sensorsystem. Linköpings universitet, Tekniska högskolan.
    Karyakin, Arkady A
    Moscow State University, Russia.
    Turner, Anthony
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biosensorer och bioelektronik. Linköpings universitet, Tekniska högskolan.
    Vagin, Mikhail Y
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Kemiska och optiska sensorsystem. Linköpings universitet, Tekniska högskolan.
    Novel single-enzyme based self-powered biosensor2014Inngår i: 15th International Conference on Electroanalysis (ESEAC), 2014Konferansepaper (Annet vitenskapelig)
  • 29.
    Sekretaryova, Alina N
    et al.
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biosensorer och bioelektronik. Linköpings universitet, Tekniska högskolan.
    Vagin, Mikhail Y
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Kemiska och optiska sensorsystem. Linköpings universitet, Tekniska högskolan.
    Turner, Anthony
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biosensorer och bioelektronik. Linköpings universitet, Tekniska högskolan.
    Eriksson, Mats
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Kemiska och optiska sensorsystem. Linköpings universitet, Tekniska högskolan.
    A screen-printed microband array biosensor for water monitoring2014Inngår i: 15th International Conference on Electroanalysis (ESEAC), 2014Konferansepaper (Annet vitenskapelig)
  • 30.
    Sekretaryova, Alina N.
    et al.
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Kemiska och optiska sensorsystem. Linköpings universitet, Tekniska fakulteten.
    Vagin, Mikhail Yu.
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Fysik och elektroteknik. Linköpings universitet, Tekniska fakulteten.
    Eriksson, Mats
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Kemiska och optiska sensorsystem. Linköpings universitet, Tekniska fakulteten.
    Evaluation of the electrochemically active surface area of microelectrodes by capacitive and faradaic currentsManuskript (preprint) (Annet vitenskapelig)
    Abstract [en]

    Two methods to estimate the electrochemically active surface area (EASA) of microelectrodes were compared. One is based on electrocapacitive measurements and the other on faradaic measuements. A systematic study revealed a strong influence of the surface roughness and the electrolyte concentration on the EASA of microelectrodes estimated from the electrocapacitive measurements, yielding a lack of reliability compared to the faradaic method.

  • 31.
    Sekretaryova, Alina N.
    et al.
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Kemiska och optiska sensorsystem. Linköpings universitet, Tekniska fakulteten.
    Vagin, Mikhail Yu.
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Fysik och elektroteknik. Linköpings universitet, Tekniska fakulteten.
    Turner, Anthony P.F.
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biosensorer och bioelektronik. Linköpings universitet, Tekniska fakulteten.
    Eriksson, Mats
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Kemiska och optiska sensorsystem. Linköpings universitet, Tekniska fakulteten.
    Electrocatalytic Currents from Single Enzyme Molecules2016Inngår i: Journal of the American Chemical Society, ISSN 0002-7863, E-ISSN 1520-5126, Vol. 138, nr 8, s. 2504-2507Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    Single molecule enzymology provides an opportunity to examine details of enzyme mechanisms that are not distinguishable in biomolecule ensemble studies. Here we report, for the first time, detection of the current produced in an electrocatalytic reaction by a single redox enzyme molecule when it collides with an ultramicroelectrode. The catalytic process provides amplification of the current from electron-transfer events at the catalyst leading to a measurable current. This new methodology monitors turnover of a single enzyme molecule. The methodology might complement existing single molecule techniques, giving further insights into enzymatic mechanisms and filling the gap between fundamental understanding of biocatalytic processes and their potential for bioenergy production.

  • 32.
    Sekretaryova, Alina
    et al.
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biosensorer och bioelektronik. Linköpings universitet, Tekniska högskolan.
    Vagin, Mikhail
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Tillämpad Fysik. Linköpings universitet, Tekniska högskolan.
    Beni, Valerio
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biosensorer och bioelektronik. Linköpings universitet, Tekniska högskolan.
    Eriksson, Mats
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Tillämpad Fysik. Linköpings universitet, Tekniska högskolan.
    Turner, Anthony
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biosensorer och bioelektronik. Linköpings universitet, Tekniska högskolan.
    Unsubstitutedand insoluble phenothiazine as an electron-transfer mediator in enzymaticelectrochemical biosensors2013Inngår i: Nano-scaled arrangements of proteins, aptamers, andother nucleic acid structures – and their potential applications , COST Thematic Workshop, 8-9 October 2013, Helmholtz Zentrum fürUmweltforschung, Leipzig, Germany, Leipzig: Helmholtz Zentrum für Umweltforschung , 2013, s. O1-Konferansepaper (Fagfellevurdert)
  • 33.
    Sekretaryova, Alina
    et al.
    Linköpings universitet, Institutionen för fysik, kemi och biologi. Linköpings universitet, Tekniska högskolan. Lomonosov Moscow State University, Russia.
    Vagin, Mikhail
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Tillämpad Fysik. Linköpings universitet, Tekniska högskolan.
    Beni, Valerio
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biosensorer och bioelektronik. Linköpings universitet, Tekniska högskolan.
    Turner, Anthony P.F.
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biosensorer och bioelektronik. Linköpings universitet, Tekniska högskolan.
    Karyakin, Arkady A.
    Lomonosov Moscow State University, Russia.
    Unsubstituted phenothiazine as a superior water-insoluble mediator for oxidases2014Inngår i: Biosensors & bioelectronics, ISSN 0956-5663, E-ISSN 1873-4235, Vol. 53, s. 275-282Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    The mediation of oxidases glucose oxidase (GOx), lactate oxidase (LOx) and cholesterol oxidase (ChOx) by a new electron shuttling mediator, unsubstituted phenothiazine (PTZ), was studied. Cyclic voltammetry and rotating-disk electrode measurements in nonaqueous media were used to determine the diffusion characteristics of the mediator and the kinetics of its reaction with GOx, giving a second-order rate constant of 7.6×103–2.1×104 M−1 s−1 for water–acetonitrile solutions containing 5–15% water. These values are in the range reported for commonly used azine-type mediators, indicating that PTZ is able to function as an efficient mediator. PTZ and GOx, LOx and ChOx were successfully co-immobilised in sol–gel membrane on a screen-printed electrode to construct glucose, lactate and cholesterol biosensors, respectively, which were then optimised in terms of stability and sensitivity. The electrocatalytic oxidation responses showed a dependence on substrate concentration ranging from 0.6 to 32 mM for glucose, from 19 to 565 mM for lactate and from 0.015 to 1.0 mM for cholesterol detection. Oxidation of substrates on the surface of electrodes modified with PTZ and enzyme membrane was investigated with double-step chronoamperometry and the results showed that the PTZ displays excellent electrochemical catalytic activities even when immobilised on the surface of the electrode.

  • 34.
    Sekretaryova, Alina
    et al.
    Linköpings universitet, Institutionen för fysik, kemi och biologi. Linköpings universitet, Tekniska fakulteten.
    Vagin, Mikhail
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Fysik och elektroteknik. Linköpings universitet, Tekniska fakulteten.
    Turner, Anthony
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biosensorer och bioelektronik. Linköpings universitet, Tekniska fakulteten.
    Eriksson, Mats
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Kemiska och optiska sensorsystem. Linköpings universitet, Tekniska fakulteten.
    Collision-based Electrochemistry for Investigation of Direct Electron Transfer of a Single Enzyme Molecule2017Inngår i: 26th Anniversary World Congress on Biosensors (Biosensors), Elsevier, 2017, s. 238-239Konferansepaper (Fagfellevurdert)
    Abstract [en]

    Eldectron transfer between a biorecognition element and an electrode is an essential element of bioelectrocatalytic systems, such as biosensors and biofuel cells. The number of working systems based on direct electron communication is limited and detailed investigations of the mechanism of the process are still required. Here, we present the use of a novel approach of collision-based bioelectrocatalysis to monitor electrocatalytic currents from individual redox enzyme molecules. This approach allowed us to calculate the individual turnover rates of these molecules and investigate the influence of the applied potential, pH and additions of inhibitor on the observed rates of direct electron transfer.

  • 35.
    Sekretaryova, Alina
    et al.
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Kemiska och optiska sensorsystem. Linköpings universitet, Tekniska fakulteten.
    Volkov, Anton V.
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Fysik och elektroteknik. Linköpings universitet, Tekniska fakulteten.
    Zozoulenko, Igor V.
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Fysik och elektroteknik. Linköpings universitet, Tekniska fakulteten.
    Turner, Anthony
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biosensorer och bioelektronik. Linköpings universitet, Tekniska fakulteten.
    Vagin, Mikhail Yu
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Fysik och elektroteknik. Linköpings universitet, Tekniska fakulteten.
    Eriksson, Mats
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Kemiska och optiska sensorsystem. Linköpings universitet, Tekniska fakulteten.
    Total phenol analysis of weakly supported water using a laccase-based microband biosensor.2016Inngår i: Analytica Chimica Acta, ISSN 0003-2670, E-ISSN 1873-4324, Vol. 907, s. 45-53Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    The monitoring of phenolic compounds in wastewaters in a simple manner is of great importance for environmental control. Here, a novel screen printed laccase-based microband array for in situ, total phenol estimation in wastewaters and for water quality monitoring without additional sample pre-treatment is presented. Numerical simulations using the finite element method were utilized for the characterization of micro-scale graphite electrodes. Anodization followed by covalent modification was used for the electrode functionalization with laccase. The functionalization efficiency and the electrochemical performance in direct and catechol-mediated oxygen reduction were studied at the microband laccase electrodes and compared with macro-scale electrode structures. The reduction of the dimensions of the enzyme biosensor, when used under optimized conditions, led to a significant improvement in its analytical characteristics. The elaborated microsensor showed fast responses towards catechol additions to tap water – a weakly supported medium – characterized by a linear range from 0.2 to 10 μM, a sensitivity of 1.35 ± 0.4 A M−1 cm−2 and a dynamic range up to 43 μM. This enhanced laccase-based microsensor was used for water quality monitoring and its performance for total phenol analysis of wastewater samples from different stages of the cleaning process was compared to a standard method.

  • 36.
    Shtepliuk, Ivan I.
    et al.
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Halvledarmaterial. Linköpings universitet, Tekniska fakulteten. NASU, Ukraine.
    Vagin, Mikhail
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Fysik och elektroteknik. Linköpings universitet, Tekniska fakulteten.
    Ivanov, Ivan Gueorguiev
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Halvledarmaterial. Linköpings universitet, Tekniska fakulteten.
    Iakimov, Tihomir
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Halvledarmaterial. Linköpings universitet, Tekniska fakulteten.
    Yazdi, Gholamreza
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Halvledarmaterial. Linköpings universitet, Tekniska fakulteten.
    Yakimova, Rositsa
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Halvledarmaterial. Linköpings universitet, Tekniska fakulteten.
    Lead (Pb) interfacing with epitaxial graphene2018Inngår i: Physical Chemistry, Chemical Physics - PCCP, ISSN 1463-9076, E-ISSN 1463-9084, Vol. 20, nr 25, s. 17105-17116Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    Here, we report the electrochemical deposition of lead (Pb) as a model metal on epitaxial graphene fabricated on silicon carbide (Gr/SiC). The kinetics of electrodeposition and morphological characteristics of the deposits were evaluated by complementary electrochemical, physical and computational methods. The use of Gr/SiC as an electrode allowed the tracking of lead-associated redox conversions. The analysis of current transients passed during the deposition revealed an instantaneous nucleation mechanism controlled by convergent mass transport on the nuclei locally randomly distributed on epitaxial graphene. This key observation of the deposit topology was confirmed by low values of the experimentally-estimated apparent diffusion coefficient, Raman spectroscopy and scanning electron microscopy (SEM) studies. First principles calculations showed that the nucleation of Pb clusters on the graphene surface leads to weakening of the interaction strength of the metal-graphene complex, and only spatially separated Pb adatoms adsorbed on bridge and/or edge-plane sites can affect the vibrational properties of graphene. We expect that the lead adatoms can merge in large metallic clusters only at defect sites that reinforce the metal-graphene interactions. Our findings provide valuable insights into both heavy metal ion electrochemical analysis and metal electroplating on graphene interfaces that are important for designing effective detectors of toxic heavy metals.

  • 37.
    Shtepliuk, Ivan
    et al.
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Halvledarmaterial. Linköpings universitet, Tekniska fakulteten. NASU, Ukraine.
    Santangelo, Maria Francesca
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Sensor- och aktuatorsystem. Linköpings universitet, Tekniska fakulteten.
    Vagin, Mikhail
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Fysik och elektroteknik. Linköpings universitet, Tekniska fakulteten.
    Ivanov, Ivan Gueorguiev
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Halvledarmaterial. Linköpings universitet, Tekniska fakulteten.
    Khranovskyy, Volodymyr
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Halvledarmaterial. Linköpings universitet, Tekniska fakulteten.
    Iakimov, Tihomir
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Halvledarmaterial. Linköpings universitet, Tekniska fakulteten.
    Eriksson, Jens
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Sensor- och aktuatorsystem. Linköpings universitet, Tekniska fakulteten.
    Yakimova, Rositsa
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Halvledarmaterial. Linköpings universitet, Tekniska fakulteten.
    Understanding Graphene Response to Neutral and Charged Lead Species: Theory and Experiment2018Inngår i: Materials, ISSN 1996-1944, E-ISSN 1996-1944, Vol. 11, nr 10, artikkel-id 2059Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    Deep understanding of binding of toxic Lead (Pb) species on the surface of two-dimensional materials is a required prerequisite for the development of next-generation sensors that can provide fast and real-time detection of critically low concentrations. Here we report atomistic insights into the Lead behavior on epitaxial graphene (Gr) on silicon carbide substrates by thorough complementary study of voltammetry, electrical characterization, Raman spectroscopy, and Density Functional Theory (DFT). It is verified that the epitaxial graphene exhibits quasi-reversible anode reactions in aqueous solutions, providing a well-defined redox peak for Pb species and good linearity over a concentration range from 1 nM to 1 mu M. The conductometric approach offers another way to investigate Lead adsorption, which is based on the formations of stable charge-transfer complexes affecting the p-type conductivity of epitaxial graphene. Our results suggest the adsorption ability of the epitaxial graphene towards divalent Lead ions is concentration-dependent and tends to saturate at higher concentrations. To elucidate the mechanisms responsible for Pb adsorption, we performed DFT calculations and estimated the solvent-mediated interaction between Lead species in different oxidative forms and graphene. Our results provide central information regarding the energetics and structure of Pb-graphene interacting complexes that underlay the adsorption mechanisms of neutral and divalent Lead species. Such a holistic understanding favors design and synthesis of new sensitive materials for water quality monitoring.

  • 38.
    Shtepliuk, Ivan
    et al.
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Halvledarmaterial. Linköpings universitet, Tekniska fakulteten. NASU, Kyiv, Ukraine.
    Vagin, Mikhail
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Laboratoriet för organisk elektronik. Linköpings universitet, Institutionen för fysik, kemi och biologi, Halvledarmaterial. Linköpings universitet, Tekniska fakulteten.
    Yakimova, Rositsa
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Halvledarmaterial. Linköpings universitet, Tekniska fakulteten.
    Insights into the Electrochemical Behavior of Mercury on Graphene/SiC Electrodes2019Inngår i: C — Journal of Carbon Research, ISSN 2311-5629, Vol. 5, nr 3, artikkel-id 51Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    Fast and real time detection of Mercury (Hg) in aqueous solutions is a great challenge due to its bio-accumulative character and the detrimental effect on human health of this toxic element. Therefore, development of reliable sensing platforms is highly desirable. Current research is aiming at deep understanding of the electrochemical response of epitaxial graphene to Mercury exposure. By performing cyclic voltammetry and chronoamperometry measurements as well as density functional theory calculations, we elucidate the nature of Hg-involved oxidation-reduction reactions at the graphene electrode and shed light on the early stages of Hg electrodeposition. The obtained critical information of Hg behavior will be helpful for the design and processing of novel graphene-based sensors.

  • 39.
    Sun, Hengda
    et al.
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Fysik och elektroteknik. Linköpings universitet, Tekniska fakulteten.
    Vagin, Mikhail
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Fysik och elektroteknik. Linköpings universitet, Institutionen för fysik, kemi och biologi. Linköpings universitet, Tekniska fakulteten.
    Wang, Suhao
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Fysik och elektroteknik. Linköpings universitet, Tekniska fakulteten.
    Crispin, Xavier
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Fysik och elektroteknik. Linköpings universitet, Tekniska fakulteten.
    Forchheimer, Robert
    Linköpings universitet, Institutionen för systemteknik, Informationskodning. Linköpings universitet, Tekniska fakulteten.
    Berggren, Magnus
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Fysik och elektroteknik. Linköpings universitet, Tekniska fakulteten.
    Fabiano, Simone
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Fysik och elektroteknik. Linköpings universitet, Tekniska fakulteten.
    Complementary Logic Circuits Based on High-Performance n-Type Organic Electrochemical Transistors2018Inngår i: Advanced Materials, ISSN 0935-9648, E-ISSN 1521-4095, Vol. 30, nr 9, artikkel-id 1704916Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    Organic electrochemical transistors (OECTs) have been the subject of intense research in recent years. To date, however, most of the reported OECTs rely entirely on p-type (hole transport) operation, while electron transporting (n-type) OECTs are rare. The combination of efficient and stable p-type and n-type OECTs would allow for the development of complementary circuits, dramatically advancing the sophistication of OECT-based technologies. Poor stability in air and aqueous electrolyte media, low electron mobility, and/or a lack of electrochemical reversibility, of available high-electron affinity conjugated polymers, has made the development of n-type OECTs troublesome. Here, it is shown that ladder-type polymers such as poly(benzimidazobenzophenanthroline) (BBL) can successfully work as stable and efficient n-channel material for OECTs. These devices can be easily fabricated by means of facile spray-coating techniques. BBL-based OECTs show high transconductance (up to 9.7 mS) and excellent stability in ambient and aqueous media. It is demonstrated that BBL-based n-type OECTs can be successfully integrated with p-type OECTs to form electrochemical complementary inverters. The latter show high gains and large worst-case noise margin at a supply voltage below 0.6 V.

  • 40.
    Tahira, Aneela
    et al.
    Lulea Univ Technol, Sweden.
    Ibupoto, Zafar Hussain
    Lulea Univ Technol, Sweden; Univ Sindh Jamshoro, Pakistan.
    Mazzaro, Raffaello
    Lulea Univ Technol, Sweden; CNR, Italy.
    You, Shuji
    Lulea Univ Technol, Sweden.
    Morandi, Vittorio
    CNR, Italy.
    Natile, Marta Maria
    CNR ICMATE CNR, Italy; Univ Padua, Italy.
    Vagin, Mikhail
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Laboratoriet för organisk elektronik. Linköpings universitet, Tekniska fakulteten.
    Vomiero, Alberto
    Lulea Univ Technol, Sweden; Ca Foscari Univ Venice, Italy.
    Advanced Electrocatalysts for Hydrogen Evolution Reaction Based on Core-Shell MoS2/TiO2 Nanostructures in Acidic and Alkaline Media2019Inngår i: ACS APPLIED ENERGY MATERIALS, ISSN 2574-0962, Vol. 2, nr 3, s. 2053-2062Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    Hydrogen production as alternative energy source is still a challenge due to the lack of efficient and inexpensive catalysts, alternative to platinum. Thus, stable, earth abundant, and inexpensive catalysts are of prime need for hydrogen production via hydrogen evolution reaction (HER). Herein, we present an efficient and stable electrocatalyst composed of earth abundant TiO2 nanorods decorated with molybdenum disulfide thin nanosheets, a few nanometers thick. We grew rutile TiO2 nanorods via the hydrothermal method on conducting glass substrate, and then we nucleated the molybdenum disulfide nanosheets as the top layer. This composite possesses excellent hydrogen evolution activity in both acidic and alkaline media at considerably low overpotentials (350 mV and 700 mV in acidic and alkaline media, respectively) and small Tafel slopes (48 and 60 mV/dec in acidic and alkaline conditions, respectively), which are better than several transition metal dichalcogenides, such as pure molybdenum disulfide and cobalt diselenide. A good stability in acidic and alkaline media is reported here for the new MoS2/TiO2 electrocatalyst. These results demonstrate the potential of composite electrocatalysts for HER based on earth abundant, cost-effective, and environmentally friendly materials, which can also be of interest for a broader range of scalable applications in renewable energies, such as lithium sulfur batteries, solar cells, and fuel cells.

  • 41.
    Tahira, Aneela
    et al.
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Fysik, elektroteknik och matematik. Linköpings universitet, Tekniska fakulteten.
    Ibupoto, Zafar Hussain
    Univ Sindh Jamshoro, Pakistan.
    Vagin, Mikhail
    Linköpings universitet, Institutionen för fysik, kemi och biologi. Linköpings universitet, Tekniska fakulteten.
    Aftab, Umair
    Mehran Univ Engn and Technol, Pakistan.
    Abro, Muhammad Ishaq
    Mehran Univ Engn and Technol, Pakistan.
    Willander, Magnus
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Fysik, elektroteknik och matematik. Linköpings universitet, Tekniska fakulteten.
    Nur, Omer
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Fysik, elektroteknik och matematik. Linköpings universitet, Tekniska fakulteten.
    An efficient bifunctional electrocatalyst based on a nickel iron layered double hydroxide functionalized Co3O4 core shell structure in alkaline media2019Inngår i: Catalysis Science & Technology, ISSN 2044-4753, E-ISSN 2044-4761, Vol. 9, nr 11, s. 2879-2887Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    Developing highly active nonprecious metal and binder free bifunctional electrocatalysts for water splitting is a challenging task. In this study, we used a simple strategy to deposit a nickel iron layered double hydroxide (NiFeLDH) onto cobalt oxide (Co3O4) nanowires. The cobalt oxide nanowires are covered with thin nanosheets of NiFeLDH forming a core shell structure. The Co3O4 nanowires contain the mixed oxidation states of Co2+ and Co3+, and the surface modification of Co3O4 nanowires has shown synergetic effects due to there being more oxygen defects, catalytic sites, and enhanced electronic conductivity. Further, the core shell structure of Co3O4 nanowires demonstrated a bifunctional activity for water splitting in 1 M KOH aqueous solution. From the hydrogen evolution reaction (HER), a current density of 10 mA cm - 2 is achieved at a potential of - 0.303 V vs. reversible hydrogen electrode (RHE). Meanwhile for the case of the oxygen evolution reaction (OER), a current density of 40 mA cm - 2 is measured at a potential of 1.49 V vs. RHE. Also, this electrocatalyst has shown a considerable long- term stability of 15 h for both the HER and the OER. Importantly, electrochemical impedance spectroscopy has shown that the NiFeLDH integration onto cobalt oxide exhibited around 3 fold decrease of charge transfer resistance for both the HER and the OER in comparison with pristine cobalt oxide films, which reveals an excellent electrocatalytic activity for both faradaic processes. All these results confirm that the proposed electrocatalyst can be integrated into an efficient water splitting system.

    Fulltekst tilgjengelig fra 2020-05-09 08:15
  • 42.
    Turner, Anthony
    et al.
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biosensorer och bioelektronik. Linköpings universitet, Tekniska högskolan.
    Karimian, Najmeh
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biosensorer och bioelektronik. Linköpings universitet, Tekniska högskolan. Ferdowsi University of Mashhad, Iran.
    Tiwari, Ashutosh
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biosensorer och bioelektronik. Linköpings universitet, Tekniska högskolan.
    Vagin, Mikhail
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Tillämpad Fysik. Linköpings universitet, Tekniska högskolan.
    Zavar, M. H. A.
    Chamsaz, M.
    Zohuri, G.
    Amperometric cardiac troponin affinity sensor based on electrochemically synthesised troponin imprinted polymer over a Au electrode2013Inngår i: 19th Iranian Seminar on Analytical Chemistry, 2013, Iran: Ferdowsi University of Mashhad , 2013Konferansepaper (Annet vitenskapelig)
  • 43.
    Turner, Anthony
    et al.
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biosensorer och bioelektronik. Linköpings universitet, Tekniska högskolan.
    Sekretaryova, Alina
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biosensorer och bioelektronik. Linköpings universitet, Tekniska högskolan. Lomonosov Moscow State University, Russia.
    Vagin, Mikhail
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Tillämpad Fysik. Linköpings universitet, Tekniska högskolan.
    Eriksson, Mats
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Tillämpad Fysik. Linköpings universitet, Tekniska högskolan.
    Karyakin, Arkady
    Lomonosov Moscow State University, Russia.
    Electrochemicalsensing platform based on sol-gel/phenothiazine/enzyme composite films2013Inngår i: Advanced Materials World Congress, 2013, VBRI , 2013Konferansepaper (Annet vitenskapelig)
  • 44.
    Vagin, Mikhail
    et al.
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Laboratoriet för organisk elektronik. Linköpings universitet, Tekniska fakulteten. Linköpings universitet, Institutionen för fysik, kemi och biologi.
    Sekretareva, Alina
    Linköpings universitet, Institutionen för fysik, kemi och biologi. Linköpings universitet, Tekniska fakulteten. Stanford Univ, CA 94305 USA; Uppsala Univ, Sweden.
    Håkansson, Anna
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Laboratoriet för organisk elektronik. Linköpings universitet, Tekniska fakulteten. Linköpings universitet, Institutionen för fysik, kemi och biologi.
    Iakimov, Tihomir
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Halvledarmaterial. Linköpings universitet, Tekniska fakulteten. Graphens AB, Teknikringen 1F, SE-58330 Linkoping, Sweden.
    Ivanov, Ivan Gueorguiev
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Halvledarmaterial. Linköpings universitet, Tekniska fakulteten.
    Syväjärvi, Mikael
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Halvledarmaterial. Linköpings universitet, Tekniska fakulteten. Graphens AB, Teknikringen 1F, SE-58330 Linkoping, Sweden.
    Yakimova, Rositsa
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Halvledarmaterial. Linköpings universitet, Tekniska fakulteten. Graphens AB, Teknikringen 1F, SE-58330 Linkoping, Sweden.
    Lundström, Ingemar
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Sensor- och aktuatorsystem. Linköpings universitet, Tekniska fakulteten.
    Eriksson, Mats
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Sensor- och aktuatorsystem. Linköpings universitet, Tekniska fakulteten.
    Bioelectrocatalysis on Anodized Epitaxial Graphene and Conventional Graphitic Interfaces2019Inngår i: CHEMELECTROCHEM, ISSN 2196-0216, Vol. 6, nr 14, s. 3791-3796Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    Graphitic materials exhibit significant anisotropy due to the difference in conductivity in a single layer and between adjacent layers. This anisotropy is manifested on epitaxial graphene (EG), which can be manipulated on the nanoscale in order to provide tailor-made properties. Insertion of defects into the EG lattice was utilized here for controllable surface modification with a model biocatalyst and the properties were quantified by both electrochemical and optical methods. A comparative evaluation of the electrode reaction kinetics on the enzyme-modified 2D material vs conventional carbon electrode materials revealed a significant enhancement of mediated bioelectrocatalysis at the nanoscale.

    Fulltekst tilgjengelig fra 2020-07-01 15:20
  • 45.
    Vagin, Mikhail
    et al.
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Kemiska och optiska sensorsystem. Linköpings universitet, Tekniska högskolan.
    Sekretareva, Alina
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Kemiska och optiska sensorsystem. Linköpings universitet, Tekniska högskolan.
    Sanchez, Rafael
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Tillämpad Fysik. Linköpings universitet, Tekniska högskolan.
    Lundström, Ingemar
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biosensorer och bioelektronik. Linköpings universitet, Tekniska högskolan.
    Winquist, Fredrik
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biosensorer och bioelektronik. Linköpings universitet, Tekniska högskolan.
    Eriksson, Mats
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Kemiska och optiska sensorsystem. Linköpings universitet, Tekniska högskolan.
    Arrays of Screen-Printed Graphite Microband Electrodes as a Versatile Electroanalysis Platform2014Inngår i: ChemElectroChem, ISSN 2196-0216, Vol. 1, nr 4, s. 755-762Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    Arrays of microband electrodes were developed by screen printing followed by cutting, which enabled the realization of microband arrays at the cut edge. The microband arrays of different designs were characterized by physical and electro-chemical methods. In both cases, the methods showed that the microband width was around 5 mm. Semi-steady-state cyclic voltammetry responses were observed for redox probes, and chronocoulometric measurements showed the establishment of convergent diffusion regimes characterized by current densities similar to those of a single microelectrode. The analytical performance of the electrode system and its versatility were illustrated with two electrochemical assays: detection of ascorbic acid through direct oxidation and a mediated glucose biosensor fabricated by dip coating. Due to convergent mass transport, both systems showed an enhancement in their analytical characteristics. The developed approach can be adapted to automated electrode recovery.

  • 46.
    Vagin, Mikhail
    et al.
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Fysik och elektroteknik. Linköpings universitet, Tekniska fakulteten.
    Trashin, Stanislav A.
    University of Antwerp, Belgium.
    Beloglazkina, Elena K.
    Moscow MV Lomonosov State University, Russia.
    Majouga, Alexander G.
    Moscow MV Lomonosov State University, Russia.
    Direct reagentless detection of the affinity binding of recombinant His-tagged firefly luciferase with a nickel-modified gold electrode2015Inngår i: Mendeleev communications (Print), ISSN 0959-9436, E-ISSN 1364-551X, Vol. 25, nr 4, s. 290-292Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    The direct reagentless electrochemical detection of recombinant firefly luciferase binding with a gold electrode modified with nickel complex of 1,16-di[4-(2,6-dihydroxycarbonyl)pyridyl]-1,16-dioxa-8,9-dithiahexadecane has been carried out.

  • 47.
    Vagin, Mikhail
    et al.
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Fysik och elektroteknik. Linköpings universitet, Tekniska fakulteten.
    Wannapob, Rodtichoti
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biosensorer och bioelektronik. Linköpings universitet, Tekniska fakulteten. Prince Songkla University, Thailand.
    Liu, Yu
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Kemi. Linköpings universitet, Tekniska fakulteten. Sichuan Agriculture University, Peoples R China.
    Mak, Wing Cheung
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biosensorer och bioelektronik. Linköpings universitet, Tekniska fakulteten.
    Potential-modulated Electrocapacitive Properties of Soft Microstructured Polypyrrole2017Inngår i: Electroanalysis, ISSN 1040-0397, E-ISSN 1521-4109, Vol. 29, nr 1, s. 203-207Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    Microstructured materials are becoming important for high performance electrochemical device especially for energy storage due to their advantageous diffusion and flux properties. Utilizing a rationally designed hollow structured polypyrrole microparticles (PPyMPs) with controllable wall thicknesses of -110 to 340 nm, we observed a significant morphological effect on electrocapacitive kinetics of the PPyMPs modulated by the voltammetric potential window and scan rate. The thinhollow architecture of PPyMPs revealed significant enhancement of charge storage performance (up to 447%), high retention at high scan rate and faster charge/dis-charge kinetics compared to the thick-hollow PPyMPs due to the larger accessible surface area and decrease of diffusion length. These findings demonstrated the electrocapacitive kinetics performance of microstructured soft materials related to morphological effect modulated by operational conditions. Our study provides new insight on electrochemistry of soft electrode materials with controlled nanostructured morphology for understanding the mechanism of charge insertion and mass diffusion for the future development of high performance porous electrode material.

  • 48.
    Vagin, Mikhail Y
    et al.
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Kemiska och optiska sensorsystem. Linköpings universitet, Tekniska högskolan.
    Lundström, Ingemar
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biosensorer och bioelektronik. Linköpings universitet, Tekniska högskolan.
    Turner, Anthony
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biosensorer och bioelektronik. Linköpings universitet, Tekniska högskolan.
    Beni, Valerio
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biosensorer och bioelektronik. Linköpings universitet, Tekniska högskolan.
    Eriksson, Mats
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Kemiska och optiska sensorsystem. Linköpings universitet, Tekniska högskolan.
    Boron-doped diamond microelectrode arrays for electrochemical monitoring of antibiotics contamination in water2014Inngår i: 15th International Conference on Electroanalysis (ESEAC), 2014Konferansepaper (Annet vitenskapelig)
    Abstract [en]

    The improvement of water management and increasing the access to safe drinking water can develop the quality of life for millions of people world-wide and reduce child mortality due to water-borne diseases [1]. Sweden was recently affected by the lack of appropriate water management which resulted in microbial contamination and tens of thousands of people falling ill [2]. Pollution with chemical compounds is also a waterworks concern. The appearance of pharmaceuticals such as antibiotics in raw water affects the cleaning processes at waterworks [3]. Substances which are not, or are only partly, eliminated in the sewage treatment plant will reach the surface water where they may affect organisms of different trophic levels and cause, for example, the of antibiotics resistance [4]. The inhibition of bacteria of waste water plants by antibiotics may seriously affect organic matter degradation. The efficiency of nitrification as an important step in waste water purification, can be decreased by antibiotics inhibition [5]. Boron-doped diamond (BDD) is an advanced electrode material that possesses the combination of good electrical conductivity achieved via film doping and the extreme chemical inertness of diamond, which gives rise to a number of highly desirable properties of BDD as electrode material: a wide potential window in aqueous media allows electrochemical measurements at both extreme anodic and cathodic potentials, very low capacitive currents leads to a sensitivity increase and extreme chemical and structural inertness prevents electrode fouling [6]. Usage of a microelectrode array as the working electrode offers a variety of benefits for electroanalysis: an improvement of the analytical performance in comparison with macroelectrodes under planar diffusion, higher signal-to-noise ratios due to low capacitive currents at the small surface area, shorter response times and less sensitivity to variations in the water flow rate. The BDD arrays of this work contain 2900 microelectrodes (10 mm diameter each) and have been used for the detection of antibiotics (ofloxacine and canamycin A) in water with high amplitude pulse voltammetry processed by multivariate data analysis. The detection limits observed in monitoring mode were comparable with the characteristics of standard protocols of antibiotics detection, which opens the possibility for continuous monitoring of water.

    [1] The United Nations, World Water Development Report 4, 2012; [2] Lindberg, A. et al.,

    FOI-R--3376--SE, 2011; Dryselius, R.; National Food Agency, Sweden, 2012; [3] Kummerer

    K. Chemosphere, 2009, 75, 417; [4] Kummerer K. Chemosphere, 2009, 75, 435; [5]

    Dokianakis, S.N. et al., Water Sci. Technol. 50, 341; [6] Goeting, C. et al.,

    NewDiam.Front.C.Tech. 1999, 9, 207; Compton, R. et al., Electroanal. 2003, 15, 1349.

     

  • 49.
    Vagin, Mikhail Y
    et al.
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Kemiska och optiska sensorsystem. Linköpings universitet, Tekniska högskolan.
    Sekretaryova, Alina N
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biosensorer och bioelektronik. Linköpings universitet, Tekniska högskolan.
    Reategui, Rafael Sanchez
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biosensorer och bioelektronik.
    Lundström, Ingemar
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biosensorer och bioelektronik.
    Turner, Anthony
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biosensorer och bioelektronik. Linköpings universitet, Tekniska högskolan.
    Eriksson, Mats
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Kemiska och optiska sensorsystem. Linköpings universitet, Tekniska högskolan.
    Screen-printed graphite microbands as a versatile biosensor platform2014Inngår i: 24th Anniversary World Congress on Biosensors – Biosensors 2014, Elsevier, 2014Konferansepaper (Annet vitenskapelig)
    Abstract [en]

    The use of extremely small working electrodes offers a variety of benefits for electroanalysis. The enhanced mass transport as a result of convergent diffusion is the most important advantage of microdimensional electrodes and results in improved of analytical performance The low detectable-currents problem can be solved by single microelectrode multiplication into an array, thus combining the advantages of enhanced mass transport and high output signals. The microband is one of the most cost-effective and easy-fabricated geometries for microelectrodes. The microband width is a critical microscopic dimension of the electrode, which maintains the dominance of convergent diffusion, whereas the microband length is macroscopic and ensures registration of high currents.

    Graphite screen-printing on a plastic support is a standard technology for large-scale production of low cost electrochemical devices. This has been combined with simple guillotine cutting to fabricate of microband arrays for autonomous environmental and clinical monitoring.

    Single-layer and multilayer microband arrays of different band lengths were produced and characterised using optical and electrochemical methods. The critical dimension for the microband width to facilitate convergent diffusion was assessed electrochemically and found to be in the order of 5 microns. The developed electrode structures were used as a versatile platform for the manufacture of model electroanalytical systems. Direct oxidation of ascorbic acid was explored at the microband arrays and a glucose biosensor based on mediated and immobilised glucose oxidase was fabricated. Both examples yielded significant enhancement of the analytical performance.

    A: the layout of the screen-printed graphite microband array of 5 electrode layers. B: voltammmetric responses obtained at the microband arrays.

    Acknowledgement: Formas and Security Link for financial support; David Nilsson (Acreo) for screen-printing.

  • 50.
    Vagin, Mikhail Y
    et al.
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Kemiska och optiska sensorsystem. Linköpings universitet, Tekniska högskolan.
    Sekretaryova, Alina N
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biosensorer och bioelektronik. Linköpings universitet, Tekniska högskolan.
    Reategui, Rafael Sanchez
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biosensorer och bioelektronik. Linköpings universitet, Tekniska högskolan.
    Lundström, Ingemar
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biosensorer och bioelektronik. Linköpings universitet, Tekniska högskolan.
    Turner, Anthony
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biosensorer och bioelektronik. Linköpings universitet, Tekniska högskolan.
    Eriksson, Mats
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Kemiska och optiska sensorsystem. Linköpings universitet, Tekniska högskolan.
    Screen-printed graphite microbands for electroanalysis2014Inngår i: 15th International Conference on Electroanalysis (ESEAC), 2014Konferansepaper (Annet vitenskapelig)
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