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  • 51.
    Berggren, Magnus
    et al.
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Fysik och elektroteknik. Linköpings universitet, Tekniska högskolan.
    Nilsson, David
    Acreo, Norrköping.
    Robinson, Nathaniel D.
    Linköpings universitet, Institutionen för teknik och naturvetenskap. Linköpings universitet, Tekniska högskolan.
    Organic materials for printed electronics2007Ingår i: Nature Materials, ISSN 1476-1122, E-ISSN 1476-4660, Vol. 6, nr 1, s. 3-5Artikel i tidskrift (Refereegranskat)
    Abstract [en]

    Organic materials can offer a low-cost alternative for printed electronics and flexible displays. However, research in these systems must exploit the differences — via molecular-level control of functionality — compared with inorganic electronics if they are to become commercially viable.

    Introduction

    Conducting and semiconducting organic materials, both polymers and molecules, are being considered for a vast array of electronic applications. The first examples, such as displays in mobile appliances, have found their way to market as replacements for traditional components in existing products. Organic electronics distinguishes itself from traditional electronics because one can define functionality at the molecular level, process the materials from solution, and make displays and circuits that are completely flexible. So far, very little of the uniqueness of organic electronics is expressed in the products promoted as manufacturable; why?

    One important opportunity for organic electronics is the area of radiofrequency identification (RFID) manufactured using an all-in-line printing process. This technology comprises fast-switching transistors, antennas operating at frequencies above 100 kHz, memory, and so on, all integrated into a plastic foil. The present target in many organic electronics labs around the world is to develop the high-speed (>10 kHz) transistors critical for such devices. The use of organic transistors instead of their inorganic equivalents is motivated by cost. So far, little effort has been devoted to exploring organic electronics in terms of its true unique electronic functionality and the possibility to add electronics to surfaces previously considered electronically inactive. For instance, paper is produced at speeds exceeding 100 km h-1 and is converted into packages and printed media at manufacturing flows typically above 100 m min-1. Adding organic electronics onto, for instance, the paper surface during the paper conversion process would demonstrate the true uniqueness of organic electronics, both from a manufacturing and an application point of view. Retail chains and transportation companies desperately seek a printed electronic technology to provide better safety and security features on packages and automatically track and trace products all the way from the manufacturer to the end customer. The financial losses related to counterfeiting, failure in transportation and damaged packages is comparable to the overall profits made on the product contained in the package. In addition, printed electronics could potentially guide the end-user to properly use the product and to guarantee brand authenticity, for example through an interactive user's guide, and electronic features to replace existing security devices such as the holographic stickers commonly used in packages and bank notes today. It turns out that, for many of these applications, high-frequency signal-processing is not required; 10 ms to 1 s response times are appropriate. These are goals that a very simple printed electronics technology may be able to fill. Silicon-based RFID devices are currently used in high-end products, but are prohibitively expensive for commodities such as food at the consumer package level. Thus, the potential value for printed organic electronics seems to exist if the expense can be kept down. For instance, TetraPak, who produces more than 100 billion packages every year, estimates that the costs for additional security and safety features cannot exceed about 0.2 Eurocents per package (Istvan Ulvros, TetraPak, private communication).

    Much of the research in organic electronics aims to optimise inherent charge transport and efficiency characteristics of the materials already in use in individual devices. This work has pushed the solar energy-to-electricity power-conversion efficiency in organic solar cells close to 5% (ref. 1) and the luminous efficiency of plastic luminescent devices to around 25 cd A-1 (ref. 2). Organic electrochromic displays now perform extraordinarily well in terms of colour contrast, memory and stability3, and polymer transistors easily run at speeds beyond 100 kHz (ref.4). These results have been achieved by improving the performance at the individual device level. Rarely are integrated circuits or high-volume manufacturing conditions considered in the research. Typically, a series of more than ten patterning, material deposition and post-processing steps are required to make one kind of device. The tradition has been to develop specific materials that exclusively function well in only one device type. RFID circuits (for example) typically require rectifiers, antennas, powering devices, transistors for signal processing, encapsulation layers and in some cases also displays. Merging today's efforts conducted at the organic electronics device level would then result in a production route that would include perhaps 50 (or even more) discrete manufacturing steps. Unfortunately, the cost for a label requiring several tens of patterning steps including exotic organic electronic materials is not compatible with the value and costs of packages.

    In traditional printers, typically five to ten printing stations are available in series (Fig. 1). Each station also includes one or two convection, infrared or ultraviolet curing steps. At ordinary printing speeds (10 to 200 m min-1) the substrate spends on the order of a tenth to several seconds in each printing station. During this time, registration, material deposition and post-processing must take place. The value structure in printing technology means that the cost for printing scales at least linearly with the number of printing steps. The yield and systematic errors in printing technology becomes a nightmare beyond ten printing steps. The cost for materials such as inks, substrates and coatings is a considerable part of the entire product value. Our own calculations indicate that each individual RFID label would cost more than 10 Eurocents (Lars-Olov Hennerdal, Acreo, private communication).

  • 52.
    Berggren, Magnus
    et al.
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Fysik och elektroteknik. Linköpings universitet, Tekniska högskolan.
    Richter Dahlfors, Agneta
    Karolinska Institutet, Institutionen för Neurovetenskap.
    Electrochemical Surface Switches and Electronic Ion Pumps Based on Conjugated Polymers2009Ingår i: Organic Electronics in Sensors and Biotechnology / [ed] R. Shinar, J. Shinar, McGraw-Hill , 2009, 1, s. 395-406Kapitel i bok, del av antologi (Övrigt vetenskapligt)
    Abstract [en]

    The latest in organic electronics-based sensing and biotechnology Develop high-performance, field-deployable organic semiconductor-based biological, chemical, and physical sensor arrays using the comprehensive information contained in this definitive volume. Organic Electronics in Sensors and Biotechnology presents state-of-the-art technology alongside real-world applications and ongoing R & D. Learn about light, temperature, and pressure monitors, integrated flexible pyroelectric sensors, sensing of organic and inorganic compounds, and design of compact photoluminescent sensors. You will also get full details on organic lasers, organic electronics in memory elements, disease and pathogen detection, and conjugated polymers for advancing cellular biology. Monitor organic and inorganic compounds with OFETs Characterize organic materials using impedance spectroscopy Work with organic LEDs, photodetectors, and photovoltaic cells Form flexible pyroelectric sensors integrated with OFETs Build PL-based chemical and biological sensing modules and arrays Design organic semiconductor lasers and memory elements Use luminescent conjugated polymers as optical biosensors Deploy polymer-based switches and ion pumps at the microfluidic level

  • 53.
    Berggren, Magnus
    et al.
    Linköpings universitet, Tekniska högskolan. Linköpings universitet, Institutionen för teknik och naturvetenskap.
    Richter-Dahlfors, Agneta
    Organic bioelectronics2007Ingår i: Advanced Materials, ISSN 0935-9648, E-ISSN 1521-4095, Vol. 19, nr 20, s. 3201-3213Artikel, forskningsöversikt (Refereegranskat)
    Abstract [en]

    During the last two decades, organic electroactive materials have been explored as the working material in a vast array of electronic devices, promising low-cost, flexible, and easily manufactured systems. The same materials also possess features that make them unique in bioelectronics applications, where electronic signals are translated into biosignals and vice versa. Here we review, in the broadest sense, the field of organic bioelectronics, describing the electronic properties and mechanisms of the organic electronic materials that are utilized in specific biological experiments.

  • 54.
    Berggren, Magnus
    et al.
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Fysik och elektroteknik. Linköpings universitet, Tekniska fakulteten.
    Simon, Daniel
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Fysik och elektroteknik. Linköpings universitet, Tekniska fakulteten.
    Nilsson, D
    Acreo Swedish ICT, Box 787, SE-601 17, Norrköping, Sweden..
    Dyreklev, P
    Acreo Swedish ICT, Box 787, SE-601 17, Norrköping, Sweden..
    Norberg, P
    Acreo Swedish ICT, Box 787, SE-601 17, Norrköping, Sweden..
    Nordlinder, S
    Acreo Swedish ICT, Box 787, SE-601 17, Norrköping, Sweden..
    Ersman, PA
    Acreo Swedish ICT, Box 787, SE-601 17, Norrköping, Sweden..
    Gustafsson, G
    Acreo Swedish ICT, Box 787, SE-601 17, Norrköping, Sweden..
    Wikner, Jacob
    Linköpings universitet, Institutionen för systemteknik, Elektroniska Kretsar och System. Linköpings universitet, Tekniska fakulteten.
    Hederén, J
    DU Radio, Ericsson AB, SE-583 30, Linköping, Sweden..
    Hentzell, H
    Swedish ICT Research, Box 1151, SE-164 26, Kista, Sweden..
    Browsing the Real World using Organic Electronics, Si-Chips, and a Human Touch.2016Ingår i: Advanced Materials, ISSN 0935-9648, E-ISSN 1521-4095, Vol. 28, nr 10, s. 1911-1916Artikel i tidskrift (Refereegranskat)
    Abstract [en]

    Organic electronics have been developed according to an orthodox doctrine advocating "all-printed, "all-organic and "ultra-low-cost primarily targeting various e-paper applications. In order to harvest from the great opportunities afforded with organic electronics potentially operating as communication and sensor outposts within existing and future complex communication infrastructures, high-quality computing and communication protocols must be integrated with the organic electronics. Here, we debate and scrutinize the twinning of the signal-processing capability of traditional integrated silicon chips with organic electronics and sensors, and to use our body as a natural local network with our bare hand as the browser of the physical world. The resulting platform provides a body network, i.e., a personalized web, composed of e-label sensors, bioelectronics, and mobile devices that together make it possible to monitor and record both our ambience and health-status parameters, supported by the ubiquitous mobile network and the resources of the "cloud".

  • 55.
    Bernacka Wojcik, Iwona
    et al.
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Laboratoriet för organisk elektronik. Linköpings universitet, Tekniska fakulteten.
    Huerta, Miriam
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Fysik och elektroteknik. Linköpings universitet, Tekniska fakulteten.
    Tybrandt, Klas
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Fysik och elektroteknik. Linköpings universitet, Tekniska fakulteten.
    Karady, Michal
    Swedish Univ Agr Sci, Sweden.
    Mulla, Yusuf
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Fysik och elektroteknik. Linköpings universitet, Tekniska fakulteten.
    Poxson, David
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Laboratoriet för organisk elektronik. Linköpings universitet, Tekniska fakulteten.
    Gabrielsson, Erik
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Laboratoriet för organisk elektronik. Linköpings universitet, Tekniska fakulteten.
    Ljung, Karin
    Swedish Univ Agr Sci, Sweden.
    Simon, Daniel
    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.
    Implantable Organic Electronic Ion Pump Enables ABA Hormone Delivery for Control of Stomata in an Intact Tobacco Plant2019Ingår i: Small, ISSN 1613-6810, E-ISSN 1613-6829, Vol. 15, nr 43, artikel-id 1902189Artikel i tidskrift (Refereegranskat)
    Abstract [en]

    Electronic control of biological processes with bioelectronic devices holds promise for sophisticated regulation of physiology, for gaining fundamental understanding of biological systems, providing new therapeutic solutions, and digitally mediating adaptations of organisms to external factors. The organic electronic ion pump (OEIP) provides a unique means for electronically-controlled, flow-free delivery of ions, and biomolecules at cellular scale. Here, a miniaturized OEIP device based on glass capillary fibers (c-OEIP) is implanted in a biological organism. The capillary form factor at the sub-100 mu m scale of the device enables it to be implanted in soft tissue, while its hyperbranched polyelectrolyte channel and addressing protocol allows efficient delivery of a large aromatic molecule. In the first example of an implantable bioelectronic device in plants, the c-OEIP readily penetrates the leaf of an intact tobacco plant with no significant wound response (evaluated up to 24 h) and effectively delivers the hormone abscisic acid (ABA) into the leaf apoplast. OEIP-mediated delivery of ABA, the phytohormone that regulates plants tolerance to stress, induces closure of stomata, the microscopic pores in leafs epidermis that play a vital role in photosynthesis and transpiration. Efficient and localized ABA delivery reveals previously unreported kinetics of ABA-induced signal propagation.

  • 56.
    Berto, Marcello
    et al.
    University of Modena and Reggio Emilia, Italy.
    Casalini, Stefano
    University of Modena and Reggio Emilia, Italy; Institute Ciencia Mat Barcelona ICMAB CSIC, Spain.
    Di Lauro, Michele
    University of Modena and Reggio Emilia, Italy.
    Marasso, Simone L.
    Politecn Torino, Italy; IMEM CNR, Italy.
    Cocuzza, Matteo
    Politecn Torino, Italy; IMEM CNR, Italy.
    Perrone, Denis
    Ist Italiano Tecnol, Italy.
    Pinti, Marcello
    University of Modena and Reggio Emilia, Italy.
    Cossarizza, Andrea
    University of Modena and Reggio Emilia, Italy.
    Pirri, Candido F.
    Politecn Torino, Italy; Ist Italiano Tecnol, Italy.
    Simon, Daniel
    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.
    Zerbetto, Francesco
    University of Bologna, Italy.
    Bortolotti, Carlo A.
    University of Modena and Reggio Emilia, Italy.
    Biscarini, Fabio
    University of Modena and Reggio Emilia, Italy.
    Biorecognition in Organic Field Effect Transistors Biosensors: The Role of the Density of States of the Organic Semiconductor2016Ingår i: ANALYTICAL CHEMISTRY, ISSN 0003-2700, Vol. 88, nr 24, s. 12330-12338Artikel i tidskrift (Refereegranskat)
    Abstract [en]

    Biorecognition is a central event in biological processes in the living systems that is also widely exploited in technological and health applications. We demonstrate that the Electrolyte Gated Organic Field Effect Transistor (EGOFET) is an ultrasensitive and specific device that allows us to quantitatively assess the thermodynamics of biomolecular recognition between a human antibody and its antigen, namely, the inflammatory cytokine TNF alpha at the solid/liquid interface. The EGOFET biosensor exhibits a superexponential response at TNF alpha concentration below 1 nM with a minimum detection level of 100 pM. The sensitivity of the device depends on the analyte concentration, reaching a maximum in the range of clinically relevant TNF alpha concentrations when the EGOFET is operated in the subthreshold regime. At concentrations greater than 1 nM the response scales linearly with the concentration. The sensitivity and the dynamic range are both modulated by the gate voltage. These results are explained by establishing the correlation between the sensitivity and the density of states (DOS) of the organic semiconductor. Then, the superexponential response arises from the energy-dependence of the tail of the DOS of the HOMO level. From the gate voltage-dependent response, we extract the binding constant, as well as the changes of the surface charge and the effective capacitance accompanying biorecognition at the electrode surface. Finally, we demonstrate the detection of TNF alpha in human-plasma derived samples as an example for point-of-care application.

  • 57.
    Berto, Marcello
    et al.
    Univ Modena and Reggio Emilia, Italy; Univ Ferrara, Italy.
    Diacci, Chiara
    Univ Modena and Reggio Emilia, Italy.
    DAgata, Roberta
    Univ Catania, Italy.
    Pinti, Marcello
    Univ Modena and Reggio Emilia, Italy.
    Bianchini, Elena
    Univ Modena and Reggio Emilia, Italy.
    Di Lauro, Michele
    Univ Modena and Reggio Emilia, Italy.
    Casalini, Stefano
    Univ Modena and Reggio Emilia, Italy; Inst Ciencia Mat Barcelona ICMAB CSIC, Spain.
    Cossarizza, Andrea
    Univ Modena and Reggio Emilia, Italy.
    Berggren, Magnus
    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.
    Spoto, Giuseppe
    Univ Catania, Italy; Univ Catania, Italy.
    Biscarini, Fabio
    Univ Modena and Reggio Emilia, Italy.
    Bortolotti, Carlo A.
    Univ Modena and Reggio Emilia, Italy.
    EGOFET Peptide Aptasensor for Label-Free Detection of Inflammatory Cytokines in Complex Fluids2018Ingår i: ADVANCED BIOSYSTEMS, ISSN 2366-7478, Vol. 2, nr 2, artikel-id 1700072Artikel i tidskrift (Refereegranskat)
    Abstract [en]

    Organic electronic transistors are rapidly emerging as ultrahigh sensitive label-free biosensors suited for point-of-care or in-field deployed applications. Most organic biosensors reported to date are based on immunorecognition between the relevant biomarkers and the immobilized antibodies, whose use is hindered by large dimensions, poor control of sequence, and relative instability. Here, an electrolyte-gated organic field effect transistor (EGOFET) biosensor where the recognition units are surface immobilized peptide aptamers (Affimer proteins) instead of antibodies is reported. Peptide aptasensor for the detection of the pro-inflammatory cytokine tumor necrosis factor alpha (TNF alpha) with a 1 x 10(-12) M limit of detection is demonstrated. Ultralow sensitivity is met even in complex solutions such as cell culture media containing 10% serum, demonstrating the remarkable ligand specificity of the device. The device performances, together with the simple one-step immobilization strategy of the recognition moieties and the low operational voltages, all prompt EGOFET peptide aptasensors as candidates for early diagnostics and monitoring at the point-of-care.

  • 58.
    Berto, Marcello
    et al.
    Univ Modena and Reggio Emilia, Italy.
    Diacci, Chiara
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Laboratoriet för organisk elektronik. Linköpings universitet, Tekniska fakulteten.
    Theuer, Lorenz
    Linköpings universitet, Institutionen för teknik och naturvetenskap. Linköpings universitet, Tekniska fakulteten. RISE Acreo, Sweden.
    Di Lauro, Michele
    Univ Modena and Reggio Emilia, Italy.
    Simon, Daniel
    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.
    Biscarini, Fabio
    Univ Modena and Reggio Emilia, Italy; Ist Italiano Tecnol, Italy.
    Beni, Valerio
    RISE Acreo, Sweden.
    Bortolotti, Carlo A.
    Univ Modena and Reggio Emilia, Italy.
    Label free urea biosensor based on organic electrochemical transistors2018Ingår i: FLEXIBLE AND PRINTED ELECTRONICS, ISSN 2058-8585, Vol. 3, nr 2, artikel-id 024001Artikel i tidskrift (Refereegranskat)
    Abstract [en]

    The quantification of urea is of the utmost importance not only in medical diagnosis, where it serves as a potential indicator of kidney and liver disfunction, but also in food safety and environmental control. Here, we describe a urea biosensor based on urease entrapped in a crosslinked gelatin hydrogel, deposited onto a fully printed PEDOT:PSS-based organic electrochemical transistor (OECT). The device response is based on the modulation of the channel conductivity by the ionic species produced upon urea hydrolysis catalyzed by the entrapped urease. The biosensor shows excellent reproducibility, a limit of detection as low as 1 mu M and a response time of a few minutes. The fabrication of the OECTs by screen-printing on flexible substrates ensures a significant reduction in manufacturing time and costs. The low dimensionality and operational voltages (0.5 V or below) of these devices contribute to make these enzymatic OECT-based biosensors as appealing candidates for high-throughput monitoring of urea levels at the point-of-care or in the field.

  • 59.
    Blaudeck, Thomas
    et al.
    Linköpings universitet, Institutionen för teknik och naturvetenskap. Linköpings universitet, Tekniska högskolan.
    Andersson Ersman, Peter
    Acreo AB, Sweden .
    Sandberg, Mats
    Acreo AB, Sweden .
    Heinz, Sebastian
    Technical University of Chemnitz, Germany .
    Laiho, Ari
    Linköpings universitet, Institutionen för teknik och naturvetenskap. Linköpings universitet, Tekniska högskolan.
    Liu, Jiang
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Fysik och elektroteknik. Linköpings universitet, Tekniska högskolan.
    Engquist, Isak
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Fysik och elektroteknik. Linköpings universitet, Tekniska högskolan.
    Berggren, Magnus
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Fysik och elektroteknik. Linköpings universitet, Tekniska högskolan.
    Baumann, Reinhard R.
    Technical University of Chemnitz, Germany Fraunhofer Institute Elect Nanosyst ENAS, Germany .
    Simplified Large-Area Manufacturing of Organic Electrochemical Transistors Combining Printing and a Self-Aligning Laser Ablation Step2012Ingår i: Advanced Functional Materials, ISSN 1616-301X, E-ISSN 1616-3028, Vol. 22, nr 14, s. 2939-2948Artikel i tidskrift (Refereegranskat)
    Abstract [en]

    A hybrid manufacturing approach for organic electrochemical transistors (OECTs) on flexible substrates is reported. The technology is based on conventional and digital printing (screen and inkjet printing), laser processing, and post-press technologies. A careful selection of the conductive, dielectric, and semiconductor materials with respect to their optical properties enables a self-aligning pattern formation which results in a significant reduction of the usual registration problems during manufacturing. For the prototype OECTs, based on this technology, on/off ratios up to 600 and switching times of 100 milliseconds at gate voltages in the range of 1 V were obtained.

  • 60.
    Bolin, Maria
    et al.
    Linköpings universitet, Institutionen för teknik och naturvetenskap. Linköpings universitet, Tekniska högskolan.
    Svennersten, Karl
    Karolinska Inst, Dept Neurosci, S-17177 Stockholm, Sweden .
    Nilsson, David
    Acreo AB, S-60117 Norrkoping, Sweden .
    Sawatdee, Anurak
    Acreo AB, S-60117 Norrkoping, Sweden .
    Jager, Edwin
    Linköpings universitet, Institutionen för teknik och naturvetenskap. Linköpings universitet, Tekniska högskolan.
    Richter-Dahlfors, Agneta
    Karolinska Inst, Dept Neurosci, S-17177 Stockholm, Sweden .
    Berggren, Magnus
    Linköpings universitet, Institutionen för teknik och naturvetenskap. Linköpings universitet, Tekniska högskolan.
    Active Control of Epithelial Cell-Density Gradients Grown Along the Channel of an Organic Electrochemical Transistor2009Ingår i: ADVANCED MATERIALS, ISSN 0935-9648, Vol. 21, nr 43, s. 4379-Artikel i tidskrift (Refereegranskat)
    Abstract [en]

    Complex patterning of the extracellular matrix, cells, and tissues under in situ electronic control is the aim of the technique presented here. The distribution of epithelial cells along the channel of an organic electrochemical transistor is shown to be actively controlled by the gate and drain voltages, as electrochemical gradients are formed along the transistor channel when the device is biased.

  • 61.
    Bolin, Maria
    et al.
    Linköpings universitet, Institutionen för teknik och naturvetenskap. Linköpings universitet, Tekniska högskolan.
    Svennersten, Karl
    Karolinska Institute.
    Wang, Xiangjun
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biomolekylär och Organisk Elektronik. Linköpings universitet, Tekniska högskolan.
    Chronakis, Ioannis S
    Industrial Research & Development Corporation.
    Richter-Dahlfors, Agneta
    Karolinska Institute.
    Jager, Edwin
    Linköpings universitet, Institutionen för teknik och naturvetenskap. Linköpings universitet, Tekniska högskolan.
    Berggren, Magnus
    Linköpings universitet, Institutionen för teknik och naturvetenskap. Linköpings universitet, Tekniska högskolan.
    Nano-fiber scaffold electrodes based on PEDOT for cell stimulation2009Ingår i: SENSORS AND ACTUATORS B-CHEMICAL, ISSN 0925-4005, Vol. 142, nr 2, s. 451-456Artikel i tidskrift (Refereegranskat)
    Abstract [en]

    Electronically conductive and electrochemically active 3D-scaffolds based on electrospun poly(ethylene terephthalate) (PET) nano-fibers are reported. Vapour phase polymerization was employed to achieve an uniform and conformal coating of poly(3,4-ethylenedioxythiophene) doped with tosylate (PEDOT:tosylate) on the nano-fibers. The PEDOT coatings had a large impact on the wettability, turning the hydrophobic PET fibers super-hydrophilic. SH-SY5Y neuroblastoma cells were grown on the PEDOT coated fibers. The SH-SY5Y cells adhered well and showed healthy morphology. These electrically active scaffolds were used to induce Ca2+ signalling in SH-SY5Y neuroblastoma cells. PEDOT:tosylate coated nano-fibers represent a class of 3D host environments that combines excellent adhesion and proliferation for neuronal cells with the possibility to regulate their signalling.

  • 62.
    Brooke, Robert
    et al.
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Laboratoriet för organisk elektronik. Linköpings universitet, Tekniska fakulteten. Acreo, Sweden.
    Edberg, Jesper
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Laboratoriet för organisk elektronik. Linköpings universitet, Tekniska fakulteten. Acreo, 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.
    Engquist, Isak
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Laboratoriet för organisk elektronik. Linköpings universitet, Tekniska fakulteten.
    Jonsson, Magnus
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Laboratoriet för organisk elektronik. Linköpings universitet, Tekniska fakulteten.
    Greyscale and Paper Electrochromic Polymer Displays by UV Patterning2019Ingår i: Polymers, ISSN 2073-4360, E-ISSN 2073-4360, Vol. 11, nr 2, artikel-id 267Artikel i tidskrift (Refereegranskat)
    Abstract [en]

    Electrochromic devices have important implications as smart windows for energy efficient buildings, internet of things devices, and in low-cost advertising applications. While inorganics have so far dominated the market, organic conductive polymers possess certain advantages such as high throughput and low temperature processing, faster switching, and superior optical memory. Here, we present organic electrochromic devices that can switch between two high-resolution images, based on UV-patterning and vapor phase polymerization of poly(3,4-ethylenedioxythiophene) films. We demonstrate that this technique can provide switchable greyscale images through the spatial control of a UV-light dose. The color space was able to be further altered via optimization of the oxidant concentration. Finally, we utilized a UV-patterning technique to produce functional paper with electrochromic patterns deposited on porous paper, allowing for environmentally friendly electrochromic displays.

  • 63.
    Brooke, Robert
    et al.
    Linköpings universitet, Institutionen för teknik och naturvetenskap. Linköpings universitet, Tekniska fakulteten.
    Edberg, Jesper
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Fysik och elektroteknik. Linköpings universitet, Tekniska fakulteten.
    Iandolo, Donata
    Linköpings universitet, Institutionen för teknik och naturvetenskap. Linköpings universitet, Tekniska fakulteten. Ecole Natl Super Mines, France.
    Berggren, 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.
    Engquist, Isak
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Fysik och elektroteknik. Linköpings universitet, Tekniska fakulteten.
    Controlling the electrochromic properties of conductive polymers using UV-light2018Ingår i: Journal of Materials Chemistry C, ISSN 2050-7526, E-ISSN 2050-7534, Vol. 6, nr 17, s. 4663-4670Artikel i tidskrift (Refereegranskat)
    Abstract [en]

    The phenomenon of electrochromism in conductive polymers is well known and has been exploited in many scientific reports. Using a newly developed patterning technique for conductive polymers, we manufactured high-resolution electrochromic devices from the complementary polymers PEDOT and polypyrrole. The technique, which combines UV-light exposure with vapor phase polymerization, has previously only been demonstrated with the conductive polymer PEDOT. We further demonstrated how the same technique can be used to control the optical properties and the electrochromic contrast in these polymers. Oxidant exposure to UV-light prior to vapor phase polymerization showed a reduction in polymer electrochromic contrast allowing high-resolution (100 mu m) patterns to completely disappear while applying a voltage bias due to their optical similarity in one redox state and dissimilarity in the other. This unique electrochromic property enabled us to construct devices displaying images that appear and disappear with the change in applied voltage. Finally, a modification of the electrochromic device architecture permitted a dual image electrochromic device incorporating patterned PEDOT and patterned polypyrrole on the same electrode, allowing the switching between two different images.

  • 64.
    Brooke, Robert
    et al.
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Fysik och elektroteknik. Linköpings universitet, Tekniska fakulteten.
    Mitraka, Evangelia
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Fysik och elektroteknik. Linköpings universitet, Tekniska fakulteten.
    Sardar, Samim
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Fysik och elektroteknik. Linköpings universitet, Tekniska fakulteten.
    Sandberg, Mats
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Fysik och elektroteknik. Linköpings universitet, Tekniska fakulteten. Acreo Swedish ICT, SE-601 74 Norrköping, Sweden.
    Sawatdee, Anurak
    Acreo Swedish ICT, SE-601 74 Norrköping, Sweden.
    Berggren, 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.
    Jonsson, Magnus P.
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Fysik och elektroteknik. Linköpings universitet, Tekniska fakulteten.
    Infrared electrochromic conducting polymer devices2017Ingår i: Journal of Materials Chemistry C, ISSN 2050-7526, E-ISSN 2050-7534, Vol. 5, nr 23, s. 5824-5830Artikel i tidskrift (Refereegranskat)
    Abstract [en]

    The conducting polymer poly(3,4-ethylenedioxythiophene) (PEDOT) is well known for its electrochromic properties in the visible region. Less focus has been devoted to the infrared (IR) wavelength range, although tunable IR properties could enable a wide range of novel applications. As an example, modern day vehicles have thermal cameras to identify pedestrians and animals in total darkness, but road and speed signs cannot be easily visualized by these imaging systems. IR electrochromism could enable a new generation of dynamic road signs that are compatible with thermal imaging, while simultaneously providing contrast also in the visible region. Here, we present the first metal-free flexible IR electrochromic devices, based on PEDOT:Tosylate as both the electrochromic material and electrodes. Lateral electrochromic devices enabled a detailed investigation of the IR electrochromism of thin PEDOT:Tosylate films, revealing large changes in their thermal signature, with effective temperature changes up to 10 [degree]C between the oxidized (1.5 V) and reduced (-1.5 V) states of the polymer. Larger scale (7 [times] 7 cm) vertical electrochromic devices demonstrate practical suitability and showed effective temperature changes of approximately 7 [degree]C, with good optical memory and fast switching (1.9 s from the oxidized state to the reduced state and 3.3 s for the reversed switching). The results are highly encouraging for using PEDOT:Tosylate for IR electrochromic applications.

  • 65.
    Bubnova, Olga
    et al.
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Fysik och elektroteknik. Linköpings universitet, Tekniska högskolan.
    Berggren, Magnus
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Fysik och elektroteknik. Linköpings universitet, Tekniska högskolan.
    Crispin, Xavier
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Fysik och elektroteknik. Linköpings universitet, Tekniska högskolan.
    Ph effect on thermoelectric properties of poly-(3,4-ethylenedioxythiophene):tosylateManuskript (preprint) (Övrigt vetenskapligt)
    Abstract [en]

    Abstract not available.

  • 66.
    Bubnova, Olga
    et al.
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Fysik och elektroteknik. Linköpings universitet, Tekniska högskolan.
    Berggren, Magnus
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Fysik och elektroteknik. Linköpings universitet, Tekniska högskolan.
    Crispin, Xavier
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Fysik och elektroteknik. Linköpings universitet, Tekniska högskolan.
    Tuning the Thermoelectric Properties of Conducting Polymers in an Electrochemical Transistor2012Ingår i: Journal of the American Chemical Society, ISSN 0002-7863, E-ISSN 1520-5126, Vol. 134, nr 40, s. 16456-16459Artikel i tidskrift (Refereegranskat)
    Abstract [en]

    While organic field-effect transistors allow the investigation of interfacial charge transport at the semiconductor-dielectric interface, an electrochemical transistor truly modifies the oxidation level and conductivity throughout the bulk of an organic semiconductor. In this work, the thermoelectric properties of the bulk of the conducting polymer poly(3,4-ethylenedioxythiophene) -poly(styrene sulfonate) were controlled electrically by varying the gate voltage. In light of the growing interest in conducting polymers as thermoelectric generators, this method provides an easy tool to study the physics behind the thermoelectric properties and to optimize polymer thermoelectrics.

  • 67.
    Bubnova, Olga
    et al.
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Fysik och elektroteknik. Linköpings universitet, Tekniska högskolan.
    Khan, Zia Ullah
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Fysik och elektroteknik. Linköpings universitet, Tekniska högskolan.
    Wang, Hui
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Fysik och elektroteknik. Linköpings universitet, Tekniska högskolan.
    Braun, Slawomir
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Ytors Fysik och Kemi. Linköpings universitet, Tekniska högskolan.
    Evans, Drew R
    University of South Australia, Mawson Institute, Mawson Lakes 5095, Australia.
    Fabretto, Manrico
    University of South Australia, Mawson Institute, Mawson Lakes 5095, Australia.
    Hojati-Talemi, Pejman
    University of South Australia, Mawson Institute, Mawson Lakes 5095, Australia.
    Dagnelund, Daniel
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Funktionella elektroniska material. Linköpings universitet, Tekniska högskolan.
    Arlin, Jean-Baptiste
    Free University of Brussels, Laboratoire de Chimie des Polymères, CP 206/1, Boulevard du Triomphe, 1050 Bruxelles, Belgium.
    Geerts, Yves H.
    Free University of Brussels, Laboratoire de Chimie des Polymères, CP 206/1, Boulevard du Triomphe, 1050 Bruxelles, Belgium.
    Desbief, Simon
    University of Mons, Laboratoire de chimie des materiaux nouveaux, Place du Parc 20, 7000 Mons, Belgium.
    Breiby, Dag W.
    Norwegian University of Science and Technology (NTNU), Department of Physics, Høgskoleringen 5, 7491 Trondheim, Norway.
    Andreasen, Jens W.
    Technical University of Denmark, Department of Energy Conversion and Storage, Frederiksborgvej 399, 4000 Roskilde, Denmark.
    Lazzaroni, Roberto
    University of Mons, Laboratoire de chimie des materiaux nouveaux, Place du Parc 20, 7000 Mons, Belgium.
    Chen, Weimin
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Funktionella elektroniska material. Linköpings universitet, Tekniska högskolan.
    Zozoulenko, Igor
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Fysik och elektroteknik. Linköpings universitet, Tekniska högskolan.
    Fahlman, Mats
    Linköpings universitet, Institutionen för fysik, kemi och biologi. Linköpings universitet, Tekniska högskolan.
    Murphy, Peter J.
    University of South Australia, Mawson Institute, Mawson Lakes 5095, Australia.
    Berggren, Magnus
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Fysik och elektroteknik. Linköpings universitet, Tekniska högskolan.
    Crispin, Xavier
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Fysik och elektroteknik. Linköpings universitet, Tekniska högskolan.
    Corrigendum: Semi-metallic polymers2014Ingår i: Nature Materials, ISSN 1476-1122, E-ISSN 1476-4660, Vol. 13, s. 662-662Artikel i tidskrift (Refereegranskat)
  • 68.
    Bubnova, Olga
    et al.
    Linköpings universitet, Institutionen för teknik och naturvetenskap. Linköpings universitet, Tekniska högskolan.
    Ullah Khan, Zia
    Linköpings universitet, Institutionen för teknik och naturvetenskap. Linköpings universitet, Tekniska högskolan.
    Malti, Abdellah
    Linköpings universitet, Institutionen för teknik och naturvetenskap. Linköpings universitet, Tekniska högskolan.
    Braun, Slawomir
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Ytors Fysik och Kemi. Linköpings universitet, Tekniska högskolan.
    Fahlman, Mats
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Ytors Fysik och Kemi. Linköpings universitet, Tekniska högskolan.
    Berggren, Magnus
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Fysik och elektroteknik. Linköpings universitet, Tekniska högskolan.
    Crispin, Xavier
    Linköpings universitet, Institutionen för teknik och naturvetenskap. Linköpings universitet, Tekniska högskolan.
    Optimization of the thermoelectric figure of merit in the conducting polymer poly(3,4-ethylenedioxythiophene)2011Ingår i: NATURE MATERIALS, ISSN 1476-1122, Vol. 10, nr 6, s. 429-433Artikel i tidskrift (Refereegranskat)
    Abstract [en]

    Thermoelectric generators (TEGs) transform a heat flow into electricity. Thermoelectric materials are being investigated for electricity production from waste heat (co-generation) and natural heat sources. For temperatures below 200 degrees C, the best commercially available inorganic semiconductors are bismuth telluride (Bi2Te3)-based alloys, which possess a figure of merit ZT close to one(1). Most of the recently discovered thermoelectric materials with ZT andgt; 2 exhibit one common property, namely their low lattice thermal conductivities(2,3). Nevertheless, a high ZT value is not enough to create a viable technology platform for energy harvesting. To generate electricity from large volumes of warm fluids, heat exchangers must be functionalized with TEGs. This requires thermoelectric materials that are readily synthesized, air stable, environmentally friendly and solution processable to create patterns on large areas. Here we show that conducting polymers might be capable of meeting these demands. The accurate control of the oxidation level in poly(3,4-ethylenedioxythiophene) (PEDOT) combined with its low intrinsic thermal conductivity (lambda = D 0.37W m(-1) K-1) yields a ZT = 0.25 at room temperature that approaches the values required for efficient devices.

  • 69.
    Bubnova, Olga
    et al.
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Fysik och elektroteknik. Linköpings universitet, Tekniska högskolan.
    Ullah Khan, Zia
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Fysik och elektroteknik. Linköpings universitet, Tekniska högskolan.
    Wang, Hui
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Fysik och elektroteknik. Linköpings universitet, Tekniska högskolan.
    Braun, Slawomir
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Ytors Fysik och Kemi. Linköpings universitet, Tekniska högskolan.
    Evans, Drew R.
    University of S Australia, Australia .
    Fabretto, Manrico
    University of S Australia, Australia .
    Hojati-Talemi, Pejman
    University of S Australia, Australia .
    Dagnelund, Daniel
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Funktionella elektroniska material. Linköpings universitet, Tekniska högskolan.
    Arlin, Jean-Baptiste
    University of Libre Brussels, Belgium .
    Geerts, Yves H.
    University of Libre Brussels, Belgium .
    Desbief, Simon
    University of Mons, Belgium .
    Breiby, Dag W.
    Norwegian University of Science and Technology NTNU, Norway .
    Andreasen, Jens W.
    Technical University of Denmark, Denmark .
    Lazzaroni, Roberto
    University of Mons, Belgium .
    Chen, Weimin
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Funktionella elektroniska material. Linköpings universitet, Tekniska högskolan.
    Zozoulenko, Igor
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Fysik och elektroteknik. Linköpings universitet, Tekniska högskolan.
    Fahlman, Mats
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Ytors Fysik och Kemi. Linköpings universitet, Tekniska högskolan.
    Murphy, Peter J.
    University of S Australia, Australia .
    Berggren, Magnus
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Fysik och elektroteknik. Linköpings universitet, Tekniska högskolan.
    Crispin, Xavier
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Fysik och elektroteknik. Linköpings universitet, Tekniska högskolan.
    Semi-metallic polymers2014Ingår i: Nature Materials, ISSN 1476-1122, E-ISSN 1476-4660, Vol. 13, nr 2, s. 190-194Artikel i tidskrift (Refereegranskat)
    Abstract [en]

    Polymers are lightweight, flexible, solution-processable materials that are promising for low-cost printed electronics as well as for mass-produced and large-area applications. Previous studies demonstrated that they can possess insulating, semiconducting or metallic properties; here we report that polymers can also be semi-metallic. Semi-metals, exemplified by bismuth, graphite and telluride alloys, have no energy bandgap and a very low density of states at the Fermi level. Furthermore, they typically have a higher Seebeck coefficient and lower thermal conductivities compared with metals, thus being suitable for thermoelectric applications. We measure the thermoelectric properties of various poly( 3,4-ethylenedioxythiophene) samples, and observe a marked increase in the Seebeck coefficient when the electrical conductivity is enhanced through molecular organization. This initiates the transition from a Fermi glass to a semi-metal. The high Seebeck value, the metallic conductivity at room temperature and the absence of unpaired electron spins makes polymer semi-metals attractive for thermoelectrics and spintronics.

  • 70.
    Bubnova, Olga
    et al.
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Fysik och elektroteknik. Linköpings universitet, Tekniska högskolan.
    Ullah Khan, Zia
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Fysik och elektroteknik. Linköpings universitet, Tekniska högskolan.
    Wang, Hui
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Fysik och elektroteknik. Linköpings universitet, Tekniska högskolan.
    Dagnelund, Daniel
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Funktionella elektroniska material. Linköpings universitet, Tekniska högskolan.
    Arlin, Jean-Baptiste
    Free University of Brussels Laboratoire de Chimie des Polymères, Bruxelles, Belgium.
    Geerts, Yves
    Free University of Brussels Laboratoire de Chimie des Polymères, Bruxelles, Belgium.
    Desbief, Simon
    University of Mons Laboratoire de chimie des materiaux nouveaux, Mons, Belgium.
    Breiby, Dag W.
    Department of Physics, Norwegian University of Science and Technology (NTNU), Trondheim, Norway.
    Andreasen, Jens W.
    Imaging and Structural Analysis Programme, Department of Energy Conversion and Storage, Technical University of Denmark, Roskilde, Denmark.
    Lazzaroni, Roberto
    University of Mons Laboratoire de chimie des materiaux nouveaux, Mons, Belgium.
    Zozoulenko, Igor
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Fysik och elektroteknik. Linköpings universitet, Tekniska högskolan.
    Berggren, Magnus
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Fysik och elektroteknik. Linköpings universitet, Tekniska högskolan.
    Crispin, Xavier
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Fysik och elektroteknik. Linköpings universitet, Tekniska högskolan.
    Advantageous thermoelectric properties of a semimetallic polymerManuskript (preprint) (Övrigt vetenskapligt)
    Abstract [en]

    Thermoelectric generation potentially holds a solution for waste heat recovery issues provided that the availability of inexpensive, biodegradable and highly efficient thermoelectric materials is insured in the near future. Plastic thermoelectrics could successfully comply with the said requirements if the thermoelectric efficiency (ZT) of conducting polymers was higher. However, given the novelty of the subject, at present there are no clear guidelines for ZT optimization in this class of materials. The most important piece of information that is currently missing is the description of a specific electronic makeup that conducting polymers must possess in order to enable good thermoelectric performance. In the present study the thermoelectric properties of poly(3,4-ethylenedioxythiophene) derivatives with two types of counterions, i.e. poly(styrenesulfonate) (PSS) and tosylate (Tos) are evaluated. A striking variation in their thermoelectric performance is attributed to structural and morphological differences between two polymers that manifest itself in dissimilar charge transport mechanism. The superior properties of PEDOT-Tos presumably originate from a high degree of crystallinity and structural order that predetermines the tendency for bipolaron band formation. Unlike polaronic PEDOT-PSS with slowly varying density of localized states (DOS) near the Fermi level (EF), the DOS in PEDOT-Tos is characterized by higher asymmetry and higher charge carrier density at EF (similar to semimetals), which allows for higher thermopower and electrical conductivity. Therefore, we conclude that the polymers with semimetallic electronic makeup are expected to exhibit promising thermoelectric properties with bigger variation in thermopower upon doping.

  • 71.
    Campana, Alessandra
    et al.
    CNR-ISMN, Bologna, Italy; University of Bologna, Italy .
    Cramer, Tobias
    CNR-ISMN, Bologna, Italy.
    Simon, Daniel
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Fysik och elektroteknik. Linköpings universitet, Tekniska högskolan.
    Berggren, Magnus
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Fysik och elektroteknik. Linköpings universitet, Tekniska högskolan. null.
    Biscarini, Fabio
    CNR-ISMN, Bologna, Italy; University of Modena and Reggio Emilia, Italy .
    Electrocardiographic recording with conformable organic electrochemical transistor fabricated on resorbable bioscaffold2014Ingår i: Advanced Materials, ISSN 0935-9648, E-ISSN 1521-4095, Vol. 26, nr 23, s. 3874-3878Artikel i tidskrift (Refereegranskat)
    Abstract [en]

    Organic electrochemical transistors are fabricated on a poly(L-lactide-co-glycolide) substrate. Fast and sensitive performance of the transistors allows recording of the electrocardiogram. The result paves the way for new types of bioelectronic interfaces with reduced invasiveness due to bioresorption and soft mechanical properties.

  • 72.
    Chaharsoughi, Mina Shiran
    et al.
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Fysik och elektroteknik. Linköpings universitet, Tekniska fakulteten.
    Tordera, Daniel
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Fysik och elektroteknik. Linköpings universitet, Tekniska fakulteten.
    Grimoldi, Andrea
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Fysik och elektroteknik. Linköpings universitet, Tekniska fakulteten.
    Engquist, Isak
    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.
    Fabiano, Simone
    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.
    Hybrid Plasmonic and Pyroelectric Harvesting of Light Fluctuations2018Ingår i: Advanced Optical Materials, ISSN 2162-7568, E-ISSN 2195-1071Artikel i tidskrift (Refereegranskat)
    Abstract [en]

    State-of-the-art solar energy harvesting systems based on photovoltaic technology require constant illumination for optimal operation. However, weather conditions and solar illumination tend to fluctuate. Here, a device is presented that extracts electrical energy from such light fluctuations. The concept combines light-induced heating of gold nanodisks (acting as plasmonic optical nanoantennas), and an organic pyroelectric copolymer film (poly(vinylidenefluoride-co-trifluoroethylene)), that converts temperature changes into electrical signals. This hybrid device can repeatedly generate current pulses, not only upon the onset of illumination, but also when illumination is blocked. Detailed characterization highlights the key role of the polarization state of the copolymer, while the copolymer thickness has minor influence on performance. The results are fully consistent with plasmon-assisted pyroelectric effects, as corroborated by combined optical and thermal simulations that match the experimental results. Owing to the tunability of plasmonic resonances, the presented concept is compatible with harvesting near infrared light while concurrently maintaining visible transparency.

  • 73.
    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 Storage2019Ingår i: Advanced Sustainable Systems, ISSN 2366-7486, Vol. 3, nr 9, artikel-id 1900039Artikel i tidskrift (Refereegranskat)
    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.

  • 74.
    Chen, Miaoxiang
    et al.
    Linköpings universitet, Tekniska högskolan. Linköpings universitet, Institutionen för teknik och naturvetenskap.
    Berggren, Magnus
    Linköpings universitet, Tekniska högskolan. Linköpings universitet, Institutionen för teknik och naturvetenskap.
    Printed electrochemical diodes based on conducting polymers2002Ingår i: E-MRS,2003, 2002Konferensbidrag (Refereegranskat)
  • 75.
    Chen, Miaoxiang
    et al.
    Linköpings universitet, Tekniska högskolan. Linköpings universitet, Institutionen för teknik och naturvetenskap. null.
    Berggren, Magnus
    Linköpings universitet, Tekniska högskolan. Linköpings universitet, Institutionen för teknik och naturvetenskap. null.
    Printed low-pass organic filters2003Ingår i: Polytronic,2003, 2003Konferensbidrag (Refereegranskat)
  • 76.
    Chen, Miaoxiang
    et al.
    Linköpings universitet, Tekniska högskolan. Linköpings universitet, Institutionen för teknik och naturvetenskap.
    Berggren, Magnus
    Linköpings universitet, Tekniska högskolan. Linköpings universitet, Institutionen för teknik och naturvetenskap.
    Remonen, Tommie
    Acreo AB, Norrköping.
    Kugler, Thomas
    Acreo AB, Norrköping.
    Robertsson, Mats
    Linköpings universitet, Tekniska högskolan. Linköpings universitet, Institutionen för teknik och naturvetenskap.
    Electrochemically Organic Rectifying Diodes Based on Flexible Substrates2003Ingår i: Material Research Society Spring Meeting,2003, 2003Konferensbidrag (Refereegranskat)
  • 77.
    Chen, Miaoxiang
    et al.
    Linköpings universitet, Institutionen för teknik och naturvetenskap. Linköpings universitet, Tekniska högskolan.
    Crispin, Xavier
    Linköpings universitet, Institutionen för teknik och naturvetenskap. Linköpings universitet, Tekniska högskolan.
    Perzon, Erik
    Department of Materials and Surface Chemistry, Polymer Technology, Chalmers University of Technology, Göteborg, Sweden .
    Andersson, Mats R
    Department of Materials and Surface Chemistry, Polymer Technology, Chalmers University of Technology, Göteborg, Sweden .
    Pullerits, Tönu
    Department of Chemical Physics, Lund University, Lund, Sweden .
    Andersson, Mattias
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biomolekylär och Organisk Elektronik. Linköpings universitet, Tekniska högskolan.
    Inganäs, Olle
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biomolekylär och Organisk Elektronik. Linköpings universitet, Tekniska högskolan.
    Berggren, Magnus
    Linköpings universitet, Institutionen för teknik och naturvetenskap. Linköpings universitet, Tekniska högskolan.
    High carrier mobility in low band gap polymer-based field-effect transistors2005Ingår i: Applied Physics Letters, ISSN 0003-6951, E-ISSN 1077-3118, Vol. 87, nr 25, s. 252105-1-252105-3Artikel i tidskrift (Refereegranskat)
    Abstract [en]

    A conjugated polymer with a low band gap of 1.21 eV, i.e., absorbing infrared light, is demonstrated as active material in field-effect transistors (FETs). The material consists of alternating fluorene units and low band gap segments with electron donor-acceptor-donor units composed of two electron-donating thiophene rings attached on both sides of a thiadiazolo-quinoxaline electron-acceptor group. The polymer is solution-processable and air-stable; the resulting FETs exhibit typical p-channel characteristics and field-effect mobility of 0.03 cm2 V−1 s−1.

  • 78.
    Chen, Miaoxiang
    et al.
    Linköpings universitet, Institutionen för teknik och naturvetenskap. Linköpings universitet, Tekniska högskolan.
    Nilsson, David
    Linköpings universitet, Institutionen för teknik och naturvetenskap. Linköpings universitet, Tekniska högskolan.
    Kugler, Thomas
    Linköpings universitet, Institutionen för teknik och naturvetenskap. Linköpings universitet, Tekniska högskolan.
    Berggren, Magnus
    Linköpings universitet, Institutionen för teknik och naturvetenskap. Linköpings universitet, Tekniska högskolan.
    Remonen, Tommie
    Acreo AB, Norrköping, Sweden.
    Electric current rectification by an all-organic electrochemical device2002Ingår i: Applied Physics Letters, ISSN 0003-6951, E-ISSN 1077-3118, Vol. 81, s. 2011-2013Artikel i tidskrift (Refereegranskat)
    Abstract [en]

    An all-organic printed electrochemical rectifier is reported. The device is based on a patterned layer of poly(3,4-ethylenedioxythiophene) poly(styrene sulfonate) (PEDOT:PSS) that interfaces a patterned electrolyte top layer. Overlap between the electrolyte layer and the conducting polymer pattern results in the formation of two electrochemically active areas within the conducting polymer pattern. When bias voltage is applied across the conducting polymer pattern, the PEDOT in the negatively biased areas is reduced electrochemically, while the PEDOT in the positively biased area is further oxidized. Reducing PEDOT from its p-doped, pristine state to the neutral state results in a marked loss of electrical conductivity. Due to the unsymmetrical device geometry, the current through the device may be shut off for one polarity of applied bias voltage with an electrical current rectification ratio of 100 compared to the opposite polarity. The output characteristics of a corresponding half wave rectifier as well as those from a full wave bridge rectifier show stable performance at frequencies below 15 Hz.

  • 79.
    Chen, Miaoxiang
    et al.
    Linköpings universitet, Institutionen för teknik och naturvetenskap. Linköpings universitet, Tekniska högskolan.
    Perzon, E.
    Materials and Surface Chemistry, Chalmers University of Technology, Göteborg, Sweden.
    Robinson, Nathaniel D
    Linköpings universitet, Institutionen för teknik och naturvetenskap. Linköpings universitet, Tekniska högskolan.
    Jönsson, Stina
    Linköpings universitet, Institutionen för teknik och naturvetenskap. Linköpings universitet, Tekniska högskolan.
    Andersson, Mike
    Materials and Surface Chemistry, Chalmers University of Technology, Göteborg, Sweden.
    Fahlman, Mats
    Linköpings universitet, Institutionen för teknik och naturvetenskap. Linköpings universitet, Tekniska högskolan.
    Berggren, Magnus
    Linköpings universitet, Institutionen för teknik och naturvetenskap. Linköpings universitet, Tekniska högskolan.
    Low band gap donor–acceptor–donor polymers for infra-red electroluminescence and transistors2004Ingår i: Synthetic metals, ISSN 0379-6779, E-ISSN 1879-3290, Vol. 146, nr 3, s. 233-236Artikel i tidskrift (Refereegranskat)
    Abstract [en]

    We report on transistors and light-emitting diodes using a conjugated polymer consisting of alternated segments of fluorene units and low-band gap donor–acceptor–donor (D–A–D) units. The D–A–D segment includes two electron-donating thiophene rings combined with a thiadiazolo-quinoxaline unit, which is electron withdrawing to its nature. The resulting polymer is conjugated and has a band gap of around 1.27 eV. Here we present the corresponding electro- and photoluminescence spectra, which both peak at approximately 1 μm. Single layer light-emitting diodes demonstrated external quantum efficiencies from 0.03% to 0.05%. The polymer was employed as active material in thin film transistors, a field-effect mobility of 3 × 10−3 cm2/V s and current on/off ratio of 104 were achieved at ambient atmosphere.

  • 80.
    Chen, Miaoxiang
    et al.
    Linköpings universitet, Institutionen för teknik och naturvetenskap. Linköpings universitet, Tekniska högskolan.
    Perzon, Erik
    Materials and Surface Chemistry, Chalmers University of Technology, Göteborg, Sweden .
    Andersson, Mats R.
    Materials and Surface Chemistry, Chalmers University of Technology, Göteborg, Sweden .
    Marcinkevicius, Saulius
    Department of Microelectronics and Information Technology, Royal Institute of Technology, Kista, Sweden .
    Jönsson, Stina
    Linköpings universitet, Institutionen för teknik och naturvetenskap. Linköpings universitet, Tekniska högskolan.
    Fahlman, Mats
    Linköpings universitet, Institutionen för teknik och naturvetenskap. Linköpings universitet, Tekniska högskolan.
    Berggren, Magnus
    Linköpings universitet, Institutionen för teknik och naturvetenskap. Linköpings universitet, Tekniska högskolan.
    1 micron wavelength photo- and electroluminescence from a conjugated polymer2004Ingår i: Applied Physics Letters, ISSN 0003-6951, E-ISSN 1077-3118, Vol. 84, nr 18, s. 3570-3572Artikel i tidskrift (Refereegranskat)
    Abstract [en]

    We report photo- and electroluminescence from an alternating conjugated polymer consisting of fluorene units and low-band gap donor-acceptor-donor (D–A–D) units. The D–A–D segment includes two electron-donating thiophene rings combined with a thiadiazolo-quinoxaline unit, which is electron withdrawing to its nature. The resulting polymer is conjugated and has a band gap of 1.27 eV. The corresponding electro- and photoluminescence spectra both peak at approximately 1 μm. Light-emitting diodes, based on a single layer of the polymer, demonstrated external quantum efficiencies from 0.03% to 0.05%.

  • 81.
    Cherian, Dennis
    et al.
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Laboratoriet för organisk elektronik. Linköpings universitet, Tekniska fakulteten.
    Armgarth, Astrid
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Laboratoriet för organisk elektronik. Linköpings universitet, Tekniska fakulteten.
    Beni, Valerio
    Res Inst Sweden, Sweden.
    Linderhed, Ulrika
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Laboratoriet för organisk elektronik. Linköpings universitet, Tekniska fakulteten. Res Inst Sweden, Sweden.
    Tybrandt, Klas
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Fysik och elektroteknik. Linköpings universitet, Tekniska fakulteten.
    Nilsson, David
    Res Inst Sweden, Sweden.
    Simon, Daniel
    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.
    Large-area printed organic electronic ion pumps2019Ingår i: FLEXIBLE AND PRINTED ELECTRONICS, ISSN 2058-8585, Vol. 4, nr 2, artikel-id 022001Artikel i tidskrift (Refereegranskat)
    Abstract [en]

    Biological systems use a large variety of ions and molecules of different sizes for signaling. Precise electronic regulation of biological systems therefore requires an interface which translates the electronic signals into chemically specific biological signals. One technology for this purpose that has been developed during the last decade is the organic electronic ion pump (OEIP). To date, OEIPs have been fabricated by micropatterning and labor-intensive manual techniques, hindering the potential application areas of this promising technology. Here we show, for the first time, fully screen-printed OEIPs. We demonstrate a large-area printed design with manufacturing yield amp;gt;90%. Screen-printed cation- and anion-exchange membranes are both demonstrated with promising ion selectivity and performance, with transport verified for both small ions (Na+,K+,Cl-) and biologically-relevant molecules (the cationic neurotransmitter acetylcholine, and the anionic anti-inflammatory salicylic acid). These advances open the iontronics toolbox to the world of printed electronics, paving the way for a broader arena for applications.

  • 82.
    Cotrone, Serafina
    et al.
    Università di Bari “Aldo Moro”.
    Ambrico, Marianna
    CNR-IMIP.
    Toss, Henrik
    Linköpings universitet, Institutionen för teknik och naturvetenskap. Linköpings universitet, Tekniska högskolan.
    Angione, M. Daniela
    Università di Bari “Aldo Moro”.
    Magliulo, Maria
    Università di Bari “Aldo Moro”.
    Mallardi, Antonia
    CNR-IPCF.
    Berggren, Magnus
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Fysik och elektroteknik. Linköpings universitet, Tekniska högskolan.
    Palazzo, Gerardo
    Università di Bari “Aldo Moro”.
    Horowitz, Gilles
    University Paris Diderot.
    Ligonzo, Teresa
    Università di Bari “Aldo Moro”.
    Torsi, Luisa
    Università di Bari “Aldo Moro”.
    Phospholipid film in electrolyte-gated organic field-effect transistors2012Ingår i: Organic electronics, ISSN 1566-1199, E-ISSN 1878-5530, Vol. 13, nr 4, s. 638-644Artikel i tidskrift (Refereegranskat)
    Abstract [en]

    A totally innovative electrolyte-gated field effect transistor, embedding a phospholipid film at the interface between the organic semiconductor and the gating solution, is described. The electronic properties of OFETs including a phospholipid film are studied in both pure water and in an electrolyte solution and compared to those of an OFET with the organic semiconductor directly in contact with the gating solution. In addition, to investigate the role of the lipid layers in the charge polarization process and quantify the field-effect mobility, impedance spectroscopy was employed. The results indicate that the integration of the biological film minimizes the penetration of ions into the organic semiconductor thus leading to a capacitive operational mode as opposed to an electrochemical one. The OFETs operate at low voltages with a field-effect mobility in the 10−3 cm2 V−1 s−1 range and an on/off current ratio of 103. This achievement opens perspectives to the development of FET biosensors potentially capable to operate in direct contact with physiological fluids.

  • 83.
    Crispin, Annica
    et al.
    Linköpings universitet, Tekniska högskolan. Linköpings universitet, Institutionen för fysik, kemi och biologi, Ytors Fysik och Kemi.
    Crispin, Xavier
    Linköpings universitet, Tekniska högskolan. Linköpings universitet, Institutionen för teknik och naturvetenskap.
    Fahlman, Mats
    Linköpings universitet, Tekniska högskolan. Linköpings universitet, Institutionen för teknik och naturvetenskap.
    Berggren, Magnus
    Linköpings universitet, Tekniska högskolan. Linköpings universitet, Institutionen för teknik och naturvetenskap.
    Salaneck, William R
    Linköpings universitet, Tekniska högskolan. Linköpings universitet, Institutionen för fysik, kemi och biologi, Ytors Fysik och Kemi.
    Transition between energy level alignment regimes at a low band gap polymer-electrode interfaces2006Ingår i: Applied Physics Letters, ISSN 0003-6951, E-ISSN 1077-3118, Vol. 89, nr 21Artikel i tidskrift (Refereegranskat)
    Abstract [en]

    The energy level alignment at interfaces between a low band gap conjugated polymer and various electrodes is investigated using ultraviolet photoemission spectroscopy. When the electrode work function is lower (higher) than the negative (positive) polaronic level of the polymer, the Fermi level is pinned to the negative (positive) polaronic level. These Fermi level pinning regimes suggest a spontaneous electron transfer from or towards the electrode resulting in an interfacial dipole of different orientation. On the contrary, when the substrate work function is intermediate, there is no charge transfer and the energy level alignment across the interface follows the Schottky-Mott limit. © 2006 American Institute of Physics.

  • 84.
    Crispin, Xavier
    et al.
    Linköpings universitet, Tekniska högskolan. Linköpings universitet, Institutionen för teknik och naturvetenskap.
    Andersson, Peter
    Linköpings universitet, Tekniska högskolan. Linköpings universitet, Institutionen för teknik och naturvetenskap.
    Robinson, Nathaniel D
    Linköpings universitet, Tekniska högskolan. Linköpings universitet, Institutionen för teknik och naturvetenskap.
    Olivier, Yoann
    Laboratory for Chemistry of Novel Materials, Université de Mons. Mons, Belgium.
    Cornil, Jerome
    Belgian National Fund for Scientific Research (FNRS), Université de Mons. Mons, Belgium.
    Berggren, Magnus
    Linköpings universitet, Tekniska högskolan. Linköpings universitet, Institutionen för teknik och naturvetenskap.
    Photochromic Diodes2006Ingår i: Semiconducting Polymers: chemistry, physics and engineering. Vol. 2 / [ed] Georges Hadziioannou, George Malliaras, Weinheim, Tyskland: WileyVCH Verlag GmbH & Co , 2006, 2, s. 579-611Kapitel i bok, del av antologi (Övrigt vetenskapligt)
    Abstract [en]

      The field of semiconducting polymers has attracted many researchers from a diversity of disciplines. Printed circuitry, flexible electronics and displays are already migrating from laboratory successes to commercial applications, but even now fundamental knowledge is deficient concerning some of the basic phenomena that so markedly influence a device's usefulness and competitiveness. This two-volume handbook describes the various approaches to doped and undoped semiconducting polymers taken with the aim to provide vital understanding of how to control the properties of these fascinating organic materials. Prominent researchers from the fields of synthetic chemistry, physical chemistry, engineering, computational chemistry, theoretical physics, and applied physics cover all aspects from compounds to devices.Since the first edition was published in 2000, significant findings and successes have been achieved in the field, and especially handheld electronic gadgets have become billion-dollar markets that promise a fertile application ground for flexible, lighter and disposable alternatives to classic silicon circuitry. The second edition brings readers up-to-date on cutting edge research in this field.

  • 85.
    Crispin, Xavier
    et al.
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Fysik och elektroteknik. Linköpings universitet, Tekniska högskolan.
    Herlogsson, Lars
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Fysik och elektroteknik. Linköpings universitet, Tekniska högskolan.
    Larsson, Oscar
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Fysik och elektroteknik. Linköpings universitet, Tekniska högskolan.
    Said, Elias
    Royal Institute of Technology, Stockholm, Sweden.
    Berggren, Magnus
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Fysik och elektroteknik. Linköpings universitet, Tekniska högskolan.
    Polyelectrolyte-Gated Organic Field-Effect Transistors2010Ingår i: Iontronics: Ionic Carriers in Organic Electronic Materials and Devices / [ed] Janell Leger, Magnus Berggren, Sue Carter, Boca Raton: CRC Press; Taylor & Francis Group , 2010, s. 193-218Kapitel i bok, del av antologi (Övrigt vetenskapligt)
    Abstract [en]

    The field of organic electronics promises exciting new technologies based on inexpensive and mechanically flexible electronic devices. It has progressed over the past three decades to the point of commercial viability and is projected to grow to a 30 billion dollar market by the year 2015. Exploring new applications and device architectures, this book sets the tone for that exploration, gathering a community of experts in this area who are focused on the use of ionic functions to define the principle of operation in polymer devices. The contributors detail relevant technologies based on organic electronics, including polymer electrochromic devices and light-emitting electrochemical cells.

  • 86.
    Crispin, Xavier
    et al.
    Linköpings universitet, Tekniska högskolan. Linköpings universitet, Institutionen för teknik och naturvetenskap.
    Jakobsson, Fredrik
    Linköpings universitet, Tekniska högskolan. Linköpings universitet, Institutionen för teknik och naturvetenskap.
    Crispin, Annica
    Linköpings universitet, Tekniska högskolan. Linköpings universitet, Institutionen för fysik, kemi och biologi, Ytors Fysik och Kemi.
    Grim, P.C.M.
    KUL, Belgien.
    Andersson, Peter
    Linköpings universitet, Tekniska högskolan. Linköpings universitet, Institutionen för teknik och naturvetenskap.
    Volodin, A.
    KUL, Belgien.
    van Haesendonch, C.
    KUL, Belgien.
    van der Auweraer, M.
    KUL, Belgien.
    Salaneck, William R
    Linköpings universitet, Tekniska högskolan. Linköpings universitet, Institutionen för fysik, kemi och biologi, Ytors Fysik och Kemi.
    Berggren, Magnus
    Linköpings universitet, Tekniska högskolan. Linköpings universitet, Institutionen för teknik och naturvetenskap.
    The origin of the high conductivity of poly(3,4-ethylenedioxythiophene)- poly(styrenesulfonate) (PEDOT-PSS) plastic electrodes2006Ingår i: Chemistry of Materials, ISSN 0897-4756, E-ISSN 1520-5002, Vol. 18, nr 18, s. 4354-4360Artikel i tidskrift (Refereegranskat)
    Abstract [en]

    The development of printed and flexible (opto)electronics requires specific materials for the device's electrodes. Those materials must satisfy a combination of properties. They must be electrically conducting, transparent, printable, and flexible. The conducting polymer poly(3,4-ethylenedioxythiophene) - poly-(styrenesulfonate) (PEDOT-PSS) is known as a promising candidate. Its conductivity can be increased by 3 orders of magnitude by the secondary dopant diethylene glycol (DEG). This "secondary doping" phenomenon is clarified in a combined photoelectron spectroscopy and scanning probe microscopy investigation. PEDOT-PSS appears to form a three-dimensional conducting network explaining the improvement of its electrical property upon addition of DEG. Polymer light emitting diodes are successfully fabricated using the transparent plastic PEDOT-PSS electrodes instead of the traditionally used indium tin oxide. © 2006 American Chemical Society.

  • 87.
    del Pozo, Freddy G.
    et al.
    Institute Ciencia Mat Barcelona ICMAB CSIC, Spain; Networking Research Centre Bioengn Biomat and Nanomed CIBER, Spain.
    Fabiano, Simone
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Fysik och elektroteknik. Linköpings universitet, Tekniska fakulteten.
    Pfattner, Raphael
    Institute Ciencia Mat Barcelona ICMAB CSIC, Spain; Networking Research Centre Bioengn Biomat and Nanomed CIBER, Spain.
    Georgakopoulos, Stamatis
    Institute Ciencia Mat Barcelona ICMAB CSIC, Spain; Networking Research Centre Bioengn Biomat and Nanomed CIBER, Spain.
    Galindo, Sergi
    Institute Ciencia Mat Barcelona ICMAB CSIC, Spain; Networking Research Centre Bioengn Biomat and Nanomed CIBER, Spain.
    Liu, Xianjie
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Ytors Fysik och Kemi. Linköpings universitet, Tekniska fakulteten.
    Braun, Slawomir
    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.
    Veciana, Jaume
    Institute Ciencia Mat Barcelona ICMAB CSIC, Spain; Networking Research Centre Bioengn Biomat and Nanomed CIBER, Spain.
    Rovira, Concepcio
    Institute Ciencia Mat Barcelona ICMAB CSIC, Spain; Networking Research Centre Bioengn Biomat and Nanomed CIBER, Spain.
    Crispin, Xavier
    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.
    Mas-Torrent, Marta
    Institute Ciencia Mat Barcelona ICMAB CSIC, Spain; Networking Research Centre Bioengn Biomat and Nanomed CIBER, Spain.
    Single Crystal-Like Performance in Solution-Coated Thin-Film Organic Field-Effect Transistors2016Ingår i: Advanced Functional Materials, ISSN 1616-301X, E-ISSN 1616-3028, Vol. 26, nr 14, s. 2379-2386Artikel i tidskrift (Refereegranskat)
    Abstract [en]

    In electronics, the field-effect transistor (FET) is a crucial cornerstone and successful integration of this semiconductor device into circuit applications requires stable and ideal electrical characteristics over a wide range of temperatures and environments. Solution processing, using printing or coating techniques, has been explored to manufacture organic field-effect transistors (OFET) on flexible carriers, enabling radically novel electronics applications. Ideal electrical characteristics, in organic materials, are typically only found in single crystals. Tiresome growth and manipulation of these hamper practical production of flexible OFETs circuits. To date, neither devices nor any circuits, based on solution-processed OFETs, has exhibited an ideal set of characteristics similar or better than todays FET technology based on amorphous silicon. Here, bar-assisted meniscus shearing of dibenzo-tetrathiafulvalene to coat-process self-organized crystalline organic semiconducting domains with high reproducibility is reported. Including these coatings as the channel in OFETs, electric field and temperature-independent charge carrier mobility and no bias stress effects are observed. Furthermore, record-high gain in OFET inverters and exceptional operational stability in both air and water are measured.

  • 88.
    Derek, Vedran
    et al.
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Fysik och elektroteknik. Linköpings universitet, Tekniska fakulteten.
    Jakesova, Marie
    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.
    Simon, Daniel
    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.
    Micropatterning of organic electronic materials using a facile aqueous photolithographic process2018Ingår i: AIP Advances, ISSN 2158-3226, E-ISSN 2158-3226, Vol. 8, nr 10, artikel-id 105116Artikel i tidskrift (Refereegranskat)
    Abstract [en]

    Patterning organic semiconductors via traditional solution-based microfabrication techniques is precluded by undesired interactions between processing solvents and the organic material. Herein we show how to avoid these problems easily and introduce a simple lift-off method to pattern organic semiconductors. Positive tone resist is deposited on the substrate, followed by conventional exposure and development. After deposition of the organic semiconductor layer, the remaining photoresist is subjected to a flood exposure, rendering it developable. Lift-off is then performed using the same aqueous developer as before. We find that the aqueous developers do not compromise the integrity of the organic layer or alter its electronic performance. We utilize this technique to pattern four different organic electronic materials: epindo-lidione (EPI), a luminescent semiconductor, p-n photovoltaic bilayers of metal-free phthalocyanine and N, N-dimethyltetracarboxylic diimide, and finally the archetypical conducting polymer poly(3,4-ethylenedioxythiophene) (PEDOT). The result of our efforts is a facile method making use of well-established techniques that can be added to the toolbox of research and industrial scientists developing organic electronics technology. (c) 2018 Author(s).

  • 89.
    Diacci, Chiara
    et al.
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Laboratoriet för organisk elektronik. Linköpings universitet, Tekniska fakulteten.
    Lee, Jee Woong
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Laboratoriet för organisk elektronik. Linköpings universitet, Tekniska fakulteten.
    Janson, Per
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Laboratoriet för organisk elektronik. Linköpings universitet, Tekniska fakulteten.
    Dufil, Gwennael
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Laboratoriet för organisk elektronik. Linköpings universitet, Tekniska fakulteten.
    Méhes, Gábor
    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.
    Simon, Daniel
    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.
    Real-Time Monitoring of Glucose Export from Isolated Chloroplasts Using an Organic Electrochemical Transistor2019Ingår i: Advanced Materials Technologies, ISSN 2365-709X, artikel-id 1900262Artikel i tidskrift (Refereegranskat)
    Abstract [en]

    Biosensors based on organic electrochemical transistors (OECT) are attractive devices for real-time monitoring of biological processes. The direct coupling between the channel of the OECT and the electrolyte enables intimate interfacing with biological environments at the same time bringing signal amplification and fast sensor response times. So far, these devices are mainly applied to mammalian systems; cells or body fluids for the development of diagnostics and various health status monitoring technology. Yet, no direct detection of biomolecules from cells or organelles is reported. Here, an OECT glucose sensor applied to chloroplasts, which are the plant organelles responsible for the light-to-chemical energy conversion of the photosynthesis, is reported. Real-time monitoring of glucose export from chloroplasts in two distinct metabolic phases is demonstrated and the transfer dynamics with a time resolution of 1 min is quantified, thus reaching monitoring dynamics being an order of magnitude better than conventional methods.

  • 90.
    Dodabalapur, A
    et al.
    Bell Laboratories, Murray Hill, USA.
    Berggren, Magnus
    Bell Laboratories, Murray Hill, USA.
    Slusher, RE
    ATandT Bell Labs, Lucent Technology, Murray Hill, NJ 07974 USA; .
    Bao, Z
    Bell Laboratories, Murray Hill, USA.
    Timko, A
    Bell Laboratories, Murray Hill, USA.
    Schiortino, P
    Bell Laboratories, Murray Hill, USA.
    Laskowski, E
    Bell Laboratories, Murray Hill, USA.
    Katz, HE
    Bell Laboratories, Murray Hill, USA.
    Nalamasu, O
    Bell Laboratories, Murray Hill, USA.
    Resonators and materials for organic lasers based on energy transfer1998Ingår i: IEEE Journal of Selected Topics in Quantum Electronics, ISSN 1077-260X, E-ISSN 1558-4542, Vol. 4, nr 1, s. 67-74Artikel i tidskrift (Refereegranskat)
    Abstract [en]

    Optically pumped lasers have been fabricated with organic/polymeric materials capable of charge transport. The active materials employed are doped films with small molecule hosts and dye, oligomer, and conjugated polymer emitters, In these materials, the excited states created in the host are transferred nonradiatively to the guest molecules which are the emitters, This energy transfer results in very low absorption losses at the emission wavelength and relatively low-threshold powers for the onset of stimulated emission. Such gain media have been successfully included in many types of resonators including whispering-gallery mode, photonic bandgap, and distributed Bragg reflector (DBR) based resonators. A number of novel patterning and fabrication procedures have been developed for organic-based lasers.

  • 91.
    Dodabalapur, A.
    et al.
    Bell Laboratories, Murray Hill, NJ, USA.
    Chandross, E. A.
    Bell Laboratories, Murray Hill, NJ, USA.
    Berggren, Magnus
    Bell Laboratories, Murray Hill, NJ, USA.
    Slusher, R. E.
    Bell Laboratories, Murray Hill, NJ, USA.
    Applied physics - Organic solid-state lasers: Past and future1997Ingår i: Science, ISSN 0036-8075, E-ISSN 1095-9203, Vol. 277, nr 5333, s. 1787-1788Artikel i tidskrift (Övrigt vetenskapligt)
    Abstract [en]

    Researchers around the world are seeking organic materials that can be made into practical and efficient lasers. In their Perspective, Dodabalapur et al. review the past history and future prospects of this important class of laser materials.                                            

  • 92.
    Dyreklev, Peter
    et al.
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Tillämpad Fysik. Linköpings universitet, Tekniska högskolan. null.
    Berggren, Magnus
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Tillämpad Fysik. Linköpings universitet, Tekniska högskolan. null.
    Inganäs, Olle
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Tillämpad Fysik. Linköpings universitet, Tekniska högskolan. null.
    Andersson, Mats R.
    Chalmers Tekniska Högskola.
    Wennerström, Olof
    Chalmers Tekniska Högskola.
    Hjertberg, Thomas
    Chalmers Tekniska Högskola.
    Polarized electroluminescence from an oriented substituted polythiophene in a light emitting diode1995Ingår i: Advanced Materials, ISSN 0935-9648, E-ISSN 1521-4095, Vol. 7, nr 1, s. 43-45Artikel i tidskrift (Refereegranskat)
    Abstract [en]

    Polarized light sources based on stretch-oriented conjugated polymers are reported. The devices, based on poly 3(4-octylphenyl)-2,2′-bithiophene, show an external quantum efficiency of 0.1% and are produced using a very simple method which may be easily extended to other polymers. The fabrication of the devices is described and factors such as the emission and spectral differences parallel and prependicular to the stretching direction discussed.

  • 93.
    Edberg, Jesper
    et al.
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Fysik och elektroteknik. Linköpings universitet, Tekniska fakulteten.
    Iandolo, Donata
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Fysik och elektroteknik. Linköpings universitet, Tekniska fakulteten.
    Brooke, Robert
    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.
    Musumeci, Chiara
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biomolekylär och Organisk Elektronik. Linköpings universitet, Tekniska fakulteten.
    Wenzel Andreasen, Jens
    Technical University of Denmark, Denmark.
    Simon, Daniel
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Fysik och elektroteknik. Linköpings universitet, Tekniska fakulteten.
    Evans, Drew
    University of South Australia, Australia.
    Engquist, Isak
    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.
    Patterning and Conductivity Modulation of Conductive Polymers by UV Light Exposure2016Ingår i: Advanced Functional Materials, ISSN 1616-301X, E-ISSN 1616-3028, Vol. 26, nr 38, s. 6950-6960Artikel i tidskrift (Refereegranskat)
    Abstract [en]

    A novel patterning technique of conductive polymers produced by vapor phase polymerization is demonstrated. The method involves exposing an oxidant film to UV light which changes the local chemical environment of the oxidant and subsequently the polymerization kinetics. This procedure is used to control the conductivity in the conjugated polymer poly(3,4-ethylenedioxythiophene): tosylate by more than six orders of magnitude in addition to producing high-resolution patterns and optical gradients. The mechanism behind the modulation in the polymerization kinetics by UV light irradiation as well as the properties of the resulting polymer are investigated.

  • 94.
    Edberg, Jesper
    et al.
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Fysik och elektroteknik. Linköpings universitet, Tekniska fakulteten. RISE Acreo, Sweden.
    Inganäs, Olle
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Biomolekylär och Organisk Elektronik. Linköpings universitet, Tekniska fakulteten.
    Engquist, Isak
    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. Stellenbosch University, South Africa.
    Boosting the capacity of all-organic paper supercapacitors using wood derivatives2018Ingår i: Journal of Materials Chemistry A, ISSN 2050-7488, Vol. 6, nr 1, s. 145-152Artikel i tidskrift (Refereegranskat)
    Abstract [en]

    Printed and flexible organic electronics is a steadily expanding field of research and applications. One of the most attractive features of this technology is the possibility of large area and high throughput production to form low-cost electronics on different flexible substrates. With an increasing demand for sustainable energy production, low-cost and large volume technologies to store high-quality energy become equally important. These devices should be environmentally friendly with respect to their entire life cycle. Supercapacitors and batteries based on paper hold great promise for such applications due to the low cost and abundance of cellulose and other forest-derived components. We report a thick-film paper-supercapacitor system based on cellulose nanofibrils, the mixed ion-electron conducting polymer PEDOT: PSS and sulfonated lignin. We demonstrate that the introduction of sulfonated lignin into the cellulose-conducting polymer system increases the specific capacitance from 110 to 230 F g(-1) and the areal capacitance from 160 mF cm(-2) to 1 F cm(-2). By introducing lignosulfonate also into the electrolyte solution, equilibrium, with respect to the concentration of the redox molecule, was established between the electrode and the electrolyte, thus allowing us to perform beyond 700 charge/discharge cycles with no observed decrease in performance.

  • 95.
    Edberg, Jesper
    et al.
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Fysik och elektroteknik. Linköpings universitet, Tekniska fakulteten.
    Malti, Abdellah
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Fysik och elektroteknik. Linköpings universitet, Tekniska fakulteten.
    Granberg, Hjalmar
    RISE Bioeconomy.
    Hamedi, Mahiar M.
    KTH Royal Institute of Technology.
    Crispin, Xavier
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Fysik och elektroteknik. Linköpings universitet, Tekniska fakulteten.
    Engquist, Isak
    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.
    Electrochemical circuits from ‘cut and stick’ PEDOT:PSS-nanocellulose composite2017Ingår i: Flexible and printed electronics, E-ISSN 2058-8585, Vol. 4, nr 2, artikel-id 045010Artikel i tidskrift (Refereegranskat)
    Abstract [en]

    We report a flexible self-standing adhesive composite made from PEDOT:PSS and nanofibrillated cellulose. The material exhibits good combined mechanical and electrical characteristics(an elastic modulus of 4.4 MPa, and an electrical conductivity of 30 S cm−1 ). The inherent self-adhesiveness of the material enables it to be laminated and delaminated repeatedly to form and reconfigure devices and circuits. This modular property opens the door for a plethora of applications where reconfigurability and ease-of-manufacturing are of prime importance. We also demonstrate a paper composite with ionic conductivity and combine the two materials to construct electrochemical devices, namely transistors, capacitors and diodes with high values of transconductance, charge storage capacity and current rectification. We have further used these devices to construct digital circuits such as NOT, NAND and NOR logic.

  • 96.
    Erdmann, Tim
    et al.
    Leibniz Institute Polymerforschung Dresden eV, Germany; Technical University of Dresden, Germany; Polyera Corp, IL 60077 USA.
    Fabiano, Simone
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Fysik och elektroteknik. Linköpings universitet, Tekniska fakulteten. Polyera Corp, IL 60077 USA.
    Milian-Medina, Begona
    University of Valencia, Spain; Ciudad University of Cantoblanco, Spain.
    Hanifi, David
    Stanford University, CA 94305 USA.
    Chen, Zhihua
    Polyera Corp, IL 60077 USA.
    Berggren, Magnus
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Fysik och elektroteknik. Linköpings universitet, Tekniska fakulteten.
    Gierschner, Johannes
    Ciudad University of Cantoblanco, Spain.
    Salleo, Alberto
    Stanford University, CA 94305 USA.
    Kiriy, Anton
    Leibniz Institute Polymerforschung Dresden eV, Germany; Technical University of Dresden, Germany.
    Voit, Brigitte
    Leibniz Institute Polymerforschung Dresden eV, Germany; Technical University of Dresden, Germany.
    Facchetti, Antonio
    Polyera Corp, IL 60077 USA; Northwestern University, IL 60208 USA; Northwestern University, IL 60208 USA.
    Naphthalenediimide Polymers with Finely Tuned In-Chain pi-Conjugation: Electronic Structure, Film Microstructure, and Charge Transport Properties2016Ingår i: ADVANCED MATERIALS, ISSN 0935-9648, Vol. 28, nr 41, s. 9169-+Artikel i tidskrift (Refereegranskat)
    Abstract [en]

    Naphthalenediimide-based random copolymers (PNDI-TVTx) with different p-conjugated dithienylvinylene (TVT) versus p-nonconjugated dithienylethane (TET) unit ratios (x = 100 -amp;gt; 0%) are investigated. The PNDI-TVTx-transistor electron/hole mobilities are affected differently, a result rationalized by molecular orbital topologies and energies, with hole mobility vanishing but electron mobility decreasing only by approximate to 2.5 times when going from x = 100% to 40%.

  • 97.
    Fabiano, Simone
    et al.
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Fysik och elektroteknik. Linköpings universitet, Tekniska fakulteten.
    Abdollahi Sani, Negar
    Linköpings universitet, Institutionen för teknik och naturvetenskap. Linköpings universitet, Tekniska fakulteten. RISE Acreo, Sweden.
    Kawahara, Jun
    RISE Acreo, Sweden; LINTEC Corp, Japan.
    Kergoat, Loig
    Linköpings universitet, Institutionen för teknik och naturvetenskap. Linköpings universitet, Tekniska fakulteten. Aix Marseille University, France.
    Nissa, Josefin
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Fysik och elektroteknik. Linköpings universitet, Tekniska fakulteten.
    Engquist, Isak
    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.
    Berggren, Magnus
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Fysik och elektroteknik. Linköpings universitet, Tekniska fakulteten.
    Ferroelectric polarization induces electronic nonlinearity in ion-doped conducting polymers2017Ingår i: Science Advances, ISSN 0036-8156, E-ISSN 2375-2548, Vol. 3, nr 6, artikel-id e1700345Artikel i tidskrift (Refereegranskat)
    Abstract [en]

    Poly(3,4-ethylenedioxythiophene): polystyrene sulfonate (PEDOT:PSS) is an organic mixed ion-electron conducting polymer. The PEDOT phase transports holes and is redox-active, whereas the PSS phase transports ions. When PEDOT is redox-switched between its semiconducting and conducting state, the electronic and optical properties of its bulk are controlled. Therefore, it is appealing to use this transition in electrochemical devices and to integrate those into large-scale circuits, such as display or memory matrices. Addressability and memory functionality of individual devices, within these matrices, are typically achieved by nonlinear current-voltage characteristics and bistability-functions that can potentially be offered by the semiconductor-conductor transition of redox polymers. However, low conductivity of the semiconducting state and poor bistability, due to self-discharge, make fast operation and memory retention impossible. We report that a ferroelectric polymer layer, coated along the counter electrode, can control the redox state of PEDOT. The polarization switching characteristics of the ferroelectric polymer, which take place as the coercive field is overcome, introduce desired nonlinearity and bistability in devices that maintain PEDOT in its highly conducting and fast-operating regime. Memory functionality and addressability are demonstrated in ferro-electrochromic display pixels and ferro-electrochemical transistors.

  • 98.
    Fabiano, Simone
    et al.
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Fysik och elektroteknik. Linköpings universitet, Tekniska högskolan.
    Braun, Slawomir
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Ytors Fysik och Kemi. Linköpings universitet, Tekniska högskolan.
    Fahlman, Mats
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Ytors Fysik och Kemi. Linköpings universitet, Tekniska högskolan.
    Crispin, Xavier
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Fysik och elektroteknik. Linköpings universitet, Tekniska högskolan.
    Berggren, Magnus
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Fysik och elektroteknik. Linköpings universitet, Tekniska högskolan.
    Effect of Gate Electrode Work-Function on Source Charge Injection in Electrolyte-Gated Organic Field-Effect Transistors2014Ingår i: Advanced Functional Materials, ISSN 1616-301X, E-ISSN 1616-3028, Vol. 24, nr 5, s. 695-700Artikel i tidskrift (Refereegranskat)
    Abstract [en]

    Systematic investigation of the contact resistance in electrolyte-gated organic field-effect transistors (OFETs) demonstrates a dependence of source charge injection versus gate electrode work function. This analysis reveals contact-limitations at the source metal-semiconductor interface and shows that the contact resistance increases as low work function metals are used as the gate electrode. These findings are attributed to the establishment of a built-in potential that is high enough to prevent the Fermi-level pinning at the metal-organic interface. This results in an unfavorable energetic alignment of the source electrode with the valence band of the organic semiconductor. Since the operating voltage in the electrolyte-gated devices is on the same order as the variation of the work functions, it is possible to tune the contact resistance over more than one order of magnitude by varying the gate metal.

  • 99.
    Fabiano, Simone
    et al.
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Fysik och elektroteknik. Linköpings universitet, Tekniska högskolan.
    Braun, Slawomir
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Ytors Fysik och Kemi. Linköpings universitet, Tekniska högskolan.
    Liu, Xianjie
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Ytors Fysik och Kemi. Linköpings universitet, Tekniska högskolan.
    Weverberghs, Eric
    University of Mons-UMONS, Belgium.
    Gerbaux, Pascal
    University of Mons-UMONS, Belgium.
    Fahlman, Mats
    Linköpings universitet, Institutionen för fysik, kemi och biologi, Ytors Fysik och Kemi. Linköpings universitet, Tekniska högskolan.
    Berggren, Magnus
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Fysik och elektroteknik. Linköpings universitet, Tekniska högskolan.
    Crispin, Xavier
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Fysik och elektroteknik. Linköpings universitet, Tekniska högskolan.
    Poly(ethylene imine) impurities induce n-doping reaction in organic (semi)conductors2014Ingår i: Advanced Materials, ISSN 0935-9648, E-ISSN 1521-4095, Vol. 26, nr 34, s. 6000-6006Artikel i tidskrift (Refereegranskat)
    Abstract [en]

    Volatile impurities contained in polyethyleneimine (PEI), and identified as ethyleneimine dimers and trimers, are reported. These N-based molecules show a strong reducing character, as demonstrated by the change in electrical conductivity of organic (semi) conductors exposed to the PEI vapor. The results prove that electron transfer rather than a dipole effect at the electrode interface is the origin of the work-function modification by the PEI-based layers.

  • 100.
    Fabiano, Simone
    et al.
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Fysik och elektroteknik. Linköpings universitet, Tekniska högskolan.
    Crispin, Xavier
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Fysik och elektroteknik. Linköpings universitet, Tekniska högskolan.
    Berggren, Magnus
    Linköpings universitet, Institutionen för teknik och naturvetenskap, Fysik och elektroteknik. Linköpings universitet, Tekniska högskolan.
    Ferroelectric Polarization Induces Electric Double Layer Bistability in Electrolyte-Gated Field-Effect Transistors2014Ingår i: ACS Applied Materials and Interfaces, ISSN 1944-8244, E-ISSN 1944-8252, Vol. 6, nr 1, s. 438-442Artikel i tidskrift (Refereegranskat)
    Abstract [en]

    The dense surface charges expressed by a ferroelectric polymeric thin film induce ion displacement within a polyelectrolyte layer and vice versa. This is because the density of dipoles along the surface of the ferroelectric thin film and its polarization switching time matches that of the (Helmholtz) electric double layers formed at the ferroelectric/polyelectrolyte and polyelectrolyte/semiconductor interfaces. This combination of materials allows for introducing hysteresis effects in the capacitance of an electric double layer capacitor. The latter is advantageously used to control the charge accumulation in the semiconductor channel of an organic field-effect transistor. The resulting memory transistors can be written at a gate voltage of around 7 V and read out at a drain voltage as low as 50 mV. The technological implication of this large. difference between write and read-out voltages lies in the non-destructive reading of this ferroelectric memory.

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