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Berggren, Magnus, ProfessorORCID iD iconorcid.org/0000-0001-5154-0291
Publications (10 of 284) Show all publications
Wu, Z., Ding, P., Gueskine, V., Boyd, R., Glowacki, E. D., Odén, M., . . . Vagin, M. (2023). Conducting Polymer‐Based e‐Refinery for Sustainable Hydrogen Peroxide Production. ENERGY & ENVIRONMENTAL MATERIALS, Article ID e12551.
Open this publication in new window or tab >>Conducting Polymer‐Based e‐Refinery for Sustainable Hydrogen Peroxide Production
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2023 (English)In: ENERGY & ENVIRONMENTAL MATERIALS, E-ISSN 2575-0356, article id e12551Article in journal (Refereed) Epub ahead of print
Abstract [en]

Electrocatalysis enables the industrial transition to sustainable production of chemicals using abundant precursors and electricity from renewable sources. De-centralized production of hydrogen peroxide (H2O2) from water and oxygen of air is highly desirable for daily life and industry. We report an effective electrochemical refinery (e-refinery) for H2O2 by means of electrocatalysis-controlled comproportionation reaction (2(H)O + O -> 2(HO)), feeding pure water and oxygen only. Mesoporous nickel (II) oxide (NiO) was used as electrocatalyst for oxygen evolution reaction (OER), producing oxygen at the anode. Conducting polymer poly(3,4-ethylenedioxythiophene): poly(styrene sulfonate) (PEDOT:PSS) drove the oxygen reduction reaction (ORR), forming H2O2 on the cathode. The reactions were evaluated in both half-cell and device configurations. The performance of the H2O2 e-refinery, assembled on anion-exchange solid electrolyte and fed with pure water, was limited by the unbalanced ionic transport. Optimization of the operation conditions allowed a conversion efficiency of 80%.

Place, publisher, year, edition, pages
Wiley-Blackwell, 2023
Keywords
conducting polymer; hydrogen peroxide; nickel (II) oxide; oxygen evolution reaction; oxygen reduction reaction
National Category
Materials Chemistry
Identifiers
urn:nbn:se:liu:diva-191801 (URN)10.1002/eem2.12551 (DOI)000932336900001 ()2-s2.0-85147681332 (Scopus ID)
Funder
Swedish Energy Agency, 42022‐1Knut and Alice Wallenberg Foundation, 2018.0058Swedish Research Council, 2016‐05990Swedish Research Council, 2019‐05577Swedish Research Council, 2021‐04427Vinnova, 2016‐05156
Note

Funding: Swedish Agency for Innovation Systems (Vinnova) [2016-05156]; Swedish Energy Agency [42022-1]; Swedish Research Council [VR 2021-04427, VR 2019-05577, VR 2016-05990]; Centre in Nanoscience and Technology (CeNano, Linkoeping Institute of Technology (LiTH), Linkoeping University, 2020, 2021); Swedish Government Strategic Research Area in Materials Science on Advanced Functional Materials at Linkoeping University (Faculty Grant SFO-Mat-LiU) [2009-00971]; Knut and Alice Wallenberg Foundation (H2O2) [KAW 2018.0058]

Available from: 2023-02-16 Created: 2023-02-16 Last updated: 2024-01-30Bibliographically approved
Tran, V. C., Mastantuoni, G. G., Zabihipour, M., Li, L., Berglund, L., Berggren, M., . . . Engquist, I. (2023). Electrical current modulation in wood electrochemical transistor. Proceedings of the National Academy of Sciences of the United States of America, 120(118), Article ID e2218380120.
Open this publication in new window or tab >>Electrical current modulation in wood electrochemical transistor
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2023 (English)In: Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, E-ISSN 1091-6490, Vol. 120, no 118, article id e2218380120Article in journal (Refereed) Published
Abstract [en]

The nature of mass transport in plants has recently inspired the development of low-cost and sustainable wood-based electronics. Herein, we report a wood electrochemical transistor (WECT) where all three electrodes are fully made of conductive wood (CW). The CW is prepared using a two-step strategy of wood delignification followed by wood amalgamation with a mixed electron-ion conducting polymer, poly(3,4-ethylenedioxythiophene)–polystyrene sulfonate (PEDOT:PSS). The modified wood has an electrical conductivity of up to 69 Sm−1 induced by the formation of PEDOT:PSS microstructures inside the wood 3D scaffold. CW is then used to fabricate the WECT, which is capable of modulating an electrical current in a porous and thick transistor channel (1 mm) with an on/off ratio of 50. The device shows a good response to gate voltage modulation and exhibits dynamic switching properties similar to those of an organic electrochemical transistor. This wood-based device and the proposed working principle demonstrate the possibility to incorporate active electronic functionality into the wood, suggesting different types of bio-based electronic devices.

Place, publisher, year, edition, pages
Proceedings of the National Academy of Sciences, 2023
Keywords
conductivity, electrochemistry, PEDOT:PSS, transistor, wood
National Category
Polymer Chemistry Other Electrical Engineering, Electronic Engineering, Information Engineering
Identifiers
urn:nbn:se:liu:diva-197080 (URN)10.1073/pnas.2218380120 (DOI)001025817800003 ()37094114 (PubMedID)2-s2.0-85153687393 (Scopus ID)
Note

QC 20230713

Available from: 2023-08-22 Created: 2023-08-22 Last updated: 2024-01-10Bibliographically approved
Roy, A., Bersellini Farinotti, A., Arbring Sjöström, T., Abrahamsson, T., Cherian, D., Karaday, M., . . . Simon, D. (2023). Electrophoretic Delivery of Clinically Approved Anesthetic Drug for Chronic Pain Therapy. Advanced Therapeutics
Open this publication in new window or tab >>Electrophoretic Delivery of Clinically Approved Anesthetic Drug for Chronic Pain Therapy
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2023 (English)In: Advanced Therapeutics, E-ISSN 2366-3987Article in journal (Refereed) Epub ahead of print
Abstract [en]

Despite a range of available pain therapies, most patients report so-called “breakthrough pain.” Coupled with global issues like opioid abuse, there is a clear need for advanced therapies and technologies for safe and effective pain management. Here the authors demonstrate a candidate for such an advanced therapy: precise and fluid-flow-free electrophoretic delivery via organic electronic ion pumps (OEIPs) of the commonly used anesthetic drug bupivacaine. Bupivacaine is delivered to dorsal root ganglion (DRG) neurons in vitro. DRG neurons are a good proxy for pain studies as they are responsible for relaying ascending sensory signals from nociceptors (pain receptors) in the peripheral nervous system to the central nervous system. Capillary based OEIPs are used due to their probe-like and free-standing form factor, ideal for interfacing with cells. By delivering bupivacaine with the OEIP and recording dose versus response (Ca2+ imaging), it is observed that only cells close to the OEIP outlet (≤75 µm) are affected (“anaesthetized”) and at concentrations up to 10s of thousands of times lower than with bulk/bolus delivery. These results demonstrate the first effective OEIP deliveryof a clinically approved and widely used analgesic pharmaceutical, and thus are a major translational milestone for this technology.

Place, publisher, year, edition, pages
John Wiley & Sons, Ltd, 2023
Keywords
anesthetic, bupivacaine, calcium imaging, drug delivery, electrophoretic, ion exchange membrane
National Category
Anesthesiology and Intensive Care
Identifiers
urn:nbn:se:liu:diva-193517 (URN)10.1002/adtp.202300083 (DOI)000977943800001 ()2-s2.0-85154059805 (Scopus ID)
Note

Funding agencies: This work was supported by the Swedish Foundation for Strategic Research, the Knut and Alice Wallenberg Foundation, the Swedish Research Council, the European Research Council (AdG 2018 Magnus Berggren, 834677 and CoG 2019 Camilla Svensson, 866075), and Vinnova. Additional support was provided by the Swedish Government Strategic Research Area in Materials Science on Advanced Functional Materials at Linköping University (Faculty Grant SFO-Mat-LiU no. 2009-00971).

Available from: 2023-05-03 Created: 2023-05-03 Last updated: 2024-01-10Bibliographically approved
Cherian, D., Roy, A., Farinotti, A. B., Abrahamsson, T., Arbring Sjöström, T., Tybrandt, K., . . . Simon, D. (2023). Flexible Organic Electronic Ion Pump Fabricated Using Inkjet Printing and Microfabrication for Precision In Vitro Delivery of Bupivacaine. Advanced Healthcare Materials
Open this publication in new window or tab >>Flexible Organic Electronic Ion Pump Fabricated Using Inkjet Printing and Microfabrication for Precision In Vitro Delivery of Bupivacaine
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2023 (English)In: Advanced Healthcare Materials, ISSN 2192-2640, E-ISSN 2192-2659Article in journal (Refereed) Epub ahead of print
Abstract [en]

The organic electronic ion pump (OEIP) is an on-demand electrophoretic drug delivery device, that via electronic to ionic signal conversion enables drug delivery without additional pressure or volume changes. The fundamental component of OEIPs is their polyelectrolyte membranes which are shaped into ionic channels that conduct and deliver ionic drugs, with high spatiotemporal resolution. The patterning of these membranes is essential in OEIP devices and is typically achieved using laborious micro processing techniques. Here, we report the development of an inkjet printable formulation of polyelectrolyte, based on a custom anionically functionalized hyperbranched polyglycerol (i-AHPG). This polyelectrolyte ink greatly simplifies the fabrication process, and is used in the production of free standing, OEIPs on flexible polyimide substrates. Both i-AHPG and the OEIP devices are characterized, exhibiting favorable iontronic characteristics of charge selectivity and ability to transport aromatic compounds. Further, the applicability of these technologies is demonstrated by transport and delivery of the pharmaceutical compound bupivacaine to dorsal root ganglion cells with high spatial precision and effective nerve-blocking, highlighting the applicability of these technologies for biomedical scenarios.

Place, publisher, year, edition, pages
John Wiley & Sons, 2023
Keywords
bioelectronics, flexible devices, inkjet printing, polyelectrolytes, polyimide
National Category
Materials Chemistry
Identifiers
urn:nbn:se:liu:diva-193520 (URN)10.1002/adhm.202300550 (DOI)001010551300001 ()37069480 (PubMedID)
Note

Funding: Swedish Foundation for Strategic Research; Knut and Alice Wallenberg Foundation; Swedish Research Council; European Research Council [834677]; Swedish Government Strategic Research Area in Materials Science on Advanced Functional Materials at Linkoping University (Faculty Grant SFO-Mat-LiU) [2009-00971]; Vinnova

Available from: 2023-05-03 Created: 2023-05-03 Last updated: 2024-01-10Bibliographically approved
Brooke, R., Lay, M., Jain, K., Francon, H., Say, M. G., Belaineh, D., . . . Berggren, M. (2023). Nanocellulose and PEDOT:PSS composites and their applications. POLYMER REVIEWS, 63(2), 437-477
Open this publication in new window or tab >>Nanocellulose and PEDOT:PSS composites and their applications
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2023 (English)In: POLYMER REVIEWS, ISSN 1558-3724, Vol. 63, no 2, p. 437-477Article, review/survey (Refereed) Published
Abstract [en]

The need for achieving sustainable technologies has encouraged research on renewable and biodegradable materials for novel products that are clean, green, and environmentally friendly. Nanocellulose (NC) has many attractive properties such as high mechanical strength and flexibility, large specific surface area, in addition to possessing good wet stability and resistance to tough chemical environments. NC has also been shown to easily integrate with other materials to form composites. By combining it with conductive and electroactive materials, many of the advantageous properties of NC can be transferred to the resulting composites. Conductive polymers, in particular poly(3,4-ethylenedioxythiophene:poly(styrene sulfonate) (PEDOT:PSS), have been successfully combined with cellulose derivatives where suspensions of NC particles and colloids of PEDOT:PSS are made to interact at a molecular level. Alternatively, different polymerization techniques have been used to coat the cellulose fibrils. When processed in liquid form, the resulting mixture can be used as a conductive ink. This review outlines the preparation of NC/PEDOT:PSS composites and their fabrication in the form of electronic nanopapers, filaments, and conductive aerogels. We also discuss the molecular interaction between NC and PEDOT:PSS and the factors that affect the bonding properties. Finally, we address their potential applications in energy storage and harvesting, sensors, actuators, and bioelectronics.

Place, publisher, year, edition, pages
TAYLOR & FRANCIS INC, 2023
Keywords
PEDOT; nanocellulose; composites; cellulose; conductive polymers
National Category
Polymer Chemistry
Identifiers
urn:nbn:se:liu:diva-187886 (URN)10.1080/15583724.2022.2106491 (DOI)000842101900001 ()
Note

Funding Agencies|Vinnova for the Digital Cellulose Competence Center (DCC) [2016-05193]; Swedish Foundation for Strategic Research [GMT14-0058]; Wallenberg Wood Science Centre

Available from: 2022-08-31 Created: 2022-08-31 Last updated: 2023-11-21Bibliographically approved
Ail, U., Nilsson, J., Jansson, M., Buyanova, I. A., Wu, Z., Björk, E., . . . Crispin, X. (2023). Optimization of Non-Pyrolyzed Lignin Electrodes for Sustainable Batteries. ADVANCED SUSTAINABLE SYSTEMS, 7(2), Article ID 2200396.
Open this publication in new window or tab >>Optimization of Non-Pyrolyzed Lignin Electrodes for Sustainable Batteries
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2023 (English)In: ADVANCED SUSTAINABLE SYSTEMS, ISSN 2366-7486, Vol. 7, no 2, article id 2200396Article in journal (Refereed) Published
Abstract [en]

Lignin, a byproduct from the pulp industry, is one of the redox active biopolymers being investigated as a component in the electrodes for sustainable energy storage applications. Due to its insulating nature, it needs to be combined with a conductor such as carbon or conducting polymer for efficient charge storage. Here, the lignin/carbon composite electrodes manufactured via mechanical milling (ball milling) are reported. The composite formation, correlation between performance and morphology is studied by comparison with manual mixing and jet milling. Superior charge storage capacity with approximate to 70% of the total contribution from the Faradaic process involving the redox functionality of lignin is observed in a mechanically milled composite. In comparison, manual mix shows only approximate to 30% from the lignin storage participation while the rest is due to the electric double layer at the carbon-electrolyte interface. The significant participation of lignin in the ball milled composite is attributed to the homogeneous, intimate mixing of the carbon and the lignin leading the electronic carrier transported in the carbon phase to reach most of the redox group of lignin. A maximum capacity of 49 mAh g(-1) is obtained at charge/discharge rate of 0.25 A g(-1) for the sample milled for 60 min.

Place, publisher, year, edition, pages
WILEY-V C H VERLAG GMBH, 2023
Keywords
ball milling; biopolymers; Faradaic and non-Faradaic charge storages; lignin-carbon composites; renewable energy storages
National Category
Materials Chemistry
Identifiers
urn:nbn:se:liu:diva-190943 (URN)10.1002/adsu.202200396 (DOI)000893500700001 ()
Note

Funding Agencies|Knut and Alice Wallenberg Foundation [KAW 2019-0344, KAW 2020-0174]; Wallenberg Wood Science Center; Vetenskapradet [2016-05990]; Swedish Government Strategic Research Area in Materials Science on Functional Materials at Linkoeping University [2009-00971]; Wallenberg Scholar grants

Available from: 2023-01-09 Created: 2023-01-09 Last updated: 2024-02-06Bibliographically approved
Kumar, D., Ail, U., Wu, Z., Björk, E., Berggren, M., Gueskine, V., . . . Khan, Z. (2023). Zinc salt in "Water-in-Polymer Salt Electrolyte" for Zinc-Lignin Batteries: Electroactivity of the Lignin Cathode. ADVANCED SUSTAINABLE SYSTEMS, 7(4), Article ID 2200433.
Open this publication in new window or tab >>Zinc salt in "Water-in-Polymer Salt Electrolyte" for Zinc-Lignin Batteries: Electroactivity of the Lignin Cathode
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2023 (English)In: ADVANCED SUSTAINABLE SYSTEMS, ISSN 2366-7486, Vol. 7, no 4, article id 2200433Article in journal (Refereed) Published
Abstract [en]

Zn-ion batteries are one of the hot candidates for low-cost and sustainable secondary batteries. The hydrogen evolution and dendritic growth upon zinc deposition are todays challenges for that technology. One of the new strategies to cope with these issues is to use "water-in-salt" electrolyte (WISE), that is, super concentrated aqueous electrolytes, to broaden its electrochemical stability window (ESW), suppressing hydrogen evolution reaction (HER), and perturbing the dendritic growth. Herein, this work proposes to use "water-in-polymer salt" electrolyte (WIPSE) concept to mitigate the challenges with Zn ion batteries and bring this technology toward one of the cheapest, greenest, and most sustainable electrodes: Lignin-carbon (L-C) electrode. Potassium polyacrylate (PAAK) as WISE bears out as better electrolyte for L-C electrodes in terms of self-discharge, cyclic stability, and specific capacity compared to conventional electrolyte based on chemically cousin molecule potassium acetate. Zinc bis(trifluoromethanesulfonyl) imide (Zn(TFSI)(2)) added into WIPSE shows deposition and dissolution of Zn in Zn//Zn symmetric cell suggesting that Zn2+ are moving into the polyanionic network. Furthermore, the added bis (trifluor omethanesul fonyl) imide (TFSI-) metal salts trigger a approximate to 40% enhancement of the capacity of L-C electrode. These results show a new promising direction toward the development of cost-effective and sustainable Zn-lignin batteries.

Place, publisher, year, edition, pages
WILEY-V C H VERLAG GMBH, 2023
Keywords
lignin; polymer electrolytes; water-in-salt electrolytes; WISE; Zn-ion Batteries
National Category
Other Chemical Engineering
Identifiers
urn:nbn:se:liu:diva-190937 (URN)10.1002/adsu.202200433 (DOI)000896916400001 ()
Note

Funding Agencies|Knut and Alice Wallenberg (KAW) foundation [KAW 2020.0174]; Swedish Research Council [2016-05990]; Swedish Government Strategic Research Area in Materials Science on Functional Materials at Linkoeping University [2009-00971]; competence center FunMat-II - Swedish Agency for Innovation Systems (Vinnova) [2016-05156]; aforsk foundation [21-130]; KAW

Available from: 2023-01-09 Created: 2023-01-09 Last updated: 2024-02-08Bibliographically approved
Ghorbani Shiraz, H., Ullah Khan, Z., Pere, D., Liu, X., Coppel, Y., Fahlman, M., . . . Crispin, X. (2022). 3R-TaS2 as an Intercalation-Dependent Electrified Interface for Hydrogen Reduction and Oxidation Reactions. The Journal of Physical Chemistry C, 126(40), 17056-17065
Open this publication in new window or tab >>3R-TaS2 as an Intercalation-Dependent Electrified Interface for Hydrogen Reduction and Oxidation Reactions
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2022 (English)In: The Journal of Physical Chemistry C, ISSN 1932-7447, E-ISSN 1932-7455, Vol. 126, no 40, p. 17056-17065Article in journal (Refereed) Published
Abstract [en]

Hydrogen technology, as a future breakthrough for the energy industry, has been defined as an environmentally friendly, renewable, and high-power energy carrier. The green production of hydrogen, which mainly relies on electrocatalysts, is limited by the high cost and/ or the performance of the catalytic system. Recently, studies have been conducted in search of bifunctional electrocatalysts accelerating both the hydrogen evolution reaction (HER) and the hydrogen oxidation reaction (HOR). Herein, we report the investigation of the high efficiency bifunctional electrocatalyst TaS2 for both the HER and the HOR along with the asymmetric effect of inhibition by organic intercalation. The linear organic agent, to boost the electron donor property and to ease the process of intercalation, provides a higher interlayer gap in the tandem structure of utilized nanosheets. XRD and XPS data reveal an increase in the interlayer distance of 22%. The HER and the HOR were characterized in a Pt group metal-free electrochemical system. The pristine sample shows a low overpotential of -0.016 Vat the onset. The intercalated sample demonstrates a large shift in its performance for the HER. It is revealed that the intercalation is a potential key strategy for tuning the performance of this family of catalysts. The inhibition of the HER by intercalation is considered as the increase in the operational window of a water-based electrolyte on a negative electrode, which is relevant to technologies of electrochemical energy storage.

Place, publisher, year, edition, pages
American Chemical Society (ACS), 2022
National Category
Other Chemical Engineering
Identifiers
urn:nbn:se:liu:diva-189795 (URN)10.1021/acs.jpcc.2c04290 (DOI)000869704900001 ()
Note

Funding Agencies|Swedish Research Council [VR 2016-05990]; Knut and Alice Wallenberg Foundation [KAW 2019.0604, 2021.0195]; Karl Erik Onnesjos Foundation; Swedish Government Strategic Research Area in Materials Science on Advanced Functional Materials at Linkoping University (Faculty Grant SFO-MatLiU) [2009-00971]

Available from: 2022-11-08 Created: 2022-11-08 Last updated: 2023-12-06Bibliographically approved
Yang, H., Gueskine, V., Berggren, M. & Engquist, I. (2022). Cross-Linked Nanocellulose Membranes for Nanofluidic Osmotic Energy Harvesting. ACS Applied Energy Materials, 5(12), 15740-15748
Open this publication in new window or tab >>Cross-Linked Nanocellulose Membranes for Nanofluidic Osmotic Energy Harvesting
2022 (English)In: ACS Applied Energy Materials, E-ISSN 2574-0962, Vol. 5, no 12, p. 15740-15748Article in journal (Refereed) Published
Abstract [en]

Osmotic energy generated from the salinity gradient is a kind of clean and renewable energy source, where the ion-exchange membranes play a critical role in its operation. The nanofluidic technique is emerging to overcome the limitations of high resistance and low mass transport of traditional ion-exchange membranes and thus improve osmotic power conversion. However, the currently reported nanofluidic materials suffer from high cost and complicated fabrication processes, which limits their practical application. Here, we report low-cost nanocellulose membranes that can be facilely prepared by a chemical cross-linking approach. The obtained membranes exhibit excellent ion transport characteristics as high-performance nanofluidic osmotic power generators. The control of cross-linker dosage enables the simultaneous tunability of the surface charge density and size of nanofluidic channels created between the interwoven cellulose nanofibrils. The maximum osmotic power generated by the membrane is reached when the cross-linker weight content is 20 wt %. Furthermore, the cross-linked nanocellulose membranes exhibit long-term working stability in osmotic energy harvesting under a wide range of pH values (3.2-9.7). This nanocellulose membrane derived from green and sustainable natural materials demonstrates a promising potential for renewable osmotic energy harvesting.

Place, publisher, year, edition, pages
American Chemical Society (ACS), 2022
Keywords
nanocellulose; membrane; osmotic energy; nanofluidic; ion selectivity
National Category
Energy Systems
Identifiers
urn:nbn:se:liu:diva-190788 (URN)10.1021/acsaem.2c03308 (DOI)000899478400001 ()
Note

Funding Agencies|Digital Cellulose Center (Swedish Innovation Agency VINNOVA); Wallenberg Wood Science Center (Knut and Alice Wallenberg Foundation); Karl-Erik Onnesjo Foundation

Available from: 2023-01-02 Created: 2023-01-02 Last updated: 2024-02-13Bibliographically approved
Keene, S. T., Gueskine, V., Berggren, M., Malliaras, G. G., Tybrandt, K. & Zozoulenko, I. (2022). Exploiting mixed conducting polymers in organic and bioelectronic devices. Physical Chemistry, Chemical Physics - PCCP, 24(32), 19144-19163
Open this publication in new window or tab >>Exploiting mixed conducting polymers in organic and bioelectronic devices
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2022 (English)In: Physical Chemistry, Chemical Physics - PCCP, ISSN 1463-9076, E-ISSN 1463-9084, Vol. 24, no 32, p. 19144-19163Article, review/survey (Refereed) Published
Abstract [en]

Efficient transport of both ionic and electronic charges in conjugated polymers (CPs) has enabled a wide range of novel electrochemical devices spanning applications from energy storage to bioelectronic devices. In this Perspective, we provide an overview of the fundamental physical processes which underlie the operation of mixed conducting polymer (MCP) devices. While charge injection and transport have been studied extensively in both ionic and electronic conductors, translating these principles to mixed conducting systems proves challenging due to the complex relationships among the individual materials properties. We break down the process of electrochemical (de)doping, the basic feature exploited in mixed conducting devices, into its key steps, highlighting recent advances in the study of these physical processes in the context of MCPs. Furthermore, we identify remaining challenges in further extending fundamental understanding of MCP-based device operation. Ultimately, a deeper understanding of the elementary processes governing operation in MCPs will drive the advancement in both materials design and device performance.

Place, publisher, year, edition, pages
Royal Society of Chemistry, 2022
National Category
Condensed Matter Physics
Identifiers
urn:nbn:se:liu:diva-187730 (URN)10.1039/d2cp02595g (DOI)000837602700001 ()35942679 (PubMedID)
Note

Funding Agencies|European Union [101022365]; Knut and Alice Wallenberg Foundation; Wallenberg Wood Science Center; Swedish Government Strategic Research Area in Materials Science on Advanced Functional Materials at Linkoping University [2009-00971]; Swedish Foundation for Strategic Research; H2020-EU-FET Open MITICS [964677]

Available from: 2022-08-30 Created: 2022-08-30 Last updated: 2023-04-11Bibliographically approved
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ORCID iD: ORCID iD iconorcid.org/0000-0001-5154-0291

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