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Reversible Electronic Solid-Gel Switching of a Conjugated Polymer
Linköping University, Department of Science and Technology, Laboratory of Organic Electronics. Linköping University, Faculty of Science & Engineering.
Linköping University, Department of Science and Technology, Laboratory of Organic Electronics. Linköping University, Faculty of Science & Engineering.
Linköping University, Department of Science and Technology, Laboratory of Organic Electronics. Linköping University, Faculty of Science & Engineering.ORCID iD: 0000-0002-3012-910X
Imperial Coll London, England.
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2020 (English)In: ADVANCED SCIENCE, ISSN 2198-3844, Vol. 7, no 2, article id 1901144Article in journal (Refereed) Published
Abstract [en]

Conjugated polymers exhibit electrically driven volume changes when included in electrochemical devices via the exchange of ions and solvent. So far, this volumetric change is limited to 40% and 100% for reversible and irreversible systems, respectively, thus restricting potential applications of this technology. A conjugated polymer that reversibly expands by about 300% upon addressing, relative to its previous contracted state, while the first irreversible actuation can achieve values ranging from 1000-10 000%, depending on the voltage applied is reported. From experimental and theoretical studies, it is found that this large and reversible volumetric switching is due to reorganization of the polymer during swelling as it transforms between a solid-state phase and a gel, while maintaining percolation for conductivity. The polymer is utilized as an electroactive cladding to reduce the void sizes of a porous carbon filter electrode by 85%.

Place, publisher, year, edition, pages
WILEY , 2020. Vol. 7, no 2, article id 1901144
Keywords [en]
conjugated polymers; electroactive materials; hydrogels; volume change
National Category
Textile, Rubber and Polymeric Materials
Identifiers
URN: urn:nbn:se:liu:diva-161843DOI: 10.1002/advs.201901144ISI: 000492740700001OAI: oai:DiVA.org:liu-161843DiVA, id: diva2:1370890
Note

Funding Agencies|Knut and Alice Wallenberg FoundationKnut & Alice Wallenberg Foundation; Wallenberg Wood Science Center [KAW 2018.0452]; Swedish Research Council (VR)Swedish Research Council; Swedish Government Strategic Research Area in Materials Science on Advanced Functional Materials at Linkoping University (Faculty Grant SFO-Mat-LiU) [2009-00971]; Engineering and Physical Sciences Research CouncilEngineering & Physical Sciences Research Council (EPSRC) [EP/G037515/1, EP/N509486/1]

Available from: 2019-11-18 Created: 2019-11-18 Last updated: 2023-09-08
In thesis
1. Investigating volume change and ion transport in conjugated polymers
Open this publication in new window or tab >>Investigating volume change and ion transport in conjugated polymers
2021 (English)Doctoral thesis, comprehensive summary (Other academic)
Abstract [en]

Volume changes are the foundation for a wide range of phenomena and applications, ranging from the movement of plants to valves and drug delivery devices. Therefore, it does not come as a surprise that controlled volume changes are an interesting topic of research. In this thesis, volume changes in polymers are the object of investigation. Polymers are a class of macromolecules that comprise repetitive units. Owing to the wide variety of such units, polymers can exhibit manifold properties, including but not limited to strong water attraction and electrical conductivity. The former is the defining property in polymer hydrogels while the latter is a core property of conducting polymers. Both the water attracting properties and conductivity are closely linked to transport events on a molecular level. In the case of hydrogels, it is predominantly water uptake, while in the case of conducting polymers it is a complex interplay between charges, ionic charge balancing entities and water. However, in either case the transport events lead to volume changes. Despite the similarities, the properties of the materials differ greatly. On the one hand volume changes in hydrogels are very large but hard to control. On the other hand, volume changes in conducting polymers are much smaller than in hydrogels, but the control is easier due to the electronic addressing.   

P(gXTX) polymers combine a conducting polymer backbone with hydrogel sidechains. As described in publication 1, this combination of molecular entities was found to enabled unique properties of an electrically controllable giant volume change and concomitant solid-gel transition. In the second publication, the effect of the side chain lengths on the volume change properties of the polymers were explored. The knowledge acquired from these studies helped us to develop an electroactive filter based on p(gXTX) polymers which enabled electrochemical modulation of flow (publication 3). The aim of the fourth publication was to study the complex electronic-ionic transport processes and volume changes in a model conducting polymer, PEDOT:Tos. 

The understanding of fundamental processes and properties of controllable volume changes may pave the way for advances in various applications, including electroactive meshes, actuators and drug delivery devices.   

Place, publisher, year, edition, pages
Linköping: Linköping University Electronic Press, 2021. p. 48
Series
Linköping Studies in Science and Technology. Dissertations, ISSN 0345-7524 ; 2150
National Category
Polymer Chemistry
Identifiers
urn:nbn:se:liu:diva-175337 (URN)10.3384/diss.diva-175337 (DOI)9789179296285 (ISBN)
Public defence
2021-06-16, Kåkenhus, Treesearch conference room and online via Zoom, Campus Norrköping, Norrköping, 15:00 (English)
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Available from: 2021-04-28 Created: 2021-04-28 Last updated: 2021-05-18Bibliographically approved

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Gladisch, JohannesStavrinidou, EleniGhosh, SarbaniZozoulenko, IgorBerggren, Magnus
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