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Reversible Electronic Solid–Gel Switching of a Conjugated Polymer

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dc.contributor.author Ghosh, Sarbani
dc.date.accessioned 2024-08-08T05:11:33Z
dc.date.available 2024-08-08T05:11:33Z
dc.date.issued 2019-10
dc.identifier.uri https://onlinelibrary.wiley.com/doi/full/10.1002/advs.201901144
dc.identifier.uri http://dspace.bits-pilani.ac.in:8080/jspui/xmlui/handle/123456789/15145
dc.description.abstract 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%. en_US
dc.language.iso en en_US
dc.publisher Wiley en_US
dc.subject Chemical Engineering en_US
dc.subject Conjugated Polymers en_US
dc.subject Carbon filter en_US
dc.title Reversible Electronic Solid–Gel Switching of a Conjugated Polymer en_US
dc.type Article en_US


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