Please use this identifier to cite or link to this item: http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/8375
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dc.contributor.authorMUKHOPADHYAY, SANCHAYITAen_US
dc.contributor.authorRAJA, ALAGARen_US
dc.contributor.authorDEVENDRACHARI, MRUTHUNJAYACHARI CHATTANAHALLIen_US
dc.contributor.authorMENDHE, RAHUL MAHADEOen_US
dc.contributor.authorKotresh, Harish Makri Nimbegondien_US
dc.contributor.authorPrabhakaran, Vinoden_US
dc.contributor.authorTHOTIYL, MUSTHAFA OTTAKAMen_US
dc.date.accessioned2024-01-02T05:31:11Z
dc.date.available2024-01-02T05:31:11Z
dc.date.issued2024-02en_US
dc.identifier.citationChemical Science, 15(05), 1726-1735.en_US
dc.identifier.issn2041-6520en_US
dc.identifier.issn2041-6539en_US
dc.identifier.urihttps://doi.org/10.1039/D3SC05639Ben_US
dc.identifier.urihttp://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/8375
dc.description.abstractContrary to the conventional beliefs, we show how a ligand functionality that do not exhibit any redox activity, elevate the charge storage capability of the electric double layer via a proton charge assembly. The non-redox active carboxy ligand compared to the unsubstituted ligand demonstrated nearly 4 times elevated charge storage, impressive capacitive retention even at 900C rate and ~2 times lowered leakage currents with an enhancement in energy density up to ~70% via a non-electrochemical route of proton charge assembly. Generalizability of these findings are presented with various non redox active functionalities that can undergo proton charge assembly in the ligand. This demonstration of non-redox active functionalities enriching the super capacitive charge storage via proton charge assembly contributes to the rationale design of ligands for energy storage applications.en_US
dc.language.isoenen_US
dc.publisherRoyal Society of Chemistryen_US
dc.subjectChemistryen_US
dc.subject2023-DEC-WEEK3en_US
dc.subjectTOC-DEC-2023en_US
dc.subject2024en_US
dc.titleElectrochemical energy storage in organic supercapacitor via a non-electrochemical proton charge assemblyen_US
dc.typeArticleen_US
dc.contributor.departmentDept. of Chemistryen_US
dc.identifier.sourcetitleChemical Scienceen_US
dc.publication.originofpublisherForeignen_US
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