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Electrochemical energy storage in an organic supercapacitor via a non-electrochemical proton charge assembly.


ABSTRACT: Contrary to conventional beliefs, we show how a functional ligand that does not exhibit any redox activity elevates the charge storage capability of an electric double layer via a proton charge assembly. Compared to an unsubstituted ligand, a non-redox active carboxy ligand demonstrated nearly a 4-fold increase in charge storage, impressive capacitive retention even at a rate of 900C, and approximately a 2-fold decrease in leakage currents with an enhancement in energy density up to approximately 70% via a non-electrochemical route of proton charge assembly. Generalizability of these findings is presented with various non-redox active functional units that can undergo proton charge assembly in the ligand. This demonstration of non-redox active functional units enriching supercapacitive charge storage via proton charge assembly contributes to the rational design of ligands for energy storage applications.

SUBMITTER: Mukhopadhyay S 

PROVIDER: S-EPMC10829031 | biostudies-literature | 2024 Jan

REPOSITORIES: biostudies-literature

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Electrochemical energy storage in an organic supercapacitor <i>via</i> a non-electrochemical proton charge assembly.

Mukhopadhyay Sanchayita S   Kottaichamy Alagar Raja AR   Devendrachari Mruthyunjayachari Chattanahalli MC   Mendhe Rahul Mahadeo RM   Nimbegondi Kotresh Harish Makri HM   Vinod Chathakudath Prabhakaran CP   Ottakam Thotiyl Musthafa M  

Chemical science 20231219 5


Contrary to conventional beliefs, we show how a functional ligand that does not exhibit any redox activity elevates the charge storage capability of an electric double layer <i>via</i> a proton charge assembly. Compared to an unsubstituted ligand, a non-redox active carboxy ligand demonstrated nearly a 4-fold increase in charge storage, impressive capacitive retention even at a rate of 900C, and approximately a 2-fold decrease in leakage currents with an enhancement in energy density up to appro  ...[more]

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