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Erschienen in: Journal of Materials Science 24/2018

12.09.2018 | Energy materials

Cr2O3 nanoparticles: a fascinating electrode material combining both surface-controlled and diffusion-limited redox reactions for aqueous supercapacitors

verfasst von: Tianli Li, Zaichun Liu, Li Zhu, Fang Dai, Lu Hu, Lei Zhang, Zubiao Wen, Yuping Wu

Erschienen in: Journal of Materials Science | Ausgabe 24/2018

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Abstract

Chromium oxide has emerged as an attractive electrode material to construct high-performance supercapacitor. Despite some available reports on Cr2O3-based supercapacitors, the charge storage of Cr2O3 electrodes in alkaline electrolytes is far from being understood unlike those of other compounds of Ti, V, Mn, Fe, Co, Ni etc in periodic table of elements. Herein, the detail kinetics analyses of electrochemical behaviors of the electrode based on Cr2O3 nanoparticles in alkaline electrolyte were demonstrated in this work. We examine that there are both surface-controlled pseudocapacitance (with a contribution of 76%) and diffusion-limited redox reactions (with a contribution of 24%) for the charge storage in electrode based on Cr2O3 nanoparticles at a low sweep rate of 1 mV s−1. The identifying pseudocapacitive contribution dominates the charge storage in electrode based on Cr2O3 nanoparticles at high sweep rates, reaching up to 96% at 50 mV s−1. In addition, the assembled hybrid supercapacitor based on Cr2O3 nanoparticles as the positive electrode displays an operating voltage of 1.45 V, an energy density of 14.7 Wh kg−1, and high stability of 3000 cycles. This work will contribute to the development of pseudocapacitive electrode materials for supercapacitors.

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Metadaten
Titel
Cr2O3 nanoparticles: a fascinating electrode material combining both surface-controlled and diffusion-limited redox reactions for aqueous supercapacitors
verfasst von
Tianli Li
Zaichun Liu
Li Zhu
Fang Dai
Lu Hu
Lei Zhang
Zubiao Wen
Yuping Wu
Publikationsdatum
12.09.2018
Verlag
Springer US
Erschienen in
Journal of Materials Science / Ausgabe 24/2018
Print ISSN: 0022-2461
Elektronische ISSN: 1573-4803
DOI
https://doi.org/10.1007/s10853-018-2743-0

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