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Self-Recovery Chemistry and Cobalt-Catalyzed Electrochemical Deposition of Cathode for Boosting Performance of Aqueous Zinc-Ion Batteries

Rechargeable Zn-ion batteries working with manganese oxide cathodes and mild aqueous electrolytes suffer from notorious cathode dissolution during galvanostatic cycling. Herein, for the first time we demonstrate the dynamic self-recovery chemistry of manganese compound during charge/discharge proces...

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Detalles Bibliográficos
Autores principales: Zhong, Yijun, Xu, Xiaomin, Veder, Jean-Pierre, Shao, Zongping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7066221/
https://www.ncbi.nlm.nih.gov/pubmed/32163897
http://dx.doi.org/10.1016/j.isci.2020.100943
Descripción
Sumario:Rechargeable Zn-ion batteries working with manganese oxide cathodes and mild aqueous electrolytes suffer from notorious cathode dissolution during galvanostatic cycling. Herein, for the first time we demonstrate the dynamic self-recovery chemistry of manganese compound during charge/discharge processes, which strongly determines the battery performance. A cobalt-modified δ-MnO(2) with a redox-active surface shows superior self-recovery capability as a cathode. The cobalt-containing species in the cathode enable efficient self-recovery by continuously catalyzing the electrochemical deposition of active Mn compound, which is confirmed by characterizations of both practical coin-type batteries and a new-design electrolyzer system. Under optimized condition, a high specific capacity over 500 mAh g(−1) is achieved, together with a decent cycling performance with a retention rate of 63% over 5,000 cycles. With this cobalt-facilitated deposition effect, the battery with low concentration (0.02 M) of additive Mn(2+) in the electrolyte (only 12 atom % to the overall Mn) maintains decent capacity retention.