Reversible Zn-driven reduction displacement reaction in aqueous zinc-ion battery

被引:99
作者
Shan, Lutong [1 ]
Zhou, Jiang [1 ]
Han, Mingming [1 ]
Fang, Guozhao [1 ]
Cao, Xinxin [1 ]
Wu, Xianwen [2 ]
Liang, Shuquan [1 ]
机构
[1] Cent South Univ, Sch Mat Sci & Engn, Changsha 410083, Hunan, Peoples R China
[2] Jishou Univ, Sch Chem & Chem Engn, Jishou 416000, Peoples R China
基金
中国国家自然科学基金;
关键词
CHEMISTRY; FRAMEWORK; VANADATES; CATHODE; STORAGE; ANODE;
D O I
10.1039/c9ta00125e
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Tremendous attention has been paid to aqueous zinc-ion batteries (ZIBs) with the merits of low cost, safety and environmental benignity. Exploration of the Zn2+ ion storage mechanism is of great significance to the fundamental understanding and future practical application of advanced aqueous Zn-ion battery systems. Herein, we have observed the reduction displacement reaction mechanism upon Zn2+ insertion/extraction into/from the structure of copper pyrovanadate (Cu-3(OH)(2)V(2)O(7)2H(2)O), i.e., Zn2+ insertion would drive the reduction of Cu2+ to metallic Cu-0 particles, and also the phase transition from Cu-3(OH)(2)V(2)O(7)2H(2)O to a new phase of Zn0.25V2O5H2O. As a result, Cu-3(OH)(2)V(2)O(7)2H(2)O is able to deliver excellent electrochemical performance (e.g., a high discharge capacity of 136 mA h g(-1) can be maintained after 3000 repetitive cycles at 10 A g(-1)).
引用
收藏
页码:7355 / 7359
页数:5
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