Observation of combination displacement/intercalation reaction in aqueous zinc-ion battery

被引:189
|
作者
Shan, Lutong [1 ]
Yang, Yongqiang [1 ]
Zhang, Wanying [1 ]
Chen, Huijie [1 ]
Fang, Guozhao [1 ]
Zhou, Jiang [1 ]
Liang, Shuquan [1 ]
机构
[1] Cent S Univ, Sch Mat Sci & Engn, Changsha 410083, Hunan, Peoples R China
基金
中国国家自然科学基金;
关键词
Ag0.4V2O5; energy storage mechanisms; metallic Ag matrix; cathode; aqueous zinc-ion battery; ANODE MATERIALS; CATHODE; LI; PERFORMANCE; CHEMISTRY; ELECTRODE; STORAGE;
D O I
10.1016/j.ensm.2018.08.008
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
Rechargeable aqueous Zinc-ion batteries (ZIBs) are regarded as the promising battery chemistry in stationary grid energy storage applications. Exploration of new zinc storage mechanism concepts is a feasible way to achieve high energy/power density. Herein, for the first time, we demonstrate the combination displacement/intercalation (CDI) reaction mechanism in aqueous ZIBs, as an example in Zn/Ag0.4V2O5 system. Unlike the classical intercalation/deintercalation storage mechanism, the CDI reaction mechanism enables more Zn2+ ions insertion into the host structure in two different sites, i.e. most of Ag+ in Ag0.4V2O5 replaced by Zn2+, and classical intercalation of Zn2+ in Ag0.4V2O5 and Zn-2(V3O8)(2). Importantly, the in-situ generation of highly conductive Ag-0 matrix within the electrode provides high electronic conductivity. As a result, the Ag0.4V2O5 cathode performs excellent rate capability as well as long-term cycling performance (stable capacity of 144 mA h g(-1) after 4000 cycles at 20 A g(-1)).
引用
收藏
页码:10 / 14
页数:5
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