插层(化学)
材料科学
电池(电)
单排替反应
水溶液
阴极
储能
电化学
离子
锌
化学工程
无机化学
电极
功率(物理)
物理化学
冶金
热力学
化学
有机化学
工程类
物理
作者
Lutong Shan,Yongqiang Yang,Wanying Zhang,Huijie Chen,Guozhao Fang,Jiang Zhou,Shuquan Liang
标识
DOI:10.1016/j.ensm.2018.08.008
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 Zn2(V3O8)2. Importantly, the in-situ generation of highly conductive Ag0 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).
科研通智能强力驱动
Strongly Powered by AbleSci AI