材料科学
阴极
储能
反应机理
电极
离子
水溶液
电化学
分析化学(期刊)
化学工程
化学
无机化学
物理化学
催化作用
有机化学
热力学
工程类
功率(物理)
物理
作者
Shiyong Zuo,Jun Liu,Weixin He,Sahar Osman,Zhengbo Liu,Xijun Xu,Jiadong Shen,Wei Jiang,Jiangwen Liu,Zhiyuan Zeng,Min Zhu
标识
DOI:10.1021/acs.jpclett.1c01776
摘要
Because they are safer and less costly than state-of-the-art Li-ion batteries, aqueous zinc-ion batteries (AZIBs) have been attracting more attention in stationary energy storage and industrial energy storage. However, the electrochemical reaction of H+ in all of the cathode materials of AZIBs has been puzzling until now. Herein, highly oriented VO2 monocrystals grown on a Ti current collector (VO2-Ti) were rationally designed as the research model, and such a well-aligned VO2 cathode also displayed excellent zinc-ion storage capability (e.g., a reversible capacity of 148.4 mAh/g at a current density of 2 A/g). To visualize the H+ reaction process, we used time-of-flight secondary-ion mass spectrometry. With the benefit of such a binder-free and conductor-free electrode design, a clear and intuitive reaction of H+ in a VO2 cathode is obtained, which is quite significant for unraveling the accurate reaction mechanism of VO2 in AZIBs.
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