A mixed-valent vanadium oxide cathode with ultrahigh rate capability for aqueous zinc-ion batteries

被引:42
|
作者
Li, Shenglong [1 ]
Wei, Xiujuan [1 ]
Chen, Haopeng [1 ]
Lai, Guoyong [1 ]
Wang, Xuanpeng [1 ,2 ]
Zhang, Shaojian [1 ]
Wu, Shuxing [1 ]
Tang, Weiting [1 ]
Lin, Zhan [1 ]
机构
[1] Guangdong Univ Technol, Sch Chem Engn & Light Ind, Guangzhou Key Lab Clean Transportat Energy Chem, Guangzhou 510006, Peoples R China
[2] Wuhan Univ Technol, Sch Sci, Dept Phys Sci & Technol, Wuhan 430070, Peoples R China
基金
中国国家自然科学基金;
关键词
RECENT PROGRESS; V2O5;
D O I
10.1039/d1ta04420f
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
The development of high-performance cathode materials is the key to realize commercial applications of zinc-ion batteries (ZIBs). Vanadium-based materials have been used as cathode candidates for ZIBs due to their low cost and high capacity. However, the low conductivity, unstable layered structure and slow diffusion kinetics of Zn2+ are still the main problems for vanadium-based oxides. Herein, V10O24 center dot nH(2)O with a large interlayer spacing and stable structure is successfully synthesized by inducing a VO2 phase transition through a simple refluxing process. As the ZIB cathode material, V10O24 center dot nH(2)O demonstrates a high reversible capacity of 365.3 mA h g(-1) at 0.2 A g(-1), ultrahigh rate performance (127.2 mA h g(-1) even at 80 A g(-1)), and long-term cycling stability (83.2% capacity retention over 3000 cycles at 5.0 A g(-1)). The excellent electrochemical performance is attributed to the synergistic effects of the ultrathin nanoribbon structures, oxygen vacancy and water molecules, which are favorable for enhancing the electron/ion transfer kinetics and maintaining structural stability of the V10O24 center dot nH(2)O electrode in the whole cycling process. Furthermore, ex situ XRD and XPS analyses elucidate the Zn2+ storage mechanism of the V10O24 center dot nH(2)O cathode.
引用
收藏
页码:22392 / 22398
页数:7
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