Ultrafast synthesis of vanadium-based oxides with crystalline-amorphous heterostructure for advanced aqueous zinc-ion batteries

被引:0
|
作者
Yan, Duan [1 ]
Li, Hanbo [1 ]
Yang, Aomen [1 ]
Wang, Menglian [1 ]
Nie, Kaiqi [2 ]
Lv, Xiaoxin [1 ]
Deng, Jiujun [1 ]
机构
[1] Jiangsu Univ, Inst Energy Res, Automot Engn Res Inst, 301 Xuefu Rd, Zhenjiang 212013, Peoples R China
[2] Chinese Acad Sci, Inst High Energy Phys, Beijing 100049, Peoples R China
基金
中国国家自然科学基金;
关键词
Amorphous; Vanadium; Heterostructure; Cathode; Zinc-ion batteries; Flash Joule heating; SPECTROSCOPY;
D O I
10.1016/j.cej.2024.158966
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The development of amorphous-crystalline hybrids shows significant promise for high-performance cathodes in aqueous zinc ion batteries (ZIBs). However, efficient and controlled synthesis remains a major challenge due to the thermodynamic instability of amorphous materials. In this study, we present a facile and ultrafast method for the controlled fabrication of crystalline V2O3 and amorphous sodium vanadate (V2O3 /a-NVO) heterostructure using the flash Joule heating technique, achieved in approximately 3 s. Benefitting from abundant storage sites and isotropic charge transfer channel of a-NVO, as well as the intimate contact between V2O3 and a-NVO, the resulting heterostructure exhibits significant pseudocapacitive contribution and accelerated reaction kinetics, further facilitated by the co-insertion of H+/Zn2+. This results in impressive electrochemical performance, with a high specific capacity of 414.6 mAh/g at 0.2 A/g and a capacity of 329.2 mAh/g at a current density of 1 A/g after 1000 cycles. Notably, it retains a high capacity of 138 mAh/g after 5000 cycles at a large current density of 10 A/g. This approach offers a facile and rapid strategy for designing efficient vanadium-based oxide cathodes through the rational design of amorphous-crystalline heterostructures.
引用
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页数:10
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