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Disorder/order-heterophase VO2 for enhanced lithium storage performance in lithium-ion capacitors
被引:2
|作者:
Hou, Jing-Feng
Gao, Jian-Fei
Kong, Ling-Bin
[1
]
机构:
[1] Lanzhou Univ Technol, State Key Lab Adv Proc & Recycling Nonferrous Met, Lanzhou 730050, Peoples R China
基金:
中国国家自然科学基金;
关键词:
Lithium-ion capacitors;
Disorder-order engineering;
Vanadium dioxide;
Heterogeneous interface;
ENERGY DENSITY;
ANODE;
INTERCALATION;
MICROSPHERES;
NANOFIBERS;
NANOWIRES;
FILMS;
D O I:
10.1016/j.est.2024.110433
中图分类号:
TE [石油、天然气工业];
TK [能源与动力工程];
学科分类号:
0807 ;
0820 ;
摘要:
Interfacial engineering has proved to be an effective strategy for improving the performance of electrode materials in many applications. Herein, we report the disorder-order engineering of VO2 nanorods, and construct a crystal core and a surface-amorphized shell heterostructure (denoted as A-VO2) by simple hydrothermal method and reduction reaction, as a promising anode of lithium ion capacitor (LIC). The tunable amorphous layer introduces a large number of oxygen vacancy, which can efficiently improve electronic conductivity and enhance Li ion storage capacity. The crystalline-amorphous heterointerface generated in A-VO2 can significantly reduce the surface energy of VO2 and Li+ diffusion barrier, as well as increase the charge storage sites. The crystalline-amorphous heterogeneous phases work synergistically to facilitate ion and electron transport and maintain structural stability in discharge/charge process. The A-VO2-2 nanorods electrode possesses high capacity of 309 mAh g(-1) at 0.1 A g(-1) after 300 cycles, obviously larger than the crystalline VO2 electrode. In addition, the LIC, assembled with A-VO2-2 nanorods as anode and commercial active carbon (AC) as cathode, exhibit great energy density of 76.75 and 22.05 W h kg(-1) at power density of 195 and 9360 W kg(-1). It can remain 38.9 % of the initial capacity after 5000 cycles, demonstrating an instructive paradigm for disorder-order engineering in LIC electrode materials.
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页数:10
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