MOF-derived heterostructured C@VO2 @V2O5 for stable aqueous zinc-ion batteries cathode

被引:36
|
作者
Tong, Yunxiao [1 ]
Zhao, Ying [1 ]
Luo, Min [1 ]
Su, Senda [1 ]
Yang, Yongqing [1 ]
Zang, Ying [1 ]
Li, Xiaoman [1 ]
Wang, Lifeng [1 ]
Fang, Junzhuo [1 ]
机构
[1] Ningxia Univ, Sch Chem & Chem Engn, State Key Lab High efficiency Utilizat Coal & Gree, Yinchuan 750021, Ningxia, Peoples R China
基金
中国国家自然科学基金;
关键词
Metal -organic framework; Heterostructure; Porous carbon skeleton; Synergistic Energy Mechanism; Aqueous Zinc -ion batteries;
D O I
10.1016/j.jallcom.2022.167681
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
Rationally designed cathode materials with high specific capacity and excellent cycling stability are in-dispensable for stable and highly efficient aqueous zinc-ion batteries (AZIBs). The mesoporous nano -composite C@VO2 @V2O5 is successfully synthesized using the vanadium-based metal-organic framework as precursor by carbonization and subsequent oxidation processes. As the AZIBs cathode, the MOF-derived heterostructured materials display a high specific capacity (376 mAh g-1 at 0.05 A g-1), excellent rate capability (178 mAh g-1 at 5 A g-1) and outstanding long-life cycling (90.3% capacity retention for 2000 cycles at 5 A g-1). The promising electrochemical performance is attributed to abundant Zn2+ active sites and rapid intercalation kinetics of Zn2+ originated from the heterojunction structure at the two-phase (VO2 @V2O5) interface and mesoporous structure, and the enhanced electron transport efficiency brought by the the porous carbon skeleton with high conductivity. Furthermore, the synergistic effect of dual-ion co -in-tercalated energy storage mechanism endows C@VO2 @V2O5 with impressive electrochemical performance. This work demonstrates MOF-derived hetero-structured materials as an alternative cathode for high cyclic stability AZIBs in the future.(c) 2022 Elsevier B.V. All rights reserved.
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页数:11
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