Competing with other polyanionic cathode materials for potassium-ion batteries via fine structure design: new layered KVOPO4 with a tailored particle morphology

被引:86
作者
Liao, Jiaying [1 ]
Hu, Qiao [1 ]
Che, Bo [1 ]
Ding, Xiang [1 ]
Chen, Fei [1 ]
Chen, Chunhua [1 ]
机构
[1] Univ Sci & Technol China, CAS Key Lab Mat Energy Convers, Dept Mat Sci & Engn, Collaborat Innovat Ctr Suzhou Nano Sci & Technol, Hefei 230026, Anhui, Peoples R China
基金
中国国家自然科学基金; 国家重点研发计划;
关键词
HYDROTHERMAL SYNTHESIS; VOPO4; NANOSHEETS; INTERCALATION; INSERTION;
D O I
10.1039/c9ta03192h
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
Layered materials with two-dimensional ion diffusion channels are attractive for fast kinetics in secondary batteries. However, it is a great challenge to tolerate the structure evolution and volume change during the insertion/extraction of large size K ions. Herein, we report new layered KVOPO4 (L-KVOP) with a controllable morphology prepared by a hydrothermal method. The L-KVOP electrodes exhibit advantageous K-storage performance, including a high average voltage of 3.65 V, a high capacity of 115 mA h g(-1) (0.2C, 1C = 120 mA h g(-1)), considerable cycling stability with 86.8% capacity retention over 100 cycles (0.5C) and superior rate capability in potassium ion batteries. A high contribution of capacitive charge storage is revealed due to the fast ion diffusion in the bulk. The reversible structural evolution during K ion insertion/extraction is verified by ex situ X-ray diffraction, and the volume change is only 9.4%. Its superior rate performance and energy density make L-KVOP a promising candidate for potassium-ion batteries.
引用
收藏
页码:15244 / 15251
页数:8
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