Dual functions of zirconium modification on improving the electrochemical performance of Ni-rich LiNi0.8Co0.1Mn0.1O2

被引:165
作者
Li, Xing [1 ]
Zhang, Kangjia [1 ]
Wang, MingShan [1 ]
Liu, Yang [1 ]
Qu, MeiZhen [2 ]
Zhao, Wengao [3 ]
Zheng, Jianming [3 ]
机构
[1] Southwest Petr Univ, Ctr New Energy Mat & Technol, Xindu Rd 8, Chengdu 610500, Sichuan, Peoples R China
[2] Chinese Acad Sci, Chengdu Inst Organ Chem, Chengdu 610041, Sichuan, Peoples R China
[3] Pacific Northwest Natl Lab, Energy & Environm Directorate, 902 Battelle Blvd, Richland, WA 99354 USA
基金
中国国家自然科学基金;
关键词
LITHIUM-ION BATTERIES; LOW-TEMPERATURE PERFORMANCE; CATHODE MATERIALS; RECHARGEABLE BATTERIES; STORAGE CHARACTERISTICS; DOPED LINI0.8CO0.2O2; LINI1/3CO1/3MN1/3O2; OXIDE; TRANSITION; AL;
D O I
10.1039/c7se00513j
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
Trace amounts of zirconium (Zr) have been adopted to modify the crystal structure and surface of the Ni-rich LiNi0.8Co0.1Mn0.1O2 (NCM811) cathode material. During cycling at 1.0C, the Zr-modified NCM811 shows an improved capacity retention of 92% after 100 cycles, higher than 75% for pristine NMC811. In addition, the Zr-modified NCM811 is capable of delivering a discharge capacity of 107 mA h g(-1) at a 10.0C rate, much higher than 28 mA h g(-1) delivered by pristine materials. These improved electrochemical performances are ascribed to the dual functions of Zr modification. On one hand, part of the Zr enters the crystal lattice, which is beneficial for reducing the Li/Ni cation mixing and enhancing the crystal stability of the cathode. On the other hand, the rest of the Zr forms a 1-2 nm thick coating layer on the surface of the NCM811 cathode, which effectively prevents direct contact between NCM and the electrolyte, thus suppressing the detrimental interfacial reactions. Therefore, the Zr-modified LiNi0.8Co0.1Mn0.1O2 exhibited significantly enhanced cycling stability and charge/discharge rate capability in comparison with its untreated counterpart.
引用
收藏
页码:413 / 421
页数:9
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