Improving the Electrochemical Performance of Ni‐Rich LiNi0.8Co0.1Mn0.1O2 by Enlarging the Li Layer Spacing

Author:

Wu Kang123,Jia Guofeng12,Shangguan Xuehui123,Yang Guowei123,Zhu Zenghu12,Peng Zhengjun12,Zhuge Qin12,Li Faqiang124,Cui Xiaoling5,Liu Suqin6

Affiliation:

1. Key Laboratory of Comprehensive and Highly Efficient Utilization of Salt Lake Resources Qinghai Institute of Salt Lakes Chinese Academy of Sciences Xining 810008 P.R. China.

2. Key Laboratory of Salt Lake Resources Chemistry of Qinghai Province Xining 810008 P.R. China.

3. University of Chinese Academy of Sciences Beijing 100049 P.R. China.

4. Qinghai Research Center of Low-temperature Lithium-ion Battery Technology Engineering Qinghai Green Grass New Energy Technology Co. Ltd. Xining 810000 P.R. China.

5. College of Petrochemical Technology Lanzhou University of Technology Lanzhou 730050 P.R. China.

6. College of Chemistry and Chemical Engineering Central South University, Hunan Changsha 410083 P.R. China.

Abstract

AbstractNi‐rich cathode materials have high capacities but exhibit serious capacity attenuation. Therefore, a strategy for modifying a LiNi0.8Co0.1Mn0.1O2 cathode material by Na doping of the Li+ sites is proposed to improve its electrochemical performance. In this work, Li1−xNaxNi0.8Co0.1Mn0.1O2 (x=0, 0.01, 0.03) materials are synthesized by a co‐precipitation and solid‐state sintering method, and their structures and electrochemical properties are analyzed. X‐ray diffraction (XRD) results suggest that all the prepared materials have a typical hexagonal layered structure with no impurities. The spacing of the Li layers increases from 2.59251 Å to 2.59805 Å, which shows that a small amount of larger Na ions (0.102 nm) occupy the Li sites (0.076 nm). Additionally, electrochemical measurements show that the high‐rate performance and cycling stability are significantly improved when some of the Li+ sites in LiNi0.8Co0.1Mn0.1O2 are occupied by Na+. Specifically, the capacity retention of Li0.99Na0.01Ni0.8Co0.1Mn0.1O2 is 91 % after 100 cycles at a rate of 10 C. Meanwhile, the mechanism about electrochemical performance was improved by doping Na+ into Li+ sites of LiNi0.8Co0.1Mn0.1O2 has been further discussed.

Funder

Natural Science Foundation of China

Publisher

Wiley

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