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B-Mg co-doping behavior of LiFePO4 cathode material: balance of oxygen vacancy and enhancement of electrochemical performance
被引:11
作者:

Wang, Li
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机构:
Kunming Univ Sci & Technol, Natl Engn Lab Vacuum Met, Kunming 650093, Yunnan, Peoples R China
Kunming Univ Sci & Technol, Natl Local Joint Engn Lab Lithium Ion Battery & M, Kunming 650093, Yunnan, Peoples R China Kunming Univ Sci & Technol, Natl Engn Lab Vacuum Met, Kunming 650093, Yunnan, Peoples R China

Wei, Runhong
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h-index: 0
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Kunming Univ Sci & Technol, Natl Engn Lab Vacuum Met, Kunming 650093, Yunnan, Peoples R China
Kunming Univ Sci & Technol, Natl Local Joint Engn Lab Lithium Ion Battery & M, Kunming 650093, Yunnan, Peoples R China Kunming Univ Sci & Technol, Natl Engn Lab Vacuum Met, Kunming 650093, Yunnan, Peoples R China

Zhang, Hui
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h-index: 0
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Kunming Univ Sci & Technol, Natl Engn Lab Vacuum Met, Kunming 650093, Yunnan, Peoples R China
Kunming Univ Sci & Technol, Natl Local Joint Engn Lab Lithium Ion Battery & M, Kunming 650093, Yunnan, Peoples R China Kunming Univ Sci & Technol, Natl Engn Lab Vacuum Met, Kunming 650093, Yunnan, Peoples R China

Zhang, Keyu
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h-index: 0
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Kunming Univ Sci & Technol, Natl Engn Lab Vacuum Met, Kunming 650093, Yunnan, Peoples R China
Kunming Univ Sci & Technol, Natl Local Joint Engn Lab Lithium Ion Battery & M, Kunming 650093, Yunnan, Peoples R China Kunming Univ Sci & Technol, Natl Engn Lab Vacuum Met, Kunming 650093, Yunnan, Peoples R China

Liang, Feng
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h-index: 0
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Kunming Univ Sci & Technol, Natl Engn Lab Vacuum Met, Kunming 650093, Yunnan, Peoples R China
Kunming Univ Sci & Technol, Natl Local Joint Engn Lab Lithium Ion Battery & M, Kunming 650093, Yunnan, Peoples R China Kunming Univ Sci & Technol, Natl Engn Lab Vacuum Met, Kunming 650093, Yunnan, Peoples R China

Yao, Yaochun
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h-index: 0
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Kunming Univ Sci & Technol, Natl Engn Lab Vacuum Met, Kunming 650093, Yunnan, Peoples R China
Kunming Univ Sci & Technol, Natl Local Joint Engn Lab Lithium Ion Battery & M, Kunming 650093, Yunnan, Peoples R China Kunming Univ Sci & Technol, Natl Engn Lab Vacuum Met, Kunming 650093, Yunnan, Peoples R China

Li, Yin
论文数: 0 引用数: 0
h-index: 0
机构:
Kunming Univ Sci & Technol, Natl Engn Lab Vacuum Met, Kunming 650093, Yunnan, Peoples R China
Kunming Univ Sci & Technol, Natl Local Joint Engn Lab Lithium Ion Battery & M, Kunming 650093, Yunnan, Peoples R China Kunming Univ Sci & Technol, Natl Engn Lab Vacuum Met, Kunming 650093, Yunnan, Peoples R China
机构:
[1] Kunming Univ Sci & Technol, Natl Engn Lab Vacuum Met, Kunming 650093, Yunnan, Peoples R China
[2] Kunming Univ Sci & Technol, Natl Local Joint Engn Lab Lithium Ion Battery & M, Kunming 650093, Yunnan, Peoples R China
来源:
基金:
中国国家自然科学基金;
关键词:
Lithium-ion batteries;
LiFePO4 cathode material;
B-Mg co-doped;
Oxygen vacancy;
Electrochemical performance;
PARTICLE-SIZE;
COMPOSITE;
IMPACT;
D O I:
10.1007/s11581-021-04349-7
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:
Increasing the intrinsic conductivity of LiFePO4 can improve its electrochemical performance. Solving this problem can be achieved by P-site doping of LiFePO4 powder. Here, B-Mg co-doped LiFePO4 is successfully synthesized by solvothermal methods. The physical and electrochemical properties of all samples are systematically characterized with various characterization methods. In particular, proper B ion doping is determined to be beneficial to electronic conductivity, which induces the rearrangement of the PO43+ electron cloud. Also, doping with Mg can balance the problems of oxygen vacancies caused by doping B, thereby smoothing the transmission path of lithium ions, resulting in enhanced electrochemical performance. Moreover, XRD and SEM results illustrated that co-doping B and Mg do not change the LiFePO4 structure but promote the formation of a uniform and small particle. Compared with other samples, LiFeMg0.02P0.98B0.02O4 demonstrates superior electrochemical performance, which showed a specific discharge capacity of 147.4 mAh g(-1) at 1 C and a corresponding capacity retention rate of 98.6% after 100 cycles. Even at 10 C, the discharge capacity still maintains 114.9 mAh g(-1). The results of this work indicate that enhancing electronic conductivity and balancing oxygen vacancy are attributed to high electrochemical performance.
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页码:593 / 600
页数:8
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