Challenges and Modification Strategies of Ni-Rich Cathode Materials Operating at High-Voltage

被引:43
|
作者
Liao, Caijian [1 ]
Li, Fangkun [1 ]
Liu, Jun [1 ]
机构
[1] South China Univ Technol, Sch Mat Sci & Engn, Guangdong Prov Key Lab Adv Energy Storage Mat, Guangzhou 510641, Guangdong, Peoples R China
关键词
Ni-rich cathode materials; high voltage; surface degradation; microcrack; modification; LITHIUM-ION BATTERIES; POSITIVE-ELECTRODE MATERIALS; TRANSITION-METAL OXIDE; HIGH-ENERGY; LAYERED CATHODE; ELECTROCHEMICAL PERFORMANCE; CYCLING PERFORMANCE; THERMAL-STABILITY; CHEMOMECHANICAL INTERPLAY; RATE CAPABILITY;
D O I
10.3390/nano12111888
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Ni-rich cathode materials have become promising candidates for lithium-based automotive batteries due to the obvious advantage of electrochemical performance. Increasing the operating voltage is an effective means to obtain a higher specific capacity, which also helps to achieve the goal of high energy density (capacity x voltage) of power lithium-ion batteries (LIBs). However, under high operating voltage, surface degradation will occur between Ni-rich cathode materials and the electrolytes, forming a solid interface film with high resistance, releasing O-2, CO2 and other gases. Ni-rich cathode materials have serious cation mixing, resulting in an adverse phase transition. In addition, the high working voltage will cause microcracks, leading to contact failure and repeated surface reactions. In order to solve the above problems, researchers have proposed many modification methods to deal with the decline of electrochemical performance for Ni-rich cathode materials under high voltage such as element doping, surface coating, single-crystal fabrication, structural design and multifunctional electrolyte additives. This review mainly introduces the challenges and modification strategies for Ni-rich cathode materials under high voltage operation. The future application and development trend of Ni-rich cathode materials for high specific energy LIBs are projected.
引用
收藏
页数:25
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