Achieving high-energy-density lithium-ion batteries through oxygen redox of cathode: From fundamentals to applications

被引:7
|
作者
Jiao, Sichen [1 ,2 ]
Li, Quan [1 ]
Xiong, Xinyun [1 ,2 ]
Yu, Xiqian [1 ,2 ]
Li, Hong [1 ,2 ]
Chen, Liquan [1 ,2 ]
Huang, Xuejie [1 ]
机构
[1] Chinese Acad Sci, Inst Phys, Beijing Adv Innovat Ctr Mat Genome Engn, Beijing 100190, Peoples R China
[2] Univ Chinese Acad Sci, Ctr Mat Sci & Optoelect Engn, Beijing 100049, Peoples R China
基金
中国国家自然科学基金;
关键词
LI-ION; HIGH-CAPACITY; ELECTRODE MATERIALS; VOLTAGE HYSTERESIS; LAYERED OXIDES; RICH CATHODE; ORIGIN; EVOLUTION; DESIGN; OPPORTUNITIES;
D O I
10.1063/5.0096578
中图分类号
O59 [应用物理学];
学科分类号
摘要
Constructions of high-energy-density lithium-ion batteries (LIBs) largely rely on the breakthrough of cathode materials. In contrast to conventional layered oxide cathodes (LiTMO2, TM denotes transition metal), invoking oxygen redox by increasing the chemical ratio of Li/O in oxide cathode can further boost the development of new types of high-capacity cathodes which theoretically enable the realization of LIBs of above 400 Wh/kg and are even attainable for 600 Wh/kg, meeting the future demands of various application scenarios for high energy density, such as electrical aircraft. However, the revolution of high-capacity cathodes is far from the realistic elevation of cell-level energy density and their practical applications in LIBs, which involves the considerations of other indispensable metrics in terms of both materials and technologies. Therefore, in this perspective, an in-depth discussion from fundamentals to applications of oxygen-based cathode materials is provided. First, we briefly summarized the representative investigations on oxygen redox mechanisms. Moreover, intrinsic properties of materials based on oxygen redox are multidimensionally evaluated. Furthermore, cell-level gravimetric energy density, potentials for practical applications, and possible design strategies are critically analyzed. Published under an exclusive license by AIP Publishing.
引用
收藏
页数:11
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