阴极
材料科学
电解质
硫代磷酸盐
氧化物
涂层
化学工程
相(物质)
扫描电子显微镜
复合材料
物理化学
电极
冶金
化学
有机化学
工程类
作者
Yaqian Zhang,Yaosen Tian,Yihan Xiao,Lincoln J. Miara,Yûichi Aihara,Tomoyuki Tsujimura,Tan Shi,Mary Scott,Gerbrand Ceder
标识
DOI:10.1002/aenm.201903778
摘要
Abstract The interfacial instability between a thiophosphate solid electrolyte and oxide cathodes results in rapid capacity fade and has driven the need for cathode coatings. In this work, the stability, evolution, and performance of uncoated, Li 2 ZrO 3 ‐coated, and Li 3 B 11 O 18 ‐coated LiNi 0.5 Co 0.2 Mn 0.3 O 2 cathodes are compared using first‐principles computations and electron microscopy characterization. Li 3 B 11 O 18 is identified as a superior coating that exhibits excellent oxidation/chemical stability, leading to substantially improved performance over cells with Li 2 ZrO 3 ‐coated or uncoated cathodes. The chemical and structural origin of the different performance is interpreted using different microscopy techniques which enable the direct observation of the phase decomposition of the Li 2 ZrO 3 coating. It is observed that Li is already extracted from the Li 2 ZrO 3 in the first charge, leading to the formation of ZrO 2 nanocrystallites with loss of protection of the cathode. After 50 cycles separated (Co, Ni)‐sulfides and Mn‐sulfides can be observed within the Li 2 ZrO 3 ‐coated material. This work illustrates the severity of the interfacial reactions between a thiophosphate electrolyte and oxide cathode and shows the importance of using coating materials that are absolutely stable at high voltage.
科研通智能强力驱动
Strongly Powered by AbleSci AI