电解质
材料科学
阴极
阳极
电极
相间
金属锂
化学工程
锂(药物)
金属
电池(电)
溶解
无机化学
化学
冶金
内分泌学
生物
工程类
量子力学
物理化学
物理
遗传学
功率(物理)
医学
作者
Qianqian Liu,Zerui Chen,Yan Liu,Youran Hong,Weina Wang,Jianghao Wang,Bo Zhao,Yifei Xu,Jiangwei Wang,Xiulin Fan,Linsen Li,Hao Wu
标识
DOI:10.1016/j.ensm.2021.02.039
摘要
Stable electrode-electrolyte interphases on both electrodes are indispensable to warrant cycling stability of high-voltage Li-metal batteries. Here, we reveal a unique cooperative reaction mechanism to form protective interphase layers on both Li-metal anode and high-voltage cathodes, which is exemplified by a multifunctional additive ethoxy(pentafluoro)cyclotriphosphazene (PFPN). The F-rich PFPN first reacts with Li-metal anode to form LiF-rich solid electrolyte interphase (SEI), which stabilizes the Li deposition/dissolution processes. Meanwhile, the in-situ generated PFPN derivatives with a de-fluorated structure are prone to be oxidized on cathode, forming a robust cathode-electrolyte interphase (CEI) to prevent electrolyte oxidation and electrode degradation at high voltage. With PFPN to harness the aggressive battery electrodes, Li-metal batteries with high-voltage LiCoO2 (4.5 V) and LiNi0.5Mn1.5O2 (4.9 V) cathodes exhibit improved cycling stability and rate capability. In particular, the LiNi0.5Mn1.5O2|Li full cell with limited Li supply (N/P =7.6) demonstrates outperformed capacity retention of 90.7 % after 100 cycles, which is almost twice that of the cell using PFPN-free conventional electrolyte (47.5 %).
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