氧化还原
电解质
硫化物
锂(药物)
再分配(选举)
化学
材料科学
无机化学
快离子导体
离子键合
电化学
金属
离子电导率
锂电池
化学工程
电导率
电子
电池(电)
电子转移
纳米技术
集聚经济
磷酸钒锂电池
不稳定性
电流密度
金属锂
化学物理
密度泛函理论
电极
离子
作者
Chong Liu,Butian Chen,Tianran Zhang,Jicheng Zhang,Ruoyu Wang,Jian Zheng,Qianjiang Mao,Xiangfeng Liu
标识
DOI:10.1002/ange.202302655
摘要
Abstract Sulfide electrolytes with high ionic conductivity hold great promise for all‐solid‐state lithium batteries. However, the parasitic redox reactions between sulfide electrolyte and Li metal result in interfacial instability and rapid decline of the battery performance. Herein, a redox‐resistible Li 6 PS 5 Cl (LPSC) electrolyte is created by regulating the electron distribution in LPSC with Mg and F incorporation. The introduction of Mg triggers the electron agglomeration around S atom, inhibiting the electron acceptance from Li, and F generates the self‐limiting interface, which hinders the redox reactions between LPSC and Li metal. This redox‐resistible Li 6 PS 5 Cl‐MgF 2 electrolyte therefore presents a high critical current density (2.3 times that of pristine electrolyte). The LiCoO 2 /Li 6 PS 5 Cl‐MgF 2 /Li cell shows an outstanding cycling stability (93.3 %@100 cycles at 0.2 C). This study highlights the electronic structure modulation to address redox issues on sulfide‐based lithium batteries.
科研通智能强力驱动
Strongly Powered by AbleSci AI