阴极
离子电导率
电导率
材料科学
电解质
成核
快离子导体
锂(药物)
电化学
硫化物
晶界
化学工程
化学物理
纳米技术
化学
物理化学
复合材料
电极
冶金
内分泌学
医学
工程类
微观结构
有机化学
作者
Niaz Ahmad,Cailing Fan,Muhammad Faheem,Chaoyuan Zeng,Sajid Mahmood,Xiaoxiao Liang,Xianzhe Yu,Qinxi Dong,Wen Yang
标识
DOI:10.1002/adsu.202400729
摘要
Abstract Inorganic solid‐state electrolytes (ISSEs) are recognized as promising candidates for safer and higher energy‐density all‐solid‐state lithium‐metal/sulfur batteries (ASSLM/SBs). Significant efforts have been directed at designing ISSEs with better chemical/electrochemical stability, superior lithium‐ion conductivity, and extensive working voltage windows. However, it has been investigated that Li‐dendrites produced within bulk ISSEs during the charge‐discharge process short‐circuit ASSLM/SBs. Notably, non‐negligble electronic conductivity (σ e ) ≈10 −8 S cm −1 can trigger nucleation of Li‐dendrites at intrinsic defects, e.g., grain boundaries, pores, and cracks of ISSEs, leading to a significant self‐discharge phenomenon in ASSLM/SBs. Furthermore, the reasons behind the insufficient utilization of cathode active materials (CAMs) in ASSLM/SBs at practical current densities or C‐rate remained overlooked. Herein, first, the strategies to reduce the σ e of sulfide‐based SSEs to prevent the Li‐dendrite formation at intrinsic defects are discussed. Second, strategies to enhance sulfur‐based cathodes' ionic and electronic conductivity (CAMs: Li 2 S and S 8 ) are addressed. How a balanced ionic and electronic conductivity in the positive cathode layer realizes fast kinetics and maximizes the utilization of CAMs and reversibility for high‐performance ASSLM/SBs is also discussed. Finally, an extensive conclusion and innovative perspectives are presented to give readers a clearer insight into ASSLM/SBs.
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