电解质
材料科学
阴极
硫化物
化学工程
降级(电信)
化学稳定性
锂(药物)
图层(电子)
无机化学
电极
纳米技术
化学
冶金
物理化学
内分泌学
工程类
电信
医学
计算机科学
作者
Chanhyun Park,Juho Lee,Sangpyo Lee,Yu Han,Jin‐Soo Kim,Sung‐Kyun Jung
标识
DOI:10.1002/aenm.202203861
摘要
Abstract Keeping both the chemical and physical state of the electrode–electrolyte interface intact is one of the greatest challenges in achieving solid‐state batteries (SSBs) with longer cycle lives. Herein, the use of organic electrolyte additives in the cathode electrolyte interphase (CEI) layer to mitigate the intertwined chemical and mechanical degradation in sulfide‐based SSBs is demonstrated. Lithium difluorobis(oxalato)phosphate (LiDFBOP) and argyrodite (Li 6 PS 5 Cl) are used as a model system, with the LiDFBOP‐derived CEI layer induced by irreversible oxidation above 4.12 V (vs Li + /Li) during the formation cycle exhibiting dual functions. This CEI layer retards the rate of chemical degradation between the cathode active particles and solid electrolytes at high charging potential and helps maintain intimate physical contact even at a low stack pressure of 0.75 MPa. The improved physical contact enables delivery of a high initial capacity, while chemical stability suppressing the sulfite or sulfate formation has a more dominant effect on the long‐term cycle stability. This study presents a new perspective and strategies for designing cathode coating materials for sulfide‐based SSBs beyond the typically used inorganic oxide materials.
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