硫代磷酸盐
电解质
材料科学
复合数
电极
电化学
无定形固体
化学工程
快离子导体
扫描电子显微镜
纳米技术
复合材料
化学
结晶学
物理化学
有机化学
工程类
作者
Patrice Perrenot,Pascale Bayle‐Guillemaud,Claire Villevieille
出处
期刊:ACS energy letters
[American Chemical Society]
日期:2023-11-01
卷期号:8 (11): 4957-4965
被引量:8
标识
DOI:10.1021/acsenergylett.3c01975
摘要
Solid-state batteries using thiophosphate solid electrolytes are believed to be the next generation solid electrolyte batteries, but they suffer from several issues, including also the engineering of the composite positive electrode. To date, the relationship between the morphology of the composite electrode and its electrochemical performance remains undetermined. By using Focused Ion Beam–Scanning Electron Microscopy (FIB-SEM) tomography, we investigated the engineering of several composite electrodes of polycrystalline NMC 622 (LiNi0.6Mn0.2Co0.2O2) particles and amorphous Li3PS4 solid electrolyte. Based on the morphological analysis of the electronic and ionic networks, it is possible to determine that the electrochemical performance limitation in this cell emerges from the surface contact between the NMC and the LPS as the sintering of the solid electrolyte (SE) is far from optimal. Additionally, similar analyses performed after the first charge show that the fading of the electrochemical is linked to the morphological evolution in the composite positive electrode.
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