Observation of Interfacial Degradation of Li6PS5Cl against Lithium Metal and LiCoO2 via In Situ Electrochemical Raman Microscopy

被引:87
|
作者
Zhou, Yundong [1 ,2 ,3 ]
Doerrer, Christopher [3 ,4 ]
Kasemchainan, Jitti [3 ,4 ]
Bruce, Peter G. [3 ,4 ]
Pasta, Mauro [3 ,4 ]
Hardwick, Laurence J. [1 ,2 ,3 ]
机构
[1] Univ Liverpool, Stephenson Inst Renewable Energy, Chadwick Bldg,Peach St, Liverpool L69 7ZF, Merseyside, England
[2] Univ Liverpool, Dept Chem, Crown St, Liverpool L69 7ZD, Merseyside, England
[3] Faraday Inst, Quad One,Becquerel Ave,Harwell Campus, Didcot OX11 0RA, Oxon, England
[4] Univ Oxford, Dept Mat, Parks Rd, Oxford OX1 3PH, England
基金
英国工程与自然科学研究理事会;
关键词
electrode-solid electrolyte interface; electrochemistry; in situ Raman microscopy; interfaces; solid-state batteries; SOLID-ELECTROLYTE; STRUCTURAL-CHARACTERIZATION; THIN-FILM; SULFUR; STABILITY; CATHODE; PERFORMANCE; SULFIDE; SURFACE;
D O I
10.1002/batt.201900218
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
Sulfide-based Li+ conducting solid electrolytes, such as argyrodite, Li6PS5Cl, for all-solid-state batteries can have comparable ionic conductivities with liquid electrolytes. However, the interface between sulfide containing solid electrolytes and Li metal and Li-ion positive electrodes has been found to be unstable, leading to poor cell performance and cycling. Understanding the in situ evolution of interfacial layers between the electrolyte and both electrodes is of paramount importance for designing stable and long-life solid-state batteries. Here, in situ Raman microscopy was used to study the interface between Li6PS5Cl electrolyte and metallic Li and LiCoO2. Under potential control, Raman microscopy identified the appearance of degradation products (Li2S, P2Sx and polysulfides) at the electrode/solid electrolyte interface.
引用
收藏
页码:647 / 652
页数:6
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