Operando hard X-ray photoelectron spectroscopy of LiCoO2 thin film in an all-solid-state lithium ion battery

Electrochemistry Communications

Eiichiro Matsubara¹  Kazuhiro Hikima²  Ryoji Kanno³  Fukunaga Toshiharu⁴  Keisuke Shimizu⁴  Hisao Kiuchi⁵ 

[1] All-Solid-State Battery Unit, Institute of Innovative Research, Tokyo Institute of Technology, 4259 Nagatsuta, Midori-ku, Yokohama, Kanagawa 226-8502, Japan;Corresponding author.;All-Solid-State Battery Unit, Institute of Innovative Research, Tokyo Institute of Technology, 4259 Nagatsuta, Midori-ku, Yokohama, Kanagawa 226-8502, Japan;Department of Chemical Science and Engineering, School of Materials and Chemical Technology, Tokyo Institute of Technology, 4259 Nagatsuta, Midori-ku, Yokohama, Kanagawa 226-8502, Japan;Office of Society-Academia Collaboration for Innovation, Kyoto University, Gokasho, Uji, Kyoto 611-0011, Japan;

关键词: All-solid-state battery;    Thin film;    LiCoO2;    In situ;    Operando;    Hard X-ray photoelectron spectroscopy;   

DOI  :  

来源: DOAJ

【 摘 要 】

A novel electrochemical setup for operando hard X-ray photoelectron spectroscopy (HAXPES) was proposed to investigate the bulk-sensitive electronic structure of cations and anions in the active materials of an all-solid-state Li-ion battery. A model all-solid-state thin film cell was prepared by depositing a LiCoO2 positive electrode and an Al current collector on the front of the solid electrolyte substrate, and a Li3PO4 buffer solid electrolyte and a Li negative electrode on the back side, to give a structure of Al (10 nm)/LiCoO2 (35 nm)/Li1+x+yAlx(Ti, Ge)2−xSiyP3−yO12 (180 μm)/Li3PO4 (500 nm)/Li (1000 nm). The reversible changes of the core levels (Al 1s, P 1s, Li 1s, Co 2p3/2, O 1s) and the valence bands in the charged (4.2 V)/discharged (3.0 V) states were observed without disassembling the LiCoO2 thin film cell inside the vacuum chamber. The operando HAXPES spectra acquired during the charge–discharge process revealed that the reversible changes in the Co 2p3/2 and O 1s spectra were attributed to the participation of cobalt cations and oxygen anions from LiCoO2 in the redox mechanism.

【 授权许可】

Unknown