TY - JOUR
T1 - Operando soft x-ray emission spectroscopy of LiMn2O4 thin film involving Li-ion extraction/insertion reaction
AU - Asakura, Daisuke
AU - Hosono, Eiji
AU - Niwa, Hideharu
AU - Kiuchi, Hisao
AU - Miyawaki, Jun
AU - Nanba, Yusuke
AU - Okubo, Masashi
AU - Matsuda, Hirofumi
AU - Zhou, Haoshen
AU - Oshima, Masaharu
AU - Harada, Yoshihisa
N1 - Funding Information:
The XAS and XES measurements were performed by the joint research in SRRO and ISSP, the University of Tokyo (Proposal Nos. 2012B7437, 2013A7445 and 2013B7460). D.A. acknowledges support from JSPS KAKENHI (25871186). This work is partially supported by the Japan–U.S. Cooperation Project for Research and Standardization of Clean Energy Technologies . A part of this work was conducted at the AIST Nano-Processing Facility, supported by “Nanotechnology Platform Program” of MEXT , Japan.
Publisher Copyright:
© 2014 Elsevier B.V. All rights reserved.
PY - 2015/1
Y1 - 2015/1
N2 - We developed an electrochemical in situ cell for soft x-ray emission spectroscopy (XES) to accurately investigate the redox reaction and electronic structure of transition metals in the cathode materials for Li-ion battery. The in situ cell consists of a Li-metal counter electrode, an organic electrolyte solution, and a cathode on a membrane window which separates the liquid electrolyte from high vacuum and can pass the incoming and emitted photons. In this study, the Mn 3d electronic structure of LiMn2O4 thin-film electrodewas clarified by the operando XES. At the charged state, the XES spectrum changed significantly from the open-circuit-voltage (OCV) state, suggesting oxidation of the Mn3+ component through Li-ion extraction. Upon discharge up to 3.0 V vs. Li/Li+, the XES spectrum almost returned to its profile at the OCV state with small difference, indicating the valence change of Mn: Mn3.6+ → Mn4+ → Mn3.3+ corresponding to the OCV, charged, and discharged states.
AB - We developed an electrochemical in situ cell for soft x-ray emission spectroscopy (XES) to accurately investigate the redox reaction and electronic structure of transition metals in the cathode materials for Li-ion battery. The in situ cell consists of a Li-metal counter electrode, an organic electrolyte solution, and a cathode on a membrane window which separates the liquid electrolyte from high vacuum and can pass the incoming and emitted photons. In this study, the Mn 3d electronic structure of LiMn2O4 thin-film electrodewas clarified by the operando XES. At the charged state, the XES spectrum changed significantly from the open-circuit-voltage (OCV) state, suggesting oxidation of the Mn3+ component through Li-ion extraction. Upon discharge up to 3.0 V vs. Li/Li+, the XES spectrum almost returned to its profile at the OCV state with small difference, indicating the valence change of Mn: Mn3.6+ → Mn4+ → Mn3.3+ corresponding to the OCV, charged, and discharged states.
KW - In situ
KW - Li-ion battery
KW - LiMno
KW - Operando
KW - Soft x-ray emission spectroscopy
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U2 - 10.1016/j.elecom.2014.09.015
DO - 10.1016/j.elecom.2014.09.015
M3 - Article
AN - SCOPUS:84919740259
SN - 1388-2481
VL - 50
SP - 93
EP - 96
JO - Electrochemistry Communications
JF - Electrochemistry Communications
ER -