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Electronic and Geometric Structures of Rechargeable Lithium Manganese Sulfate Li2Mn(SO4)2 Cathode
Author(s) -
Disha Gupta,
Aravind Muthiah,
Minh Phuong,
Gopinathan Sankar,
Timothy I. Hyde,
Mark Copley,
Tom Baikie,
Yonghua Du,
Shibo Xi,
Madhavi Srinivasan,
Zhili Dong
Publication year - 2019
Publication title -
acs omega
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.779
H-Index - 40
ISSN - 2470-1343
DOI - 10.1021/acsomega.9b00356
Subject(s) - manganese , cathode , lithium (medication) , sulfate , materials science , inorganic chemistry , chemistry , metallurgy , medicine , endocrinology
Here, we report the use of Li 2 Mn(SO 4 ) 2 as a potential energy storage material and describe its route of synthesis and structural characterization over one electrochemical cycle. Li 2 Mn(SO 4 ) 2 is synthesized by ball milling of MnSO 4 ·H 2 O and Li 2 SO 4 ·H 2 O and characterized using a suite of techniques, in particular, ex situ X-ray diffraction, X-ray photoelectron spectroscopy, and X-ray absorption spectroscopy on the Mn and S K-edges to investigate the electronic and local geometry around the absorbing atoms. The prepared Li 2 Mn(SO 4 ) 2 electrodes undergo electrochemical cycles to different potential points on the charge-discharge curve and are then extracted from the cells at these points for ex situ structural analysis. Analysis of X-ray absorption spectroscopy (both near and fine structure part of the data) data suggests that there are minimal changes to the oxidation state of Mn and S ions during charge-discharge cycles. However, X-ray photoelectron spectroscopy analysis suggests that there are changes in the oxidation state of Mn, which appears to be different from the conclusion drawn from X-ray absorption spectroscopy. This difference in results during cycling can thus be attributed to electrochemical reactions being dominant at the surface of the Li 2 Mn(SO 4 ) 2 particles rather than in the bulk.

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