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Electronic and Geometric Structures of Rechargeable Lithium Manganese Sulfate Li(2)Mn(SO(4))(2) Cathode

[Image: see text] 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 charact...

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Autores principales: Gupta, Disha, Muthiah, Aravind, Do, Minh Phuong, Sankar, Gopinathan, Hyde, Timothy I., Copley, Mark Patrick, Baikie, Tom, Du, Yonghua, Xi, Shibo, Srinivasan, Madhavi, Dong, ZhiLi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2019
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6682148/
https://www.ncbi.nlm.nih.gov/pubmed/31460237
http://dx.doi.org/10.1021/acsomega.9b00356
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author Gupta, Disha
Muthiah, Aravind
Do, Minh Phuong
Sankar, Gopinathan
Hyde, Timothy I.
Copley, Mark Patrick
Baikie, Tom
Du, Yonghua
Xi, Shibo
Srinivasan, Madhavi
Dong, ZhiLi
author_facet Gupta, Disha
Muthiah, Aravind
Do, Minh Phuong
Sankar, Gopinathan
Hyde, Timothy I.
Copley, Mark Patrick
Baikie, Tom
Du, Yonghua
Xi, Shibo
Srinivasan, Madhavi
Dong, ZhiLi
author_sort Gupta, Disha
collection PubMed
description [Image: see text] 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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spelling pubmed-66821482019-08-27 Electronic and Geometric Structures of Rechargeable Lithium Manganese Sulfate Li(2)Mn(SO(4))(2) Cathode Gupta, Disha Muthiah, Aravind Do, Minh Phuong Sankar, Gopinathan Hyde, Timothy I. Copley, Mark Patrick Baikie, Tom Du, Yonghua Xi, Shibo Srinivasan, Madhavi Dong, ZhiLi ACS Omega [Image: see text] 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. American Chemical Society 2019-07-01 /pmc/articles/PMC6682148/ /pubmed/31460237 http://dx.doi.org/10.1021/acsomega.9b00356 Text en Copyright © 2019 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes.
spellingShingle Gupta, Disha
Muthiah, Aravind
Do, Minh Phuong
Sankar, Gopinathan
Hyde, Timothy I.
Copley, Mark Patrick
Baikie, Tom
Du, Yonghua
Xi, Shibo
Srinivasan, Madhavi
Dong, ZhiLi
Electronic and Geometric Structures of Rechargeable Lithium Manganese Sulfate Li(2)Mn(SO(4))(2) Cathode
title Electronic and Geometric Structures of Rechargeable Lithium Manganese Sulfate Li(2)Mn(SO(4))(2) Cathode
title_full Electronic and Geometric Structures of Rechargeable Lithium Manganese Sulfate Li(2)Mn(SO(4))(2) Cathode
title_fullStr Electronic and Geometric Structures of Rechargeable Lithium Manganese Sulfate Li(2)Mn(SO(4))(2) Cathode
title_full_unstemmed Electronic and Geometric Structures of Rechargeable Lithium Manganese Sulfate Li(2)Mn(SO(4))(2) Cathode
title_short Electronic and Geometric Structures of Rechargeable Lithium Manganese Sulfate Li(2)Mn(SO(4))(2) Cathode
title_sort electronic and geometric structures of rechargeable lithium manganese sulfate li(2)mn(so(4))(2) cathode
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6682148/
https://www.ncbi.nlm.nih.gov/pubmed/31460237
http://dx.doi.org/10.1021/acsomega.9b00356
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