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Anionic redox reaction in layered NaCr(2/3)Ti(1/3)S(2) through electron holes formation and dimerization of S–S
The use of anion redox reactions is gaining interest for increasing rechargeable capacities in alkaline ion batteries. Although anion redox coupling of S(2−) and (S(2))(2−) through dimerization of S–S in sulfides have been studied and reported, an anion redox process through electron hole formation...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6773774/ https://www.ncbi.nlm.nih.gov/pubmed/31575867 http://dx.doi.org/10.1038/s41467-019-12310-6 |
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author | Wang, Tian Ren, Guo-Xi Shadike, Zulipiya Yue, Ji-Li Cao, Ming-Hui Zhang, Jie-Nan Chen, Ming-Wei Yang, Xiao-Qing Bak, Seong-Min Northrup, Paul Liu, Pan Liu, Xiao-Song Fu, Zheng-Wen |
author_facet | Wang, Tian Ren, Guo-Xi Shadike, Zulipiya Yue, Ji-Li Cao, Ming-Hui Zhang, Jie-Nan Chen, Ming-Wei Yang, Xiao-Qing Bak, Seong-Min Northrup, Paul Liu, Pan Liu, Xiao-Song Fu, Zheng-Wen |
author_sort | Wang, Tian |
collection | PubMed |
description | The use of anion redox reactions is gaining interest for increasing rechargeable capacities in alkaline ion batteries. Although anion redox coupling of S(2−) and (S(2))(2−) through dimerization of S–S in sulfides have been studied and reported, an anion redox process through electron hole formation has not been investigated to the best of our knowledge. Here, we report an O3-NaCr(2/3)Ti(1/3)S(2) cathode that delivers a high reversible capacity of ~186 mAh g(−1) (0.95 Na) based on the cation and anion redox process. Various charge compensation mechanisms of the sulfur anionic redox process in layered NaCr(2/3)Ti(1/3)S(2), which occur through the formation of disulfide-like species, the precipitation of elemental sulfur, S–S dimerization, and especially through the formation of electron holes, are investigated. Direct structural evidence for formation of electron holes and (S(2))(n−) species with shortened S–S distances is obtained. These results provide valuable information for the development of materials based on the anionic redox reaction. |
format | Online Article Text |
id | pubmed-6773774 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-67737742019-10-03 Anionic redox reaction in layered NaCr(2/3)Ti(1/3)S(2) through electron holes formation and dimerization of S–S Wang, Tian Ren, Guo-Xi Shadike, Zulipiya Yue, Ji-Li Cao, Ming-Hui Zhang, Jie-Nan Chen, Ming-Wei Yang, Xiao-Qing Bak, Seong-Min Northrup, Paul Liu, Pan Liu, Xiao-Song Fu, Zheng-Wen Nat Commun Article The use of anion redox reactions is gaining interest for increasing rechargeable capacities in alkaline ion batteries. Although anion redox coupling of S(2−) and (S(2))(2−) through dimerization of S–S in sulfides have been studied and reported, an anion redox process through electron hole formation has not been investigated to the best of our knowledge. Here, we report an O3-NaCr(2/3)Ti(1/3)S(2) cathode that delivers a high reversible capacity of ~186 mAh g(−1) (0.95 Na) based on the cation and anion redox process. Various charge compensation mechanisms of the sulfur anionic redox process in layered NaCr(2/3)Ti(1/3)S(2), which occur through the formation of disulfide-like species, the precipitation of elemental sulfur, S–S dimerization, and especially through the formation of electron holes, are investigated. Direct structural evidence for formation of electron holes and (S(2))(n−) species with shortened S–S distances is obtained. These results provide valuable information for the development of materials based on the anionic redox reaction. Nature Publishing Group UK 2019-10-01 /pmc/articles/PMC6773774/ /pubmed/31575867 http://dx.doi.org/10.1038/s41467-019-12310-6 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Wang, Tian Ren, Guo-Xi Shadike, Zulipiya Yue, Ji-Li Cao, Ming-Hui Zhang, Jie-Nan Chen, Ming-Wei Yang, Xiao-Qing Bak, Seong-Min Northrup, Paul Liu, Pan Liu, Xiao-Song Fu, Zheng-Wen Anionic redox reaction in layered NaCr(2/3)Ti(1/3)S(2) through electron holes formation and dimerization of S–S |
title | Anionic redox reaction in layered NaCr(2/3)Ti(1/3)S(2) through electron holes formation and dimerization of S–S |
title_full | Anionic redox reaction in layered NaCr(2/3)Ti(1/3)S(2) through electron holes formation and dimerization of S–S |
title_fullStr | Anionic redox reaction in layered NaCr(2/3)Ti(1/3)S(2) through electron holes formation and dimerization of S–S |
title_full_unstemmed | Anionic redox reaction in layered NaCr(2/3)Ti(1/3)S(2) through electron holes formation and dimerization of S–S |
title_short | Anionic redox reaction in layered NaCr(2/3)Ti(1/3)S(2) through electron holes formation and dimerization of S–S |
title_sort | anionic redox reaction in layered nacr(2/3)ti(1/3)s(2) through electron holes formation and dimerization of s–s |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6773774/ https://www.ncbi.nlm.nih.gov/pubmed/31575867 http://dx.doi.org/10.1038/s41467-019-12310-6 |
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