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Antisite occupation induced single anionic redox chemistry and structural stabilization of layered sodium chromium sulfide
The intercalation compounds with various electrochemically active or inactive elements in the layered structure have been the subject of increasing interest due to their high capacities, good reversibility, simple structures, and ease of synthesis. However, their reversible intercalation/deintercala...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5603526/ https://www.ncbi.nlm.nih.gov/pubmed/28924149 http://dx.doi.org/10.1038/s41467-017-00677-3 |
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author | Shadike, Zulipiya Zhou, Yong-Ning Chen, Lan-Li Wu, Qu Yue, Ji-Li Zhang, Nian Yang, Xiao-Qing Gu, Lin Liu, Xiao-Song Shi, Si-Qi Fu, Zheng-Wen |
author_facet | Shadike, Zulipiya Zhou, Yong-Ning Chen, Lan-Li Wu, Qu Yue, Ji-Li Zhang, Nian Yang, Xiao-Qing Gu, Lin Liu, Xiao-Song Shi, Si-Qi Fu, Zheng-Wen |
author_sort | Shadike, Zulipiya |
collection | PubMed |
description | The intercalation compounds with various electrochemically active or inactive elements in the layered structure have been the subject of increasing interest due to their high capacities, good reversibility, simple structures, and ease of synthesis. However, their reversible intercalation/deintercalation redox chemistries in previous compounds involve a single cationic redox reaction or a cumulative cationic and anionic redox reaction. Here we report an anionic redox chemistry and structural stabilization of layered sodium chromium sulfide. It was discovered that the sulfur in sodium chromium sulfide is electrochemically active, undergoing oxidation/reduction rather than chromium. Significantly, sodium ions can successfully move out and into without changing its lattice parameter c, which is explained in terms of the occurrence of chromium/sodium vacancy antisite during desodiation and sodiation processes. Our present work not only enriches the electrochemistry of layered intercalation compounds, but also extends the scope of investigation on high-capacity electrodes. |
format | Online Article Text |
id | pubmed-5603526 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-56035262017-09-22 Antisite occupation induced single anionic redox chemistry and structural stabilization of layered sodium chromium sulfide Shadike, Zulipiya Zhou, Yong-Ning Chen, Lan-Li Wu, Qu Yue, Ji-Li Zhang, Nian Yang, Xiao-Qing Gu, Lin Liu, Xiao-Song Shi, Si-Qi Fu, Zheng-Wen Nat Commun Article The intercalation compounds with various electrochemically active or inactive elements in the layered structure have been the subject of increasing interest due to their high capacities, good reversibility, simple structures, and ease of synthesis. However, their reversible intercalation/deintercalation redox chemistries in previous compounds involve a single cationic redox reaction or a cumulative cationic and anionic redox reaction. Here we report an anionic redox chemistry and structural stabilization of layered sodium chromium sulfide. It was discovered that the sulfur in sodium chromium sulfide is electrochemically active, undergoing oxidation/reduction rather than chromium. Significantly, sodium ions can successfully move out and into without changing its lattice parameter c, which is explained in terms of the occurrence of chromium/sodium vacancy antisite during desodiation and sodiation processes. Our present work not only enriches the electrochemistry of layered intercalation compounds, but also extends the scope of investigation on high-capacity electrodes. Nature Publishing Group UK 2017-09-18 /pmc/articles/PMC5603526/ /pubmed/28924149 http://dx.doi.org/10.1038/s41467-017-00677-3 Text en © The Author(s) 2017 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 Shadike, Zulipiya Zhou, Yong-Ning Chen, Lan-Li Wu, Qu Yue, Ji-Li Zhang, Nian Yang, Xiao-Qing Gu, Lin Liu, Xiao-Song Shi, Si-Qi Fu, Zheng-Wen Antisite occupation induced single anionic redox chemistry and structural stabilization of layered sodium chromium sulfide |
title | Antisite occupation induced single anionic redox chemistry and structural stabilization of layered sodium chromium sulfide |
title_full | Antisite occupation induced single anionic redox chemistry and structural stabilization of layered sodium chromium sulfide |
title_fullStr | Antisite occupation induced single anionic redox chemistry and structural stabilization of layered sodium chromium sulfide |
title_full_unstemmed | Antisite occupation induced single anionic redox chemistry and structural stabilization of layered sodium chromium sulfide |
title_short | Antisite occupation induced single anionic redox chemistry and structural stabilization of layered sodium chromium sulfide |
title_sort | antisite occupation induced single anionic redox chemistry and structural stabilization of layered sodium chromium sulfide |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5603526/ https://www.ncbi.nlm.nih.gov/pubmed/28924149 http://dx.doi.org/10.1038/s41467-017-00677-3 |
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