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Alloying Motif Confined in Intercalative Frameworks toward Rapid Li‐Ion Storage
High‐capacity alloying‐type anodes suffer poor rate capability due to their great volume expansion, while high‐rate intercalation‐type anodes are troubled with low theoretical capacity. Herein, a novel mechanism of alloying in the intercalative frameworks is proposed to confer both high‐capacity and...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9376843/ https://www.ncbi.nlm.nih.gov/pubmed/35713282 http://dx.doi.org/10.1002/advs.202202026 |
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author | Lin, Xueyu Dong, Chenlong Zhao, Siwei Peng, Baixin Zhou, Ce Wang, Ruiqi Huang, Fuqiang |
author_facet | Lin, Xueyu Dong, Chenlong Zhao, Siwei Peng, Baixin Zhou, Ce Wang, Ruiqi Huang, Fuqiang |
author_sort | Lin, Xueyu |
collection | PubMed |
description | High‐capacity alloying‐type anodes suffer poor rate capability due to their great volume expansion, while high‐rate intercalation‐type anodes are troubled with low theoretical capacity. Herein, a novel mechanism of alloying in the intercalative frameworks is proposed to confer both high‐capacity and high‐rate performances on anodes. Taking the indium‐vanadium oxide (IVO) as a typical system, alloying‐typed In is dispersed in the stable intercalative V(2)O(3) to form a solid solution. The alloying‐typed In element provides high lithium storage capacity, while the robust, Li‐conductive V−O frameworks effectively alleviate the volume expansion and aggregation of In. Benefiting from the above merits, the anode exhibits a high specific capacity of 1364 mA h g(−1) at 1 A g(−1) and an extraordinary cyclic performance of 814 mA h g(−1) at 10 A g(−1) after 600 cycles (124.9 mA h g(−1) after 10 000 cycles at 50 A g(−1)). The superior electrochemical rate capability of (In,V)(2)O(3) solid solution anode rivals that of the reported alloying anode materials. This strategy can be extended for fabricating other alloying/intercalation hybrid anodes, such as (Sn,V)O(2) and (Sn,Ti)O(2), which demonstrates the universality of confining alloying motifs in intercalative frameworks for rapid and high‐capacity lithium storage. |
format | Online Article Text |
id | pubmed-9376843 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-93768432022-08-18 Alloying Motif Confined in Intercalative Frameworks toward Rapid Li‐Ion Storage Lin, Xueyu Dong, Chenlong Zhao, Siwei Peng, Baixin Zhou, Ce Wang, Ruiqi Huang, Fuqiang Adv Sci (Weinh) Research Articles High‐capacity alloying‐type anodes suffer poor rate capability due to their great volume expansion, while high‐rate intercalation‐type anodes are troubled with low theoretical capacity. Herein, a novel mechanism of alloying in the intercalative frameworks is proposed to confer both high‐capacity and high‐rate performances on anodes. Taking the indium‐vanadium oxide (IVO) as a typical system, alloying‐typed In is dispersed in the stable intercalative V(2)O(3) to form a solid solution. The alloying‐typed In element provides high lithium storage capacity, while the robust, Li‐conductive V−O frameworks effectively alleviate the volume expansion and aggregation of In. Benefiting from the above merits, the anode exhibits a high specific capacity of 1364 mA h g(−1) at 1 A g(−1) and an extraordinary cyclic performance of 814 mA h g(−1) at 10 A g(−1) after 600 cycles (124.9 mA h g(−1) after 10 000 cycles at 50 A g(−1)). The superior electrochemical rate capability of (In,V)(2)O(3) solid solution anode rivals that of the reported alloying anode materials. This strategy can be extended for fabricating other alloying/intercalation hybrid anodes, such as (Sn,V)O(2) and (Sn,Ti)O(2), which demonstrates the universality of confining alloying motifs in intercalative frameworks for rapid and high‐capacity lithium storage. John Wiley and Sons Inc. 2022-06-17 /pmc/articles/PMC9376843/ /pubmed/35713282 http://dx.doi.org/10.1002/advs.202202026 Text en © 2022 The Authors. Advanced Science published by Wiley‐VCH GmbH https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Articles Lin, Xueyu Dong, Chenlong Zhao, Siwei Peng, Baixin Zhou, Ce Wang, Ruiqi Huang, Fuqiang Alloying Motif Confined in Intercalative Frameworks toward Rapid Li‐Ion Storage |
title | Alloying Motif Confined in Intercalative Frameworks toward Rapid Li‐Ion Storage |
title_full | Alloying Motif Confined in Intercalative Frameworks toward Rapid Li‐Ion Storage |
title_fullStr | Alloying Motif Confined in Intercalative Frameworks toward Rapid Li‐Ion Storage |
title_full_unstemmed | Alloying Motif Confined in Intercalative Frameworks toward Rapid Li‐Ion Storage |
title_short | Alloying Motif Confined in Intercalative Frameworks toward Rapid Li‐Ion Storage |
title_sort | alloying motif confined in intercalative frameworks toward rapid li‐ion storage |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9376843/ https://www.ncbi.nlm.nih.gov/pubmed/35713282 http://dx.doi.org/10.1002/advs.202202026 |
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