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Orthorhombic Nb(2)O(5) Decorated Carbon Nanoreactors Enable Bidirectionally Regulated Redox Behaviors in Room‐Temperature Na–S Batteries
Regulating redox kinetics is able to spur the great‐leap‐forward development of room‐temperature sodium–sulfur (RT Na–S) batteries, especially on propelling their Na‐ion storage capability. Here, an innovative metal oxide kinetics accelerator, orthorhombic Nb(2)O(5) Na‐ion conductor, is proposed to...
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/PMC9896060/ https://www.ncbi.nlm.nih.gov/pubmed/36470655 http://dx.doi.org/10.1002/advs.202206558 |
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author | Huang, Xiang Long Zhang, Xiaofeng Zhou, Liujiang Guo, Zaiping Liu, Hua Kun Dou, Shi Xue Wang, Zhiming |
author_facet | Huang, Xiang Long Zhang, Xiaofeng Zhou, Liujiang Guo, Zaiping Liu, Hua Kun Dou, Shi Xue Wang, Zhiming |
author_sort | Huang, Xiang Long |
collection | PubMed |
description | Regulating redox kinetics is able to spur the great‐leap‐forward development of room‐temperature sodium–sulfur (RT Na–S) batteries, especially on propelling their Na‐ion storage capability. Here, an innovative metal oxide kinetics accelerator, orthorhombic Nb(2)O(5) Na‐ion conductor, is proposed to functionalize porous carbon nanoreactors (CNR) for S cathodes. The Nb(2)O(5) is shown to chemically immobilize sodium polysulfides via strong affinity. Theoretical and experimental evidence reveals that the Nb(2)O(5) can bidirectionally regulate redox behaviors of S cathodes, which accelerates reduction conversions from polysulfides to sulfides as well as promotes oxidation reactions from sulfides to S. In situ and ex situ characterization techniques further verify its electrochemical lasting endurance in catalyzing S conversions. The well‐designed S cathode demonstrates a high specific capacity of 1377 mA h g(−1) at 0.1 A g(−1), outstanding rate capability of 405 mA h g(−1) at 2 A g(−1), and stable cyclability with a capacity retention of 617 mA h g(−1) over 600 cycles at 0.5 A g(−1). An ultralow capacity decay rate of 0.0193% per cycle is successfully realized, superior to those of current state‐of‐the‐art RT Na–S batteries. This design also suits emerging Na–Se batteries, which contribute to outstanding electrochemical performance as well. |
format | Online Article Text |
id | pubmed-9896060 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-98960602023-02-08 Orthorhombic Nb(2)O(5) Decorated Carbon Nanoreactors Enable Bidirectionally Regulated Redox Behaviors in Room‐Temperature Na–S Batteries Huang, Xiang Long Zhang, Xiaofeng Zhou, Liujiang Guo, Zaiping Liu, Hua Kun Dou, Shi Xue Wang, Zhiming Adv Sci (Weinh) Research Articles Regulating redox kinetics is able to spur the great‐leap‐forward development of room‐temperature sodium–sulfur (RT Na–S) batteries, especially on propelling their Na‐ion storage capability. Here, an innovative metal oxide kinetics accelerator, orthorhombic Nb(2)O(5) Na‐ion conductor, is proposed to functionalize porous carbon nanoreactors (CNR) for S cathodes. The Nb(2)O(5) is shown to chemically immobilize sodium polysulfides via strong affinity. Theoretical and experimental evidence reveals that the Nb(2)O(5) can bidirectionally regulate redox behaviors of S cathodes, which accelerates reduction conversions from polysulfides to sulfides as well as promotes oxidation reactions from sulfides to S. In situ and ex situ characterization techniques further verify its electrochemical lasting endurance in catalyzing S conversions. The well‐designed S cathode demonstrates a high specific capacity of 1377 mA h g(−1) at 0.1 A g(−1), outstanding rate capability of 405 mA h g(−1) at 2 A g(−1), and stable cyclability with a capacity retention of 617 mA h g(−1) over 600 cycles at 0.5 A g(−1). An ultralow capacity decay rate of 0.0193% per cycle is successfully realized, superior to those of current state‐of‐the‐art RT Na–S batteries. This design also suits emerging Na–Se batteries, which contribute to outstanding electrochemical performance as well. John Wiley and Sons Inc. 2022-12-05 /pmc/articles/PMC9896060/ /pubmed/36470655 http://dx.doi.org/10.1002/advs.202206558 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 Huang, Xiang Long Zhang, Xiaofeng Zhou, Liujiang Guo, Zaiping Liu, Hua Kun Dou, Shi Xue Wang, Zhiming Orthorhombic Nb(2)O(5) Decorated Carbon Nanoreactors Enable Bidirectionally Regulated Redox Behaviors in Room‐Temperature Na–S Batteries |
title | Orthorhombic Nb(2)O(5) Decorated Carbon Nanoreactors Enable Bidirectionally Regulated Redox Behaviors in Room‐Temperature Na–S Batteries |
title_full | Orthorhombic Nb(2)O(5) Decorated Carbon Nanoreactors Enable Bidirectionally Regulated Redox Behaviors in Room‐Temperature Na–S Batteries |
title_fullStr | Orthorhombic Nb(2)O(5) Decorated Carbon Nanoreactors Enable Bidirectionally Regulated Redox Behaviors in Room‐Temperature Na–S Batteries |
title_full_unstemmed | Orthorhombic Nb(2)O(5) Decorated Carbon Nanoreactors Enable Bidirectionally Regulated Redox Behaviors in Room‐Temperature Na–S Batteries |
title_short | Orthorhombic Nb(2)O(5) Decorated Carbon Nanoreactors Enable Bidirectionally Regulated Redox Behaviors in Room‐Temperature Na–S Batteries |
title_sort | orthorhombic nb(2)o(5) decorated carbon nanoreactors enable bidirectionally regulated redox behaviors in room‐temperature na–s batteries |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9896060/ https://www.ncbi.nlm.nih.gov/pubmed/36470655 http://dx.doi.org/10.1002/advs.202206558 |
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