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Highly Stable Aqueous Zinc Metal Batteries Enabled by an Ultrathin Crack‐Free Hydrophobic Layer with Rigid Sub‐Nanochannels

Aqueous zinc‐metal batteries (AZMBs) have received tremendous attentions due to their high safety, low cost, environmental friendliness, and simple process. However, zinc‐metal still suffer from uncontrollable dendrite growth and surface parasitic reactions that reduce the Coulombic efficiency (CE)...

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Autores principales: Xu, Dongming, Ren, Xueting, Xu, Yan, Wang, Yijiang, Zhang, Shibin, Chen, Benqiang, Chang, Zhi, Pan, Anqiang, Zhou, Haoshen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10520658/
https://www.ncbi.nlm.nih.gov/pubmed/37515370
http://dx.doi.org/10.1002/advs.202303773
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author Xu, Dongming
Ren, Xueting
Xu, Yan
Wang, Yijiang
Zhang, Shibin
Chen, Benqiang
Chang, Zhi
Pan, Anqiang
Zhou, Haoshen
author_facet Xu, Dongming
Ren, Xueting
Xu, Yan
Wang, Yijiang
Zhang, Shibin
Chen, Benqiang
Chang, Zhi
Pan, Anqiang
Zhou, Haoshen
author_sort Xu, Dongming
collection PubMed
description Aqueous zinc‐metal batteries (AZMBs) have received tremendous attentions due to their high safety, low cost, environmental friendliness, and simple process. However, zinc‐metal still suffer from uncontrollable dendrite growth and surface parasitic reactions that reduce the Coulombic efficiency (CE) and lifetime of AZMBs. These problems which are closely related to the active water are not well‐solved. Here, an ultrathin crack‐free metal–organic framework (ZIF‐7 (x) ‐8) with rigid sub‐nanopore (0.3 nm) is constructed on Zn‐metal to promote the de‐solvation of zinc‐ions before approaching Zn‐metal surface, reduce the contacting opportunity between water and Zn, and consequently eliminate water‐induced corrosion and side‐reactions. Due to the presence of rigid and ordered sub‐nanochannels, Zn‐ions deposits on Zn‐metal follow a highly ordered manner, resulting in a dendrite‐free Zn‐metal with negligible by‐products, which significantly improve the reversibility and lifespan of Zn‐metals. As a result, Zn‐metal protected by ultrathin crack‐free ZIF‐7 (x) ‐8 layer exhibits excellent cycling stability (over 2200 h) and extremely‐high 99.96% CE during 6000 cycles. The aqueous PANI‐V(2)O(5)//ZIF‐7 (x) ‐8@Zn full‐cell preserves 86% high‐capacity retention even after ultra‐long 2000 cycles. The practical pouch‐cell can also be cycled for more than 120 cycles. It is believed that the simple strategy demonstrated in this work can accelerate the practical utilizations of AZMBs.
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spelling pubmed-105206582023-09-27 Highly Stable Aqueous Zinc Metal Batteries Enabled by an Ultrathin Crack‐Free Hydrophobic Layer with Rigid Sub‐Nanochannels Xu, Dongming Ren, Xueting Xu, Yan Wang, Yijiang Zhang, Shibin Chen, Benqiang Chang, Zhi Pan, Anqiang Zhou, Haoshen Adv Sci (Weinh) Research Articles Aqueous zinc‐metal batteries (AZMBs) have received tremendous attentions due to their high safety, low cost, environmental friendliness, and simple process. However, zinc‐metal still suffer from uncontrollable dendrite growth and surface parasitic reactions that reduce the Coulombic efficiency (CE) and lifetime of AZMBs. These problems which are closely related to the active water are not well‐solved. Here, an ultrathin crack‐free metal–organic framework (ZIF‐7 (x) ‐8) with rigid sub‐nanopore (0.3 nm) is constructed on Zn‐metal to promote the de‐solvation of zinc‐ions before approaching Zn‐metal surface, reduce the contacting opportunity between water and Zn, and consequently eliminate water‐induced corrosion and side‐reactions. Due to the presence of rigid and ordered sub‐nanochannels, Zn‐ions deposits on Zn‐metal follow a highly ordered manner, resulting in a dendrite‐free Zn‐metal with negligible by‐products, which significantly improve the reversibility and lifespan of Zn‐metals. As a result, Zn‐metal protected by ultrathin crack‐free ZIF‐7 (x) ‐8 layer exhibits excellent cycling stability (over 2200 h) and extremely‐high 99.96% CE during 6000 cycles. The aqueous PANI‐V(2)O(5)//ZIF‐7 (x) ‐8@Zn full‐cell preserves 86% high‐capacity retention even after ultra‐long 2000 cycles. The practical pouch‐cell can also be cycled for more than 120 cycles. It is believed that the simple strategy demonstrated in this work can accelerate the practical utilizations of AZMBs. John Wiley and Sons Inc. 2023-07-28 /pmc/articles/PMC10520658/ /pubmed/37515370 http://dx.doi.org/10.1002/advs.202303773 Text en © 2023 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
Xu, Dongming
Ren, Xueting
Xu, Yan
Wang, Yijiang
Zhang, Shibin
Chen, Benqiang
Chang, Zhi
Pan, Anqiang
Zhou, Haoshen
Highly Stable Aqueous Zinc Metal Batteries Enabled by an Ultrathin Crack‐Free Hydrophobic Layer with Rigid Sub‐Nanochannels
title Highly Stable Aqueous Zinc Metal Batteries Enabled by an Ultrathin Crack‐Free Hydrophobic Layer with Rigid Sub‐Nanochannels
title_full Highly Stable Aqueous Zinc Metal Batteries Enabled by an Ultrathin Crack‐Free Hydrophobic Layer with Rigid Sub‐Nanochannels
title_fullStr Highly Stable Aqueous Zinc Metal Batteries Enabled by an Ultrathin Crack‐Free Hydrophobic Layer with Rigid Sub‐Nanochannels
title_full_unstemmed Highly Stable Aqueous Zinc Metal Batteries Enabled by an Ultrathin Crack‐Free Hydrophobic Layer with Rigid Sub‐Nanochannels
title_short Highly Stable Aqueous Zinc Metal Batteries Enabled by an Ultrathin Crack‐Free Hydrophobic Layer with Rigid Sub‐Nanochannels
title_sort highly stable aqueous zinc metal batteries enabled by an ultrathin crack‐free hydrophobic layer with rigid sub‐nanochannels
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10520658/
https://www.ncbi.nlm.nih.gov/pubmed/37515370
http://dx.doi.org/10.1002/advs.202303773
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