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Interfacial Engineering of Polymer Membranes with Intrinsic Microporosity for Dendrite‐Free Zinc Metal Batteries

Rui Tan Orcid Logo, Hongzhen He Orcid Logo, Anqi Wang Orcid Logo, Toby Wong, Yilin Yang, Sunshine Iguodala, Chunchun Ye Orcid Logo, Dezhi Liu, Zhiyu Fan, Mate Furedi, Guanjie He Orcid Logo, Stefan Guldin Orcid Logo, Dan J. L. Brett Orcid Logo, Neil B. McKeown Orcid Logo, Qilei Song Orcid Logo

Angewandte Chemie International Edition, Volume: 63, Issue: 49, Start page: e202409322

Swansea University Author: Rui Tan Orcid Logo

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DOI (Published version): 10.1002/anie.202409322

Abstract

Metallic zinc has emerged as a promising anode material for high-energy battery systems due to its high theoretical capacity (820 mAh g−1), low redox potential for two-electron reactions, cost-effectiveness and inherent safety. However, current zinc metal batteries face challenges in low coulombic e...

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Published in: Angewandte Chemie International Edition
ISSN: 1433-7851 1521-3773
Published: Wiley 2024
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URI: https://cronfa.swan.ac.uk/Record/cronfa68344
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However, current zinc metal batteries face challenges in low coulombic efficiency and limited longevity due to uncontrollable dendrite growth, the corrosive hydrogen evolution reaction (HER) and decomposition of the aqueous ZnSO4 electrolyte. Here, we report an interfacial-engineering approach to mitigate dendrite growth and reduce corrosive reactions through the design of ultrathin selective membranes coated on the zinc anodes. The submicron-thick membranes derived from polymers of intrinsic microporosity (PIMs), featuring pores with tunable interconnectivity, facilitate regulated transport of Zn2+-ions, thereby promoting a uniform plating/stripping process. Benefiting from the protection by PIM membranes, zinc symmetric cells deliver a stable cycling performance over 1500&#x2005;h at 1&#x2005;mA/cm2 with a capacity of 0.5&#x2005;mAh while full cells with NaMnO2 cathode operate stably at 1&#x2005;A&#x2009;g&#x2212;1 over 300&#x2005;cycles without capacity decay. 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spelling 2025-01-13T15:44:33.9040205 v2 68344 2024-11-26 Interfacial Engineering of Polymer Membranes with Intrinsic Microporosity for Dendrite‐Free Zinc Metal Batteries 774c33a0a76a9152ca86a156b5ae26ff 0009-0001-9278-7327 Rui Tan Rui Tan true false 2024-11-26 EAAS Metallic zinc has emerged as a promising anode material for high-energy battery systems due to its high theoretical capacity (820 mAh g−1), low redox potential for two-electron reactions, cost-effectiveness and inherent safety. However, current zinc metal batteries face challenges in low coulombic efficiency and limited longevity due to uncontrollable dendrite growth, the corrosive hydrogen evolution reaction (HER) and decomposition of the aqueous ZnSO4 electrolyte. Here, we report an interfacial-engineering approach to mitigate dendrite growth and reduce corrosive reactions through the design of ultrathin selective membranes coated on the zinc anodes. The submicron-thick membranes derived from polymers of intrinsic microporosity (PIMs), featuring pores with tunable interconnectivity, facilitate regulated transport of Zn2+-ions, thereby promoting a uniform plating/stripping process. Benefiting from the protection by PIM membranes, zinc symmetric cells deliver a stable cycling performance over 1500 h at 1 mA/cm2 with a capacity of 0.5 mAh while full cells with NaMnO2 cathode operate stably at 1 A g−1 over 300 cycles without capacity decay. Our work represents a new strategy of preparing multi-functional membranes that can advance the development of safe and stable zinc metal batteries. Journal Article Angewandte Chemie International Edition 63 49 e202409322 Wiley 1433-7851 1521-3773 Energy storage , Zinc metal batteries, Ion-selective membranes, Polymers of intrinsic microporosity, Coating 2 12 2024 2024-12-02 10.1002/anie.202409322 COLLEGE NANME Engineering and Applied Sciences School COLLEGE CODE EAAS Swansea University Another institution paid the OA fee This project has received funding from the European Research Council (ERC) under the European Union's Horizon 2020 research and innovation programme (grant agreement No 851272, ERC-StG-PE8-NanoMMES). This work was also funded by the Engineering and Physical Sciences Research Council (EPSRC, UK, EP/V047078/1), and UK Research and Innovation (UKRI) under the UK government's Horizon Europe funding (101077226; EP/Y008707/1). M.F. is grateful for funding by an UCL Engineering Impact Studentship sponsored by Semilab Co. Ltd. A.A.F. and S.G. are grateful for funding by an EPSRC New Investigator Award (EP/R035105/1). 2025-01-13T15:44:33.9040205 2024-11-26T14:56:59.1666361 Faculty of Science and Engineering School of Engineering and Applied Sciences - Chemical Engineering Rui Tan 0009-0001-9278-7327 1 Hongzhen He 0000-0002-8053-3389 2 Anqi Wang 0000-0003-3409-823x 3 Toby Wong 4 Yilin Yang 5 Sunshine Iguodala 6 Chunchun Ye 0000-0003-0171-6468 7 Dezhi Liu 8 Zhiyu Fan 9 Mate Furedi 10 Guanjie He 0000-0002-7365-9645 11 Stefan Guldin 0000-0002-4413-5527 12 Dan J. L. Brett 0000-0002-8545-3126 13 Neil B. McKeown 0000-0002-6027-261x 14 Qilei Song 0000-0001-8570-3626 15
title Interfacial Engineering of Polymer Membranes with Intrinsic Microporosity for Dendrite‐Free Zinc Metal Batteries
spellingShingle Interfacial Engineering of Polymer Membranes with Intrinsic Microporosity for Dendrite‐Free Zinc Metal Batteries
Rui Tan
title_short Interfacial Engineering of Polymer Membranes with Intrinsic Microporosity for Dendrite‐Free Zinc Metal Batteries
title_full Interfacial Engineering of Polymer Membranes with Intrinsic Microporosity for Dendrite‐Free Zinc Metal Batteries
title_fullStr Interfacial Engineering of Polymer Membranes with Intrinsic Microporosity for Dendrite‐Free Zinc Metal Batteries
title_full_unstemmed Interfacial Engineering of Polymer Membranes with Intrinsic Microporosity for Dendrite‐Free Zinc Metal Batteries
title_sort Interfacial Engineering of Polymer Membranes with Intrinsic Microporosity for Dendrite‐Free Zinc Metal Batteries
author_id_str_mv 774c33a0a76a9152ca86a156b5ae26ff
author_id_fullname_str_mv 774c33a0a76a9152ca86a156b5ae26ff_***_Rui Tan
author Rui Tan
author2 Rui Tan
Hongzhen He
Anqi Wang
Toby Wong
Yilin Yang
Sunshine Iguodala
Chunchun Ye
Dezhi Liu
Zhiyu Fan
Mate Furedi
Guanjie He
Stefan Guldin
Dan J. L. Brett
Neil B. McKeown
Qilei Song
format Journal article
container_title Angewandte Chemie International Edition
container_volume 63
container_issue 49
container_start_page e202409322
publishDate 2024
institution Swansea University
issn 1433-7851
1521-3773
doi_str_mv 10.1002/anie.202409322
publisher Wiley
college_str Faculty of Science and Engineering
hierarchytype
hierarchy_top_id facultyofscienceandengineering
hierarchy_top_title Faculty of Science and Engineering
hierarchy_parent_id facultyofscienceandengineering
hierarchy_parent_title Faculty of Science and Engineering
department_str School of Engineering and Applied Sciences - Chemical Engineering{{{_:::_}}}Faculty of Science and Engineering{{{_:::_}}}School of Engineering and Applied Sciences - Chemical Engineering
document_store_str 0
active_str 0
description Metallic zinc has emerged as a promising anode material for high-energy battery systems due to its high theoretical capacity (820 mAh g−1), low redox potential for two-electron reactions, cost-effectiveness and inherent safety. However, current zinc metal batteries face challenges in low coulombic efficiency and limited longevity due to uncontrollable dendrite growth, the corrosive hydrogen evolution reaction (HER) and decomposition of the aqueous ZnSO4 electrolyte. Here, we report an interfacial-engineering approach to mitigate dendrite growth and reduce corrosive reactions through the design of ultrathin selective membranes coated on the zinc anodes. The submicron-thick membranes derived from polymers of intrinsic microporosity (PIMs), featuring pores with tunable interconnectivity, facilitate regulated transport of Zn2+-ions, thereby promoting a uniform plating/stripping process. Benefiting from the protection by PIM membranes, zinc symmetric cells deliver a stable cycling performance over 1500 h at 1 mA/cm2 with a capacity of 0.5 mAh while full cells with NaMnO2 cathode operate stably at 1 A g−1 over 300 cycles without capacity decay. Our work represents a new strategy of preparing multi-functional membranes that can advance the development of safe and stable zinc metal batteries.
published_date 2024-12-02T20:36:19Z
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