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

被引:0
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作者
Tan, Rui [1 ,2 ]
He, Hongzhen [3 ]
Wang, Anqi [1 ]
Wong, Toby [1 ]
Yang, Yilin [1 ]
Iguodala, Sunshine [1 ]
Ye, Chunchun [4 ]
Liu, Dezhi [1 ]
Fan, Zhiyu [1 ]
Furedi, Mate [3 ]
He, Guanjie [5 ]
Guldin, Stefan [3 ]
Brett, Dan J. L. [3 ]
McKeown, Neil B. [4 ]
Song, Qilei [1 ]
机构
[1] Department of Chemical Engineering, Imperial College London, London,SW7 2AZ, United Kingdom
[2] Department of Chemical Engineering, Swansea University, Swansea,SA1 8EN, United Kingdom
[3] Department of Chemical Engineering, University College London, London,WC1E 7JE, United Kingdom
[4] EaStChem School of Chemistry, University of Edinburgh, Edinburgh,EH9 3FJ, United Kingdom
[5] Department of Chemistry, University College London, London,WC1E 7JE, United Kingdom
关键词
Ion selective membranes;
D O I
10.1002/anie.202409322
中图分类号
学科分类号
摘要
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. © 2024 The Authors. Angewandte Chemie International Edition published by Wiley-VCH GmbH.
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