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Regulating Zn2+/H+ selectivity through functional group design of separators for long-lifespan aqueous zinc batteries
State Key Laboratory of Physical Chemistry of Solid Surfaces, Tan Kah Kee Innovation Laboratory (IKKEM), College of Chemistry and Chemical Engineering, Xiamen University, Xiamen 361005, China; College of Materials Engineering, Fujian Agriculture and Forestry University, Fuzhou 350002, China.
Luleå University of Technology, Department of Engineering Sciences and Mathematics, Material Science.ORCID iD: 0000-0002-4507-2759
State Key Laboratory of Physical Chemistry of Solid Surfaces, Tan Kah Kee Innovation Laboratory (IKKEM), College of Chemistry and Chemical Engineering, Xiamen University, Xiamen 361005, China.
State Key Laboratory of Physical Chemistry of Solid Surfaces, Tan Kah Kee Innovation Laboratory (IKKEM), College of Chemistry and Chemical Engineering, Xiamen University, Xiamen 361005, China.
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2025 (English)In: Materials Horizons, ISSN 2051-6347, E-ISSN 2051-6355, Vol. 12, p. 6252-6260Article in journal (Refereed) Published
Abstract [en]

Zn anodes in aqueous rechargeable zinc batteries (AZBs) are plagued by irreversibility issues stemming from dendrite growth, hydrogen evolution, and corrosion. The design of separator offers a promising approach to enhance the reversibility of Zn anodes, but a universal strategy for rational separator design remains elusive. In this study, we propose a comprehensive design principle that takes into account the selective binding with Zn2+, H+ and H2O, and further suggest that separators should ideally exhibit strong binding strength with H+ and H2O but weak with Zn2+. We explore four typical scenarios based on varying binding strengths and identify polyethersulfone (PES) as a highly promising separator through screening of various commercial separators. Both experiment and theoretical calculations reveal that PES effectively regulates the transfer of Zn2+, H+ and H2O, thereby concurrently suppressing dendrite growth, hydrogen evolution, and corrosion. As a result, the Zn‖Zn symmetric battery can operate for over 4000 h at 1 mA cm−2 and 1 mA h cm−2. Furthermore, the full battery can deliver an impressive lifespan of over 6400 cycles at 3 A g−1. This work not only introduces a new separator for high-performance AZBs but also provides guiding principles for functional separator design.

Place, publisher, year, edition, pages
Royal Society of Chemistry , 2025. Vol. 12, p. 6252-6260
National Category
Materials Chemistry
Research subject
Applied Physics
Identifiers
URN: urn:nbn:se:ltu:diva-112904DOI: 10.1039/d5mh00358jISI: 001487405600001PubMedID: 40365928Scopus ID: 2-s2.0-105005621450OAI: oai:DiVA.org:ltu-112904DiVA, id: diva2:1963277
Note

Validerad;2025;Nivå 2;2025-08-14 (u5);

Funder: National Key R&D Program of China (2020YFE0204500); Natural Science Foundation of Xiamen, China (3502Z202473021); Fujian Provincial Science and Technology Program for External Cooperation (2024I0001); Fundamental Research Funds for the Central Universities, China (20720240066);

Funder (see correction): Knut och Alice Wallenberg Foundation; Kempe-stiftelserna; Wallenberg Initiative Materials Science (WISE); Swedish Research Council (2023-03894, 2022-06725);

For correction, see: Zheng J. et al (2025) Correction: Regulating Zn2+/H+ selectivity through functional group design of separators for long-lifespan aqueous zinc batteries. Materials Horizons. DOI: https://doi.org/10.1039/D5MH90080H

Available from: 2025-06-03 Created: 2025-06-03 Last updated: 2025-10-21Bibliographically approved

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Sufyan, AliLarsson, J. Andreas

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