{"title":"用于水电解的一体化双极膜电极组件","authors":"Weisheng Yu, , , Fen Luo, , , Xiaojiang Li, , , Jingjing Tu, , , Xian Liang, , , Yan Xu, , , Zhiru Liu, , , Wenfeng Li, , , Jihao Zhang, , , Luxin Xiong, , , Huijuan Wang, , , Liang Wu*, , and , Tongwen Xu*, ","doi":"10.1021/acsami.5c13717","DOIUrl":null,"url":null,"abstract":"<p >Water dissociation (WD, H<sub>2</sub>O → H<sup>+</sup> + OH<sup>–</sup>) occurring at the bipolar membrane (BPM) junction can be leveraged in water electrolyzers for green hydrogen production, enabling the anode and cathode reactions to operate in kinetically favorable pH environments. However, practical application of BPM-integrated membrane electrode assemblies (BPMEAs) in electrolyzers faces formidable challenges due to the sluggish WD efficiency and insufficient stability at the bipolar junction. Here, we develop a convenient serial spraying approach to fabricate an all-in-one BPMEA. This approach endows the BPMEA with a wrinkled bipolar junction and integrated membrane/electrode interfaces, expanding the active interfaces and thereby enhancing WD efficiency and mass transport within BPMEA. As a result, the BPMEA exhibits competitive pure water and asymmetric acid/alkali electrolyzer voltages of 3.25 and 2.69 V at a high current density of 3000 mA cm<sup>–2</sup>, achieving 32% and 23% savings in energy consumption. Moreover, the wrinkled architecture imparts physical reinforcement to the bipolar junction and membrane/electrode interfaces, leading to an appropriate durability at current densities of 500–1000 mA cm<sup>–2</sup>. This work provides insights into the performance degradation mechanisms of BPM electrolyzers, and the proposed all-in-one approach is applicable to a broader range of electrochemical applications beyond water electrolysis.</p>","PeriodicalId":5,"journal":{"name":"ACS Applied Materials & Interfaces","volume":"17 40","pages":"56189–56196"},"PeriodicalIF":8.2000,"publicationDate":"2025-09-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"All-in-One Bipolar Membrane Electrode Assembly for Water Electrolysis\",\"authors\":\"Weisheng Yu, , , Fen Luo, , , Xiaojiang Li, , , Jingjing Tu, , , Xian Liang, , , Yan Xu, , , Zhiru Liu, , , Wenfeng Li, , , Jihao Zhang, , , Luxin Xiong, , , Huijuan Wang, , , Liang Wu*, , and , Tongwen Xu*, \",\"doi\":\"10.1021/acsami.5c13717\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >Water dissociation (WD, H<sub>2</sub>O → H<sup>+</sup> + OH<sup>–</sup>) occurring at the bipolar membrane (BPM) junction can be leveraged in water electrolyzers for green hydrogen production, enabling the anode and cathode reactions to operate in kinetically favorable pH environments. However, practical application of BPM-integrated membrane electrode assemblies (BPMEAs) in electrolyzers faces formidable challenges due to the sluggish WD efficiency and insufficient stability at the bipolar junction. Here, we develop a convenient serial spraying approach to fabricate an all-in-one BPMEA. This approach endows the BPMEA with a wrinkled bipolar junction and integrated membrane/electrode interfaces, expanding the active interfaces and thereby enhancing WD efficiency and mass transport within BPMEA. As a result, the BPMEA exhibits competitive pure water and asymmetric acid/alkali electrolyzer voltages of 3.25 and 2.69 V at a high current density of 3000 mA cm<sup>–2</sup>, achieving 32% and 23% savings in energy consumption. Moreover, the wrinkled architecture imparts physical reinforcement to the bipolar junction and membrane/electrode interfaces, leading to an appropriate durability at current densities of 500–1000 mA cm<sup>–2</sup>. 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引用次数: 0
摘要
在双极膜(BPM)连接处发生的水解离(WD, H2O→H+ + OH -)可以在水电解槽中用于绿色制氢,使阳极和阴极反应能够在动力学有利的pH环境中进行。然而,由于电解效率低下和双极稳定性不足,集成bpm的膜电极组件(bpmea)在电解槽中的实际应用面临巨大挑战。在这里,我们开发了一种方便的连续喷涂方法来制造一体化的BPMEA。这种方法使BPMEA具有皱褶的双极结和集成的膜/电极界面,扩大了活性界面,从而提高了BPMEA内部的WD效率和质量传递。结果表明,在3000 mA cm-2的高电流密度下,BPMEA具有具有竞争力的纯水和不对称酸/碱电解槽电压分别为3.25 V和2.69 V,实现了32%和23%的能耗节约。此外,褶皱结构为双极结和膜/电极界面提供了物理增强,从而在500-1000 mA cm-2的电流密度下具有适当的耐久性。这项工作提供了对BPM电解槽性能退化机制的见解,并且所提出的一体化方法适用于水电解以外的更广泛的电化学应用。
All-in-One Bipolar Membrane Electrode Assembly for Water Electrolysis
Water dissociation (WD, H2O → H+ + OH–) occurring at the bipolar membrane (BPM) junction can be leveraged in water electrolyzers for green hydrogen production, enabling the anode and cathode reactions to operate in kinetically favorable pH environments. However, practical application of BPM-integrated membrane electrode assemblies (BPMEAs) in electrolyzers faces formidable challenges due to the sluggish WD efficiency and insufficient stability at the bipolar junction. Here, we develop a convenient serial spraying approach to fabricate an all-in-one BPMEA. This approach endows the BPMEA with a wrinkled bipolar junction and integrated membrane/electrode interfaces, expanding the active interfaces and thereby enhancing WD efficiency and mass transport within BPMEA. As a result, the BPMEA exhibits competitive pure water and asymmetric acid/alkali electrolyzer voltages of 3.25 and 2.69 V at a high current density of 3000 mA cm–2, achieving 32% and 23% savings in energy consumption. Moreover, the wrinkled architecture imparts physical reinforcement to the bipolar junction and membrane/electrode interfaces, leading to an appropriate durability at current densities of 500–1000 mA cm–2. This work provides insights into the performance degradation mechanisms of BPM electrolyzers, and the proposed all-in-one approach is applicable to a broader range of electrochemical applications beyond water electrolysis.
期刊介绍:
ACS Applied Materials & Interfaces is a leading interdisciplinary journal that brings together chemists, engineers, physicists, and biologists to explore the development and utilization of newly-discovered materials and interfacial processes for specific applications. Our journal has experienced remarkable growth since its establishment in 2009, both in terms of the number of articles published and the impact of the research showcased. We are proud to foster a truly global community, with the majority of published articles originating from outside the United States, reflecting the rapid growth of applied research worldwide.