{"title":"电解水用薄膜精确铂杂化实现超高效氢交叉抑制","authors":"Xuyang Xie, Jingnan Song, Xiaoxuan Fan, Wutong Zhao, Ke Liu, Yanxin Zhao, LiBo Zhou, Yu Xiao, Shaobo Li, Haibo Wang, Guanlei Zhao, Fei Xie, Baoyu Song, Qiaoyu Guo, Xuechen Jiao, Ping He, Feng Liu, Yongming Zhang","doi":"10.1002/adfm.202504467","DOIUrl":null,"url":null,"abstract":"Reducing the thickness of proton exchange membranes (PEMs) is a highly effective strategy to enhance the operational efficiency of proton exchange membrane water electrolyzer (PEMWE). However, this often leads to hydrogen crossover, raising concerns about system stability. Perfluorosulfonic acid (PFSA)-stabilized Pt nanoparticles (Pt NPs) are synthesized and introduced into fabricate PFSA bilayer membrane. Electron microscopy and scattering analyses confirm the precise localization of Pt NPs within the hydrophilic domains without disturbing the overall membrane morphology. This precise doping strategy enables the on-site scavenging of the hydrogen diffusing across the membrane at an ultralow Pt loading (0.002 mg cm<sup>−2</sup>). In contrast, conventional Pt doping without a stabilizing matrix induces severe aggregation, restricting nanoparticle entry into hydrophilic domains and resulting in inefficient hydrogen elimination even at elevated loadings. Moreover, the approach significantly enhances operational durability: hydrogen crossover suppression remained stable after 500 h of operation in a practical PEMWE device at current densities of 1.0 and 2.0 A·cm<sup>−</sup><sup>2</sup>, confirming the membrane's excellent durability.","PeriodicalId":112,"journal":{"name":"Advanced Functional Materials","volume":"44 1","pages":""},"PeriodicalIF":19.0000,"publicationDate":"2025-05-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Ultra-Efficient Hydrogen Crossover Suppression Achieved by Precise Pt Hybridization in Thin Nafion Membranes for Water Electrolyzer\",\"authors\":\"Xuyang Xie, Jingnan Song, Xiaoxuan Fan, Wutong Zhao, Ke Liu, Yanxin Zhao, LiBo Zhou, Yu Xiao, Shaobo Li, Haibo Wang, Guanlei Zhao, Fei Xie, Baoyu Song, Qiaoyu Guo, Xuechen Jiao, Ping He, Feng Liu, Yongming Zhang\",\"doi\":\"10.1002/adfm.202504467\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Reducing the thickness of proton exchange membranes (PEMs) is a highly effective strategy to enhance the operational efficiency of proton exchange membrane water electrolyzer (PEMWE). However, this often leads to hydrogen crossover, raising concerns about system stability. Perfluorosulfonic acid (PFSA)-stabilized Pt nanoparticles (Pt NPs) are synthesized and introduced into fabricate PFSA bilayer membrane. Electron microscopy and scattering analyses confirm the precise localization of Pt NPs within the hydrophilic domains without disturbing the overall membrane morphology. This precise doping strategy enables the on-site scavenging of the hydrogen diffusing across the membrane at an ultralow Pt loading (0.002 mg cm<sup>−2</sup>). In contrast, conventional Pt doping without a stabilizing matrix induces severe aggregation, restricting nanoparticle entry into hydrophilic domains and resulting in inefficient hydrogen elimination even at elevated loadings. Moreover, the approach significantly enhances operational durability: hydrogen crossover suppression remained stable after 500 h of operation in a practical PEMWE device at current densities of 1.0 and 2.0 A·cm<sup>−</sup><sup>2</sup>, confirming the membrane's excellent durability.\",\"PeriodicalId\":112,\"journal\":{\"name\":\"Advanced Functional Materials\",\"volume\":\"44 1\",\"pages\":\"\"},\"PeriodicalIF\":19.0000,\"publicationDate\":\"2025-05-16\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Advanced Functional Materials\",\"FirstCategoryId\":\"88\",\"ListUrlMain\":\"https://doi.org/10.1002/adfm.202504467\",\"RegionNum\":1,\"RegionCategory\":\"材料科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Advanced Functional Materials","FirstCategoryId":"88","ListUrlMain":"https://doi.org/10.1002/adfm.202504467","RegionNum":1,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0
摘要
减小质子交换膜厚度是提高质子交换膜水电解槽运行效率的有效措施。然而,这通常会导致氢气交叉,引起对系统稳定性的担忧。合成了全氟磺酸(PFSA)稳定铂纳米粒子(Pt NPs)并将其引入到PFSA双层膜的制备中。电子显微镜和散射分析证实了Pt NPs在亲水性域内的精确定位,而不影响整个膜的形态。这种精确的掺杂策略能够在超低铂负载(0.002 mg cm - 2)下现场清除扩散在膜上的氢。相比之下,没有稳定基质的传统铂掺杂会导致严重的聚集,限制纳米颗粒进入亲水结构域,即使在高负荷下也会导致低效的氢消除。此外,该方法显著提高了操作耐久性:在实际的PEMWE装置中,在1.0和2.0 a·cm−2的电流密度下,氢交叉抑制在500 h后保持稳定,证实了膜的优异耐久性。
Ultra-Efficient Hydrogen Crossover Suppression Achieved by Precise Pt Hybridization in Thin Nafion Membranes for Water Electrolyzer
Reducing the thickness of proton exchange membranes (PEMs) is a highly effective strategy to enhance the operational efficiency of proton exchange membrane water electrolyzer (PEMWE). However, this often leads to hydrogen crossover, raising concerns about system stability. Perfluorosulfonic acid (PFSA)-stabilized Pt nanoparticles (Pt NPs) are synthesized and introduced into fabricate PFSA bilayer membrane. Electron microscopy and scattering analyses confirm the precise localization of Pt NPs within the hydrophilic domains without disturbing the overall membrane morphology. This precise doping strategy enables the on-site scavenging of the hydrogen diffusing across the membrane at an ultralow Pt loading (0.002 mg cm−2). In contrast, conventional Pt doping without a stabilizing matrix induces severe aggregation, restricting nanoparticle entry into hydrophilic domains and resulting in inefficient hydrogen elimination even at elevated loadings. Moreover, the approach significantly enhances operational durability: hydrogen crossover suppression remained stable after 500 h of operation in a practical PEMWE device at current densities of 1.0 and 2.0 A·cm−2, confirming the membrane's excellent durability.
期刊介绍:
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