{"title":"核/壳纳米阵列对800 h稳定碱性海水电解界面水活性和H2气泡的调节","authors":"Xiaodong Yang, Haochen Shen, Xiaoming Xiao, Zhichao Li, Haiqi Liang, Shuai Chen, Yongli Sun, Bin Jiang, Guobin Wen, Shuangyin Wang, Luhong Zhang","doi":"10.1002/adma.202416658","DOIUrl":null,"url":null,"abstract":"<p>The catalytic activity and stability under high current densities for hydrogen evolution reactions (HER) are impeded by firm adherence and coverage of H<sub>2</sub> bubbles to the catalytic sites. Herein, we systematically synthesize core/shell nanoarrays to engineer bubble transport channels, which further remarkably regulate interfacial H<sub>2</sub>O activity, and swift H<sub>2</sub> bubble generation and release. The self-supported catalyst holds uniform ultra-low Ru active sites of 0.38 wt% and promotes the rapid formation of plentiful small H<sub>2</sub> bubbles, which are rapidly released by the upright channels, mitigating the blockage of active sites and avoiding surface damage from bubble movements. As a result, these core/shell nanoarrays achieve ultralow overpotentials of 18 and 24 mV to reach 10 mA cm<sup>−2</sup> for HER in 1 M KOH freshwater and seawater, respectively. Additionally, the assembled electrolyzer demonstrates stable durability over 800 hours with a high current density of 2 A cm<sup>−2</sup> in 1 M KOH seawater. The techno-economic analysis (TEA) indicates that the unit cost of the hydrogen production system is nearly half of the DOE's (Department of Energy) 2026 target. Our work addresses the stability challenges of HER and highlights its potential as a sustainable and economically feasible solution for large-scale hydrogen production of seawater.</p>","PeriodicalId":114,"journal":{"name":"Advanced Materials","volume":"37 19","pages":""},"PeriodicalIF":26.8000,"publicationDate":"2025-03-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Regulating Interfacial H2O Activity and H2 Bubbles by Core/Shell Nanoarrays for 800 h Stable Alkaline Seawater Electrolysis\",\"authors\":\"Xiaodong Yang, Haochen Shen, Xiaoming Xiao, Zhichao Li, Haiqi Liang, Shuai Chen, Yongli Sun, Bin Jiang, Guobin Wen, Shuangyin Wang, Luhong Zhang\",\"doi\":\"10.1002/adma.202416658\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>The catalytic activity and stability under high current densities for hydrogen evolution reactions (HER) are impeded by firm adherence and coverage of H<sub>2</sub> bubbles to the catalytic sites. Herein, we systematically synthesize core/shell nanoarrays to engineer bubble transport channels, which further remarkably regulate interfacial H<sub>2</sub>O activity, and swift H<sub>2</sub> bubble generation and release. The self-supported catalyst holds uniform ultra-low Ru active sites of 0.38 wt% and promotes the rapid formation of plentiful small H<sub>2</sub> bubbles, which are rapidly released by the upright channels, mitigating the blockage of active sites and avoiding surface damage from bubble movements. As a result, these core/shell nanoarrays achieve ultralow overpotentials of 18 and 24 mV to reach 10 mA cm<sup>−2</sup> for HER in 1 M KOH freshwater and seawater, respectively. Additionally, the assembled electrolyzer demonstrates stable durability over 800 hours with a high current density of 2 A cm<sup>−2</sup> in 1 M KOH seawater. The techno-economic analysis (TEA) indicates that the unit cost of the hydrogen production system is nearly half of the DOE's (Department of Energy) 2026 target. Our work addresses the stability challenges of HER and highlights its potential as a sustainable and economically feasible solution for large-scale hydrogen production of seawater.</p>\",\"PeriodicalId\":114,\"journal\":{\"name\":\"Advanced Materials\",\"volume\":\"37 19\",\"pages\":\"\"},\"PeriodicalIF\":26.8000,\"publicationDate\":\"2025-03-24\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Advanced Materials\",\"FirstCategoryId\":\"88\",\"ListUrlMain\":\"https://advanced.onlinelibrary.wiley.com/doi/10.1002/adma.202416658\",\"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 Materials","FirstCategoryId":"88","ListUrlMain":"https://advanced.onlinelibrary.wiley.com/doi/10.1002/adma.202416658","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
析氢反应(HER)在高电流密度下的催化活性和稳定性受到H2气泡对催化位点的牢固粘附和覆盖的影响。在此,我们系统地合成了核/壳纳米阵列来设计气泡传输通道,从而进一步显著调节界面水活性,并快速生成和释放H2气泡。自支撑催化剂具有均匀的超低Ru活性位点(0.38 wt%),促进大量小H2气泡的快速形成,这些小H2气泡通过直立通道快速释放,减轻了活性位点的堵塞,避免了气泡运动对表面的破坏。因此,这些核/壳纳米阵列在1 M KOH的淡水和海水中分别实现了18和24 mV的超低过电位,达到10 mA cm−2。此外,组装的电解槽在1m KOH海水中具有2 a cm - 2的高电流密度,稳定耐用超过800小时。技术经济分析(TEA)表明,氢气生产系统的单位成本几乎是美国能源部2026年目标的一半。我们的工作解决了HER的稳定性挑战,并强调了其作为大规模海水制氢的可持续和经济可行解决方案的潜力。
Regulating Interfacial H2O Activity and H2 Bubbles by Core/Shell Nanoarrays for 800 h Stable Alkaline Seawater Electrolysis
The catalytic activity and stability under high current densities for hydrogen evolution reactions (HER) are impeded by firm adherence and coverage of H2 bubbles to the catalytic sites. Herein, we systematically synthesize core/shell nanoarrays to engineer bubble transport channels, which further remarkably regulate interfacial H2O activity, and swift H2 bubble generation and release. The self-supported catalyst holds uniform ultra-low Ru active sites of 0.38 wt% and promotes the rapid formation of plentiful small H2 bubbles, which are rapidly released by the upright channels, mitigating the blockage of active sites and avoiding surface damage from bubble movements. As a result, these core/shell nanoarrays achieve ultralow overpotentials of 18 and 24 mV to reach 10 mA cm−2 for HER in 1 M KOH freshwater and seawater, respectively. Additionally, the assembled electrolyzer demonstrates stable durability over 800 hours with a high current density of 2 A cm−2 in 1 M KOH seawater. The techno-economic analysis (TEA) indicates that the unit cost of the hydrogen production system is nearly half of the DOE's (Department of Energy) 2026 target. Our work addresses the stability challenges of HER and highlights its potential as a sustainable and economically feasible solution for large-scale hydrogen production of seawater.
期刊介绍:
Advanced Materials, one of the world's most prestigious journals and the foundation of the Advanced portfolio, is the home of choice for best-in-class materials science for more than 30 years. Following this fast-growing and interdisciplinary field, we are considering and publishing the most important discoveries on any and all materials from materials scientists, chemists, physicists, engineers as well as health and life scientists and bringing you the latest results and trends in modern materials-related research every week.