Decoupling fast hydrogen oxidation reaction on a tandem electrocatalyst.

IF 15.7 1区 综合性期刊 Q1 MULTIDISCIPLINARY SCIENCES
Wei Guo, Guoqiang Zhao, Ziang Sun, Bingxing Zhang, Dongyue Xin, Mingxia Gao, Yongfeng Liu, Zhongbin Zhuang, Hai-Wei Liang, Hongge Pan, Wenping Sun
{"title":"Decoupling fast hydrogen oxidation reaction on a tandem electrocatalyst.","authors":"Wei Guo, Guoqiang Zhao, Ziang Sun, Bingxing Zhang, Dongyue Xin, Mingxia Gao, Yongfeng Liu, Zhongbin Zhuang, Hai-Wei Liang, Hongge Pan, Wenping Sun","doi":"10.1038/s41467-025-62160-8","DOIUrl":null,"url":null,"abstract":"<p><p>The hydrogen oxidation reaction (HOR) shows fast kinetics in proton exchange membrane fuel cells (PEMFCs), and has not drawn intense attention. Here, we propose a tandem electrocatalysis concept, decoupling HOR on two independent active sites for accelerated kinetics. As a proof-of-concept application, a Ru-based tandem HOR catalyst is designed, with Ru nanoclusters decorated with Pt single atoms. Experimental and theoretical studies suggest that H<sub>2</sub> dissociation occurs at Ru sites, and then the produced H species migrate to Pt sites followed by the desorption of H<sup>+</sup>. The strong Ru-H interaction promotes the H<sub>2</sub> dissociation step, while the optimum Pt-H interaction ensures the fast desorption, thereby substantially enhancing the HOR kinetics. In H<sub>2</sub>-O<sub>2</sub> fuel cells, this catalyst enables a peak power density of 1.91 W cm<sup>-2</sup> and a high anodic mass activity of 23.12 A mg<sup>-1</sup> at 0.9 V<sub>iR-free</sub> with an ultralow noble metal loading of 5 μg cm<sup>-2</sup>. This work advances the development of low-cost anode catalysts for fuel cells and provides more insight into understanding hydrogen electrocatalysis.</p>","PeriodicalId":19066,"journal":{"name":"Nature Communications","volume":"16 1","pages":"6741"},"PeriodicalIF":15.7000,"publicationDate":"2025-07-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Nature Communications","FirstCategoryId":"103","ListUrlMain":"https://doi.org/10.1038/s41467-025-62160-8","RegionNum":1,"RegionCategory":"综合性期刊","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"MULTIDISCIPLINARY SCIENCES","Score":null,"Total":0}
引用次数: 0

Abstract

The hydrogen oxidation reaction (HOR) shows fast kinetics in proton exchange membrane fuel cells (PEMFCs), and has not drawn intense attention. Here, we propose a tandem electrocatalysis concept, decoupling HOR on two independent active sites for accelerated kinetics. As a proof-of-concept application, a Ru-based tandem HOR catalyst is designed, with Ru nanoclusters decorated with Pt single atoms. Experimental and theoretical studies suggest that H2 dissociation occurs at Ru sites, and then the produced H species migrate to Pt sites followed by the desorption of H+. The strong Ru-H interaction promotes the H2 dissociation step, while the optimum Pt-H interaction ensures the fast desorption, thereby substantially enhancing the HOR kinetics. In H2-O2 fuel cells, this catalyst enables a peak power density of 1.91 W cm-2 and a high anodic mass activity of 23.12 A mg-1 at 0.9 ViR-free with an ultralow noble metal loading of 5 μg cm-2. This work advances the development of low-cost anode catalysts for fuel cells and provides more insight into understanding hydrogen electrocatalysis.

串联电催化剂上的解耦快速氢氧化反应。
质子交换膜燃料电池(PEMFCs)中氢氧化反应(HOR)具有快速动力学,但尚未引起广泛关注。在这里,我们提出了串联电催化的概念,将HOR在两个独立的活性位点上解耦以加速动力学。作为一种概念验证应用,我们设计了一种Ru基串联HOR催化剂,Ru纳米团簇用Pt单原子修饰。实验和理论研究表明,H2在Ru位点发生解离,生成的H迁移到Pt位点,H+被解吸。强的Ru-H相互作用促进了H2的解离步骤,而最佳的Pt-H相互作用确保了快速的脱附,从而大大提高了HOR动力学。在H2-O2燃料电池中,该催化剂可实现1.91 W cm-2的峰值功率密度和23.12 a mg-1的高阳极质量活性,在0.9 virfree下,超低贵金属负载为5 μg cm-2。这项工作推动了燃料电池低成本阳极催化剂的发展,并为理解氢电催化提供了更多的见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Nature Communications
Nature Communications Biological Science Disciplines-
CiteScore
24.90
自引率
2.40%
发文量
6928
审稿时长
3.7 months
期刊介绍: Nature Communications, an open-access journal, publishes high-quality research spanning all areas of the natural sciences. Papers featured in the journal showcase significant advances relevant to specialists in each respective field. With a 2-year impact factor of 16.6 (2022) and a median time of 8 days from submission to the first editorial decision, Nature Communications is committed to rapid dissemination of research findings. As a multidisciplinary journal, it welcomes contributions from biological, health, physical, chemical, Earth, social, mathematical, applied, and engineering sciences, aiming to highlight important breakthroughs within each domain.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信