External electric field modulation of cation-induced interfacial potential during hydrogen evolution on polycrystalline platinum surfaces

IF 9.4 1区 化学 Q1 CHEMISTRY, PHYSICAL
Pengbo Ding , Qitao Lian , Dan Xing , Lixiu Guan , Zhuoao Li , Shuo Zhang , Junguang Tao
{"title":"External electric field modulation of cation-induced interfacial potential during hydrogen evolution on polycrystalline platinum surfaces","authors":"Pengbo Ding ,&nbsp;Qitao Lian ,&nbsp;Dan Xing ,&nbsp;Lixiu Guan ,&nbsp;Zhuoao Li ,&nbsp;Shuo Zhang ,&nbsp;Junguang Tao","doi":"10.1016/j.jcis.2025.138259","DOIUrl":null,"url":null,"abstract":"<div><div>The impact of alkaline media on the hydrogen evolution reaction (HER) rate is crucial for water electrolysis. This study provides new insights into how alkali metal cations (AM<sup>+</sup>) influence the HER performance of Pt electrodes. We quantified interfacial potential drops modulated by an external electric field and discovered that the local surface concentration of AM<sup>+</sup> is 5.0 to 8.6 times higher than in the bulk solution. The accumulation of AM<sup>+</sup> in the outer Helmholtz plane (OHP) diminishes the interaction between H<sub>2</sub>O and Pt surface, thereby impeding H<sub>2</sub>O dissociation. The external electric field drives AM<sup>+</sup> away from the OHP, mitigating this effect. Theoretical calculations indicate that AM<sup>+</sup> enhance proton transfer by reorganizing interfacial water, with Li<sup>+</sup> orienting surrounding O<img>H bonds favorably towards the Pt surface, thus facilitating the HER process. Our combined experimental and theoretical studies elucidate the role of AM<sup>+</sup> in the HER by influencing double-layer potential and interfacial water formation.</div></div>","PeriodicalId":351,"journal":{"name":"Journal of Colloid and Interface Science","volume":"699 ","pages":"Article 138259"},"PeriodicalIF":9.4000,"publicationDate":"2025-06-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Colloid and Interface Science","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0021979725016509","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
引用次数: 0

Abstract

The impact of alkaline media on the hydrogen evolution reaction (HER) rate is crucial for water electrolysis. This study provides new insights into how alkali metal cations (AM+) influence the HER performance of Pt electrodes. We quantified interfacial potential drops modulated by an external electric field and discovered that the local surface concentration of AM+ is 5.0 to 8.6 times higher than in the bulk solution. The accumulation of AM+ in the outer Helmholtz plane (OHP) diminishes the interaction between H2O and Pt surface, thereby impeding H2O dissociation. The external electric field drives AM+ away from the OHP, mitigating this effect. Theoretical calculations indicate that AM+ enhance proton transfer by reorganizing interfacial water, with Li+ orienting surrounding OH bonds favorably towards the Pt surface, thus facilitating the HER process. Our combined experimental and theoretical studies elucidate the role of AM+ in the HER by influencing double-layer potential and interfacial water formation.

Abstract Image

多晶铂表面析氢过程中阳离子诱导界面电位的外电场调制
碱性介质对析氢反应(HER)速率的影响是电解水的关键。这项研究为碱金属阳离子(AM+)如何影响Pt电极的HER性能提供了新的见解。我们量化了外电场调制的界面电位下降,发现AM+的局部表面浓度比本体溶液高5.0 ~ 8.6倍。AM+在外亥姆霍兹平面(OHP)的积累减少了H2O与Pt表面的相互作用,从而阻碍了H2O的解离。外部电场驱动AM+远离OHP,减轻了这种影响。理论计算表明,AM+通过重组界面水来增强质子转移,Li+使周围的OH键向Pt表面倾斜,从而促进了HER过程。我们的实验和理论结合研究阐明了AM+通过影响双层电位和界面水形成在HER中的作用。
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
CiteScore
16.10
自引率
7.10%
发文量
2568
审稿时长
2 months
期刊介绍: The Journal of Colloid and Interface Science publishes original research findings on the fundamental principles of colloid and interface science, as well as innovative applications in various fields. The criteria for publication include impact, quality, novelty, and originality. Emphasis: The journal emphasizes fundamental scientific innovation within the following categories: A.Colloidal Materials and Nanomaterials B.Soft Colloidal and Self-Assembly Systems C.Adsorption, Catalysis, and Electrochemistry D.Interfacial Processes, Capillarity, and Wetting E.Biomaterials and Nanomedicine F.Energy Conversion and Storage, and Environmental Technologies
×
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