Edge sites on platinum electrocatalysts are responsible for discharge in the hydrogen evolution reaction†

IF 10.7 2区 材料科学 Q1 CHEMISTRY, PHYSICAL Journal of Materials Chemistry A Pub Date : 2024-10-14 DOI:10.1039/D4TA04887C
Vipin Adavan Kiliyankil, Wei Mao, Yurie Takahashi, Wei Gong, Shigeru Kabayama, Yuki Hamasaki, Katsuyuki Fukutani, Hiroyuki Matsuzaki, Ichiro Sakata, Kenji Takeuchi, Morinobu Endo and Bunshi Fugetsu
{"title":"Edge sites on platinum electrocatalysts are responsible for discharge in the hydrogen evolution reaction†","authors":"Vipin Adavan Kiliyankil, Wei Mao, Yurie Takahashi, Wei Gong, Shigeru Kabayama, Yuki Hamasaki, Katsuyuki Fukutani, Hiroyuki Matsuzaki, Ichiro Sakata, Kenji Takeuchi, Morinobu Endo and Bunshi Fugetsu","doi":"10.1039/D4TA04887C","DOIUrl":null,"url":null,"abstract":"<p >The hydrogen evolution reaction (HER) on platinum (Pt) electrocatalysts involves the generation of hydrogen atoms and the formation of hydrogen molecules. It is commonly believed that the sites on the surfaces of the terrace (111, 110, and 100) domains are responsible for the formation of hydrogen molecules. However, the electrochemistry of the hydrogen atom generation is not well understood. We created edge-rich platinum electrocatalysts using nano-fabrics comprising entire single-walled carbon nanotubes (SWCNTs) as templates and supports. We then conducted the HER on the edge-rich Pt/SWCNT hybridized electrocatalysts and gained new insights into the electrochemical properties and functions of the edge sites. We propose that the edge sites are oxidized and serve two important functions: they act as atomic barriers, allowing electrons to accumulate within the terrace (111, 110, and 100) domains, and they transfer the electrons to the hydronium ions in the electrical double layer through discharge. Enhancing the discharge capability of the electrocatalysts is an efficient way to reduce the amount of platinum required, and this can be applied to various precious metal-based electrocatalysts to enhance their electrocatalytic activities and durability.</p>","PeriodicalId":82,"journal":{"name":"Journal of Materials Chemistry A","volume":" 42","pages":" 28731-28743"},"PeriodicalIF":10.7000,"publicationDate":"2024-10-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://pubs.rsc.org/en/content/articlepdf/2024/ta/d4ta04887c?page=search","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Materials Chemistry A","FirstCategoryId":"88","ListUrlMain":"https://pubs.rsc.org/en/content/articlelanding/2024/ta/d4ta04887c","RegionNum":2,"RegionCategory":"材料科学","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 hydrogen evolution reaction (HER) on platinum (Pt) electrocatalysts involves the generation of hydrogen atoms and the formation of hydrogen molecules. It is commonly believed that the sites on the surfaces of the terrace (111, 110, and 100) domains are responsible for the formation of hydrogen molecules. However, the electrochemistry of the hydrogen atom generation is not well understood. We created edge-rich platinum electrocatalysts using nano-fabrics comprising entire single-walled carbon nanotubes (SWCNTs) as templates and supports. We then conducted the HER on the edge-rich Pt/SWCNT hybridized electrocatalysts and gained new insights into the electrochemical properties and functions of the edge sites. We propose that the edge sites are oxidized and serve two important functions: they act as atomic barriers, allowing electrons to accumulate within the terrace (111, 110, and 100) domains, and they transfer the electrons to the hydronium ions in the electrical double layer through discharge. Enhancing the discharge capability of the electrocatalysts is an efficient way to reduce the amount of platinum required, and this can be applied to various precious metal-based electrocatalysts to enhance their electrocatalytic activities and durability.

Abstract Image

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
铂电催化剂上的边缘位在氢气进化反应中起放电作用
铂电催化剂上的氢进化反应(HER)涉及氢原子的生成和氢分子的形成。人们普遍认为,台阶(111、110 和 100)表面的位点是形成氢分子的原因。然而,人们对氢原子生成的电化学原理并不十分了解。我们利用由整根单壁碳纳米管(SWCNT)组成的纳米织物作为模板和支撑,制造出了富集边缘的铂电催化剂。然后,我们对富集边缘铂/SWCNT 杂化电催化剂进行了 HER 研究,对边缘位点的电化学性质和功能有了新的认识。我们认为,边缘位点是氧化的,具有两个重要功能:作为原子屏障,允许电子在台阶(111、110 和 100)畴内聚集;通过放电将电子转移到电双层中的氢离子。增强电催化剂的放电能力是减少铂金用量的有效方法,可应用于各种贵金属电催化剂,以提高其电催化活性和耐久性。
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 去求助
来源期刊
Journal of Materials Chemistry A
Journal of Materials Chemistry A CHEMISTRY, PHYSICAL-ENERGY & FUELS
CiteScore
19.50
自引率
5.00%
发文量
1892
审稿时长
1.5 months
期刊介绍: The Journal of Materials Chemistry A, B & C covers a wide range of high-quality studies in the field of materials chemistry, with each section focusing on specific applications of the materials studied. Journal of Materials Chemistry A emphasizes applications in energy and sustainability, including topics such as artificial photosynthesis, batteries, and fuel cells. Journal of Materials Chemistry B focuses on applications in biology and medicine, while Journal of Materials Chemistry C covers applications in optical, magnetic, and electronic devices. Example topic areas within the scope of Journal of Materials Chemistry A include catalysis, green/sustainable materials, sensors, and water treatment, among others.
期刊最新文献
Functional Carbon-Based Covalent Bridging Bonds Unlocking Superior Sodium-Ion Storage From Waste to Energy and Fuel: Novel CuxNiy/CN catalysts from waste melamine resin for efficient nitrate reduction to ammonia Fluorinated catalysts for the oxygen evolution reaction: a comprehensive review of synthesis, structure, and performance Tuning of the Ionic Conductivity of Ba7Nb4MoO20 by Pressure: A Neutron Diffraction and Atomistic Modelling Study Calix[4]arene@MIL-101 as host@MOF for cage-in-cage pore space partitioning for enhanced CO2 separation and catalysis†
×
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
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 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 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1