Unveiling the Promotion of Sulfides Heterostructure on the Urea Oxidation Reaction: Role of Interface Engineering and Sulfate Adsorption

IF 12.1 2区 材料科学 Q1 CHEMISTRY, MULTIDISCIPLINARY Small Pub Date : 2025-02-03 DOI:10.1002/smll.202410987
Yulan Song, Cuilan Tang, Jinglin Huang, Tao Wang, Xiaoshan He, Chunping Xie, Guo Chen, Yansong Liu, Zhibing He
{"title":"Unveiling the Promotion of Sulfides Heterostructure on the Urea Oxidation Reaction: Role of Interface Engineering and Sulfate Adsorption","authors":"Yulan Song,&nbsp;Cuilan Tang,&nbsp;Jinglin Huang,&nbsp;Tao Wang,&nbsp;Xiaoshan He,&nbsp;Chunping Xie,&nbsp;Guo Chen,&nbsp;Yansong Liu,&nbsp;Zhibing He","doi":"10.1002/smll.202410987","DOIUrl":null,"url":null,"abstract":"<p>The pursuit of efficient and stable urea oxidation reaction (UOR) electrocatalysts is paramount for the sustainable utilization of renewable energy sources and the treatment of wastewater with urea content. This research introduces the successful fabrication of (Fe<sub>0.5</sub>Ni<sub>0.5</sub>)<sub>0.96</sub>S/Co<sub>9</sub>S<sub>8</sub>/NF mesh heterojunction materials, which are replete with interfaces that facilitate enhanced catalytic activity. Benefiting from the electron transfer behavior from (Fe<sub>0.5</sub>Ni<sub>0.5</sub>)<sub>0.96</sub>S to Co<sub>9</sub>S<sub>8</sub>, and the promotion of surface adsorption of SO<sub>4</sub><sup>2−</sup>, the (Fe<sub>0.5</sub>Ni<sub>0.5</sub>)<sub>0.96</sub>S/Co<sub>9</sub>S<sub>8</sub>/NF electrocatalyst has excellent UOR catalytic performance. The experimental characterization and theoretical simulation show that the d-band center/thermodynamic barrier of (Fe<sub>0.5</sub>Ni<sub>0.5</sub>)<sub>0.96</sub>S/Co<sub>9</sub>S<sub>8</sub>/NF is regulated by the redistribution of electrons at the heterojunction interface, and the adsorption of SO<sub>4</sub><sup>2−</sup> on the surface. The reaction barrier of the adsorption strength/rate-controlling step of urea and reaction intermediates is optimized, which promotes the catalytic kinetics and thermodynamics of UOR, offering a promising strategy for advancing energy and environmental technologies.</p>","PeriodicalId":228,"journal":{"name":"Small","volume":"21 9","pages":""},"PeriodicalIF":12.1000,"publicationDate":"2025-02-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Small","FirstCategoryId":"88","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/smll.202410987","RegionNum":2,"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

Abstract

The pursuit of efficient and stable urea oxidation reaction (UOR) electrocatalysts is paramount for the sustainable utilization of renewable energy sources and the treatment of wastewater with urea content. This research introduces the successful fabrication of (Fe0.5Ni0.5)0.96S/Co9S8/NF mesh heterojunction materials, which are replete with interfaces that facilitate enhanced catalytic activity. Benefiting from the electron transfer behavior from (Fe0.5Ni0.5)0.96S to Co9S8, and the promotion of surface adsorption of SO42−, the (Fe0.5Ni0.5)0.96S/Co9S8/NF electrocatalyst has excellent UOR catalytic performance. The experimental characterization and theoretical simulation show that the d-band center/thermodynamic barrier of (Fe0.5Ni0.5)0.96S/Co9S8/NF is regulated by the redistribution of electrons at the heterojunction interface, and the adsorption of SO42− on the surface. The reaction barrier of the adsorption strength/rate-controlling step of urea and reaction intermediates is optimized, which promotes the catalytic kinetics and thermodynamics of UOR, offering a promising strategy for advancing energy and environmental technologies.

Abstract Image

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
揭示硫化物异质结构对尿素氧化反应的促进作用:界面工程和硫酸盐吸附的作用
寻求高效、稳定的尿素氧化反应电催化剂对可再生能源的可持续利用和含尿素废水的处理具有重要意义。本研究成功制备了(Fe0.5Ni0.5)0.96S/Co9S8/NF网状异质结材料,该材料具有丰富的界面,有利于提高催化活性。得益于(Fe0.5Ni0.5)0.96S向Co9S8的电子转移行为,以及促进SO42−的表面吸附,(Fe0.5Ni0.5)0.96S/Co9S8/NF电催化剂具有优异的UOR催化性能。实验表征和理论模拟表明,(Fe0.5Ni0.5)0.96S/Co9S8/NF的d带中心/热力学势垒受电子在异质结界面的重分布和表面对SO42−的吸附调节。优化了尿素和反应中间体吸附强度/速率控制步骤的反应屏障,促进了UOR的催化动力学和热力学,为推进能源和环境技术提供了有前途的策略。
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
Small
Small 工程技术-材料科学:综合
CiteScore
17.70
自引率
3.80%
发文量
1830
审稿时长
2.1 months
期刊介绍: Small serves as an exceptional platform for both experimental and theoretical studies in fundamental and applied interdisciplinary research at the nano- and microscale. The journal offers a compelling mix of peer-reviewed Research Articles, Reviews, Perspectives, and Comments. With a remarkable 2022 Journal Impact Factor of 13.3 (Journal Citation Reports from Clarivate Analytics, 2023), Small remains among the top multidisciplinary journals, covering a wide range of topics at the interface of materials science, chemistry, physics, engineering, medicine, and biology. Small's readership includes biochemists, biologists, biomedical scientists, chemists, engineers, information technologists, materials scientists, physicists, and theoreticians alike.
期刊最新文献
Electrochemiluminescent COFs and HOFs as Porous Material Engineering Systems for Bioanalysis and Environmental Monitoring Titanium Carbide MXene Synthesis by Etching of Titanium Aluminum Carbide in Acetic Acid Solution Laser-Induced Porosity Engineering of Metal-Organic Frameworks for Enhanced CO2/CH4 Adsorption Properties Dopamine and Rotenone Modulate α-Synuclein Phase Separation and Liquid to Solid Transition Electrofabricated Oxygen-Terminated Zincophilic ZnCoAl-LDH Functional Layers for Reversible Zinc Metal Anodes
×
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:604180095
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