Hierarchical NiFe-Layered Double Hydroxide Coupled with Bimetallic NiFe-MOF Electrocatalysts for the Oxygen Evolution Reaction

IF 5.3 2区 材料科学 Q2 MATERIALS SCIENCE, MULTIDISCIPLINARY
Weipeng Wang, Chunbo Liu, Jihui Lang, Tianyu Zhou, FeiFan Guo, Wei Jiang, Jingdong Feng, Xiaotian Yang*, Guangbo Che* and Yuanyuan Wu*, 
{"title":"Hierarchical NiFe-Layered Double Hydroxide Coupled with Bimetallic NiFe-MOF Electrocatalysts for the Oxygen Evolution Reaction","authors":"Weipeng Wang,&nbsp;Chunbo Liu,&nbsp;Jihui Lang,&nbsp;Tianyu Zhou,&nbsp;FeiFan Guo,&nbsp;Wei Jiang,&nbsp;Jingdong Feng,&nbsp;Xiaotian Yang*,&nbsp;Guangbo Che* and Yuanyuan Wu*,&nbsp;","doi":"10.1021/acsanm.4c0481510.1021/acsanm.4c04815","DOIUrl":null,"url":null,"abstract":"<p >It is crucial to utilize extremely efficient and economical catalysts for the energy-intensive and kinetically slow oxygen evolution process. Here, we fabricated a NiFeLDH coupled with the NiFe-MOF catalyst with a unique hierarchical structure using a facile and rapid electrodeposition and electrochemical activation strategy. With a low overpotential of about 187 mV at 10 mA cm<sup>–2</sup>, the NiFeLDH/NiFe-MOF/NF demonstrates exceptional stability for more than 1000 h. Additionally, the produced NiFeLDH/NiFe-MOF/NF could provide high current densities of 500 and 1000 mA cm<sup>–2</sup> in 6 M KOH at relatively low overpotentials of 293 and 353 mV, respectively. The construction of heterojunctions provides abundant interfacial active sites and optimizes catalytic activity by adjusting the surface electronic structure and energy levels. This serves to enhance the intrinsic activity of the catalyst. Density functional theory (DFT) calculations further prove that the construction of NiFeLDH regulates the band structure of metal sites, enhances the catalytic performance for the oxygen evolution reaction (OER), and lowers the intermediate medium’s adsorption free energy.</p>","PeriodicalId":6,"journal":{"name":"ACS Applied Nano Materials","volume":"7 23","pages":"26863–26872 26863–26872"},"PeriodicalIF":5.3000,"publicationDate":"2024-11-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACS Applied Nano Materials","FirstCategoryId":"88","ListUrlMain":"https://pubs.acs.org/doi/10.1021/acsanm.4c04815","RegionNum":2,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"MATERIALS SCIENCE, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0

Abstract

It is crucial to utilize extremely efficient and economical catalysts for the energy-intensive and kinetically slow oxygen evolution process. Here, we fabricated a NiFeLDH coupled with the NiFe-MOF catalyst with a unique hierarchical structure using a facile and rapid electrodeposition and electrochemical activation strategy. With a low overpotential of about 187 mV at 10 mA cm–2, the NiFeLDH/NiFe-MOF/NF demonstrates exceptional stability for more than 1000 h. Additionally, the produced NiFeLDH/NiFe-MOF/NF could provide high current densities of 500 and 1000 mA cm–2 in 6 M KOH at relatively low overpotentials of 293 and 353 mV, respectively. The construction of heterojunctions provides abundant interfacial active sites and optimizes catalytic activity by adjusting the surface electronic structure and energy levels. This serves to enhance the intrinsic activity of the catalyst. Density functional theory (DFT) calculations further prove that the construction of NiFeLDH regulates the band structure of metal sites, enhances the catalytic performance for the oxygen evolution reaction (OER), and lowers the intermediate medium’s adsorption free energy.

Abstract Image

分层nife层状双氢氧化物与双金属NiFe-MOF电催化剂的析氧反应
对于能量密集型和动力学缓慢的析氧过程,使用高效和经济的催化剂是至关重要的。在这里,我们采用简单快速的电沉积和电化学激活策略制备了具有独特分层结构的NiFeLDH与nfe - mof催化剂偶联。NiFeLDH/ nfe - mof /NF在10 mA cm-2下的过电位约为187 mV,稳定性超过1000小时。此外,制备的NiFeLDH/ nfe - mof /NF在6 M KOH下的过电位分别为293和353 mV,可提供500和1000 mA cm-2的高电流密度。异质结的构建提供了丰富的界面活性位点,并通过调节表面电子结构和能级来优化催化活性。这有助于提高催化剂的内在活性。密度泛函理论(DFT)计算进一步证明了NiFeLDH的构建调节了金属位点的能带结构,提高了析氧反应(OER)的催化性能,降低了中间介质的吸附自由能。
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
8.30
自引率
3.40%
发文量
1601
期刊介绍: ACS Applied Nano Materials is an interdisciplinary journal publishing original research covering all aspects of engineering, chemistry, physics and biology relevant to applications of nanomaterials. The journal is devoted to reports of new and original experimental and theoretical research of an applied nature that integrate knowledge in the areas of materials, engineering, physics, bioscience, and chemistry into important applications of nanomaterials.
×
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