A hollow CuS–CuO nanocube core and NiFe-LDH nanosheet shell electrocatalyst for enhanced oxygen evolution reaction†

IF 2.5 3区 化学 Q2 CHEMISTRY, MULTIDISCIPLINARY
Runmiao Chen, Long Ma, Qingdan Hui, Pengjing Yin, Pengpeng Du, Qiufang Liu, Yan Yan, Qi Xue, Yuan Dang and Yuanzhen Zhou
{"title":"A hollow CuS–CuO nanocube core and NiFe-LDH nanosheet shell electrocatalyst for enhanced oxygen evolution reaction†","authors":"Runmiao Chen, Long Ma, Qingdan Hui, Pengjing Yin, Pengpeng Du, Qiufang Liu, Yan Yan, Qi Xue, Yuan Dang and Yuanzhen Zhou","doi":"10.1039/D5NJ01317H","DOIUrl":null,"url":null,"abstract":"<p >Developing highly efficient and durable non-noble metal electrocatalysts for the oxygen evolution reaction (OER) remains a significant challenge. Herein, we synthesized a core–shell electrocatalyst, which consists of a hollow CuS–CuO nanocube core coated with a NiFe-LDH nanosheet shell (CuS–CuO@NiFe-LDH). Compared with the mono-structured electrocatalyst, the hybrid electrocatalyst, a CuS–CuO core coupled with a NiFe-LDH shell, offers a significantly larger specific surface area and a richer variety of pores. This architecture ensures more accessible active sites and provides abundant channels for ionic, electrolyte and product transport. Moreover, the strong interfacial interaction between CuS–CuO and NiFe-LDH promotes the electron rearrangement, promoting the formation of oxidation intermediates to facilitate the activity and dynamics of the OER. Electrochemical tests show that the optimized CuS–CuO@NiFe-LDH exhibits a low overpotential of 285 mV at 10 mA cm<small><sup>−2</sup></small>, a Tafel slope of 47.65 mV dec<small><sup>−1</sup></small>, and stable performance for up to 15 h under alkaline conditions. This work provides valuable insights into the design of core–shell structured anode catalysts for efficient OER.</p>","PeriodicalId":95,"journal":{"name":"New Journal of Chemistry","volume":" 25","pages":" 10832-10840"},"PeriodicalIF":2.5000,"publicationDate":"2025-06-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"New Journal of Chemistry","FirstCategoryId":"92","ListUrlMain":"https://pubs.rsc.org/en/content/articlelanding/2025/nj/d5nj01317h","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0

Abstract

Developing highly efficient and durable non-noble metal electrocatalysts for the oxygen evolution reaction (OER) remains a significant challenge. Herein, we synthesized a core–shell electrocatalyst, which consists of a hollow CuS–CuO nanocube core coated with a NiFe-LDH nanosheet shell (CuS–CuO@NiFe-LDH). Compared with the mono-structured electrocatalyst, the hybrid electrocatalyst, a CuS–CuO core coupled with a NiFe-LDH shell, offers a significantly larger specific surface area and a richer variety of pores. This architecture ensures more accessible active sites and provides abundant channels for ionic, electrolyte and product transport. Moreover, the strong interfacial interaction between CuS–CuO and NiFe-LDH promotes the electron rearrangement, promoting the formation of oxidation intermediates to facilitate the activity and dynamics of the OER. Electrochemical tests show that the optimized CuS–CuO@NiFe-LDH exhibits a low overpotential of 285 mV at 10 mA cm−2, a Tafel slope of 47.65 mV dec−1, and stable performance for up to 15 h under alkaline conditions. This work provides valuable insights into the design of core–shell structured anode catalysts for efficient OER.

Abstract Image

一种用于增强析氧反应的中空cu - cuo纳米立方核和NiFe-LDH纳米片壳电催化剂
为析氧反应(OER)开发高效、耐用的非贵金属电催化剂仍然是一个重大挑战。在此,我们合成了一种核-壳电催化剂,它由一个中空的cu - cuo纳米立方核和一层NiFe-LDH纳米片壳(cu - CuO@NiFe-LDH)组成。与单结构电催化剂相比,cu - cuo核与NiFe-LDH壳相结合的混合电催化剂具有更大的比表面积和更丰富的孔隙种类。这种结构确保了更容易接近的活性位点,并为离子、电解质和产品运输提供了丰富的通道。此外,cu - cuo和NiFe-LDH之间的强界面相互作用促进了电子重排,促进了氧化中间体的形成,从而促进了OER的活性和动力学。电化学测试表明,优化后的cu - CuO@NiFe-LDH在10 mA cm−2下的过电位为285 mV, Tafel斜率为47.65 mV dec−1,在碱性条件下稳定性能可达15 h。这项工作为高效OER的核壳结构阳极催化剂的设计提供了有价值的见解。
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
New Journal of Chemistry
New Journal of Chemistry 化学-化学综合
CiteScore
5.30
自引率
6.10%
发文量
1832
审稿时长
2 months
期刊介绍: A journal for new directions in chemistry
×
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