The strong-weak adsorption pair motif of cuFe bimetallic composite as an efficient catalyst for CO2 RR toward the C2product ethylene and ethanol

IF 4.1 3区 化学 Q1 CHEMISTRY, ANALYTICAL
Yiman Kang , Honglin Zhu , Miao Shui
{"title":"The strong-weak adsorption pair motif of cuFe bimetallic composite as an efficient catalyst for CO2 RR toward the C2product ethylene and ethanol","authors":"Yiman Kang ,&nbsp;Honglin Zhu ,&nbsp;Miao Shui","doi":"10.1016/j.jelechem.2025.119450","DOIUrl":null,"url":null,"abstract":"<div><div>Currently, with the proposal of the dual‑carbon goal, the conversion of carbon dioxide has become a hot topic. Electro-catalysis occupies a prominent position in various catalytic technologies. Carbon dioxide reduction to C<sub>2</sub> product or C<sub>2</sub>+ product is of great importance to the deep utilization of carbon dioxide. However, it is prone to disadvantages such as slow speed, low selectivity, and high over potential toward C<sub>2</sub>+ products. Here, a neighboring strong weak metal atom pair strategy is proposed to design a new bimetallic catalyst aiming at significantly reduce the over potential of C<sub>2</sub>+ products. The strong (Fe) and weak (cu) motif owns a negligible energy barrier of 0.06 eV from CO<sub>2</sub> to surface adsorbed CO molecule. Afterwards, it significantly reduces the energy barrier of the C<img>C coupling process to 0.48 eV and makes the limiting potential (LP) of the reduction to ethylene 0.28 eV and 0.49 eV to ethanol. The high efficiency of this neighboring strong weak metal atom pair strategy offers new guidance to the electro-catalysis of C1 compound to C<sub>2</sub>+ products</div></div>","PeriodicalId":355,"journal":{"name":"Journal of Electroanalytical Chemistry","volume":"997 ","pages":"Article 119450"},"PeriodicalIF":4.1000,"publicationDate":"2025-09-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Electroanalytical Chemistry","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1572665725005247","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, ANALYTICAL","Score":null,"Total":0}
引用次数: 0

Abstract

Currently, with the proposal of the dual‑carbon goal, the conversion of carbon dioxide has become a hot topic. Electro-catalysis occupies a prominent position in various catalytic technologies. Carbon dioxide reduction to C2 product or C2+ product is of great importance to the deep utilization of carbon dioxide. However, it is prone to disadvantages such as slow speed, low selectivity, and high over potential toward C2+ products. Here, a neighboring strong weak metal atom pair strategy is proposed to design a new bimetallic catalyst aiming at significantly reduce the over potential of C2+ products. The strong (Fe) and weak (cu) motif owns a negligible energy barrier of 0.06 eV from CO2 to surface adsorbed CO molecule. Afterwards, it significantly reduces the energy barrier of the CC coupling process to 0.48 eV and makes the limiting potential (LP) of the reduction to ethylene 0.28 eV and 0.49 eV to ethanol. The high efficiency of this neighboring strong weak metal atom pair strategy offers new guidance to the electro-catalysis of C1 compound to C2+ products

Abstract Image

cuFe双金属复合材料的强-弱吸附对基序作为CO2向CO2产物乙烯和乙醇的有效催化剂
目前,随着双碳目标的提出,二氧化碳的转化已成为一个热门话题。电催化在各种催化技术中占有突出的地位。二氧化碳还原为C2产物或C2+产物对二氧化碳的深度利用具有重要意义。然而,它容易存在速度慢、选择性低、对C2+产物超电位高的缺点。本文提出了邻近强弱金属原子对策略,设计了一种新的双金属催化剂,旨在显著降低C2+产物的过电位。强(Fe)和弱(cu)基序从CO2到表面吸附的CO分子具有可忽略的0.06 eV的能垒。之后,将CC耦合过程的能垒显著降低至0.48 eV,还原乙烯的极限电位(LP)为0.28 eV,还原乙醇的极限电位(LP)为0.49 eV。这种相邻强弱金属原子对策略的高效率为C1化合物电催化生成C2+产物提供了新的指导
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
7.80
自引率
6.70%
发文量
912
审稿时长
2.4 months
期刊介绍: The Journal of Electroanalytical Chemistry is the foremost international journal devoted to the interdisciplinary subject of electrochemistry in all its aspects, theoretical as well as applied. Electrochemistry is a wide ranging area that is in a state of continuous evolution. Rather than compiling a long list of topics covered by the Journal, the editors would like to draw particular attention to the key issues of novelty, topicality and quality. Papers should present new and interesting electrochemical science in a way that is accessible to the reader. The presentation and discussion should be at a level that is consistent with the international status of the Journal. Reports describing the application of well-established techniques to problems that are essentially technical will not be accepted. Similarly, papers that report observations but fail to provide adequate interpretation will be rejected by the Editors. Papers dealing with technical electrochemistry should be submitted to other specialist journals unless the authors can show that their work provides substantially new insights into electrochemical processes.
×
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