关于 Cu(110) 上电化学将 CO2 还原成 C1 和 C2 产物的反应机理的第一性原理研究

Catalysts Pub Date : 2024-07-22 DOI:10.3390/catal14070468
Yangyang Xu, Lixin Zhang
{"title":"关于 Cu(110) 上电化学将 CO2 还原成 C1 和 C2 产物的反应机理的第一性原理研究","authors":"Yangyang Xu, Lixin Zhang","doi":"10.3390/catal14070468","DOIUrl":null,"url":null,"abstract":"The mechanism of the electrochemical CO2 reduction reaction on a Cu(110) surface has yet to be fully revealed. In this work, based on first-principles calculations, we investigate the mechanisms of the CO2 reduction reaction to produce C1 (including one C atom) and C2 (including two C atoms) products on a Cu(110) surface. The results show that CH4 and C2H5OH are the main C1 and C2 products on the Cu(110) surface, respectively. CH4 is produced along the pathway CO2 → COOH* → CO* → CHO* → CH2O* → CH3O* → CH4. C2H5OH is produced via the C-C coupling pathway between CO* and CH2O* intermediates, which is the key reaction step. This is because CO* and CH2O* coupling to CO-CH2O* has the lowest barrier among the CHxO* (x = 0–2) coupling pathways. Therefore, it is the most likely C-C coupling pathway. Further, CO-CH2O* is gradually hydrogenated to C2H5OH along the following pathway: CO-CH2O* → CHO-CH2O* → CHOH-CH2* → CH2OH-CH2* → CH2OH-CH3* → C2H5OH.","PeriodicalId":505577,"journal":{"name":"Catalysts","volume":"31 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-07-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"A First-Principles Study on the Reaction Mechanisms of Electrochemical CO2 Reduction to C1 and C2 Products on Cu(110)\",\"authors\":\"Yangyang Xu, Lixin Zhang\",\"doi\":\"10.3390/catal14070468\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"The mechanism of the electrochemical CO2 reduction reaction on a Cu(110) surface has yet to be fully revealed. In this work, based on first-principles calculations, we investigate the mechanisms of the CO2 reduction reaction to produce C1 (including one C atom) and C2 (including two C atoms) products on a Cu(110) surface. The results show that CH4 and C2H5OH are the main C1 and C2 products on the Cu(110) surface, respectively. CH4 is produced along the pathway CO2 → COOH* → CO* → CHO* → CH2O* → CH3O* → CH4. C2H5OH is produced via the C-C coupling pathway between CO* and CH2O* intermediates, which is the key reaction step. This is because CO* and CH2O* coupling to CO-CH2O* has the lowest barrier among the CHxO* (x = 0–2) coupling pathways. Therefore, it is the most likely C-C coupling pathway. Further, CO-CH2O* is gradually hydrogenated to C2H5OH along the following pathway: CO-CH2O* → CHO-CH2O* → CHOH-CH2* → CH2OH-CH2* → CH2OH-CH3* → C2H5OH.\",\"PeriodicalId\":505577,\"journal\":{\"name\":\"Catalysts\",\"volume\":\"31 1\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2024-07-22\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Catalysts\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.3390/catal14070468\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Catalysts","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.3390/catal14070468","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

摘要

Cu(110) 表面的二氧化碳电化学还原反应机理尚未完全揭示。在这项工作中,我们基于第一性原理计算,研究了 CO2 还原反应在 Cu(110) 表面生成 C1(包括一个 C 原子)和 C2(包括两个 C 原子)产物的机理。结果表明,CH4 和 C2H5OH 分别是 Cu(110) 表面上的主要 C1 和 C2 产物。CH4 是沿着 CO2 → COOH* → CO* → CHO* → CH2O* → CH3O* → CH4 的路径生成的。C2H5OH 是通过 CO* 和 CH2O* 中间体之间的 C-C 偶联途径生成的,这是关键的反应步骤。这是因为在 CHxO*(x = 0-2)耦合途径中,CO* 和 CH2O* 耦合成 CO-CH2O* 的阻力最小。因此,这是最可能的 C-C 偶联途径。此外,CO-CH2O* 会沿着以下路径逐渐氢化为 C2H5OH:co-ch2o* → cho-ch2o* → choh-ch2* → ch2oh-ch2* → ch2oh-ch3* → c2h5oh。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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
A First-Principles Study on the Reaction Mechanisms of Electrochemical CO2 Reduction to C1 and C2 Products on Cu(110)
The mechanism of the electrochemical CO2 reduction reaction on a Cu(110) surface has yet to be fully revealed. In this work, based on first-principles calculations, we investigate the mechanisms of the CO2 reduction reaction to produce C1 (including one C atom) and C2 (including two C atoms) products on a Cu(110) surface. The results show that CH4 and C2H5OH are the main C1 and C2 products on the Cu(110) surface, respectively. CH4 is produced along the pathway CO2 → COOH* → CO* → CHO* → CH2O* → CH3O* → CH4. C2H5OH is produced via the C-C coupling pathway between CO* and CH2O* intermediates, which is the key reaction step. This is because CO* and CH2O* coupling to CO-CH2O* has the lowest barrier among the CHxO* (x = 0–2) coupling pathways. Therefore, it is the most likely C-C coupling pathway. Further, CO-CH2O* is gradually hydrogenated to C2H5OH along the following pathway: CO-CH2O* → CHO-CH2O* → CHOH-CH2* → CH2OH-CH2* → CH2OH-CH3* → C2H5OH.
求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
Facile Immersing Synthesis of Pt Single Atoms Supported on Sulfide for Bifunctional toward Seawater Electrolysis Construction of Cu2O-ZnO/Cellulose Composites for Enhancing the Photocatalytic Performance The Hydrodeoxygenation of Phenol over Ni-P/Hβ and Ni-P/Ce-β: Modifying the Effects in Dispersity and Acidity BiVO4-Based Photocatalysts for the Degradation of Antibiotics in Wastewater: Calcination Role after Solvothermal Synthesis Green Synthesis of Copper Oxide Nanoparticles from Waste Solar Panels Using Piper nigrum Fruit Extract and Their Antibacterial Activity
×
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