Concerted Proton-Coupled Electron Transfer by Mo5+/Mo6+ Reversible Transformation for CO2 Photoreduction with Nearly 100% CH4 Selectivity

IF 11.3 1区 化学 Q1 CHEMISTRY, PHYSICAL ACS Catalysis Pub Date : 2024-11-07 DOI:10.1021/acscatal.4c04994
Qian Liang, Jingshan Fan, Jiawen Ding, Xiuzheng Deng, Yingtang Zhou, Jun Cai, Zheng Peng, Zhongyu Li, Zhenhui Kang
{"title":"Concerted Proton-Coupled Electron Transfer by Mo5+/Mo6+ Reversible Transformation for CO2 Photoreduction with Nearly 100% CH4 Selectivity","authors":"Qian Liang, Jingshan Fan, Jiawen Ding, Xiuzheng Deng, Yingtang Zhou, Jun Cai, Zheng Peng, Zhongyu Li, Zhenhui Kang","doi":"10.1021/acscatal.4c04994","DOIUrl":null,"url":null,"abstract":"Regulation of the proton-coupled electron transfer (PCET) process to avoid the unbalanced proton and electron regions on the reduction active sites is key to dictating product selectivity in a photocatalytic CO<sub>2</sub> reduction reaction. Here, we show that reversible Mo<sup>5+</sup>/Mo<sup>6+</sup> as a mediator can regulate the proton and electron transfer process at the Bi<sub>2</sub>MoO<sub>6</sub> nanosheet/In<sub>2</sub>O<sub>3</sub> microtube (BI) catalyst. The formed concerted proton-coupled electron transfer enables a champion solar-to-methane efficiency of 0.15%, resulting in nearly 100% CH<sub>4</sub> selectivity and a competitive CH<sub>4</sub> yield of 46.37 μmol g<sup>–1</sup> h<sup>–1</sup> in pure water. The experiments, together with theoretical calculations, clearly validate that In sites as H<sub>2</sub>O oxidation centers provide protons, and the regulation of protons and electrons by using Mo sites forms approximate electroneutral proton/electron pairs, which are conjointly transferred to Bi sites as CO<sub>2</sub> adsorption/reduction centers, thus achieving precise hydrogenation on Bi sites for binding of the *CH<sub>3</sub>O key intermediate to form CH<sub>4</sub>.","PeriodicalId":9,"journal":{"name":"ACS Catalysis ","volume":null,"pages":null},"PeriodicalIF":11.3000,"publicationDate":"2024-11-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACS Catalysis ","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1021/acscatal.4c04994","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
引用次数: 0

Abstract

Regulation of the proton-coupled electron transfer (PCET) process to avoid the unbalanced proton and electron regions on the reduction active sites is key to dictating product selectivity in a photocatalytic CO2 reduction reaction. Here, we show that reversible Mo5+/Mo6+ as a mediator can regulate the proton and electron transfer process at the Bi2MoO6 nanosheet/In2O3 microtube (BI) catalyst. The formed concerted proton-coupled electron transfer enables a champion solar-to-methane efficiency of 0.15%, resulting in nearly 100% CH4 selectivity and a competitive CH4 yield of 46.37 μmol g–1 h–1 in pure water. The experiments, together with theoretical calculations, clearly validate that In sites as H2O oxidation centers provide protons, and the regulation of protons and electrons by using Mo sites forms approximate electroneutral proton/electron pairs, which are conjointly transferred to Bi sites as CO2 adsorption/reduction centers, thus achieving precise hydrogenation on Bi sites for binding of the *CH3O key intermediate to form CH4.

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
通过 Mo5+/Mo6+ 可逆转化实现协同质子耦合电子转移,以接近 100% 的 CH4 选择性进行 CO2 光还原
调节质子耦合电子转移(PCET)过程以避免还原活性位点上质子和电子区域的不平衡,是决定光催化二氧化碳还原反应中产物选择性的关键。在这里,我们展示了可逆的 Mo5+/Mo6+ 作为介质可以调节 Bi2MoO6 纳米片/In2O3 微管(BI)催化剂上的质子和电子转移过程。所形成的质子耦合电子传递使太阳能转化为甲烷的效率达到了 0.15%,从而使甲烷的选择性接近 100%,在纯水中的甲烷产率高达 46.37 μmol g-1 h-1。实验和理论计算清楚地验证了 In 位点作为 H2O 氧化中心提供质子,通过使用 Mo 位点调节质子和电子,形成近似电中性的质子/电子对,这些质子/电子对同时转移到作为 CO2 吸附/还原中心的 Bi 位点,从而在 Bi 位点上实现精确氢化,结合 *CH3O 关键中间产物形成 CH4。
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
ACS Catalysis
ACS Catalysis CHEMISTRY, PHYSICAL-
CiteScore
20.80
自引率
6.20%
发文量
1253
审稿时长
1.5 months
期刊介绍: ACS Catalysis is an esteemed journal that publishes original research in the fields of heterogeneous catalysis, molecular catalysis, and biocatalysis. It offers broad coverage across diverse areas such as life sciences, organometallics and synthesis, photochemistry and electrochemistry, drug discovery and synthesis, materials science, environmental protection, polymer discovery and synthesis, and energy and fuels. The scope of the journal is to showcase innovative work in various aspects of catalysis. This includes new reactions and novel synthetic approaches utilizing known catalysts, the discovery or modification of new catalysts, elucidation of catalytic mechanisms through cutting-edge investigations, practical enhancements of existing processes, as well as conceptual advances in the field. Contributions to ACS Catalysis can encompass both experimental and theoretical research focused on catalytic molecules, macromolecules, and materials that exhibit catalytic turnover.
期刊最新文献
Trend and Progress in Catalysis for Ethylene Production from Bioethanol Using ZSM-5 Fe-Doped Ni-Based Catalysts Surpass Ir-Baselines for Oxygen Evolution Due to Optimal Charge-Transfer Characteristics Photoreforming of Lignocellulose into CO and Lactic Acid over a Single-Atom Fe-Dispersed Order/Disorder Polymeric Carbon Nitride Homojunction Asymmetric Csp3–Csp3 Bond Formation via Ni-Catalyzed Regio- and Enantioselective Hydroalkylation of Linear 1,3-Diene through Carbonyl Umpolung Improved Catalyst Performance for the Oxygen Evolution Reaction under a Chiral Bias
×
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