Mengqian Li, Zequn Han, Qinyuan Hu, Wenya Fan, Qing Hu, Dongpo He, QingXia Chen, Xingchen Jiao and Yi Xie
{"title":"Recent progress in solar-driven CO2 reduction to multicarbon products","authors":"Mengqian Li, Zequn Han, Qinyuan Hu, Wenya Fan, Qing Hu, Dongpo He, QingXia Chen, Xingchen Jiao and Yi Xie","doi":"10.1039/D4CS00186A","DOIUrl":null,"url":null,"abstract":"<p >Currently, most catalysts used for photoconverting carbon dioxide (CO<small><sub>2</sub></small>) typically produce C<small><sub>1</sub></small> products. Achieving multicarbon (C<small><sub>2+</sub></small>) products, which are highly desirable due to their greater energy density and economic potential, still remains a significant challenge. This difficulty is primarily due to the kinetic hurdles associated with the C–C coupling step in the process. Given this, devising diverse strategies to accelerate C–C coupling for generating multicarbon products is requisite. Herein, we first give a classification of catalysts involved in the photoconversion of CO<small><sub>2</sub></small> to C<small><sub>2+</sub></small> fuels. We summarize metallic oxides, metallic sulfides, MXenes, and metal–organic frameworks as catalysts for CO<small><sub>2</sub></small> photoreduction to C<small><sub>2+</sub></small> products, attributing their efficacy to the inherent dual active sites facilitating C–C coupling. In addition, we survey covalent organic frameworks, carbon nitrides, metal phosphides, and graphene as cocatalysts for CO<small><sub>2</sub></small> photoreduction to C<small><sub>2+</sub></small> products, owing to the incorporated dual active sites that induce C–C coupling. In the end, we provide a brief conclusion and an outlook on designing new photocatalysts, understanding the catalytic mechanisms, and considering the practical application requirements for photoconverting CO<small><sub>2</sub></small> into multicarbon products.</p>","PeriodicalId":68,"journal":{"name":"Chemical Society Reviews","volume":" 20","pages":" 9964-9975"},"PeriodicalIF":40.4000,"publicationDate":"2024-09-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Chemical Society Reviews","FirstCategoryId":"92","ListUrlMain":"https://pubs.rsc.org/en/content/articlelanding/2024/cs/d4cs00186a","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0
Abstract
Currently, most catalysts used for photoconverting carbon dioxide (CO2) typically produce C1 products. Achieving multicarbon (C2+) products, which are highly desirable due to their greater energy density and economic potential, still remains a significant challenge. This difficulty is primarily due to the kinetic hurdles associated with the C–C coupling step in the process. Given this, devising diverse strategies to accelerate C–C coupling for generating multicarbon products is requisite. Herein, we first give a classification of catalysts involved in the photoconversion of CO2 to C2+ fuels. We summarize metallic oxides, metallic sulfides, MXenes, and metal–organic frameworks as catalysts for CO2 photoreduction to C2+ products, attributing their efficacy to the inherent dual active sites facilitating C–C coupling. In addition, we survey covalent organic frameworks, carbon nitrides, metal phosphides, and graphene as cocatalysts for CO2 photoreduction to C2+ products, owing to the incorporated dual active sites that induce C–C coupling. In the end, we provide a brief conclusion and an outlook on designing new photocatalysts, understanding the catalytic mechanisms, and considering the practical application requirements for photoconverting CO2 into multicarbon products.
期刊介绍:
Chemical Society Reviews is published by: Royal Society of Chemistry.
Focus: Review articles on topics of current interest in chemistry;
Predecessors: Quarterly Reviews, Chemical Society (1947–1971);
Current title: Since 1971;
Impact factor: 60.615 (2021);
Themed issues: Occasional themed issues on new and emerging areas of research in the chemical sciences