Mengqian Li, Zequn Han, Qinyuan Hu, Wenya Fan, Qing Hu, Dongpo He, QingXia Chen, Xingchen Jiao and Yi Xie
{"title":"太阳能驱动二氧化碳还原为多碳产品的最新进展","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":"{\"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}","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
摘要
目前,大多数用于光化学转化二氧化碳(CO2)的催化剂通常生产 C1 产品。多碳(C2+)产品因其更高的能量密度和经济潜力而备受青睐,但实现多碳(C2+)产品仍然是一项重大挑战。造成这一困难的主要原因是工艺中的 C-C 偶联步骤存在动力学障碍。有鉴于此,有必要设计多种策略来加速 C-C 偶联生成多碳产品。在此,我们首先对涉及 CO2 光转化为 C2+ 燃料的催化剂进行了分类。我们总结了金属氧化物、金属硫化物、MXenes 和金属有机框架作为 CO2 光还原为 C2+ 产物的催化剂,并将其功效归因于促进 C-C 偶联的固有双活性位点。此外,我们还研究了共价有机框架、碳氮化物、金属磷化物和石墨烯作为 CO2 光还原成 C2+ 产物的协同催化剂,这是因为它们具有可诱导 C-C 偶联的双活性位点。最后,我们对设计新型光催化剂、了解催化机理以及考虑将 CO2 光转化为多碳产品的实际应用要求进行了简要总结和展望。
Recent progress in solar-driven CO2 reduction to multicarbon products
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