Feng Hong , Yanan Qi , Zuodong Yang , Lijun Yu , Xiaoguang Guan , Jiangyong Diao , Bo Sun , Hongyang Liu
{"title":"Recent advances of CO2 hydrogenation to methanol","authors":"Feng Hong , Yanan Qi , Zuodong Yang , Lijun Yu , Xiaoguang Guan , Jiangyong Diao , Bo Sun , Hongyang Liu","doi":"10.1016/j.decarb.2025.100111","DOIUrl":null,"url":null,"abstract":"<div><div>The increasingly serious climate issue compels urgent greenhouse gas mitigation strategies. As a budget, plentiful, renewable feedstock and major contributor to global warming, the large-scale catalytic transformation of CO<sub>2</sub> has attracted widespread attention from society due to its potential as a solution to the environment and energy crises. At present, catalytic hydrogenation of carbon dioxide to organic chemicals is the primary approach in its industrial applications. In recent decades, various materials containing Cu-, precious metal-, In-, Zn-, and Ga-based catalysts have been designed for CO<sub>2</sub> hydrogenation to methanol. Likewise, great advances have been made in CO<sub>2</sub>-to-chemicals, such as olefins, aromatics, and gasoline by combining CO<sub>2</sub>-to-CH<sub>3</sub>OH with methanol transformation or tandem reaction of reverse water-gas shift and Fischer-Tropsch (FT) synthesis. This review exhibits the recent advances in the hydrogenation of CO<sub>2</sub>-to-CH<sub>3</sub>OH including the catalyst system, CO<sub>2</sub> activation, nature of active sites, intermediate species (formate or carboxyl), structure-activity relationship, and reaction mechanism. Finally, challenges and outlooks in CO<sub>2</sub> hydrogenation to methanol are summarized.</div></div>","PeriodicalId":100356,"journal":{"name":"DeCarbon","volume":"8 ","pages":"Article 100111"},"PeriodicalIF":0.0000,"publicationDate":"2025-04-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"DeCarbon","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2949881325000149","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
The increasingly serious climate issue compels urgent greenhouse gas mitigation strategies. As a budget, plentiful, renewable feedstock and major contributor to global warming, the large-scale catalytic transformation of CO2 has attracted widespread attention from society due to its potential as a solution to the environment and energy crises. At present, catalytic hydrogenation of carbon dioxide to organic chemicals is the primary approach in its industrial applications. In recent decades, various materials containing Cu-, precious metal-, In-, Zn-, and Ga-based catalysts have been designed for CO2 hydrogenation to methanol. Likewise, great advances have been made in CO2-to-chemicals, such as olefins, aromatics, and gasoline by combining CO2-to-CH3OH with methanol transformation or tandem reaction of reverse water-gas shift and Fischer-Tropsch (FT) synthesis. This review exhibits the recent advances in the hydrogenation of CO2-to-CH3OH including the catalyst system, CO2 activation, nature of active sites, intermediate species (formate or carboxyl), structure-activity relationship, and reaction mechanism. Finally, challenges and outlooks in CO2 hydrogenation to methanol are summarized.