Lujie Liu*, Hao Zheng, Angjian Wu, Hangjie Li, Ang Cao, Jianhua Yan*, Liang Wang and Feng-Shou Xiao*,
{"title":"金属基催化剂对CO2加氢制C1产物的稳定性研究","authors":"Lujie Liu*, Hao Zheng, Angjian Wu, Hangjie Li, Ang Cao, Jianhua Yan*, Liang Wang and Feng-Shou Xiao*, ","doi":"10.1021/acs.energyfuels.5c03153","DOIUrl":null,"url":null,"abstract":"<p >The structural evolution and migration of metal species strongly influence the performance and durability of catalysts for carbon dioxide (CO<sub>2</sub>) hydrogenation, which are critical for the development of stable metal-based catalysts. This review focuses on the recent progress in stabilizing metal-based catalysts for C<sub>1</sub> products by suppressing undesirable metal migration or harnessing dynamic restructuring to generate new active sites with different metal oxidation states and/or variable metal–support/metal–metal interfaces. Strategies such as strengthening metal–support interactions, confining metal species, and regulating wetting behavior could modulate metal sintering to enhance catalytic activities. Particular attention is given to the relationship between the structural dynamics and reaction conditions, including atmosphere, temperature, and pressure. <i>In situ</i> and <i>operando</i> techniques have provided valuable insights, yet limitations in spatial and temporal resolution remain. Moreover, zeolites have emerged as promising supports due to their tunable defect structures and confinement effects, which enable the formation of well-dispersed and stable metal centers. These insights will advance the design of effective catalysts for the production of value-added C<sub>1</sub> chemicals.</p>","PeriodicalId":35,"journal":{"name":"Energy & Fuels","volume":"39 30","pages":"14483–14499"},"PeriodicalIF":5.3000,"publicationDate":"2025-07-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Stabilization of Metal-Based Catalysts for Hydrogenation of CO2 to C1 Products\",\"authors\":\"Lujie Liu*, Hao Zheng, Angjian Wu, Hangjie Li, Ang Cao, Jianhua Yan*, Liang Wang and Feng-Shou Xiao*, \",\"doi\":\"10.1021/acs.energyfuels.5c03153\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >The structural evolution and migration of metal species strongly influence the performance and durability of catalysts for carbon dioxide (CO<sub>2</sub>) hydrogenation, which are critical for the development of stable metal-based catalysts. This review focuses on the recent progress in stabilizing metal-based catalysts for C<sub>1</sub> products by suppressing undesirable metal migration or harnessing dynamic restructuring to generate new active sites with different metal oxidation states and/or variable metal–support/metal–metal interfaces. Strategies such as strengthening metal–support interactions, confining metal species, and regulating wetting behavior could modulate metal sintering to enhance catalytic activities. Particular attention is given to the relationship between the structural dynamics and reaction conditions, including atmosphere, temperature, and pressure. <i>In situ</i> and <i>operando</i> techniques have provided valuable insights, yet limitations in spatial and temporal resolution remain. Moreover, zeolites have emerged as promising supports due to their tunable defect structures and confinement effects, which enable the formation of well-dispersed and stable metal centers. These insights will advance the design of effective catalysts for the production of value-added C<sub>1</sub> chemicals.</p>\",\"PeriodicalId\":35,\"journal\":{\"name\":\"Energy & Fuels\",\"volume\":\"39 30\",\"pages\":\"14483–14499\"},\"PeriodicalIF\":5.3000,\"publicationDate\":\"2025-07-18\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Energy & Fuels\",\"FirstCategoryId\":\"5\",\"ListUrlMain\":\"https://pubs.acs.org/doi/10.1021/acs.energyfuels.5c03153\",\"RegionNum\":3,\"RegionCategory\":\"工程技术\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"ENERGY & FUELS\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Energy & Fuels","FirstCategoryId":"5","ListUrlMain":"https://pubs.acs.org/doi/10.1021/acs.energyfuels.5c03153","RegionNum":3,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"ENERGY & FUELS","Score":null,"Total":0}
Stabilization of Metal-Based Catalysts for Hydrogenation of CO2 to C1 Products
The structural evolution and migration of metal species strongly influence the performance and durability of catalysts for carbon dioxide (CO2) hydrogenation, which are critical for the development of stable metal-based catalysts. This review focuses on the recent progress in stabilizing metal-based catalysts for C1 products by suppressing undesirable metal migration or harnessing dynamic restructuring to generate new active sites with different metal oxidation states and/or variable metal–support/metal–metal interfaces. Strategies such as strengthening metal–support interactions, confining metal species, and regulating wetting behavior could modulate metal sintering to enhance catalytic activities. Particular attention is given to the relationship between the structural dynamics and reaction conditions, including atmosphere, temperature, and pressure. In situ and operando techniques have provided valuable insights, yet limitations in spatial and temporal resolution remain. Moreover, zeolites have emerged as promising supports due to their tunable defect structures and confinement effects, which enable the formation of well-dispersed and stable metal centers. These insights will advance the design of effective catalysts for the production of value-added C1 chemicals.
期刊介绍:
Energy & Fuels publishes reports of research in the technical area defined by the intersection of the disciplines of chemistry and chemical engineering and the application domain of non-nuclear energy and fuels. This includes research directed at the formation of, exploration for, and production of fossil fuels and biomass; the properties and structure or molecular composition of both raw fuels and refined products; the chemistry involved in the processing and utilization of fuels; fuel cells and their applications; and the analytical and instrumental techniques used in investigations of the foregoing areas.