{"title":"通过热解将金属有机框架转化为高效的单原子催化剂,重点是氧还原反应催化剂","authors":"Linyu Hu , Wenrui Li , Lu Wang , Bo Wang","doi":"10.1016/j.enchem.2021.100056","DOIUrl":null,"url":null,"abstract":"<div><p>Single-atom catalysts (SACs) have attracted extensive attention because of their maximal atom utilization, unique electronic structure and high activity. Metal-organic frameworks (MOFs) could be used as perfect self-sacrificed precursors/templates for preparing SACs due to their uniformly distributed and spatially separated metal nodes and organic linkers as well as designable pore structures. Recently, numerous studies have been devoted to utilizing MOFs to prepare SACs through pyrolysis. Herein, this review summarizes the most recent strategies of turning selected MOFs into SACs, focusing on oxygen reduction reaction (ORR) catalysts. First, the inherent metal sites in MOFs are directly turned into single-atom sites <em>via</em> the high-temperature treatment with/without acid etching. Second, additional metal precursors are introduced into MOFs by various methods to further supplement active sites in the obtained SACs. Third, nonmetal heteroatom-rich (<em>i.e.</em>, N, P and S) precursors are combined with MOFs to provide more coordination sites to anchor metal atoms. Finally, perspectives on future opportunities for selecting and designing MOFs as SAC precursors are also proposed.</p></div>","PeriodicalId":307,"journal":{"name":"EnergyChem","volume":"3 3","pages":"Article 100056"},"PeriodicalIF":22.2000,"publicationDate":"2021-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.enchem.2021.100056","citationCount":"37","resultStr":"{\"title\":\"Turning metal-organic frameworks into efficient single-atom catalysts via pyrolysis with a focus on oxygen reduction reaction catalysts\",\"authors\":\"Linyu Hu , Wenrui Li , Lu Wang , Bo Wang\",\"doi\":\"10.1016/j.enchem.2021.100056\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>Single-atom catalysts (SACs) have attracted extensive attention because of their maximal atom utilization, unique electronic structure and high activity. Metal-organic frameworks (MOFs) could be used as perfect self-sacrificed precursors/templates for preparing SACs due to their uniformly distributed and spatially separated metal nodes and organic linkers as well as designable pore structures. Recently, numerous studies have been devoted to utilizing MOFs to prepare SACs through pyrolysis. Herein, this review summarizes the most recent strategies of turning selected MOFs into SACs, focusing on oxygen reduction reaction (ORR) catalysts. First, the inherent metal sites in MOFs are directly turned into single-atom sites <em>via</em> the high-temperature treatment with/without acid etching. Second, additional metal precursors are introduced into MOFs by various methods to further supplement active sites in the obtained SACs. Third, nonmetal heteroatom-rich (<em>i.e.</em>, N, P and S) precursors are combined with MOFs to provide more coordination sites to anchor metal atoms. Finally, perspectives on future opportunities for selecting and designing MOFs as SAC precursors are also proposed.</p></div>\",\"PeriodicalId\":307,\"journal\":{\"name\":\"EnergyChem\",\"volume\":\"3 3\",\"pages\":\"Article 100056\"},\"PeriodicalIF\":22.2000,\"publicationDate\":\"2021-05-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1016/j.enchem.2021.100056\",\"citationCount\":\"37\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"EnergyChem\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S2589778021000063\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"EnergyChem","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2589778021000063","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
Turning metal-organic frameworks into efficient single-atom catalysts via pyrolysis with a focus on oxygen reduction reaction catalysts
Single-atom catalysts (SACs) have attracted extensive attention because of their maximal atom utilization, unique electronic structure and high activity. Metal-organic frameworks (MOFs) could be used as perfect self-sacrificed precursors/templates for preparing SACs due to their uniformly distributed and spatially separated metal nodes and organic linkers as well as designable pore structures. Recently, numerous studies have been devoted to utilizing MOFs to prepare SACs through pyrolysis. Herein, this review summarizes the most recent strategies of turning selected MOFs into SACs, focusing on oxygen reduction reaction (ORR) catalysts. First, the inherent metal sites in MOFs are directly turned into single-atom sites via the high-temperature treatment with/without acid etching. Second, additional metal precursors are introduced into MOFs by various methods to further supplement active sites in the obtained SACs. Third, nonmetal heteroatom-rich (i.e., N, P and S) precursors are combined with MOFs to provide more coordination sites to anchor metal atoms. Finally, perspectives on future opportunities for selecting and designing MOFs as SAC precursors are also proposed.
期刊介绍:
EnergyChem, a reputable journal, focuses on publishing high-quality research and review articles within the realm of chemistry, chemical engineering, and materials science with a specific emphasis on energy applications. The priority areas covered by the journal include:Solar energy,Energy harvesting devices,Fuel cells,Hydrogen energy,Bioenergy and biofuels,Batteries,Supercapacitors,Electrocatalysis and photocatalysis,Energy storage and energy conversion,Carbon capture and storage