{"title":"用于碳、氮、氧元素电化学转化的Fe-N-C单原子催化剂","authors":"Jian Huang , Qiao Zhang , Jie Ding , Yueming Zhai","doi":"10.1016/j.matre.2022.100141","DOIUrl":null,"url":null,"abstract":"<div><p>Single atom catalysts (SACs) are constituted by isolated active metal centers, which are heterogenized on inert supports such as graphene, porous carbon, and amorphous carbon. The thermal stability, electronic properties, and catalytic activities of the metal center can be controlled via manipulating the neighboring heteroatoms such as nitrogen, oxygen, and sulfur. Due to the atomical dispersion of the active catalytic centers, the amount of metal required for catalysis can be decreased. Furthermore, new possibilities are offered to easily control the selectivity of a given transformation process as well as to improve turnover frequencies and turnover numbers of target reactions. Among them, Fe–N–C single atom catalysts own special electronic structure, and have been widely used in many fields of electrocatalysis. This review aims to summarize the synthesis of Fe–N–C based on anchoring individual iron atoms on carbon/graphene. The spin-related properties of Fe–N–C catalysts are described, including the relation between spin and electron structure of Fe–N<sub><em>x</em></sub> as well as the coupling between electronic structure of Fe–N<sub><em>x</em></sub> and electronic (orbit) of CO<sub>2</sub>, N<sub>2</sub> and O<sub>2</sub>. Next, mechanistic investigations conducted to understand the specific behavior of Fe–N–C catalysts are highlighted, including C, N, O electro-reduction. Finally, some issues related to the future developments of Fe–N–C are put forward and corresponding feasible solutions are offered.</p></div>","PeriodicalId":61638,"journal":{"name":"材料导报:能源(英文)","volume":"2 3","pages":"Article 100141"},"PeriodicalIF":0.0000,"publicationDate":"2022-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2666935822000799/pdfft?md5=43580845397a61756e641330cbdea783&pid=1-s2.0-S2666935822000799-main.pdf","citationCount":"6","resultStr":"{\"title\":\"Fe–N–C single atom catalysts for the electrochemical conversion of carbon, nitrogen and oxygen elements\",\"authors\":\"Jian Huang , Qiao Zhang , Jie Ding , Yueming Zhai\",\"doi\":\"10.1016/j.matre.2022.100141\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>Single atom catalysts (SACs) are constituted by isolated active metal centers, which are heterogenized on inert supports such as graphene, porous carbon, and amorphous carbon. The thermal stability, electronic properties, and catalytic activities of the metal center can be controlled via manipulating the neighboring heteroatoms such as nitrogen, oxygen, and sulfur. Due to the atomical dispersion of the active catalytic centers, the amount of metal required for catalysis can be decreased. Furthermore, new possibilities are offered to easily control the selectivity of a given transformation process as well as to improve turnover frequencies and turnover numbers of target reactions. Among them, Fe–N–C single atom catalysts own special electronic structure, and have been widely used in many fields of electrocatalysis. This review aims to summarize the synthesis of Fe–N–C based on anchoring individual iron atoms on carbon/graphene. The spin-related properties of Fe–N–C catalysts are described, including the relation between spin and electron structure of Fe–N<sub><em>x</em></sub> as well as the coupling between electronic structure of Fe–N<sub><em>x</em></sub> and electronic (orbit) of CO<sub>2</sub>, N<sub>2</sub> and O<sub>2</sub>. Next, mechanistic investigations conducted to understand the specific behavior of Fe–N–C catalysts are highlighted, including C, N, O electro-reduction. Finally, some issues related to the future developments of Fe–N–C are put forward and corresponding feasible solutions are offered.</p></div>\",\"PeriodicalId\":61638,\"journal\":{\"name\":\"材料导报:能源(英文)\",\"volume\":\"2 3\",\"pages\":\"Article 100141\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2022-08-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.sciencedirect.com/science/article/pii/S2666935822000799/pdfft?md5=43580845397a61756e641330cbdea783&pid=1-s2.0-S2666935822000799-main.pdf\",\"citationCount\":\"6\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"材料导报:能源(英文)\",\"FirstCategoryId\":\"1087\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S2666935822000799\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"材料导报:能源(英文)","FirstCategoryId":"1087","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2666935822000799","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 6
摘要
单原子催化剂(SACs)是由孤立的活性金属中心构成的,它们在石墨烯、多孔碳和非晶碳等惰性载体上异质化。金属中心的热稳定性、电子性质和催化活性可以通过操纵邻近的杂原子如氮、氧和硫来控制。由于活性催化中心的原子分散,催化所需的金属量可以减少。此外,还提供了新的可能性,以方便地控制给定转化过程的选择性,以及提高目标反应的周转频率和周转数。其中Fe-N-C单原子催化剂具有特殊的电子结构,已广泛应用于电催化的诸多领域。本文综述了基于锚定单个铁原子在碳/石墨烯上的Fe-N-C的合成。描述了Fe-N-C催化剂的自旋相关性质,包括Fe-Nx的自旋与电子结构的关系,以及Fe-Nx的电子结构与CO2、N2和O2的电子(轨道)的耦合。接下来,重点介绍了Fe-N-C催化剂的机理研究,包括C, N, O电还原。最后,提出了Fe-N-C未来发展中存在的问题,并提出了相应的可行解决方案。
Fe–N–C single atom catalysts for the electrochemical conversion of carbon, nitrogen and oxygen elements
Single atom catalysts (SACs) are constituted by isolated active metal centers, which are heterogenized on inert supports such as graphene, porous carbon, and amorphous carbon. The thermal stability, electronic properties, and catalytic activities of the metal center can be controlled via manipulating the neighboring heteroatoms such as nitrogen, oxygen, and sulfur. Due to the atomical dispersion of the active catalytic centers, the amount of metal required for catalysis can be decreased. Furthermore, new possibilities are offered to easily control the selectivity of a given transformation process as well as to improve turnover frequencies and turnover numbers of target reactions. Among them, Fe–N–C single atom catalysts own special electronic structure, and have been widely used in many fields of electrocatalysis. This review aims to summarize the synthesis of Fe–N–C based on anchoring individual iron atoms on carbon/graphene. The spin-related properties of Fe–N–C catalysts are described, including the relation between spin and electron structure of Fe–Nx as well as the coupling between electronic structure of Fe–Nx and electronic (orbit) of CO2, N2 and O2. Next, mechanistic investigations conducted to understand the specific behavior of Fe–N–C catalysts are highlighted, including C, N, O electro-reduction. Finally, some issues related to the future developments of Fe–N–C are put forward and corresponding feasible solutions are offered.