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Fully Exposed Metal Clusters: Fabrication and Application in Alkane Dehydrogenation
Chen, Xiaowen1,2; Peng, Mi3; Xiao, Dequan4; Liu, Hongyang1,2; Ma, Ding3
通讯作者Liu, Hongyang(liuhy@imr.ac.cn) ; Ma, Ding(dma@pku.edu.cn)
2022-10-21
发表期刊ACS CATALYSIS
ISSN2155-5435
卷号12期号:20页码:12720-12743
摘要Alkanes are the foremost basic energy sources and represent an important basic chemical material for industrial applications. Highly efficient activation of C-H bonds can convert abundant alkanes into value-added products, such as alkenes and their corresponding polymers. Therefore, C-H bond activation of alkanes has attracted widespread attention in heterogeneous catalysis. Fully exposed cluster catalysts (FECCs), as a bridge linking metal single atoms (SAs) and nanoparticles (NPs), have been widely studied for many catalytic reactions, especially for alkane dehydrogenation. On FECCs, the highly exposed active sites with multiple metal atoms can promote adsorption of alkanes and intermediates, thus enabling facile C-H activation. Moreover, the electron-rich surface can facilitate the desorption of products to suppress overdehydrogenation and coke formation. Therefore, FECCs have exhibited remarkable catalytic performance in alkane dehydrogenation, compared with SAs and NPs. In this Review, we highlight the developments on FECCs, including the structure design and their unique catalytic performance in dehydrogenation of alkanes. The synthetic methods to fabricate FECCs are discussed for alkane dehydrogenation. Subsequently, recent progresses on understanding the relationship between catalytic performance and geometric/electronic structure of FECCs are summarized, to provide the insights into the nature of structure dependence and metal dependence in alkane dehydrogenation. The strategies to stabilize FECCs for alkane dehydrogenation, including support confining and bimetallic system construction, are systematically reviewed to provide a useful guidance for the catalyst design. Lastly, major prospects in FECCs are illustrated from the viewpoint of alkane dehydrogenation.
关键词metal clusters alkane dehydrogenation structure-dependence metal-dependence heterogeneous catalysis
资助者National Key R&D Program of China ; National Natural Science Foundation of China ; Liaoning Revitalization Talents Program ; Dalian National Lab for Clean Energy (DNL Cooperation Fund) ; China Petroleum& Chemical Corporation
DOI10.1021/acscatal.2c04008
收录类别SCI
语种英语
资助项目National Key R&D Program of China[2021YFA1502802] ; National Natural Science Foundation of China[92145301] ; National Natural Science Foundation of China[U21B2092] ; National Natural Science Foundation of China[21961160722] ; National Natural Science Foundation of China[91845201] ; National Natural Science Foundation of China[22072162] ; Liaoning Revitalization Talents Program[XLYC1907055] ; Dalian National Lab for Clean Energy (DNL Cooperation Fund)[202001] ; China Petroleum& Chemical Corporation[420043-2]
WOS研究方向Chemistry
WOS类目Chemistry, Physical
WOS记录号WOS:000877019600001
出版者AMER CHEMICAL SOC
引用统计
被引频次:66[WOS]   [WOS记录]     [WOS相关记录]
文献类型期刊论文
条目标识符http://ir.imr.ac.cn/handle/321006/176523
专题中国科学院金属研究所
通讯作者Liu, Hongyang; Ma, Ding
作者单位1.Univ Sci & Technol China, Sch Mat Sci & Engn, Shenyang 110016, Peoples R China
2.Chinese Acad Sci, Inst Met Res, Shenyang Natl Lab Mat Sci, Shenyang 110016, Peoples R China
3.Peking Univ, Coll Chem & Mol Engn, Beijing Natl Lab Mol Sci, Beijing 100871, Peoples R China
4.Univ New Haven, Ctr Integrat Mat Discovery, Dept Chem & Chem & Biomed Engn, West Haven, CT 06516 USA
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GB/T 7714
Chen, Xiaowen,Peng, Mi,Xiao, Dequan,et al. Fully Exposed Metal Clusters: Fabrication and Application in Alkane Dehydrogenation[J]. ACS CATALYSIS,2022,12(20):12720-12743.
APA Chen, Xiaowen,Peng, Mi,Xiao, Dequan,Liu, Hongyang,&Ma, Ding.(2022).Fully Exposed Metal Clusters: Fabrication and Application in Alkane Dehydrogenation.ACS CATALYSIS,12(20),12720-12743.
MLA Chen, Xiaowen,et al."Fully Exposed Metal Clusters: Fabrication and Application in Alkane Dehydrogenation".ACS CATALYSIS 12.20(2022):12720-12743.
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