期刊
ENERGYCHEM
卷 3, 期 3, 页码 -出版社
ELSEVIER
DOI: 10.1016/j.enchem.2021.100056
关键词
Metal-organic frameworks; Single-atom catalysts; Oxygen reduction reaction; Pyrolysis; Electrocatalysis
类别
资金
- National Natural Science Foundation of China [21901019, 21625102, 21971017]
- National Key Research and Development Program of China [2020YFB1506300]
- Beijing Institute of Technology Research Fund Program
This review summarizes the recent strategies of converting selected MOFs into SACs, with a focus on ORR catalysts. The strategies include direct transformation of metal sites in MOFs into single-atom sites, introduction of additional metal precursors to supplement active sites in SACs, and combination of nonmetal heteroatom-rich precursors with MOFs to provide more coordination sites for anchoring metal atoms.
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.
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