期刊
ADVANCED FUNCTIONAL MATERIALS
卷 31, 期 41, 页码 -出版社
WILEY-V C H VERLAG GMBH
DOI: 10.1002/adfm.202103597
关键词
defect engineering; hydrogenation; metal-organic frameworks; single-atom catalysts
类别
资金
- NSFC [22035003, 21905142]
- Program of Introducing Talents of Discipline to Universities [B18030]
- Natural Science Fund of Tianjin [19JCZDJC37200, 19JCQNJC02600]
- China Postdoctoral Science Foundation [2019M651008]
A versatile synthetic strategy was demonstrated to generate transition metal single-atom catalysts (M SAs/NC, M = Co, Cu, Mn) through defect engineering of metal-organic frameworks. By deliberately introducing structural defects within the MOF framework, the interatomic distance between metal sites was increased, inhibiting metal aggregation and resulting in a 70% increase in single metal atom yield. The optimized Co SAs/NC-800 showed superior activity and reusability for the selective hydrogenation of nitroarenes, surpassing several state-of-art non-noble-metal catalysts.
Single-atom catalysts (SACs) have garnered enormous interest due to their remarkable catalysis activity. However, the exploitation of universal synthesis strategy and regulation of coordination environment of SACs remain a great challenge. Herein, a versatile synthetic strategy is demonstrated to generate a series of transition metal SACs (M SAs/NC, M = Co, Cu, Mn; NC represents the nitrogen-doped carbon) through defect engineering of metal-organic frameworks (MOFs). The interatomic distance between metal sites can be increased by deliberately introducing structural defects within the MOF framework, which inhibits metal aggregation and consequently results in an approximately 70% increase in single metal atom yield. Additionally, the coordination structures of metal sites can also be facilely tuned. The optimized Co SAs/NC-800 exhibits superior activity and excellent reusability for the selective hydrogenation of nitroarenes, surpassing several state-of-art non-noble-metal catalysts. This study provides a new avenue for the universal fabrication of transition metal SACs.
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