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A covalent organic framework-based route to the in situ encapsulation of metal nanoparticles in N-rich hollow carbon spheres
被引:92
|作者:
Chen, Liyu
[1
]
Zhang, Lei
[1
]
Chen, Zhijie
[1
]
Liu, Hongli
[1
]
Luque, Rafael
[2
]
Li, Yingwei
[1
]
机构:
[1] South China Univ Technol, Key Lab Fuel Cell Technol Guangdong Prov, Sch Chem & Chem Engn, Guangzhou 510640, Peoples R China
[2] Univ Cordoba, Dept Quim Organ, Edif Marie Curie,Ctra Nnal 4-A,Km 396, E-14014 Cordoba, Spain
基金:
国家教育部博士点专项基金资助;
关键词:
OXYGEN REDUCTION REACTION;
LITHIUM-ION BATTERIES;
SUPPORTED GOLD CATALYSTS;
GRAPHENE-BASED MATERIALS;
PD NANOPARTICLES;
POROUS CARBON;
GENERAL FORMATION;
ANODE MATERIALS;
NITRO-COMPOUNDS;
BENZYL ALCOHOL;
D O I:
10.1039/c6sc01659f
中图分类号:
O6 [化学];
学科分类号:
0703 ;
摘要:
Metal nanoparticles (NPs) encapsulated in hollow nanostructures hold great promise for a variety of applications. Herein, we demonstrate a new concept where covalent organic frameworks (COFs) doped with metal cations can be readily used as novel precursors for the in situ encapsulation of metal NPs into N doped hollow carbon spheres (NHCS) through a controlled carbonization process. The obtained Pd@NHCS composites show a significantly enhanced catalytic activity and selectivity in the hydrogenation of nitrobenzene in ethanol and oxidation of cinnamyl alcohol compared with that of the conventional Pd/N-C and commercial Pd/C catalysts. The excellent catalytic performance should be related to the synergism of the porous hollow spheric structure, highly dispersed Pd NPs, and uniform distribution of N dopants on the materials. We believe that this newly developed methodology could be extended to the synthesis of other metal NPs@NHCS composites for a variety of advanced applications.
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页码:6015 / 6020
页数:6
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