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.
引用
收藏
页码:6015 / 6020
页数:6
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