Probing the catalytic activity of porous graphene oxide and the origin of this behaviour

被引:559
作者
Su, Chenliang [1 ]
Acik, Muge [2 ]
Takai, Kazuyuki [3 ]
Lu, Jiong [1 ]
Hao, Si-Jia [3 ]
Zheng, Yi [1 ]
Wu, Pingping [1 ]
Bao, Qiaoliang [1 ]
Enoki, Toshiaki [3 ]
Chabal, Yves J. [2 ]
Loh, Kian Ping [1 ]
机构
[1] Natl Univ Singapore, Dept Chem, Graphene Res Ctr, Singapore 117543, Singapore
[2] Univ Texas Dallas, Dept Mat Sci & Engn, Richardson, TX 75080 USA
[3] Tokyo Inst Technol, Dept Chem, Meguro Ku, Tokyo 1528550, Japan
来源
NATURE COMMUNICATIONS | 2012年 / 3卷
基金
新加坡国家研究基金会;
关键词
GRAPHITE OXIDE; GREEN CHEMISTRY; SUSTAINABLE CHEMISTRY; REDUCTION; OXIDATION; CARBOCATALYST; EFFICIENT; CARBON; IMINES; AMINES;
D O I
10.1038/ncomms2315
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Graphene oxide, a two-dimensional aromatic scaffold decorated by oxygen-containing functional groups, possesses rich chemical properties and may present a green alternative to precious metal catalysts. Graphene oxide-based carbocatalysis has recently been demonstrated for aerobic oxidative reactions. However, its widespread application is hindered by the need for high catalyst loadings. Here we report a simple chemical treatment that can create and enlarge the defects in graphene oxide and impart on it enhanced catalytic activities for the oxidative coupling of amines to imines (up to 98% yield at 5 wt% catalyst loading, under solvent-free, open-air conditions). This study examines the origin of the enhanced catalytic activity, which can be linked to the synergistic effect of carboxylic acid groups and unpaired electrons at the edge defects. The discovery of a simple chemical processing step to synthesize highly active graphene oxide allows the premise of industrial-scale carbocatalysis to be explored.
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页数:9
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