Thiourea sole doping reagent approach for controllable N, S co-doping of pre-synthesized large-sized carbon nanospheres as electrocatalyst for oxygen reduction reaction

被引:57
作者
Chen, Jiangyao [1 ,2 ,3 ]
Zhang, Haimin [1 ,4 ]
Liu, Porun [1 ]
Li, Yibing [1 ]
Li, Guiying [2 ,3 ]
An, Taicheng [2 ,3 ]
Zhao, Huijun [1 ,4 ]
机构
[1] Griffith Univ, Ctr Clean Environm & Energy, Nathan, Qld 4222, Australia
[2] Chinese Acad Sci, Guangzhou Inst Geochem, State Key Lab Organ Geochem, Guangzhou 510640, Guangdong, Peoples R China
[3] Chinese Acad Sci, Guangzhou Inst Geochem, Guangdong Key Lab Environm Protect & Resources Ut, Guangzhou 510640, Guangdong, Peoples R China
[4] Chinese Acad Sci, Inst Solid State Phys, Ctr Environm & Energy Nanomat, Hefei 230031, Peoples R China
关键词
METAL-FREE ELECTROCATALYSTS; ORDERED MESOPOROUS CARBONS; DOPED GRAPHENE; RECENT PROGRESS; NITROGEN; SULFUR; CATALYSTS; OXIDE; NANOSHEETS; BORON;
D O I
10.1016/j.carbon.2015.04.090
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The co-doping of heteroatoms into the pre-synthesized graphitic carbons normally requires the use of different doping reagents as heteroatom sources, leading to difficulties in controlling the contents of doped heteroatoms and their chemical bonding forms with graphitic structures. Graphitic carbon-based electrocatalysts with a relatively large size, rich microporous structure and high surface area could possess better structural stability and enhanced conductivity than those of small-sized carbon nanostructures (e.g., nanodots). This study reported the use of a sole reagent (thiourea) as heteroatoms doping source to achieve controllable N, S co-doping of the pre-synthesized graphitic microporous carbon nanospheres (similar to 100 nm in diameter) via a facial thermolysis process to produce high performance oxygen reduction reaction electrocatalysts. Results showed that the contents of the doped N, S and their chemical bonds with graphitic carbon structures could be simply controlled by controlling the thermolysis temperatures. With the experimental conditions investigated, the best performed electrocatalyst was obtained from 1100 degrees C doping process that possessed the most suitable N, S doping contents with 100% of doped N being in electrocatalytically active pyridinic-N and graphitic-N forms. The approach reported in this work could be useful for controllable heteroatoms co-doping of other types of new generation graphitic carbon materials. (C) 2015 Elsevier Ltd. All rights reserved.
引用
收藏
页码:339 / 347
页数:9
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