Deflagration synthesis of nitrogen/ fluorine codoped hollow carbon nanoparticles with excellent oxygen reduction performance

被引:16
|
作者
Liu, Yousong [1 ]
Huang, Bing [1 ]
Peng, Shengjie [2 ,3 ,4 ]
Wang, Tao [2 ]
Ji, Guangbin [2 ]
Yang, Guangcheng [1 ]
Ramakrishna, Seeram [3 ]
机构
[1] China Acad Engn Phys, Inst Chem Mat, Mianyang 621900, Sichuan, Peoples R China
[2] Nanjing Univ Aeronaut & Astronaut, Coll Mat Sci & Technol, Nanjing 210016, Jiangsu, Peoples R China
[3] Natl Univ Singapore, Dept Mech Engn, Singapore 117574, Singapore
[4] Nankai Univ, Key Lab Adv Energy Mat Chem, Minist Educ, Tianjin 300071, Peoples R China
来源
INORGANIC CHEMISTRY FRONTIERS | 2018年 / 5卷 / 06期
基金
中国国家自然科学基金; 中国博士后科学基金;
关键词
METAL-FREE ELECTROCATALYSTS; N-DOPED GRAPHENE; POROUS CARBON; EFFICIENT ELECTROCATALYSTS; ORGANIC FRAMEWORK; FREE CATALYST; NANOSHEETS; NANOTUBES;
D O I
10.1039/c8qi00200b
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Critical factors such as doping content, electronic conductivity and porosity need to be addressed to obtain excellent oxygen reduction reaction (ORR) performance with metal-free carbon-based materials. However, creating a facile approach to obtain carbon materials with a high doping level, high graphitization degree and high surface area still remains a great challenge. In this work, we develop a NaN3/C5F5N deflagration method to synthesize high N/F co-doped carbon hollow nanospheres (N/F-HC) with a high graphitization degree. The deflagration of NaN3 can produce Na nanoclusters, which can not only capture partial F atoms from C5F5N but can also be used as templates for the formation of a hollow structure. The heat liberation from deflagration and the subsequent F-capturing reaction could generate an extremely high temperature for graphitic structure formation. Moreover, the ultra-fast deflagration and F-capturing reaction allow carbon growth to be completed in seconds, which can ensure a high N/F doping content. The optimized N/F-HC catalyst exhibits superior ORR performance with long-term stability compared to a commercial Pt/C electrocatalyst in an alkaline medium. The synthetic strategy described in this work is facile and is expected to underpin future research efforts to develop metal-free electrocatalysts for the ORR and other applications.
引用
收藏
页码:1307 / 1313
页数:7
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