A comparative study of undoped, boron-doped, and boron/fluorine dual-doped carbon nanoparticles obtained via solution plasma as catalysts for the oxygen reduction reaction

被引:26
作者
Chokradjaroen, Chayanaphat [1 ]
Kato, Shuhei [2 ]
Fujiwara, Kensuke [2 ]
Watanabe, Hiroko [2 ]
Ishii, Takahiro [2 ]
Ishizaki, Takahiro [2 ,3 ]
机构
[1] Shibaura Inst Technol, SIT Res Labs, Tokyo 1358548, Japan
[2] Shibaura Inst Technol, Grad Sch Engn & Sci, Mat Sci & Engn, Tokyo 1358548, Japan
[3] Shibaura Inst Technol, Coll Engn, Dept Mat Sci & Engn, Tokyo 1358548, Japan
基金
日本科学技术振兴机构; 日本学术振兴会;
关键词
METAL-FREE ELECTROCATALYSTS; MESOPOROUS GRAPHENE; TUNGSTEN CARBIDE; NITROGEN; NANOTUBES; SULFUR;
D O I
10.1039/d0se00708k
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
Boron/fluorine dual-doped carbons, which have never been reported for their oxygen reduction reaction (ORR) activity, were successfully synthesized through a one-step solution plasma (SP) process using mixtures of toluene, as a carbon source, and heterocyclic compounds containing boron and fluorine atoms,i.e., 2,4,6-tris(4-fluorophenyl)boroxin, 2,4,6-tris(3,4-difluorophenyl)boroxin and 2,4,6-tris(3,4,5-trifluorophenyl) boroxin. Therefore, in this study, the obtained undoped, boron-doped, and boron/fluorine dual-doped carbons, synthesized using SP, were investigated and compared to find their catalytic activity toward the ORR. The FE-SEM observation showed that the obtained carbons had a diameter in the nanoscale range. XRD and Raman measurements revealed that the synthesisviaSP led to the generation of turbostratic carbons with structural defect sites. The carbon atoms were found to mainly interact with fluorine atoms through semi-ionic C-F bonding. All SP-synthesized carbon nanoparticles showed acceptable ORR activity in alkaline solution. However, boron/fluorine dual-doped carbon nanoparticles also drove the ORR through a two-electron pathway with low generation of the unstable peroxide, HO2-, compared to undoped and boron-doped carbon nanoparticles.
引用
收藏
页码:4570 / 4580
页数:11
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