Simple synthesis of nitrogen-doped carbon spheres as a highly efficient metal-free electrocatalyst for the oxygen reduction reaction

被引:16
作者
Tong, Jinhui [1 ]
Li, Wenyan [1 ]
Bo, Lili [2 ]
Wang, Wenhui [1 ]
Li, Yuliang [1 ]
Li, Tao [1 ]
Zhang, Qi [1 ]
Fan, Haiyan [3 ]
机构
[1] Northwest Normal Univ, Coll Chem & Chem Engn, Key Lab Ecoenvironm Related Polymer Mat, Minist Educ,Key Lab Polymer Mat Gansu Prov, Lanzhou 730070, Gansu, Peoples R China
[2] Gansu Agr Univ, Coll Sci, Lanzhou 730070, Gansu, Peoples R China
[3] Nazarbayev Univ, Sch Sci & Technol, Dept Chem, Astana 010000, Kazakhstan
基金
中国国家自然科学基金;
关键词
Nitrogen doping; Carbon spheres; Metal-free catalyst; Oxygen reduction reaction; CONTAINING MESOPOROUS CARBON; POROUS CARBON; FORMALDEHYDE RESIN; GRAPHENE; POLYMER; NANOSPHERES; PERFORMANCE; CATALYSTS; NANOPARTICLES; NANOTUBES;
D O I
10.1016/S1872-2067(18)63078-5
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
In the present work, nitrogen-doped carbon spheres were synthesized through a simple hydro thermal treatment using glucose and melamine as inexpensive carbon and nitrogen sources, respectively. The ratio of melamine to glucose and annealing temperature were optimized. The final optimal sample exhibited a catalytic activity for the oxygen reduction reaction (ORR) that was superior than that of commercial 20%Pt/C in 0.1 mol/L KOH. It revealed an onset potential of -22.6 mV and a half-wave potential of -133.6 mV (vs. Ag/AgCl), which are 7.2 and 5.9 mV more positive than those of the 20%Pt/C catalyst, respectively, as well as a limiting current density of 4.6 mA/cm(2), which is 0.2 mA/cm(2) higher than that of the 20%Pt/C catalyst. The catalyst also exhibited higher stability and superior durability against methanol than 20%Pt/C. Moreover, ORRs on this catalyst proceed through a more effective 4e(-) path. The above mentioned superiority of the as-prepared catalyst makes it promising for fuel cells. (C) 2018, Dalian Institute of Chemical Physics, Chinese Academy of Sciences. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:1138 / 1145
页数:8
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