Fluorine and sulfur atoms induced N-doped 3D porous carbon catalyzing oxygen reduction in the zinc-air battery

被引:2
作者
Li, Mengwei [2 ]
Li, Gai [3 ]
Ye, Qilong [2 ]
Deng, Yijie [2 ]
Chi, Bin [4 ]
Hua, Yingjie [3 ]
Tian, Xinlong [1 ]
Rao, Peng [1 ]
机构
[1] Hainan Univ, Sch Marine Sci & Engn, State Key Lab Marine Resource Utilizat South China, Haikou 570228, Peoples R China
[2] Univ South China, Sch Resource Environm & Safety Engn, Hengyang 421001, Peoples R China
[3] Hainan Normal Univ, Sch Chem & Chem Engn, Haikou 571158, Peoples R China
[4] Beijing Inst Technol, Shenzhen Automot Res Inst, Shenzhen 518118, Guangdong, Peoples R China
基金
海南省自然科学基金;
关键词
Carbon catalyst; Heteroatom; Oxygen reduction reaction; Zinc-air battery; ELECTROCATALYST; CATALYSTS; NITROGEN; NANOCAGES; ORR; FE;
D O I
10.1016/j.ijhydene.2024.08.165
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
Introducing other heteroatom is considered to be a highly effective approach to improve the limited catalytic activity from single nitrogen element doping in nitrogen-doped porous carbon materials. In this work, F and Smodified nitrogen-doped porous carbon (F-S-N-C) is prepared by annealing the assembly material of poly3-fluoro aniline, hydroxyethyl sulfonic acid and g-C3N4, in which the g-C3N4 is employed as template agent and poreforming agent. A series of characterization techniques indicate that simultaneous doping of F and the S atoms enhance the electron transfer and construct more defects for N-doped 3D porous carbon, resulting in improved electrocatalytic performance. The prepared F and S-cooperated nitrogen-doped porous carbon (F-S-N-C) exhibits significantly improved oxygen reduction reaction electrocatalytic activity in alkaline media with a half-wave potential of 0.808 V. The zinc-air battery (ZAB) with F-S-N-C as the air cathode catalyst demonstrates a peak power density of 167 mW cm- 2, which is higher than that of commercial Pt/C (158 mW cm- 2). Moreover, the specific capacity of the F-S-N-C-based ZAB reaches to 817 mAh & sdot;g- 1.
引用
收藏
页码:1107 / 1112
页数:6
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