Porous N-C catalyst synthesized by pyrolyzing g-C3N4 embedded in carbon as highly efficient oxygen reduction electrocatalysts for primary Zn-air battery

被引:62
|
作者
Zhang, Li [1 ]
Xiong, Jing [2 ]
Qin, Yuan-Hang [1 ]
Wang, Cun-Wen [2 ]
机构
[1] Wuhan Inst Technol, Sch Chem Engn & Pharm, Minist Educ, Key Lab Green Chem Proc, Wuhan 430205, Hubei, Peoples R China
[2] Wuhan Inst Technol, Sch Chem Engn & Pharm, Key Lab Novel Reactor & Green Chem Technol Hubei, Wuhan 430205, Hubei, Peoples R China
基金
中国国家自然科学基金;
关键词
DOPED-CARBON; ACTIVE-SITES; BIFUNCTIONAL ELECTROCATALYSTS; FE; NANOSHEETS; IRON; METALS; COBALT;
D O I
10.1016/j.carbon.2019.05.044
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
Nitrogen-doped carbon (N-C) materials are promising low-cost catalysts for oxygen reduction reaction (ORR). However, the commonly used route for N-C synthesis, viz., the high-temperature pyrolysis of Nand C-containing precursors, usually results in a great loss of N-containing species determining the ORR catalytic performance. Herein, porous N-C materials are synthesized by using g-C3N4 embedded in glucose-derived carbon as template and N source. The N-C sample synthesized at 900 degrees C with a mass ratio of glucose to g-C3N4 being 4:1 exhibits a positive half-wave potential (E-1/2 = 0.823 V), good long-term stability and dominant 4 e pathway for ORR in alkaline media, which can be attributed to its large specific surface area, high porosity, and large fraction of pyridinic and graphitic N. When a small amount of Fe is doped into the N-C sample, its ORR performance can be greatly improved and outperforms the commercial Pt/C catalyst in terms of ORR activity (E-1/2 = 0.880 V), long-term stability and methanol tolerance. Notably, primary Zn-air batteries with N-C and Fe-N-C being the cathode catalysts exhibit peak power densities of 88 and 100 mW cm(-2), respectively. This work offers a promising route for the synthesis of porous carbon-based materials highly efficient as ORR catalyst for Zn-air battery. (C) 2019 Elsevier Ltd. All rights reserved.
引用
收藏
页码:475 / 484
页数:10
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