A hierarchically ordered porous Fe, N, S tri-doped carbon electrocatalyst with densely accessible Fe-Nx active sites and uniform sulfur-doping for efficient oxygen reduction reaction

被引:21
作者
Han, Hao [1 ]
Wang, Xiaomei [1 ]
Zhang, Xu [1 ]
机构
[1] Hebei Univ Technol, Sch Chem Engn & Technol, Hebei key Lab Funct Polymers, Tianjin, Peoples R China
关键词
Oxygen reduction reaction; Sulfur; Single-atom Fe; Hierarchically ordered porous; Zn-air battery; MEMBRANE FUEL-CELLS; NITROGEN; CATALYSTS; NANOSHEETS; CATHODE; ORR;
D O I
10.1016/j.jcis.2022.02.030
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
Doping Fe-N-C catalysts with heteroatoms has been widely recognized as a most promising way to improve the electrocatalytic activity to achieve the replacement of Pt-based electrocatalysts for efficient oxygen reduction reaction (ORR). However, it is still a challenge to combine delicate control of the catalyst structure with heteroatom-doping to achieve optimal electrocatalytic efficiency. Herein, a strategy of combining chemical vapor deposition (CVD) with dual-template cooperative pyrolysis was rationally designed to synthesize the novel electrocatalyst with densely isolated single Fe atoms scattered on hierarchically ordered porous N and S codoped carbon (ISA-Fe/HOPNSC). The three-dimensional hierarchically ordered interconnected macro/mesoporous structure and uniform sulfur-doping make ISA-Fe/ HOPNSC exhibit superb ORR performance in both alkaline and acidic electrolytes with a positive halfwave potential (0.920 V in 0.1 M KOH and 0.795 Vin 0.5 M H2SO4) as well as outstanding methanol tolerance and long-time stability. As cathode catalyst in Zn-air battery, ISA-Fe/HOPNSC also provides much better maximum power density (210.7 mW cm(2)) and specific capacity (796.7 mAh g(Zn)(1)) than those of Pt/C (112.6 mW cm(-2) and 712.6 mAh g(Zn)(1)). Remarkably, the synthesis strategy in this work proposes myriad opportunities for combining delicate control of the catalyst structure with heteroatom doping to synthesize high-performance ORR catalysts. (C) 2022 Elsevier Inc. All rights reserved.
引用
收藏
页码:617 / 626
页数:10
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