Aging effect on the structure formation of active sites in single-atomic catalysts and their electrochemical properties for oxygen reduction reaction

被引:6
|
作者
Lee, Seon Yeong [1 ]
Lee, Jong Yoon [1 ]
Jang, Han-Wool [1 ]
Son, U. Hyeok [1 ]
Lee, Sungho [2 ]
Joh, Han-Ik [1 ]
机构
[1] Konkuk Univ, Dept Energy Engn, 120 Neungdong Ro, Seoul 05029, South Korea
[2] Korea Inst Sci & Technol KIST, Carbon Composite Mat Res Ctr, 92 Chudong Ro, Wonju 55324, Jeonrabug Do, South Korea
关键词
Single-atom catalysts; Active sites; Iron dispersion; ORR electrocatalysts; Anion exchange membrane fuel cells; METAL-CATALYSTS; FE; FUEL; CARBON; ELECTROCATALYSTS; ALKALINE; IDENTIFICATION; TEMPERATURE; HYDROGEN; DENSITY;
D O I
10.1016/j.jiec.2022.10.031
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Fe-N-C catalysts have attracted attention because of their superior oxygen reduction reaction (ORR) performance in alkaline media. However, there is a conflict between the active sites of Fe-N-C catalysts, namely single-atomic Fe-Nx sites and dual active sites consisting of atomic sites/iron carbide nanoparti-cles. Herein, we synthesized catalysts with different types of active sites by controlling the facile aging process. The main active sites varied from single active sites to dual active sites when the aging time and Fe content was decreased and increased. A catalyst with 0.6 wt% Fe that is aged for 24 h (FeNC-24-0.6) has dual active sites, whereas a catalyst with 0.9 wt% Fe that is aged for 48 h (FeNC-48-0.9) consists mainly of single active sites. The catalysts showed outstanding ORR activity, exceeding the half-wave potential of the commercial 20 wt% Pt/C catalysts by 11 mV. Interestingly, the FeNC-48-0.9 catalyst exhibited a rare negative shift compared to the FeNC-24-0.6 catalyst in the durability tests. Therefore, it is believed that increasing the number of single-atomic Fe-Nx sites is an effective approach to enhance the ORR performance of Fe-N-C catalyst in alkaline media.(c) 2022 The Korean Society of Industrial and Engineering Chemistry. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:434 / 441
页数:8
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