Highly Dispersed Ruthenium-Based Multifunctional Electrocatalyst

被引:121
|
作者
Bai, Lu [1 ]
Duan, Zhiyao [2 ]
Wen, Xudong [1 ]
Si, Rui [3 ]
Zhang, Qiaoqiao [1 ]
Guan, Jingqi [1 ]
机构
[1] Jilin Univ, Coll Chem, Key Lab Surface & Interface Chem Jilin Prov, Changchun 130021, Jilin, Peoples R China
[2] Univ Texas Austin, Oden Inst Computat Engn & Sci, Austin, TX 78712 USA
[3] Chinese Acad Sci, Shanghai Inst Appl Phys, Shanghai 201204, Peoples R China
来源
ACS CATALYSIS | 2019年 / 9卷 / 11期
关键词
density functional theory; hydrogen evolution reaction; nitrogen-doped graphene; oxygen evolution reaction; oxygen reduction reaction; ruthenium; OXYGEN REDUCTION REACTION; WATER OXIDATION; HYDROGEN EVOLUTION; CATALYSTS; EFFICIENT; STABILITY; DESIGN; RU;
D O I
10.1021/acscatal.9b03514
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
A high-efficiency trifunctional electrocatalyst is required for practical applications of regenerative fuel cells, because the hydrogen evolution reaction (HER), oxygen reduction reaction (ORR), and oxygen evolution reaction (OER) are their core electrode reactions. However, implementation of both hydrogen and oxygen electrodes is hindered by low activity and poor stability of electrocatalysts for both water splitting and oxygen reduction. Herein, we report a high-temperature annealing strategy to fabricate a highly dispersed ruthenium-based catalyst embedded onto nitrogen-doped graphene (0.4-Ru@NG-750). The 0.4-Ru@NG-750 catalyst exhibits high trifunctional electrocatalytic activity and good stability in HER, ORR, and OER. The 0.4-Ru@NG-750 electrocatalyst exhibits a low overpotential of only 0.04 and 0.09 V at the current density of 10 mA.cm(-2) for HER in 1.0 M KOH and 0.5 M H2SO4, respectively, and 0.372 V for OER in 1.0 M KOH. Moreover, it shows a high half-wave potential of 0.826 and 0.723 V for ORR in 0.1 M KOH and 0.1 M HClO4, respectively. Structural characterizations show that RuN4Cx is one of the main structures in 0.4-Ru@NG-750. Density functional theory calculations indicate that the surface states of RuN4Cx sites evolve in different reaction conditions. In HER, ORR, and OER, the most stable states should be RuN4Cx, RuN4(OH)C-x, and RuN4(O)C-x, respectively, on which the theoretical overpotential is the lowest.
引用
收藏
页码:9897 / 9904
页数:15
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