Strontium-doped lanthanum iron nickelate oxide as highly efficient electrocatalysts for oxygen evolution reaction

被引:25
|
作者
Li, Mengran [1 ]
Insani, Abi Rafdi [1 ]
Zhuang, Linzhou [1 ]
Wang, Zhanke [1 ]
Rehman, Ateeq Ur [1 ]
Liu, Lian X. [2 ]
Zhu, Zhonghua [1 ]
机构
[1] Univ Queensland, Sch Chem Engn, St Lucia, Qld 4067, Australia
[2] Univ Surrey, Sch Chem & Proc Engn, Senate House, Guildford GU2 7XH, Surrey, England
基金
澳大利亚研究理事会;
关键词
Oxygen evolution reaction; Perovskite; Electrocatalysis; Heterogeneous catalyst; PEROVSKITE OXIDE; CATALYTIC-ACTIVITY; OXIDATION; STORAGE; DESIGN;
D O I
10.1016/j.jcis.2019.06.054
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
Pursuing efficient and low-cost catalysts for the sluggish oxygen evolution reaction (OER) is imperative for the large-scale deployment of promising electrochemical technologies such as water splitting and CO2 electrochemical reduction. The earth-abundant perovskite catalysts based on LaNiO3-delta show promise in OER catalysis because of their relatively low cost and their optimal electronic structure but suffer from low electrode-area normalized activity. In this work, we partially substituted La with Sr and Ni with Fe to enable a remarkably high OER activity with an ultra-low overpotential of 374 +/- 3 mV vs RHE at a current density of 10 mA cm(-2) normalized by electrode geometric area. This performance even surpasses the performance of benchmark RuO2. Our results show that Sr could promote OER-active sites including Ni (III), O-2(2-)/O-, and optimal Ni/Fe ratios, which significantly improve the surface intrinsic activity at the perovskite surface. Therefore, this work not only developed a highly efficient earth-abundant catalyst towards OER, but also demonstrated the effective modulation of catalyst surface interactions through A-site doping for perovskite oxides for key applications such as water splitting, CO2 electrochemical reduction and N-2 electrochemical fixations. (C) 2019 Elsevier Inc. All rights reserved.
引用
收藏
页码:813 / 819
页数:7
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