Recent Advances in Nickel-Based Perovskite Oxides for the Electrocatalytic Oxygen Evolution Reaction in Alkaline Electrolytes

被引:0
|
作者
Falqueto, Juliana Bruneli [1 ]
Hales, Natasha [1 ]
Schimidt, Thomas J. [1 ,2 ]
Fabbri, Emiliana [1 ]
机构
[1] Paul Scherrer Inst, Ctr Energy & Environm Sci, CH-5232 Villigen, Switzerland
[2] Swiss Fed Inst Technol, Inst Mol Phys Sci, CH-8093 Zurich, Switzerland
来源
ACS MATERIALS LETTERS | 2024年 / 6卷 / 12期
基金
瑞士国家科学基金会;
关键词
CATALYSTS; REDUCTION; STABILITY; OXIDATION; BANIO3;
D O I
10.1021/acsmaterialslett.4c01471
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Perovskites ABO3 are very versatile catalysts that can change their structure in several ways to enhance their electrocatalytic properties. Among nickel-based perovskites, those containing lanthanum or alkaline earth elements at the A-site display notable potential for the oxygen evolution reaction (OER) in alkaline electrolytes. Properties of nickel-based perovskites include the formation of mixed nickel oxidation states and the remarkable ability to accommodate numerous oxygen vacancies within their lattice. Oxygen vacancy content is an effective method to boost the electrocatalytic performance, and nickelate perovskites include a fascinating family of materials that exhibit oriented lattice oxygen vacancies: the infinite layer nickelates. However, nickelate perovskites remain a relatively underexplored area of research, likely due to the challenges associate with their synthesis. A major challenge lies in understanding the dynamic self-reconstruction of nickel-based perovskites under OER conditions. Monitoring this self-reconstruction through operando characterization is essential for precisely unraveling the causes of catalyst transformation and understanding the OER mechanisms. Leveraging these findings enables the design of more effective catalysts. In this Perspective, we aim to provide a summary of recent advances, insights, and suggestions for the development of nickel-based perovskites for electrocatalytic OER in alkaline electrolytes.
引用
收藏
页码:5227 / 5241
页数:15
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