A review on research progress of double perovskite oxides for oxygen evolution reaction electrocatalysts and supercapacitors†

Liangdong Chen, Jie Ding and Xinhua Zhu
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Abstract

In the past decade, the rapidly increasing global demand for energy and extensive concerns about the greenhouse effect and environmental problems from fossil fuels have stimulated intensive research interest in developing sustainable and clean energies and new electrochemical energy storage systems. Practical utilization of clean energies requires energy conversion involving different processes such as electricity-driven water splitting facilitating the storage of electrical energy in the form of hydrogen gas, and energy storage devices such as fuel cells and supercapacitors. A key issue to realize a high-efficiency conversion process is to find stable, low-cost and environment-friendly functional materials. Due to their extreme structural and compositional flexibilities, double perovskite (DP) oxides have gained much attention in the fields of electrocatalysis and supercapacitors. Recently, high-level theoretical studies have led to significant progress in the atomic-scale understanding of the catalytic mechanism of the DP oxide-driven oxygen evolution reaction (OER) and the electrochemical energy storage mechanism in DP oxide-based supercapacitors. In parallel, numerous experimental studies have been carried out to explore novel catalytic materials with advanced properties and kinetics, and more promising pseudocapacitive DP oxides have been developed. This review first introduces the structural and compositional flexibilities of DP perovskite oxides, and their prepared methods are described. Several strategies (e.g., nanostructure designs, elemental doping, tuning morphologies, crystallinity and surface defect engineering for improving oxygen vacancies) for modulating their electrochemical performance are also described. The recent progress of their applications in the electrochemical OER and supercapacitors is summarized. Finally, we conclude this review by giving some challenges and future perspectives of DP oxides in renewable energy conversion and energy storage devices.

Abstract Image

双钙钛矿氧化物在析氧反应电催化剂和超级电容器中的研究进展
在过去的十年中,全球能源需求的快速增长以及对化石燃料温室效应和环境问题的广泛关注,激发了人们对开发可持续清洁能源和新型电化学储能系统的强烈研究兴趣。清洁能源的实际利用需要涉及不同过程的能量转换,如电力驱动的水分解,便于以氢气形式储存电能,以及燃料电池和超级电容器等储能装置。寻找稳定、低成本、环保的功能材料是实现高效转化过程的关键问题。双钙钛矿(DP)氧化物由于其具有极强的结构和组成灵活性,在电催化和超级电容器领域受到了广泛的关注。近年来,高水平的理论研究使得对DP氧化物驱动的析氧反应(OER)的催化机理和基于DP氧化物的超级电容器的电化学储能机理的原子尺度理解取得了重大进展。与此同时,许多实验研究也在探索具有先进性能和动力学的新型催化材料,并开发了更多有前途的假电容性DP氧化物。本文首先介绍了DP钙钛矿氧化物的结构和组成的灵活性,并介绍了它们的制备方法。几种策略(例如,纳米结构设计,元素掺杂,调整形态,结晶度和表面缺陷工程,以改善氧空位)调节其电化学性能也被描述。综述了近年来它们在电化学OER和超级电容器中的应用进展。最后,我们总结了DP氧化物在可再生能源转换和储能设备中的一些挑战和未来的展望。
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