Design and Optimization of Nanoporous Materials as Catalysts for Oxygen Evolution Reaction-A Review

With the growing demand for new energy sources, electrochemical water splitting for hydrogen production is a technology that must be vigorously promoted. Therefore, to improve the efficiency of the oxygen evolution reaction (OER) at the anode, high-performance OER catalysts are essential. Given thei...

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Published inMolecules (Basel, Switzerland) Vol. 29; no. 19; p. 4562
Main Authors Cao, Zhen, Zhang, Wenbin, Zhou, Tingting, Yan, Wenhui, Wang, Kaili
Format Journal Article
LanguageEnglish
Published Switzerland MDPI AG 25.09.2024
MDPI
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Summary:With the growing demand for new energy sources, electrochemical water splitting for hydrogen production is a technology that must be vigorously promoted. Therefore, to improve the efficiency of the oxygen evolution reaction (OER) at the anode, high-performance OER catalysts are essential. Given their advantages in electrocatalysis, nanoporous materials have garnered considerable attention in previous studies for OER applications. This review provides a comprehensive overview of various strategies to optimize active site utilization in nanoporous materials. These strategies include regulating pore size and porosity, constructing hierarchical nanoporous structures, and enhancing material conductivity. Additionally, it covers approaches to boost the intrinsic OER activity of nanoporous materials, such as tuning the composition of anions and cations, creating vacancies, constructing interfaces, and forming boundary active sites. While nanoporous materials offer significant potential for advancing OER, challenges remain, including difficulties in quantifying activity within nanopores, the unclear impact of nanoporous material morphology, challenges in accessing nanopore interiors with in situ techniques, and a lack of theoretical calculations on pore structure. However, these challenges also present opportunities, and we hope this review provides a fresh perspective to inspire future research.
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ISSN:1420-3049
1420-3049
DOI:10.3390/molecules29194562