Superaerophobic/superhydrophilic surfaces as advanced electrocatalysts for the hydrogen evolution reaction: a comprehensive review
High-efficiency electrocatalysts are crucial for a fossil fuel-free future. Although many strategies have been proposed to boost the electrocatalysts' performance, efficient and cost-effective methods are rare. Recently, hydrogen (H 2 ) and oxygen (O 2 ) production via water electrolysis has se...
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Published in | Journal of materials chemistry. A, Materials for energy and sustainability Vol. 1; no. 1; pp. 5147 - 5173 |
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Main Authors | , , , |
Format | Journal Article |
Language | English |
Published |
Cambridge
Royal Society of Chemistry
08.03.2022
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Subjects | |
Online Access | Get full text |
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Summary: | High-efficiency electrocatalysts are crucial for a fossil fuel-free future. Although many strategies have been proposed to boost the electrocatalysts' performance, efficient and cost-effective methods are rare. Recently, hydrogen (H
2
) and oxygen (O
2
) production
via
water electrolysis has seen increased interest. To efficiently produce using electrochemical water splitting (EWS), there are many resistances in electrolysis systems that must be reduced. One of the major resistances in the system that dramatically reduces the system's efficiency is the adhesion of evolved gas bubbles to the surface of the electrode. Blocked active sites occur when bubbles adhere to the surface. As a result, a decrease in mass transfer ability can be expected, which can severely damage the gas production efficiency. One of the main techniques that is able to reduce bubble adhesion is to make electrocatalysts with superaerophobic and/or superhydrophilic surfaces. These surfaces can be created using different morphologies, such as nanosheets, nanotubes, and nanowires. In this review, in addition to getting acquainted with the mechanism of separation of bubbles from the surface and the application of superaerophobic/superhydrophilic surfaces as efficient electrocatalysts for the hydrogen evolution reaction and other electrochemical reactions, the latest research in this field will be reviewed.
In this review, the application of superaerophobic/superhydrophilic nanostructured surfaces as efficient and durable electrocatalysts for hydrogen production form electrochemical water splitting have been reviewed and discussed. |
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Bibliography: | Reza Andaveh is currently pursuing his M.S. degree in Prof. Sabour Rouhaghdam's group at Tarbiat Modares University, Tehran. Before that he completed his B.S. degree at Shahid Chamran University - Ahvaz in 2020. His research interests include electrochemical energy storage and conversion. Ghasem Barati Darband received his PhD degree in Materials Science and Engineering from Tarbiat Modares University in 2019. He is currently an assistant professor in the Materials and Metallurgical Engineering Department of Ferdowsi University of Mashhad, Iran. His research interests focus on electrochemistry and energy materials, especially the development of cost-effective, active and durable electrode materials for application in electrochemical energy conversion and storage systems. He has published over 45 papers in peer-reviewed international journals. Meysam Maleki graduated from Yazd University (Iran) with a B.S. in Materials Science and Engineering in 2019. He received his M.S. in Materials Science and Engineering at Tarbiat Modares University (Iran) in 2021. Currently, he works as a research assistant in Prof. Sabour Rouhaghdam's group at Tarbiat Modares University. His current research is focused on the design, fabrication and characterization of functional nanostructures for electrochemical energy conversion. Prof. Alireza Sabour Rouh Aghdam received his PhD degree in Materials Science and Engineering from RWTH Aachen in 1991. He is currently a full professor in the Department of Materials Engineering, Faculty of Engineering, Tarbiat Modares University, Iran. His current research interests focus on surface engineering, corrosion and protection of materials and energy materials. He has published more than 200 refereed journal papers. |
ISSN: | 2050-7488 2050-7496 |
DOI: | 10.1039/d1ta10519a |