Crystal facet and phase engineering for advanced water splitting
Water splitting is a promising approach to producing renewable hydrogen energy with zero carbon dioxide emission, and it has been intensively studied to improve conversion efficiencies over the past decades. As a result, crystal facet and phase engineering have been attracted as unique strategies fo...
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Published in | CrystEngComm Vol. 24; no. 33; pp. 5838 - 5864 |
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Main Authors | , , , |
Format | Journal Article |
Language | English |
Published |
Cambridge
Royal Society of Chemistry
22.08.2022
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Subjects | |
Online Access | Get full text |
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Summary: | Water splitting is a promising approach to producing renewable hydrogen energy with zero carbon dioxide emission, and it has been intensively studied to improve conversion efficiencies over the past decades. As a result, crystal facet and phase engineering have been attracted as unique strategies for designing (photo)electrocatalysts. However, there are few specialized review articles on facet and phase engineering for various water splitting systems so far. In this review, we start by concisely introducing the principle of three water splitting systems. The subsequent section explains notable tactics of crystal facet and phase engineering to modify the intrinsic properties of catalysts and construct the junction. Then, we discuss recent advances in facet and phase-engineered catalysts for water splitting. Finally, the last section outlines the challenges and invigorating perspectives for future research on crystal facets and phase-engineered catalysts for practical water splitting systems. We believe this review enables us to strengthen the basis of crystal facet and phase engineering to promote the development of water splitting cells.
This review covers the principles and recent advances in facet and phase engineering of catalysts for photocatalytic, photoelectrochemical, and electrochemical water splitting. It suggests the basis of catalyst design for advanced water splitting. |
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Bibliography: | Ho Won Jang is a full professor at the Department of Materials Science and Engineering in Seoul National University. He received his Ph.D. from the Department of Materials Science and Engineering at Pohang University of Science and Technology in 2004. He worked as a research associate at the University of Madison-Wisconsin from 2006 to 2009. Before he joined Seoul National University in 2012, he worked at the Korea Institute of Science and Technology (KIST) as a senior research scientist. His research interest includes materials synthesis and device fabrication for (photo)electrocatalysis, chemical sensors, memristors, micro-LEDs, and thin film transistors. 2 Jin Wook Yang is currently a Ph.D. candidate under the supervision of Prof. Ho Won Jang at the Department of Materials Science and Engineering of Seoul National University. He received his B.S. degree in Department of Materials Science and Engineering from Korea University in 2018. His research interest is focused on the design of nanostructured heterojunction photoelectrodes for overall solar water splitting. reduction, and carbon upgrading). Mi Gyoung Lee received her Ph.D. degree from the Department of Materials Science and Engineering, Seoul National University, South Korea, under the supervision of Prof. Ho Won Jang in 2019. She is currently working as a postdoc fellow at the University of Toronto, Canada, under the supervision of Prof. Sargent from 2020. Her research focuses on the development of electrocatalysts for diverse applications (water splitting, CO Hee Ryeong Kwon is currently a Ph.D. candidate under the supervision of Prof. Ho Won Jang at the Department of Materials Science and Engineering of Seoul National University. She received her B.S. degree in Department of Material Science and Engineering from Korea University in 2021. Her current research focuses on the design of transition-metal-based catalysts and photoelectrochemical water splitting. ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 |
ISSN: | 1466-8033 1466-8033 |
DOI: | 10.1039/d2ce00585a |