Design strategies of phosphorus-containing catalysts for photocatalytic, photoelectrochemical and electrocatalytic water splitting
Photocatalytic, photoelectrochemical and electrocatalytic water splitting provide advanced approaches to produce green hydrogen as a sustainable and renewable energy carrier. The development of highly efficient catalysts is the key to achieving cost-effective and large-scale production of hydrogen....
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Published in | Green chemistry : an international journal and green chemistry resource : GC Vol. 24; no. 2; pp. 713 - 747 |
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Main Authors | , , |
Format | Journal Article |
Language | English |
Published |
Cambridge
Royal Society of Chemistry
24.01.2022
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Subjects | |
Online Access | Get full text |
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Summary: | Photocatalytic, photoelectrochemical and electrocatalytic water splitting provide advanced approaches to produce green hydrogen as a sustainable and renewable energy carrier. The development of highly efficient catalysts is the key to achieving cost-effective and large-scale production of hydrogen. Recently, P-containing catalysts have gained a great deal of attention owing to their diverse chemical valence states, tunable structure and unique physicochemical properties. In this review, an overview of up-to-date progress in water splitting of P-containing photo- and electro-catalysts including elemental P, transition metal phosphides, metal phosphates/phosphonates and metal phosphorus trichalcogenides is provided. A general introduction to the water splitting mechanism and the activity origin of P-containing catalysts is briefly presented to provide rational guidance for the design of highly efficient catalysts. Notably, innovational strategies to design P-containing catalysts with enhanced catalytic activity are summarized with respect to modifying the phase, introducing foreign elements, tailoring morphology and engineering interfaces. In each section, we aim to deeply clarify the theory-structure-property relationship and provide underlying reasons behind enhanced catalytic performance. Finally, some challenges and research orientations of P-containing catalysts toward water splitting are briefly proposed from the perspectives of practical application and mechanism investigation.
The innovational strategies to design P-containing catalysts with enhanced photo-/electro-catalytic water splitting activity are reviewed with respect to phase modifying, foreign elements introducing, morphology tailoring and interface engineering. |
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Bibliography: | Jin-Tao Ren received his Ph.D. degree from Nankai University in 2020 under the supervision of Prof. Zhong-Yong Yuan. He is currently a postdoctoral fellow at Nankai University. His research interests focus on advanced nanomaterials for applications in electrocatalysis, metal-air batteries, fuel cells and as editorial board member of several journals. His research interests are mainly focused on the self-assembly of hierarchically nanoporous and nanostructured materials for energy and environmental applications. etc Lei Chen received her BEng degree from Northeast Forestry University in 2017 and obtained her MEng degree from Nankai University in 2020. She is currently a PhD candidate under the supervision of Prof. Zhong-Yong Yuan at Nankai University. Her current research focuses on the fabrication of nanostructured materials for energy-related applications. RSC Advances . Zhong-Yong Yuan received his PhD degree from Nankai University in 1999. After his postdoctoral research at the Institute of Physics, Chinese Academy of Sciences, he joined the Laboratory of Inorganic Materials Chemistry at the University of Namur, Belgium in 2001. In 2005, he was appointed Professor in Nankai University. In 2006, he was awarded the "Program for New Century Excellent Talents in University" by the Ministry of Education. In 2016, he was elected as a fellow of the Royal Society of Chemistry. He is currently serving as an Associate Editor of ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 content type line 23 |
ISSN: | 1463-9262 1463-9270 1463-9270 |
DOI: | 10.1039/d1gc03768d |