Pt and Pt–Ni(OH)2 Electrodes for the Hydrogen Evolution Reaction in Alkaline Electrolytes and Their Nanoscaled Electrocatalysts
The design and synthesis of Pt‐based electrocatalysts for the hydrogen evolution reaction (HER) are of great importance for the successful development of hydrogen‐based alternative energy technologies. Although Pt is considered to be the most active catalyst for the HER, its reaction performance is...
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Published in | ChemSusChem Vol. 11; no. 16; pp. 2643 - 2653 |
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Main Authors | , |
Format | Journal Article |
Language | English |
Published |
Germany
Wiley Subscription Services, Inc
22.08.2018
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Subjects | |
Online Access | Get full text |
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Summary: | The design and synthesis of Pt‐based electrocatalysts for the hydrogen evolution reaction (HER) are of great importance for the successful development of hydrogen‐based alternative energy technologies. Although Pt is considered to be the most active catalyst for the HER, its reaction performance is limited in alkaline solutions owing to a slow rate for water dissociation. Therefore, many research groups have intensively investigated reaction mechanisms and developed system designs and efficient Pt‐based catalysts to enhance the alkaline HER. Herein, we summarize the catalytic surface specificity of Pt and Pt–Ni(OH)2 materials to control the kinetics of the alkaline HER. In particular, we increase our understanding of Ni(OH)2‐modified Pt surfaces and the corresponding nanoscaled Pt–Ni(OH)2 electrocatalysts to improve the sluggish water‐dissociation step, and this knowledge will guide us to future sustainable energy applications of advanced nanomaterials.
Alkaline hydrogen: The alkaline hydrogen evolution reaction (HER) at Pt surfaces proceeds through Volmer–Heyrovsky and Volmer–Tafel mechanisms. If the Pt surface is modified with Ni(OH)2 clusters, the Volmer–Tafel mechanism with a promoted rate‐determining Volmer step and subsequent H2 generation will dominate. Benefitting from bifunctionality, the nanoscaled Pt–Ni(OH)2‐based electrocatalyst shows highly improved HER performance in alkaline electrolytes. |
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Bibliography: | ObjectType-Article-2 SourceType-Scholarly Journals-1 ObjectType-Feature-3 content type line 23 ObjectType-Review-1 |
ISSN: | 1864-5631 1864-564X |
DOI: | 10.1002/cssc.201800781 |