Hydrogen Evolution by Ni2P Catalysts Derived from Phosphine MOFs
Source abstract
Abstract
Strategies to improve the catalytic efficiency of the hydrogen evolution reaction (HER), an integral electrochemical reaction in solar-to-hydrogen technologies, frequently include the use of porous precursors to make electrocatalysts. Researchers have used high-surface-area metal organic frameworks (MOFs) as precursors to synthesize active metal phosphide catalysts, but these MOFs must be mixed with a second phosphorus precursor to produce the metal phosphide. In this work, we synthesized nickel phosphide catalysts in one step from single-MOF precursors. Our MOFs contain phosphine coordination sites within the organic framework, allowing us to produce metal phosphide catalysts without the need for an exogenous phosphorus source. This strategy is convenient because the use of a crystalline precursor may offer the possibility of greater control over both the phase and resulting properties of the as-formed metal phosphide materials. The best MOF-derived Ni2P HER electrocatalyst delivered current densities of −10 mA/cm2 at an overpotential of 120 mV on glassy carbon substrate electrodes. A long-term test showed our sample could evolve hydrogen for over 1 h under physically and chemically harsh conditions.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Electrocatalysts for Energy Conversion · Advanced battery technologies research · Advanced Photocatalysis Techniques
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Chemistry, University of Texas at Austin, Austin, Texas 78712, United States
Texas Materials Institute, University of Texas at Austin, Austin, Texas 78712, United States
Department of Chemical Engineering, University of Texas at Austin, Austin, Texas 78712, United States
Funding
Welch Foundation · National Science Foundation
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