4.6 Article

Controllable synthesis of MOFs-derived porous and tubular bimetallic Fe-Ni phosphides for efficient electrocatalytic water splitting

Journal

CATALYSIS SCIENCE & TECHNOLOGY
Volume 13, Issue 5, Pages 1512-1517

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/d2cy02112a

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To enhance the electrocatalytic performance, efficient electrocatalysts should have suitable adsorption/desorption intensity for intermediates and good transportation capability of mass and electrons. This study proposes a MOF-derived route to prepare composition-tunable Fe-Ni bimetallic phosphides as efficient electrocatalysts for water splitting. The crystallinity, morphology, and composition of the electrocatalysts can be well controlled by adjusting the phosphating temperature. Overall water splitting was achieved with an overpotential of about 1.63 V@10 mA cm(-2), demonstrating the potential of these electrocatalysts.
To boost electrocatalytic performance, efficient electrocatalysts generally require an appropriate adsorption/desorption intensity for intermediates, and a favorable transportation capability of mass and electrons. For preparing electrocatalysts with excellent performance, the crystallinity, morphology and composition of the materials should be considered. Aiming to split water, here we proposed a MOF-derived route to prepare a series of composition-tunable Fe-Ni bimetallic phosphides as efficient electrocatalysts. By controlling the phosphating temperature, electrocatalysts with tubular or porous nanostructures can be selectively obtained, and crystallinity, morphology and composition of the electrocatalysts can be well tuned. The effects of synergistic modulation of the above parameters for electrocatalytic hydrogen evolution reaction (HER) and oxygen evolution reaction (OER) were deeply explored, and overall water splitting was achieved with an overpotential of about 1.63 V@10 mA cm(-2). This work not only provides a facile method to obtain composition- and morphology-tunable phosphide electrocatalysts for water splitting, but also sheds new light on designing efficient electrocatalysts from a systematic viewpoint.

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