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Transition metal-doped nickel phosphide nanoparticles as electro- and photocatalysts for hydrogen generation reactions

[Display omitted] •Transition metal-doped nickel phosphides prepared by wet-chemical method.•Fe, Co, Ni and Mo atomic substitute Ni in phosphide lattice as a single phase.•Electro- and photocatalysts for hydrogen evolution reactions.•Tunable activities dependent on electron filling. Transition metal...

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Published in:Applied catalysis. B, Environmental Environmental, 2019-03, Vol.242, p.186-193
Main Authors: Man, Ho-Wing, Tsang, Chui-Shan, Li, Molly Meng-Jung, Mo, Jiaying, Huang, Bolong, Lee, Lawrence Yoon Suk, Leung, Yun-chung, Wong, Kwok-Yin, Tsang, Shik Chi Edman
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Language:English
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Summary:[Display omitted] •Transition metal-doped nickel phosphides prepared by wet-chemical method.•Fe, Co, Ni and Mo atomic substitute Ni in phosphide lattice as a single phase.•Electro- and photocatalysts for hydrogen evolution reactions.•Tunable activities dependent on electron filling. Transition metal-doped nickel phosphide nanoparticles with metallic properties are prepared by a simple and facile wet-chemical method. It is shown for the first time that these transition metals: iron, cobalt, manganese, and molybdenum, can atomically substitute nickel in the parent hcp phosphide lattice as a single phase without significant change in its metallic structure and morphology. They are employed as electro- and photocatalysts for hydrogen evolution reaction, which show highly tunable activities dependent on electron filling of their metallic bands and H coverage according to our experimental and theoretical rationalizations. Molybdenum-doped nickel phosphide nanoparticle with lower H coverage exhibits the best hydrogen evolution performance in electrocatalytic hydrogen evolution reaction, which also shows excellent photocatalytic hydrogen production with organic photosensitizer. In addition, cobalt-doped nickel phosphide nanoparticle with higher H coverage with aqueous photosensitizer gives more superior hydrogen evolution rate.
ISSN:0926-3373
1873-3883
DOI:10.1016/j.apcatb.2018.09.103