Journal article
Transition metal-doped nickel phosphide nanoparticles as electro- and photocatalysts for hydrogen generation reactions
- Abstract:
- 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.
- Publication status:
- Published
- Peer review status:
- Peer reviewed
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- Files:
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(Preview, Accepted manuscript, pdf, 1.8MB, Terms of use)
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- Publisher copy:
- 10.1016/j.apcatb.2018.09.103
Authors
- Publisher:
- Elsevier
- Journal:
- Applied Catalysis B: Environmental More from this journal
- Volume:
- 242
- Pages:
- 186-193
- Publication date:
- 2018-10-02
- Acceptance date:
- 2018-09-30
- DOI:
- ISSN:
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0926-3373
- Keywords:
- Pubs id:
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pubs:928881
- UUID:
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uuid:95046884-5be7-45c1-9548-5f84c7ce0efc
- Local pid:
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pubs:928881
- Source identifiers:
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928881
- Deposit date:
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2018-10-26
- ARK identifier:
Terms of use
- Copyright holder:
- Elsevier BV
- Copyright date:
- 2018
- Notes:
- © 2018 Elsevier B.V. All rights reserved. This is the accepted manuscript version of the article. The final version is available online from Elsevier at: 10.1016/j.apcatb.2018.09.103
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