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Activity and stability of cobalt phosphides for hydrogen evolution upon water splitting
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“(011) is predominantly exposed facet for CoP.[38]”
From Sub‐1.5 nm Ultrathin CoP Nanosheet Aerogel: Efficient Electrocatalyst for Hydrogen Evolution Reaction at All pH Values (2018) · cites this paper as [38]
Experimental — accuracy not yet measuredThe source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“CoP surface, thus reducing the exposure of P atoms and the degree of P oxidation, resulting in the reduction of O/Co ratio, so that more CoP can participates in HER process and enhance its catalytic ability [49].”
From CoP aerogels assisted by selenite etching as high activity electrocatalysts for water splitting (2023) · cites this paper as [49]
Experimental — accuracy not yet measuredThe source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“CoP surface, thus reducing the exposure of P atoms and the degree of P oxidation, resulting in the reduction of O/Co ratio, so that more CoP can participates in HER process and enhance its catalytic ability [49].”
From CoP aerogels assisted by selenite etching as high activity electrocatalysts for water splitting (2023) · cites this paper as [49]
Experimental — accuracy not yet measuredThe source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“CoP surface, thus reducing the exposure of P atoms and the degree of P oxidation, resulting in the reduction of O/Co ratio, so that more CoP can participates in HER process and enhance its catalytic ability [49].”
From CoP aerogels assisted by selenite etching as high activity electrocatalysts for water splitting (2023) · cites this paper as [49]
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In the citing paper
“the adsorption of H on the P sites of (011) is more active than others”
From Sub‐1.5 nm Ultrathin CoP Nanosheet Aerogel: Efficient Electrocatalyst for Hydrogen Evolution Reaction at All pH Values (2018) · cites this paper as [38]
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Metadata
- Authors
- Ha, D.-H., Han, B., Risch, M., Giordano, L., Yao, K. P. C., Karayaylali, P., & Shao-Horn, Y.
- Affiliations
- Massachusetts Institute of Technology (US)
- Venue
- Nano Energy
- Publisher
- Elsevier BV
- Published
- 2016-11
- Volume
- 29
- Pages
- 37-45
- ISSN
- 2211-2855 (ISSN-L)
- OpenAlex
- W2341234305
- Cited by
- 199
- References
- 0
- Citations by year
- 2026: 8 · 2025: 11 · 2024: 17 · 2023: 16 · 2022: 21 · 2021: 23 · 2020: 21 · 2019: 30 · 2018: 36 · 2017: 13 · 2016: 3
- FWCI
- 7.42
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- Locations
- Nano Energy (acceptedVersion)
- BOA (University of Milano-Bicocca) (submittedVersion, other-oa)
- DSpace@MIT (Massachusetts Institute of Technology) (submittedVersion, cc-by-nc-nd)
- OSTI OAI (U.S. Department of Energy Office of Scientific and Technical Information) (submittedVersion)
- Funders
- BASF (022278)
- U.S. Department of Energy
- Argonne National Laboratory
- National Science Foundation (DMR-1419807)
- Topics
- Physical Sciences › Energy › Renewable Energy, Sustainability and the Environment › Electrocatalysts for Energy Conversion
- Physical Sciences › Energy › Renewable Energy, Sustainability and the Environment › Advanced Photocatalysis Techniques
- Physical Sciences › Energy › Renewable Energy, Sustainability and the Environment › CO2 Reduction Techniques and Catalysts
- Keywords
- cobalt phosphide, hydrogen evolution reaction, water splitting, electrocatalysis, catalyst stability, phosphate formation, colloidal synthesis, photoelectrochemical hydrogen production
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