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Hydrogen production by water reduction on Si photocathode coupled with Ni2P.
- Source :
-
International Journal of Hydrogen Energy . Mar2019, Vol. 44 Issue 14, p7241-7251. 11p. - Publication Year :
- 2019
-
Abstract
- Abstract While searching for an efficient, non-noble, earth-abundant catalyst for the hydrogen evolution reaction (HER), we synthesized hexagonal dinickel phosphide with different nanostructures using solvothermal phosphidation. Coupled atop p- type Si, this catalyst performed as a p-n heterojunction photocathode assembly and the performance varied when under different electrolyte media. Apart from changing the surface morphology, Ni 2 P was crystallized with an increase in the Niδ+/Ni2+ ratio as the phosphidation temperature gradually increased. A systematic evaluation of the water splitting reaction shows that a very small amount of catalyst (>85% transmittance for the catalyst layer) exhibits a photocurrent of −10 mA cm−2 with a positive applied potential of 0.05 V versus reversible hydrogen electrode under simulated solar irradiation of AM 1.5G. We discuss the substantial charge transfer process at the depletion layer of the electrode/catalyst and the catalyst/electrolyte interface. Mott–Shottky analysis showed a shift in the flat band potential for Ni 2 P, which reveals the underlying mechanism for the role of the p-n junction for enhanced photoelectrochemical cell performance. Highlights • The Hexagonal phase Ni 2 P is changing Niδ+/Ni2+ ratio with phosphidation temperature. • p- Si coupled with as-prepared Ni 2 P performed as p-n heterojunction photocathode unit. • Optimized photocurrent obtained with 10 mA cm−2 at positive applied potential of 0.05 V. • Shifting of flat-band potential validated the charge transfer process. [ABSTRACT FROM AUTHOR]
Details
- Language :
- English
- ISSN :
- 03603199
- Volume :
- 44
- Issue :
- 14
- Database :
- Academic Search Index
- Journal :
- International Journal of Hydrogen Energy
- Publication Type :
- Academic Journal
- Accession number :
- 135077765
- Full Text :
- https://doi.org/10.1016/j.ijhydene.2019.01.258