4.8 Article

Photoelectrochemical Water Oxidation Using Cobalt Phosphate-Modified Nitrogen-Doped Titania Nanotube Arrays

Journal

SMALL STRUCTURES
Volume 4, Issue 6, Pages -

Publisher

WILEY
DOI: 10.1002/sstr.202200229

Keywords

artificial photosynthesis; hydrogen production; mixed-anion compounds; solar fuels; water splitting

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The synthesis of cobalt phosphate (CoPi)-modified, nitrogen-doped TiO2 nanotube arrays (N-TNAs) for photoelectrochemical (PEC) oxygen evolution under visible light is reported. The N-TNAs exhibit enhanced visible-light activity due to nitrogen doping, but their performance is diminished by self-oxidation. However, CoPi/N-TNAs prepared under optimal conditions show improved photocurrent generation and sensitivity to long wavelength light. Stable oxygen evolution with high Faradaic efficiency is achieved using CoPi/N-TNA photoanodes under simulated sunlight for at least 2 hours.
The synthesis of cobalt phosphate (CoPi)-modified, nitrogen-doped TiO2 nanotube arrays (N-TNAs) for photoelectrochemical (PEC) oxygen evolution under visible light is reported. Because of the nitrogen doping, the N-TNAs exhibit enhanced visible-light activity toward the PEC water oxidation reaction. However, the performance is diminished as a result of self-oxidation by photogenerated holes in the valence band of the N-TNAs. Compared with the N-TNAs, the CoPi/N-TNAs prepared under optimal conditions show a twofold improvement in photocurrent generation and are also sensitive to light with wavelengths as long as 580 nm. Stable oxygen evolution with a Faradaic efficiency approaching unity is demonstrated using the CoPi/N-TNA photoanodes under simulated sunlight for at least 2 h of operation.

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