Journal
ACS APPLIED ENERGY MATERIALS
Volume 2, Issue 5, Pages 3274-3282Publisher
AMER CHEMICAL SOC
DOI: 10.1021/acsaem.9b00126
Keywords
titanium dioxide; reduced rutile; visible light; water oxidation; photoexcited electron dynamics; chromium; tantalum
Funding
- General Sekiyu Research Scholarship Foundation
- JST, Precursory Research for Embryonic Science and Technology (PRESTO) [JPMJPR18T1]
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The importance of electron concentration in rutile TiO2 photocatalysts motivated us to apply H-2 reduction treatment to visible-light-responsive TiO2 photocatalysts sensitized by chromium ion doping. We found that H-2 reduction treatment of rutile TiO2 particles codoped with Ta and Cr (TiO2:Ta/Cr) enhanced photocatalytic activity for O-2 evolution by water oxidation under visible irradiation (>2.2 eV). The enhanced visible light activity of H-2-treated TiO2:Ta/Cr was attributed to the increase of electron concentration, which was confirmed by UV-vis diffuse reflectance and electron spin resonance (ESR) spectroscopy. The H-2-treated TiO2:Ta/Cr photocatalyst was repeatedly used in aqueous media in spite of the presence of doped electrons. Photoluminescence and transient absorption spectroscopies revealed that electron doping with H-2 treatment decreased the midgap states working as deep traps of photoexcited electrons and increased the accumulation of the photoexcited electrons in the conduction band. The optimized H-2 reduction temperature was decreased with an increase in the amount of higher valence Ta5+ used as a donor-type dopant. This study shows that the precise control of the bulk electronic structure of rutile TiO2 by a combination of codoping and H-2 reduction treatment improves the visible-light-driven photocatalytic activity because of the decrease of the trapping sites at deep energy levels and the recombination between deeply trapped electrons and valence band holes.
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