Journal
APPLIED CATALYSIS B-ENVIRONMENTAL
Volume 158, Issue -, Pages 202-208Publisher
ELSEVIER SCIENCE BV
DOI: 10.1016/j.apcatb.2014.04.025
Keywords
Defect chemistry; Hydrogenation; Oxygen vacancy; Structure-activity relationships; Titanium dioxide
Funding
- Japan Society for the Promotion of Science [23655187, 23686114]
- General Sekiyu Research Scholarship Foundation
- Grants-in-Aid for Scientific Research [23686114, 23655187] Funding Source: KAKEN
Ask authors/readers for more resources
Rutile titania (TiO2) is an efficient photocatalyst for oxidizing water to O-2. The photocatalytic activity of particulate rutile for water oxidation was significantly improved by H-2 reduction at 700 degrees C, after calcination at 1100 degrees C. The improved activity was due to an increase in crystalline size during calcination, and an increase in conduction band electron concentration by the creation of oxygen vacancies. In contrast to the consideration that oxygen vacancy increases the recombination of electron and holes, the hydrogenated TiO2 exhibited high apparent quantum efficiency for O-2 evolution, 41% under irradiation at 365 nm. It was found that H-2 treatment improved the photocatalytic activity per unit of surface area not only for O-2 evolution but also for H-2 evolution and acetic acid decomposition. The effect of H-2 reduction treatment was obtained only if the rutile particle was previously calcined at temperatures higher than 1000 degrees C. This suggests that space charge layer in large crystalline particles is involved in the activation mechanism of hydrogenated rutile TiO2 particles. (C) 2014 Elsevier B.V. All rights reserved.
Authors
I am an author on this paper
Click your name to claim this paper and add it to your profile.
Reviews
Recommended
No Data Available