Effect of precursor dopant valence state on the photocatalytic performance of Mo3+- or Mo5+-Doped TiO2 thin films. (March 2019)
- Record Type:
- Journal Article
- Title:
- Effect of precursor dopant valence state on the photocatalytic performance of Mo3+- or Mo5+-Doped TiO2 thin films. (March 2019)
- Main Title:
- Effect of precursor dopant valence state on the photocatalytic performance of Mo3+- or Mo5+-Doped TiO2 thin films
- Authors:
- Cui, Yajing
Chen, Wen-Fan
Bastide, Arnaud
Zhang, Xichao
Koshy, Pramod
Sorrell, Charles Christopher - Abstract:
- Abstract: Mo 3+ - or Mo 5+ -doped TiO2 sol-gel thin films (≤0.100 mol%) were spin coated on fused silica glass substrates and annealed at 450 °C for 2 h. The effect of the valence of the dopant precursor is significant to the nanostructural development and resultant properties. Mo 3+ or Mo 5+ doping yields converse trends with doping level, thus reflecting the competing influences of lattice distortion and destabilization (dominating Mo 3+ doping) and nucleation and recrystallization (dominating Mo 5+ doping). Mo doping results in oxidation of Mo 3+ and reduction of Mo 5+, both of which alter to Mo (5−x)+, as well as oxidation of Ti 3+ to Ti (4+x)+ ; all of these result in V O annihilation. Although the absorption edges were largely indistinguishable, Mo 3+ doping causes a red shift and Mo 5+ doping causes a blue shift. These data suggest that the performances are controlled by the synergistic effects of crystallinity, surface area, and band gap, with the latter's exhibiting the dominant effect. This suggests that the defect structure governs the photocatalytic performance but also that the defect chemistry at these low annealing temperatures is indicative of nonequilibrium conditions, thereby explaining the significance of the dopant valence. Highlights: The dominant effects are lattice distortion (Mo 3+ ) and recrystallization (Mo 5+ ). Charge transfer causes Mo 3+ and Ti 3+ oxidation, Mo 5+ reduction and V O removal. Synergistic effect of crystallinity, surface area, andAbstract: Mo 3+ - or Mo 5+ -doped TiO2 sol-gel thin films (≤0.100 mol%) were spin coated on fused silica glass substrates and annealed at 450 °C for 2 h. The effect of the valence of the dopant precursor is significant to the nanostructural development and resultant properties. Mo 3+ or Mo 5+ doping yields converse trends with doping level, thus reflecting the competing influences of lattice distortion and destabilization (dominating Mo 3+ doping) and nucleation and recrystallization (dominating Mo 5+ doping). Mo doping results in oxidation of Mo 3+ and reduction of Mo 5+, both of which alter to Mo (5−x)+, as well as oxidation of Ti 3+ to Ti (4+x)+ ; all of these result in V O annihilation. Although the absorption edges were largely indistinguishable, Mo 3+ doping causes a red shift and Mo 5+ doping causes a blue shift. These data suggest that the performances are controlled by the synergistic effects of crystallinity, surface area, and band gap, with the latter's exhibiting the dominant effect. This suggests that the defect structure governs the photocatalytic performance but also that the defect chemistry at these low annealing temperatures is indicative of nonequilibrium conditions, thereby explaining the significance of the dopant valence. Highlights: The dominant effects are lattice distortion (Mo 3+ ) and recrystallization (Mo 5+ ). Charge transfer causes Mo 3+ and Ti 3+ oxidation, Mo 5+ reduction and V O removal. Synergistic effect of crystallinity, surface area, and band gap improved efficiency. … (more)
- Is Part Of:
- Journal of physics and chemistry of solids. Volume 126(2019)
- Journal:
- Journal of physics and chemistry of solids
- Issue:
- Volume 126(2019)
- Issue Display:
- Volume 126, Issue 2019 (2019)
- Year:
- 2019
- Volume:
- 126
- Issue:
- 2019
- Issue Sort Value:
- 2019-0126-2019-0000
- Page Start:
- 314
- Page End:
- 321
- Publication Date:
- 2019-03
- Subjects:
- Titania -- Anatase -- Thin film -- Photocatalysis -- Dopant valence
Solids -- Periodicals
Solides -- Périodiques
Solids
Periodicals
530.41 - Journal URLs:
- http://www.sciencedirect.com/science/journal/00223697 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.jpcs.2018.11.018 ↗
- Languages:
- English
- ISSNs:
- 0022-3697
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 5036.500000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 11165.xml