Abstract
Mesoporous TiO2−xAy (A = N, S) thin films were fabricated using thiourea as a doping resource by a combination of sol-gel and evaporation-induced self-assembly (EISA) processes. The results showed that thiourea could serve two functions of co-doping nitrogen and sulfur and changing the mesoporous structure of TiO2 thin films. The resultant mesoporous TiO2−xAy (A = N, S) exhibited anatase framework with a high porosity and a narrow pore distribution. The formation of the O–Ti–N and O–Ti–S bonds in the mesoporous TiO2−xAy (A = N, S) were substantiated by the XPS spectra. A new bandgap in visible light region (520 nm) corresponding to 2.38 eV could be formed by the co-doping. After being illuminated for 3 h, methyl orange could be degraded nearly completely by the co-doped sample under both ultraviolet irradiation and visible light illumination. While pure mesoporous TiO2 could only degrade 60% methyl orange under UV illumination and showed negligible photodegradation capability in the visible light range. Furthermore, the photo-induced hydrophilic activity of TiO2 film was improved by the co-doping. The mesoporous microstructure and high visible light absorption could be attributed to their good photocatalytic acitivity and hydrophilicity.
Keywords: Mesoporous film; TiO2−xAy (A = N, S); Visible-light-response; Photocatalyst
Article Outline
- 1. Introduction
- 2. Experimental section
- 2. Experimental section
- 2.1. Catalyst synthesis
- 2.2. Characterization
- 2.3. Photocatalytic activity testing
- 2.4. Photo-induced hydrophilicity study
- 2.2. Characterization
- 3. Results and discussion
- 3.1. Composition of the samples
- 3.2. Morphology and pore size of the samples
- 3.3. Light absorption capability
- 3.4. Photocatalytic activity of the samples
- 3.5. Hydrophilicity of the samples
- 3.2. Morphology and pore size of the samples
- 4. Conclusions
- Acknowledgements
- References
- Acknowledgements
Fig. 3. FESEM images of the synthesized samples: (a) SN-1 (without adding thiourea), (b) SN-2 (added 2.5 mol% thiourea), (c) SN-3 (added 5 mol% thiourea), (d) SN-4 (added 7.5 mol% thiourea), (e) SN-5 (added 10 mol% thiourea).
Fig. 4. N2 adsorption–desorption isotherms and the corresponding BJH pore size distribution curves (inset) of the prepared samples, (a) SN-1, (b) SN-2, (c) SN-3, (d) SN-4 and (e) SN-5.
Fig. 6. The photocatalytic activity of the prepared mesoporous TiO2 samples. The residual concentration ratios of MO solution under (a) UV irradiation and (b) visible-light irradiation.
Fig. 7. The water contact angle of the obtained mesoporous TiO2 films without light illumination and under the visible light illumination for 10 min. (a) SN-1, (b) SN-2, (c) SN-3, (d) SN-4, (e) SN-5.