Issue 44, 2008

Correlation between the band positions of (SrTiO3)1−x·(LaTiO2N)x solid solutions and photocatalytic properties under visible light irradiation

Abstract

N-doped SrTiO3 and (SrTiO3)1−x·(LaTiO2N)x samples were prepared by the thermal ammonolysis method. The photocatalytic activities of the samples were investigated in a water suspension system. Aqueous methanol solution (50 mL CH3OH + 220 mL H2O) for H2 evolution and aqueous silver nitrate solution (270 mL, 0.01 mol L−1) for O2 evolution were used as sacrificial reagents. The oxynitrides showed photocatalytic activities under visible light irradiation. The maximum rates of photocatalytic hydrogen and oxygen evolution under visible light irradiation (λ > 420 nm) were 10 and 8 μmol h−1, respectively. The samples were characterized by X-ray diffractometry, UV-Vis spectrophotometry, Fourier transform infrared spectrometry, and laser Raman spectroscopy. The unit cell edge length of (SrTiO3)1−x·(LaTiO2N)x increased linearly and their band gaps reduced from 3.18 to 2.04 eV with increasing x from 0 to 0.30. Moreover, the calculation results of (SrTiO3)0.75·(LaTiO2N)0.25 by density functional theory suggested that the band gap narrowing of the solid solutions came from the hybridization of N2p and O2p orbital. The band positions of the solid solutions were further investigated by Mott-Schottky and the onset potential method. The results suggested that the conduction band of the solid solution was lowered, which led to decrement of the hydrogen evolution rate.

Graphical abstract: Correlation between the band positions of (SrTiO3)1−x·(LaTiO2N)x solid solutions and photocatalytic properties under visible light irradiation

Supplementary files

Article information

Article type
Paper
Submitted
07 Mar 2008
Accepted
05 Aug 2008
First published
25 Sep 2008

Phys. Chem. Chem. Phys., 2008,10, 6717-6723

Correlation between the band positions of (SrTiO3)1−x·(LaTiO2N)x solid solutions and photocatalytic properties under visible light irradiation

W. Luo, Z. Li, X. Jiang, T. Yu, L. Liu, X. Chen, J. Ye and Z. Zou, Phys. Chem. Chem. Phys., 2008, 10, 6717 DOI: 10.1039/B803996H

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