International Journal of Hydrogen Energy, Vol.37, No.7, 5532-5539, 2012
Electronic structure and water splitting under visible-light irradiation of Zn and Ag co-doped In(OH)(y)S-z photocatalysts
Zinc and silver co-doped In(OH)(y)S-z with nanocubic blocks morphology were prepared by a one-step hydrothermal method and their photocatalytic activities were investigated. The as-synthesized products were characterized by transmission electron microscopy (TEM), powder X-ray diffraction (XRD), scanning electron microscopy (SEM), inductively coupled plasma (ICP) and UV-visible spectroscopy. The electron microscope observations revealed that the particle sizes of Zn-doped In(OH)(y)S-z crystals were smaller than that of the non-doped In(OH)(y)S-z, which accords with BET results. While Zn-Ag co-doped In(OH)(y)S-z showed the nanocubic blocks with different particle sizes. The UV-vis spectra indicate that the single Zn ions doping leads to the absorbance band shifts toward lower wavelength upon increasing the Zn doping. Consequently, the band gap of In(OH)(y)S-z also increases gradually with increasing the Zn doping. In contrast, an obvious red-shift is observed for Zn-Ag co-doped In(OH)(y)S-z solid solution, which mainly attributed to the transition from Ag 4d + S 3p orbitals to Zn 4s + In Ss orbitals. The sample doped with 4 mol% Ag and Zn was found to have the highest activity, which is 20 times that of the In(OH)(y)S-z. Copyright (C) 2012, Hydrogen Energy Publications, LLC. Published by Elsevier Ltd. All rights reserved.