期刊
INTERNATIONAL JOURNAL OF HYDROGEN ENERGY
卷 35, 期 23, 页码 12954-12960出版社
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.ijhydene.2010.04.057
关键词
ANb(2)O(6); Crystal structure; Band structure; Photocatalytic activity; Water splitting; Hydrogen production
资金
- National Research Foundation of Korea [R31-2008-000-10075-0] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)
Alkali earth metaniobate compounds ANb(2)O(6) (A = Ca Sr Ba) were prepared by the conventional solid state reaction route and their electronic band structures and photo catalytic activities were investigated The prepared powders were characterized using X ray diffraction (XRD) field emission electron microscopy (FE SEM) UV-vis diffuse reflectance spectroscopy and fluorescence spectroscopy It was found that the particle sizes (similar to 1 mu m) and BET surface areas (similar to 1 m(2)/g) of the metaniobate compounds were nearly identical From the electronic band structure calculations however the band gap energies of these metaniobate compounds were found to be in the order of CaNb2O6 > SrNb2O6 > BaNb2O6 These calculated band gap energies were consistent with those estimated from the UV-vis diffuse reflectance spectra Moreover the conduction band edge (reduction potential) of SrNb2O6 calculated from the electronegativity data was higher than those of CaNb2O6 and BaNb2O6 The photoluminescence spectra revealed that CaNb2O6 exhibited a strong blue luminescence emission (at 300K) while no obvious emissions were observed in either SrNb2O6 or BaNb2O6 The luminescence behaviors of these metaniobate compounds and their band structure variations originating from their crystal structures play an important role in their photocatalytic activity for the evolution of H-2 from pure water SrNb2O6 which has a higher conduction band edge potential than the other compounds exhibited higher photocatalytic activity (C) 2010 Professor T Nejat Veziroglu Published by Elsevier Ltd All rights reserved
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