IntroductionThe most efficient way of hydrogen production using solar energy is water splitting induced by solar light. In order to achieve it, a photo-semiconductor capable of absorbing solar energy efficiently is needed. Efficient photocatalysts should satisfy several conditions: suitable band gap (about 2e2.2 eV) for visible light absorption and appropriate band edge potentials for water splitting, capability to separate excited electrons and holes, minimal energy losses during charge transport, chemical stability to corrosion, suitable electron transfer properties from photocatalysts' surface to water and low cost [1,2]. However the applicability of semiconductor photocatalyst is, without any doubt, primarily determined by its electronic structure.Titanium dioxide TiO 2 , in both rutile and anatase form, is one of the most promising photocatalysts. However, the wide energy gaps of pure TiO 2 phases allow efficient absorption of only ultraviolet light and are not suitable for efficient use of solar energy. In this sense, an extensive experimental [3,4] and theoretical [5e14] work has been carried out in order to shift the TiO 2 absorption edge from the UV to the visible-light region and thus increase its efficiency for solar-driven photocatalysis. For achieving that purpose mostly doping with transition metals was used [15e22]. However, the transition metals as dopants can increase the number of carrierrecombination centers and thus reduce the carrier mobility, * Corresponding author. Tel.: þ381 11 3408 549; fax: þ381 11 3408 681. E-mail address: cjeca@vinca.rs (J. Belosevic-Cavor).Available online at www.sciencedirect.com ScienceDirect j ou rnal h ome pag e: www.elsevier.com/loca te/he i n t e r n a t i o n a l j o u r n a l o f h y d r o g e n e n e r g y 4 0 ( 2 0 1 5 ) 9 6 9 6 e9 7 0 3http://dx