The hydrogen photo-evolution was successfully achieved in aqueous (Fe(1-x)Cr(x))(2)O(3) suspensions (0 <= x <= 1). The solid solution has been prepared by incipient wetness impregnation and characterized by X-ray diffraction, BET, transport properties and photo-electrochemistry. The oxides crystallize in the corundum structure, they exhibit n-type conductivity with activation energy of similar to 0.1 eV and the conduction occurs via adiabatic polaron hops. The characterization of the band edges has been studied by the Mott Schottky plots. The onset potential of the photo-current is similar to 0.2 V cathodic with respect to the flat band potential, implying a small existence of surface states within the gap region. The absorption of visible light promotes electrons into (Fe(1-x)Cr(x))(2)O(3)-CB with a potential (similar to-0.5 V(SCE)) sufficient to reduce water into hydrogen. As expected, the quantum yield increases with decreasing the electro affinity through the substitution of iron by the more electropositive chromium which increases the band bending at the interface and favours the charge separation. The generated photo-voltage was sufficient to promote simultaneously H(2)O reduction and SO(3)(2-) oxidation in the energetically downhill reaction (H(2)O + SO(3)(2-) -> H(2) + SO(4)(2-), Delta G = -17.68 kJ mol(-1). The best activity occurs over Fe(1.2)Cr(0.8)O(3) in SO(3)(2-) (0.1 M) solution with H(2) liberation rate of 21.7 mu mol g(-1) min(-1) and a quantum yield 0.06% under polychromatic light. Over time, a pronounced deceleration occurs, due to the competitive reduction of the end product S(2)O(6)(2-). (C) 2010 Professor T. Nejat Veziroglu. Published by Elsevier Ltd. All rights reserved.