A new series visible-light driven photocatalysts (CuIn)(x)Cd(2(1-x))S(2) was successfully synthesized by a simple and facile, low-temperature hydrothermal method. The synthesized materials were characterized by means of X-ray diffraction (XRD), scanning electron microscopy (SEM), Brunauer-Emmett-Teller (BET) surface area measurement, X-ray photoelectron spectroscopy (XPS) and ultraviolet-visible spectroscopy (UV-Vis DRS). The results show that the morphology of the photocatalysts changes with the increase of x from 0.01 to 0.3 and their band gap can be correspondingly tuned from 2.37 eV to 2.30 eV. The (CuIn)(x)Cd(2(1-x))S(2) nanocomposite show highly photocatalytic activities for H(2) evolution from aqueous solutions containing sacrificial reagents, SO(3)(2-) and S(2-) under visible light. Substantially, (CuIn)(0.05)Cd(1.9)S(2) with the band gap of 2.36 eV exhibits the highest photocatalytic activity even without a Pt cocatalyst (649.9 mu mol/(g h)). Theoretical calculations about electronic property of the (CuIn)(x)Cd(2(1-x))S(2) indicate that Cu 3d and In 5s5p states should be responsible for the photocatalytic activity. Moreover, the deposition of Pt on the doping sample results in a substantial improvement in H(2) evolution than the Pt-loaded pure CdS and the amount of H(2) produced (2456 mu mol/(g h)) in the Pt-loaded doping system is much higher than that of the latter (40.2 mu mol/(g h)). The (CuIn)(0.05)Cd(1.9)S(2) nanocomposite can keep the activity for a long time due to its stability in the photocatalytic process. Therefore, the doping of CuInS(2) not only facilitates the photocatalytic activity of CdS for H(2) evolution, but also improves its stability in photocatalytic process. (C) 2010 Professor T. Nejat Veziroglu. Published by Elsevier Ltd. All rights reserved.