Morphology control and phase transformation of ZIS/TiO2 into CdSe(en)0.5/CIS/TiO2 photoanode for enhanced solar hydrogen generation

An inorganic-organic CdSe(en)(0.5)/CdIn2S4/TiO2 complex heterostructure was successfully synthesized using a facile solvothermal method. The morphology of a CdSe(en)(0.5)/CdIn2S4/TiO2 heterostructure was controlled by varying the concentrations of cadmium nitrate and selenium precursors in ethylenediamine. Intentionally controlling the morphology enhances the absorption within the visible region compared to a ZnIn2S4/TiO2 photoanode. The photoelectrochemical (PEC) study shows that the CdSe(en)(0.5)/CdIn2S4/TiO2 photoanode complex heterostructure exhibits a photocurrent density of 2.43 mA cm(-2) at 0 V versus Ag/AgCl, which is 180% higher than that of a ZnIn2S4/TiO2 photoanode. The extra-delayed lifetime and photostability of CdSe(en)(0.5)/CdIn2S4/TiO2 complex heterojunction is cause of efficient hole scavenging. During the PEC measurement, the Se and ethylenediamine leaches out into the electrolyte while S-2- from the Na2S + Na2SO3 electrolyte reacts with surface of the CdSe(en)(0)(.5)/CdIn2S4/TiO2 complex heterojunction. Such structure can effectively separate the charge carrier and yields 100 mu mol of hydrogen within 3 h. The possible charge transfer mechanism during solar hydrogen generation in an inorganic-organic CdSe(en)(0)(.5)/CdIn2S4/TiO2 complex heterojunction structure has also been proposed.