Fe(2)O(3)/TiO(2) heterogeneous photocatalysts with different mass ratios of Fe(2)O(3)vs. TiO(2) were synthesized by impregnation of Fe(3+) on the surface of TiO(2) microrods and calcination at 300 degrees C. Scanning electron microscopy (SEM), high resolution transmission electron microscopy (HRTEM), photoluminescence spectra and X-ray diffraction (XRD) have been used to characterize the samples. The photocatalytic activities of Fe(2)O(3)/TiO(2) heterocomposites, pure Fe(2)O(3) and pure TiO(2) were evaluated by the photodegrading efficiency of Orange II under visible light (lambda > 420 nm). The experiments demonstrated that Orange II in aqueous solution was more efficiently photodegraded using Fe(2)O(3)/TiO(2) heterogeneous photocatalysts than either pure Fe(2)O(3) or TiO(2) under visible light irradiation. With an optimal mass ratio of 7:3 in Fe(2)O(3)/TiO(2) the highest rate of Orange II photodegradation was achieved under the experimental conditions. We have also compared the photoelectric properties of Fe(2)O(3)/TiO(2) heterogeneous photocatalysts with that of pure Fe(2)O(3) by surface photovoltage (SPV) and transient photovoltage (TPV) techniques. Based on the photovoltage responses, we discussed the influence of the hetero-interface between Fe(2)O(3) and TiO(2) on transfer characteristics of photogenerated charge carriers. We demonstrated that the formation of heterojunctions between Fe(2)O(3) and TiO(2) for Fe(2)O(3)/TiO(2) composites was pivotal for improving the separation and thus restraining the recombination of photogenerated electrons and holes, which accounts for the enhancement of photocatalytic activity.

ZnO/Cu(2)O heterostructure films were prepared by a two-step electrodeposition method in aqueous solution on fluorine-doped tin oxide (FTO) substrates. Scanning electron microscopy (SEM), X-ray powder diffraction (XRD) and UV-vis transmission measurements were utilized to characterize the films. Surface photovoltage (SPV) technique was used to investigate the process of photoinduced charge transfer. The results show that there is an electric field located at the interface between ZnO and Cu(2)O film and the photoinduced electrons in Cu(2)O film inject into ZnO under the effect of interfacial electric field with visible light irradiation. While under ultraviolet light illumination, the photoinduced electrons in Cu(2)O film accumulate at the surface of Cu(2)O film instead of injecting into ZnO under the action of surface built-in electric field of Cu(2)O film. The work function measurements confirm that the direction of interfacial electric field is from ZnO to Cu(2)O. These results are help to future design of high performance heterostructure photovoltaic devices.

ZnO nanorod arrays on an ITO substrate and nanorod powder have been prepared via a chemical method in aqueous solution at low temperature. Two dimensions of composite nanorods in the arrays were obtained by controlling the reaction time. SEM, XRD, UV-vis transmission, and PL measurements have been utilized to characterize the samples. The surface photovoltage (SPV) spectra of the three samples have been comparatively investigated by a lock-in amplifier with dc bias and Kelvin probe (KP) based measurements. The kinetic features of SPV responses are interpreted in terms of ac SPV phase spectra and SPV transients on a KP. We demonstrate that the photovoltaic properties of ZnO nanorods not only depend on the rod size, but also rely on the crystallographic orientation. The mechanisms therein have been discussed in detail. Our results could lead to better understanding of the photovoltaic properties in ZnO nanostructures.

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A vertically aligned array of ZnO nanorods, fabricated on conductive ITO substrate in aqueous solution, was characterized by scanning electron microscopy (SEM), x-ray diffraction (XRD), and UV-visible transmission spectroscopy. Surface photovoltage (SPV) techniques based on a lock-in amplifier and a Kelvin probe were both employed to study the photogenerated charges in the system. The effects of ethanol solvent and a liquid-crystalline porphyrin, [5-(para-dodecyloxy)phenyl-10,15,20-tri-phenyl] porphyrin (DPTPP), on the photovoltage enhancement in the ZnO nanorod array were studied via SPV comparison between different irradiation directions on the system. We demonstrate that the ethanol adsorption could induce the space charge region to expand towards the ZnO/ITO interface. In the absence of ethanol, the ZnO nanorod array with the DPTPP adsorption showed enhanced SPV with reduced attenuation rate of photogenerated charge carriers. We found that the separation of photogenerated charges could be further improved by coating the surface with DPTPP and ethanol together. Furthermore, the SPV spectra patterns of the composite system with opposite incident-light directions reveal that the DPTPP molecules adsorbed just at the surface of ZnO nanorods adopt a more monomeric alignment in contrast to the aggregative state in the DPTPP bulk.