Semiconductor photocatalysis has long been considered as a promising approach for water pollution remediation. However, limited by the recombination of electrons and holes, low kinetics of photocatalysts and slow reaction rate impede large-scale applications. Herein, we addressed this limitation by developing a triphase photocatalytic system in which a photocatalytic reaction is carried out at air-liquid-solid joint interfaces. Such a triphase system allows the rapid delivery of oxygen, a natural electron scavenger, from air to the reaction interface. This enables the efficient removal of photogenerated electrons from the photocatalyst surface and minimization of electron-hole recombination even at high light intensities, thereby resulting in an approximate 10-fold enhancement in the photocatalytic reaction rate as compared to a conventional liquid/solid diphase system. The triphase system appears an enabling platform for understanding and maximizing photocatalyst kinetics, aiding in the application of semiconductor photocatalysis.
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.
In this paper, we have engineered the interface electronic structure in Cu2O/ZnO nanorod arrays, via adjusting the carrier concentration of Cu2O, and applied them to photocatalysis. The photoinduced charge transfer kinetics at the interface between Cu2O and ZnO were systematically investigated. The Cu2O (pH 11.0)/ZnO nanorod arrays have the largest magnitude of interfacial electric field, and photoinduced charge carriers can be separated rapidly and efficiently, which generates the highest photocatalytic efficiency for the reduction of methylviologen. Heterojunction construction is an exciting direction to pursue for highly active photocatalysts, and also offers opportunities to investigate the relationship between the electronic structure and the photocatalytic performance.
The improvement of photoinduced charge separation is the key for light-harvesting systems in both photovoltaic and photoelectrochemical solar cells. In this study, the charge separation efficiency has been modulated through varying the magnitude of interfacial electric field in p–n Cu2O homojunction films prepared by simple electrodeposition method. The photoelectrochemical and surface photovoltage measurements were used to investigate the behaviors of photoinducded charge carriers in different p–n Cu2O homojunction films. The results confirmed that the p–n Cu2O homojunction film which exhibited the highest charge separation efficiency resulted in the highest activity in photocatalytic reduction of methyl viologen. These implied that it is possible to achieve high charge separation efficiency via constructing a large magnitude of interfacial electric field within a semiconductor using a simple electrodeposition method.
In 2 O 3 -sensitized flowerlike ZnO with visible light photoelectric response properties were synthesized by a facile two-step process, and characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), EDAX, HRTEM and UV-vis diffuse reflectance spectroscopy. The results revealed that In 2 O 3 nanoparticles have grown and eventually coalesced on the surface of the flowerlike ZnO successfully, and the samples exhibited significant response to visible light. The photoelectric gas-sensing of the In 2 O 3 -sensitized ZnO was also studied to formaldehyde (HCHO) under 460 nm light irradiation at room temperature with the help of surface photocurrent technique. It was found that ZnO sensitized with In 2 O 3 could enhance the gas response to HCHO under the visible light illumination. This may be due to the fact that the composite structure of In 2 O 3 -ZnO extends the photo absorbing range to visible light area, inhibits the recombination of photo-generated electrons and holes, and thus increases the utilization of photo-generated carriers in photoelectric gas detection, resulting in the higher sensing response in some extent. The gas response to 5 ppm and 100 ppm formaldehyde can reach to 19% and 419% under visible light irradiation at room temperature, respectively. These results should be valuable for designing a new type of visible-light assisted gas sensor at room temperature.
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