Core-Shell Structural CdS@SnO2 Nanorods with Excellent Visible-Light Photocatalytic Activity for the Selective Oxidation of Benzyl Alcohol to Benzaldehyde

Core-shell structural CdS@SnO2 nanorods (NRs) were fabricated by synthesizing SnO2 nanoparticles with a solvent-assisted interfacial reaction and further anchoring them on the surface of CdS NRs under ultrasonic stirring. The morphology, composition, and microstructures of the obtained samples were characterized by field-emission scanning electron microscopy, transmission electron microscopy, X-ray diffraction, X-ray photoelectron spectroscopy, and nitrogen adsorption-desorption. It was found that SnO2 nanoparticles can be tightly anchored on the surface of CdS NRs, and the thickness of SnO2 shells can be conveniently adjusted by simply changing the addition amount of SnO2 quantum dots. UV-vis diffuse reflectance spectrum indicated that SnO2 shell layer also can enhance the visible light absorption of CdS NRs to a certain extent. The results of transient photocurrents and photoluminescence spectra revealed that the core-shell structure can effectively promote the separation rate of electron-hole pairs and prolong the lifetime of electrons. Compared with the single CdS NRs, the core-shell structural CdS@SnO2 exhibited a remarkably enhanced photocatalytic activity for selective oxidation of benzyl alcohol (BA) to benzaldehyde (BAD) under visible light irradiation, attributed to the more efficient separation of electrons and holes, improved surface area, and enhanced visible light absorption of core-shell structure. The radical scavenging experiments proved that in acetonitrile solution, O-center dot(2)- and holes are the main reactive species responsible for BA to BAD transformation, and the lack of (OH)-O-center dot radicals is favorable to obtaining high reaction selectivity.