ABSTRACT
Adsorption of methanol and ethanol on the clean Pt (111) surface was studied at temperatures between 80 and 130 K using polarization-modulation infrared reflection absorption spectroscopy (PM-IRRAS). It was shown that adsorption of methanol at 80 K leads to the formation of amorphous solid methanol, and fast crystallization of the amorphous phase occurs upon warming at 100 K. Vapor deposition of methanol at 100 K directly leads to the formation of well-crystallized layers of solid methanol. According to PM-IRRAS, these crystalline layers consist of chains of hydrogen-bonded methanol molecules lying in a plane oriented close to the normal to the platinum surface. Adsorbed methanol is removed completely from platinum after heating to 120 K. Vapor deposition of ethanol at 80 K also leads to the formation of amorphous solid ethanol. However, subsequent warming does not lead to ordering of the adsorption layers, and at 130 K, ethanol is also completely desorbed.
ABSTRACT
Photocatalysts based on zinc hydroxide and a solid solution of CdS and ZnS were prepared via the precipitation method and used for photocatalytic hydrogen production from aqueous solutions of inorganic (Na2S/Na2SO3) and organic (ethanol) sacrificial agents. The photocatalysts were tested in cyclic experiments for hydrogen evolution and studied using X-ray diffraction (XRD), UV-Vis diffuse reflectance spectroscopy, high-resolution transmission electron microscopy (HRTEM), energy-dispersive X-ray spectroscopy (EDX), and X-ray photoelectron spectroscopy (XPS) techniques. Different transformations of the ß-Zn(OH)2 co-catalyst were observed in the presence of inorganic and organic sacrificial agents; namely, ZnS was formed in Na2S/Na2SO3 solution, whereas the formation of ε-Zn(OH)2 was detected in solution with ethanol. The composite Zn(OH)2/Cd1-x Zn x S photocatalysts have great potential in various photocatalysis processes (e.g., hydrogen production, CO2 reduction, and the oxidation of organic contaminants) under visible light.
