Title :
Convenient and green soft chemical route to cuprous oxide films and their visible-light photocatalytic properties
Author :
Haiyan Zheng ; Qing Li ; Yongping Zhang ; Lizhao Qin ; Hua Lin ; Ming Nie
Author_Institution :
Fac. of Mater. & Energy, Southwest Univ., Chongqing, China
Abstract :
Cuprous oxide (Cu2O) films have been synthesised by a convenient and green soft chemical route at room temperature. The films were obtained through the chemical reduction of copper acetate by ascorbic acid in solutions with ethylene glycol and deionised water. X-ray diffraction, energy-dispersive X-ray spectrometry, scanning electron microscopy (SEM), atomic force microscopy, as well as UV-Vis spectroscopy (UV-Vis) were used to characterise the resulting films. It was obvious from the SEM image that the obtained films were composed of nanosphere particles with a size of 100-400 nm. The photocatalytic activity of degradation of methyl orange (MO) of the obtained Cu2O films, H2O2 and H2O2/Cu2O films system under visible light irradiation was also investigated. The results have shown that the system exhibits high catalytic ability under visible light irradiation. Also, there was a strong synergistic effect between the obtained Cu2O films and H2O2 when the system was used to degrade MO.
Keywords :
X-ray chemical analysis; X-ray diffraction; atomic force microscopy; catalysis; copper compounds; dyes; liquid phase deposition; nanofabrication; nanoparticles; photochemistry; scanning electron microscopy; semiconductor growth; semiconductor materials; semiconductor thin films; ultraviolet spectra; visible spectra; Cu2O; SEM; UV-vis spectroscopy; X-ray diffraction; ascorbic acid; atomic force microscopy; chemical reduction; copper acetate; cuprous oxide films; deionised water; energy-dispersive X-ray spectrometry; ethylene glycol; green soft chemical synthesis; methyl orange degradation; nanosphere particles; scanning electron microscopy; temperature 293 K to 298 K; visible light irradiation; visible-light photocatalytic properties;
Journal_Title :
Micro Nano Letters, IET
DOI :
10.1049/mnl.2015.0100