Fabrication of visible light-triggered photocatalytic materials from the coupling of n-type zinc oxide and p-type copper oxide

2nd International Symposium on Frontier of Applied Physics

Gorospe, A.B.^1 ; Herrera, M.U.^1

Institute of Mathematical Sciences and Physics, University of the Philippines Los Banos, College Laguna

4031, Philippines^1

关键词: Chemical precipitation method;    N-type zinc oxides;    Photo catalytic degradation;    Photocatalytic activities;    Photocatalytic materials;    Sodium hydroxide solutions;    X-ray diffraction measurements;    Zinc oxide powder;   

Others  :  https://iopscience.iop.org/article/10.1088/1742-6596/817/1/012058/pdf
DOI  :  10.1088/1742-6596/817/1/012058

来源: IOP

【 摘 要 】

Coupling of copper oxide (CuO) and zinc oxide (ZnO) was done by chemical precipitation method. In this method, copper sulfate pentahydrate and zinc sulfate heptahydrate salt precursors were separately dissolved in distilled water; then were mixed together. The copper sulfate-zinc sulfate solution was then combined with a sodium hydroxide solution. The precipitates were collected and washed in distilled water and ethanol several times, then filtered and dried. The dried sample was grounded, and then undergone heat treatment. After heating, the sample was grounded again. Zinc oxide powder and copper oxide powder were also fabricated using chemical precipitation method. X-Ray Diffraction measurements of the coupled CuO/ZnO powder showed the presence of CuO and ZnO in the fabricated sample. Furthermore, other peaks shown by XRD were also identified corresponding to copper, copper (II) oxide, copper sulfate and zinc sulfate. Results of the photocatalytic activity investigation show that the sample exhibited superior photocatalytic degradation of methyl orange under visible light illumination compared to copper oxide powder and zinc oxide powder. This may be attributed to the lower energy gap at the copper oxide-zinc oxide interface, compared to zinc oxide, allowing visible light to trigger its photocatalytic activity.