LAUSR.org creates dashboard-style pages of related content for over 1.5 million academic articles. Sign Up to like articles & get recommendations!

Photoelectrocatalytic activity of immobilized Yb doped WO 3 photocatalyst for degradation of methyl orange dye

Photo by nikhilmitra from unsplash

Pure WO3 and Yb:WO3 thin films have been synthesized by spray pyrolysis technique. Effect of Yb doping concentration on photoelectrochemical, structural, morphological and optical properties of thin films are studied.… Click to show full abstract

Pure WO3 and Yb:WO3 thin films have been synthesized by spray pyrolysis technique. Effect of Yb doping concentration on photoelectrochemical, structural, morphological and optical properties of thin films are studied. X-ray diffraction analysis shows that all thin films are polycrystalline nature and exhibit monoclinic crystal structure. The 3 at% Yb:WO3 film shows superior photoelectrochemical (PEC) performance than that of pure WO3 film and it shows maximum photocurrent density (Iph = 1090 µA/cm2) having onset potentials around +0.3 V/SCE in 0.01 M HClO4. The photoelectrocatalytic process is more effective than that of the photocatalytic process for degradation of methyl orange (MO) dye. Yb doping in WO3 photocatalyst is greatly effective to degrade MO dye. The enhancement in photoelectrocatalytic activity is mainly due to the suppressing the recombination rate of photogenerated electron-hole pairs. The mineralization of MO dye in aqueous solution is studied by measuring chemical oxygen demand (COD) values.

Keywords: photoelectrocatalytic activity; degradation methyl; methyl orange; orange dye; wo3

Journal Title: Journal of Energy Chemistry
Year Published: 2017

Link to full text (if available)


Share on Social Media:                               Sign Up to like & get
recommendations!

Related content

More Information              News              Social Media              Video              Recommended



                Click one of the above tabs to view related content.