Abstract
Hetero-structured CoTiO3 nano-composite photocatalyst was produced by a modified sol–gel process diethylene glycol as as stabilizer and coated on glass as a thin film by Doctor Blade coating. CoTiO3 nano-composites were calcinated at 550, 650 and 750 °C to study the structure and phase formation of CoTiO3 nano-composites. X-ray diffraction results showed that the pure CoTiO3 nano-crystalline phase is formed at 650 °C while Co3O4 and TiO2 were present as impurities at 550 and 750 °C annealing temperatures. Field emission scanning electron microscopy and energy dispersive X-ray spectroscopy analysis of hetero-structured CoTiO3 nano-composite coated on a glass reveal the formation of spherical shape of nano-crystalline phases with an average size of 75 nm. The Fourier transform infrared spectroscopy results showed the existence of Co–O, Ti–O, and Ti–O–Co bonds. Thermogravimetric and derivative thermogravimetric analysis show that the weight loss phases are completed at 750 °C with peak temperatures of 107 and 345 °C. The UV–vis diffuse reflectance spectra reveal the optical band gaps of 1.587 eV (781 nm) and 2.079 eV (596 nm). Photocatalytic activity of hetero-structured CoTiO3 nano-composite photocatalyst was examined for degradation of Nile blue dye and the results showed complete degradation in 2.5 h of light irradiation. This is attributed to the efficient separation of electron–hole pairs of the CoTiO3 nano-composite, narrow band gap, and visible-light harvesting ability.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
More From: Journal of Materials Science: Materials in Electronics
Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.