Abstract

This work reports an efficient method to prepare In2O3/TiO2 heterojunction photocatalysts containing different micro-structures including nanorods (ITNR) and nanocubes (ITNC) with a coordination chemical approach followed by thermal treatments. The as-prepared materials were characterized by various physicochemical tests, to verify the structural properties and the associated photocatalytic properties. In addition, malachite green (MG) dye and ethanol were used to examine their photooxidation properties. Both experiments demonstrated the photocatalytic activity of the as-prepared samples were in the order of ITNC > ITNR > TiO2 > In2O3. This tendency implied that the formation of semiconductor-semiconductor heterojunction in ITNC and ITNR. Reduced the lower recombination rate of electron-hole pair, along with the lower electrical resistance, and higher OH adsorption sites. In addition, ITNC has a larger surface area and a wide absorption spectrum under visible light region than that of the ITNR. The scavenger study of dye degradation shows that more than 70% of the MG dye was degraded through OH radicals, which was further confirmed by the diffuse reflectance infrared Fourier transform spectroscopy (DRIFT). The results illustrated the adsorbed gas-phase ethanol was converted to CO2 and H2O through different reaction pathways, which revealed that both surface-adsorbed OH radicals and the photogenerated holes were contributed to the higher photocatalytic activity.

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

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.