Abstract

In this work, Co-doped titanate nanotubes decorated with Cu2O/CuO nanoparticle heterostructures (TNTs-Co-Cu) were successfully synthesized by hydrothermal method followed by an impregnation method. The photocatalysts were characterized by TEM, XRD, Raman spectroscopy, XPS, N2 adsorption/desorption, DRS, and Photoluminescence. The results confirm the success of the TNTs-Co-Cu heterojunctions synthesis and the excellent absorption exhibited in the visible light region. Furthermore, the photocatalytic activity of the TNTs-Co-Cu materials was higher than that of pure titanate nanotubes (TNTs) and doped with cobalt (TNTs-Co) for Methyl Blue (MB) photodegradation under UV and visible light irradiation. The improved photocatalytic activity may can explained due to the increased the lifetime of photogenerated electron/hole pairs. The photocatalytic mechanism study suggested that the photogenerated electrons in conduction band (CB) of the Cu2O flow through the CuO CB to CB of TNTs-Co, whereas the photogenerated holes migrate in the opposite direction. These transfers result in the production of O2– and OH radicals to promote the photooxidation reaction of MB. This study provides the understanding on the heterojunction mechanism of the MB photodegradation by TNTs-Co-Cu under UV irradiation and shows their high photocatalytic activity after 5 cycles, which make the TNTs-Co-Cu a promising photocatalyst for the multifunctional heterogeneous photocatalysis applications.

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.