Abstract

Photocatalysis has emerged as an environmentally friendly technology to develop selective reactions such as the oxidation of alcohol to aldehydes. Graphitic carbon nitride (CN) is a metal-free polymeric structure easily photoactivated under radiation. This work focuses on the enhancement of the photocatalytic activity of bare CN by doping it with phosphorous (P-CN). Different doping levels of P (2–12 wt.) have been explored and the samples were fully characterized by XRD, FTIR, N2 physisorption, elemental analysis, XPS, DRS-UV–visible, and photoluminescence. A better activity and enhanced selectivity were observed in the P-CN samples if compared to the undoped CN in the oxidation of cinnamyl alcohol to cinnamaldehyde in aqueous solution. The presence of P was demonstrated to contribute to a better delocalization of photo-generated charges. Moreover, the reactivity and selectivity of the CN and P-CN samples were analyzed in water-acetonitrile mixtures, appreciating a better selectivity in the presence of acetonitrile to the detriment of the conversion of the cinnamyl alcohol. The photocatalytic oxidation mechanism over P-CN in aqueous media has been tentatively proposed based on the influence of the reactive oxidative species generated in the process by chemical scavenger tests. They suggested the contribution of superoxide radicals with more selectivity than the photo-generated holes, the second reactive species of importance in the overall oxidation scheme. The contribution of hydroxyl radicals was discharged since its presence was negligible in a probe test based on the formation of 2-hydroxy-terephthalic acid.

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.