Please use this identifier to cite or link to this item: http://cmuir.cmu.ac.th/jspui/handle/6653943832/71840
Title: Simple preparation of nitrogen-doped TiO<inf>2</inf> and its performance in selective oxidation of benzyl alcohol and benzylamine under visible light
Authors: Mattawan Japa
Doldet Tantraviwat
Witchaya Phasayavan
Andrew Nattestad
Jun Chen
Burapat Inceesungvorn
Keywords: Chemical Engineering
Chemistry
Physics and Astronomy
Issue Date: 5-Feb-2021
Abstract: © 2020 Elsevier B.V. N-doped TiO2, denoted as T_400, was prepared simply by the facile thermal hydrolysis of TiOSO4 using NH4OH as both a precipitating agent and a nitrogen source. Compared to TiO2 without nitrogen doping, T_400 provides superior photocatalytic activity toward the selective oxidation of benzyl alcohol and benzylamine under visible light irradiation, with > 85 % conversion and > 95 % selectivity to benzaldehyde and N-benzylidenebenzylamine products, respectively. The increased photoactivity of T_400 is ascribed to enhanced visible-light absorption and efficient photogenerated charge transfer and separation as supported by UV–vis DRS, photoelectrochemical and VB-XPS results. The catalyst can tolerate the presence of substituent groups in benzyl alcohol and benzelamine molecules as > 80 % conversion and > 95 % selectivity are still achieved, which expands the scope of substrates and catalyst utilization. Band energy level of N-doped TiO2 compared to that of undoped TiO2 is determined using Mott-Schottky and UV–vis DRS measurements. Possible mechanisms for the formation of benzaldehyde and N-benzylidenebenzylamine over N-doped TiO2 are proposed. This work presents a simple synthesis of N-doped TiO2, using a low-cost and easily handled inorganic titanium salt instead of air/moisture-sensitive alkoxide precursors and reveals its potential application toward photocatalytic synthesis of organic fine chemicals under visible light.
URI: https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85094937765&origin=inward
http://cmuir.cmu.ac.th/jspui/handle/6653943832/71840
ISSN: 18734359
09277757
Appears in Collections:CMUL: Journal Articles

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