Photocatalytic efficiency improvement of Z-scheme CeO<inf>2</inf>/BiOI heterostructure for RHB degradation and benzylamine oxidation under visible light irradiation

© 2020 Taiwan Institute of Chemical Engineers The Z-scheme CeO2/BiOI (C/B) was prepared and evaluated for its photocatalytic RhB degradation and selective oxidation of benzylamine to N-benzylidenebenzylamine under visible light irradiation. Close contacts and chemical interactions between CeO2 and B...

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Main Authors: Kanlayawat Wangkawong, Sukon Phanichphant, Doldet Tantraviwat, Burapat Inceesungvorn
Format: Journal
Published: 2020
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http://cmuir.cmu.ac.th/jspui/handle/6653943832/68286
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Institution: Chiang Mai University
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spelling th-cmuir.6653943832-682862020-04-02T15:24:37Z Photocatalytic efficiency improvement of Z-scheme CeO<inf>2</inf>/BiOI heterostructure for RHB degradation and benzylamine oxidation under visible light irradiation Kanlayawat Wangkawong Sukon Phanichphant Doldet Tantraviwat Burapat Inceesungvorn Chemical Engineering Chemistry © 2020 Taiwan Institute of Chemical Engineers The Z-scheme CeO2/BiOI (C/B) was prepared and evaluated for its photocatalytic RhB degradation and selective oxidation of benzylamine to N-benzylidenebenzylamine under visible light irradiation. Close contacts and chemical interactions between CeO2 and BiOI which are important for efficient charge transfer in the heterojunction were revealed by HRTEM and XPS studies. The C/B heterostructure presented nearly 1.5 and 8.0 times higher RhB degradation activity than BiOI and CeO2, respectively. The activity of C/B in oxidative coupling of benzylamine was also firstly revealed and found to be more than 2 times higher than both BiOI and CeO2. Such enhanced photocatalytic performance of the C/B is ascribed to the combined effects of extended visible-light absorption range, increased surface area and improved charge transfer efficiency as evidenced from BET, UV–vis DRS and photoelectrochemical studies. Based on XPS, UV–vis DRS, Mott-Schottky plots and active species quenching results, a Z-scheme charge transfer where photogenerated electron-hole pairs can be effectively separated is proposed for the C/B and h+ and O2●– are key active species responsible for RhB degradation and N-benzylidenebenzylamine formation. The present work highlights the enhancement of photocatalytic activity based on Z-scheme heterojunction formation and reveals a further application of photocatalysts in organic fine chemical syntheses. 2020-04-02T15:24:21Z 2020-04-02T15:24:21Z 2020-03-01 Journal 18761070 2-s2.0-85078735518 10.1016/j.jtice.2020.01.003 https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85078735518&origin=inward http://cmuir.cmu.ac.th/jspui/handle/6653943832/68286
institution Chiang Mai University
building Chiang Mai University Library
country Thailand
collection CMU Intellectual Repository
topic Chemical Engineering
Chemistry
spellingShingle Chemical Engineering
Chemistry
Kanlayawat Wangkawong
Sukon Phanichphant
Doldet Tantraviwat
Burapat Inceesungvorn
Photocatalytic efficiency improvement of Z-scheme CeO<inf>2</inf>/BiOI heterostructure for RHB degradation and benzylamine oxidation under visible light irradiation
description © 2020 Taiwan Institute of Chemical Engineers The Z-scheme CeO2/BiOI (C/B) was prepared and evaluated for its photocatalytic RhB degradation and selective oxidation of benzylamine to N-benzylidenebenzylamine under visible light irradiation. Close contacts and chemical interactions between CeO2 and BiOI which are important for efficient charge transfer in the heterojunction were revealed by HRTEM and XPS studies. The C/B heterostructure presented nearly 1.5 and 8.0 times higher RhB degradation activity than BiOI and CeO2, respectively. The activity of C/B in oxidative coupling of benzylamine was also firstly revealed and found to be more than 2 times higher than both BiOI and CeO2. Such enhanced photocatalytic performance of the C/B is ascribed to the combined effects of extended visible-light absorption range, increased surface area and improved charge transfer efficiency as evidenced from BET, UV–vis DRS and photoelectrochemical studies. Based on XPS, UV–vis DRS, Mott-Schottky plots and active species quenching results, a Z-scheme charge transfer where photogenerated electron-hole pairs can be effectively separated is proposed for the C/B and h+ and O2●– are key active species responsible for RhB degradation and N-benzylidenebenzylamine formation. The present work highlights the enhancement of photocatalytic activity based on Z-scheme heterojunction formation and reveals a further application of photocatalysts in organic fine chemical syntheses.
format Journal
author Kanlayawat Wangkawong
Sukon Phanichphant
Doldet Tantraviwat
Burapat Inceesungvorn
author_facet Kanlayawat Wangkawong
Sukon Phanichphant
Doldet Tantraviwat
Burapat Inceesungvorn
author_sort Kanlayawat Wangkawong
title Photocatalytic efficiency improvement of Z-scheme CeO<inf>2</inf>/BiOI heterostructure for RHB degradation and benzylamine oxidation under visible light irradiation
title_short Photocatalytic efficiency improvement of Z-scheme CeO<inf>2</inf>/BiOI heterostructure for RHB degradation and benzylamine oxidation under visible light irradiation
title_full Photocatalytic efficiency improvement of Z-scheme CeO<inf>2</inf>/BiOI heterostructure for RHB degradation and benzylamine oxidation under visible light irradiation
title_fullStr Photocatalytic efficiency improvement of Z-scheme CeO<inf>2</inf>/BiOI heterostructure for RHB degradation and benzylamine oxidation under visible light irradiation
title_full_unstemmed Photocatalytic efficiency improvement of Z-scheme CeO<inf>2</inf>/BiOI heterostructure for RHB degradation and benzylamine oxidation under visible light irradiation
title_sort photocatalytic efficiency improvement of z-scheme ceo<inf>2</inf>/bioi heterostructure for rhb degradation and benzylamine oxidation under visible light irradiation
publishDate 2020
url https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85078735518&origin=inward
http://cmuir.cmu.ac.th/jspui/handle/6653943832/68286
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