Synthesis of the TiO2/g-C3N4 photocatalyst and its photocatalytic performance for selective oxidation of alcohols

A composite photocatalyst, xTCN (xOTiO2/g-C3N4, where x represents the added quantity of graphite carbon nitride (g-C3N4)), was synthesized using a straightforward one-step hydrothermal method with H2O2 as an oxidant. The H2O2 incorporation into the xTCN composite facilitated the enrichment of oxyge...

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Main Authors: Shuangyan Meng, Bin Liu, Minglin Xie, Chaoxin Yun, Jin Qiang, Kaizhou He, Zhiwang Yang, Xiangqian Wang
Format: Article
Language:English
Published: Sociedade Brasileira de Química 2025-07-01
Series:Química Nova
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Online Access:http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0100-40422025000700303&lng=en&tlng=en
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author Shuangyan Meng
Bin Liu
Minglin Xie
Chaoxin Yun
Jin Qiang
Kaizhou He
Zhiwang Yang
Xiangqian Wang
author_facet Shuangyan Meng
Bin Liu
Minglin Xie
Chaoxin Yun
Jin Qiang
Kaizhou He
Zhiwang Yang
Xiangqian Wang
author_sort Shuangyan Meng
collection DOAJ
description A composite photocatalyst, xTCN (xOTiO2/g-C3N4, where x represents the added quantity of graphite carbon nitride (g-C3N4)), was synthesized using a straightforward one-step hydrothermal method with H2O2 as an oxidant. The H2O2 incorporation into the xTCN composite facilitated the enrichment of oxygen (O) in titanium dioxide (TiO2). This synthesis process effectively reduced the bandgap energy, minimizing the recombination of photogenerated carriers. Concurrently, an O atom was integrated into the g-C3N4 molecule, which altered its bandgap structure and enhanced the photogenerated electron-hole separation efficiency. The dual modification effect was observed when 0.9TCN was used as the catalyst, which converted 77% of benzalcohol with a selectivity exceeding 99%. Additionally, five cycles of reuse only slightly decreased the benzalcohol conversion (by 16%) and selectivity (by 9%), indicating good reusability of the xTCN photocatalyst. The xTCN photocatalyst had an unchanged molecular structure before and after the photocatalytic reaction, demonstrating its superior light stability. The potential photocatalytic reaction mechanism was explored through an active species capture experiment and a Mott-Schottky (M-S) curve test. The results of these studies suggested that •O2- and •OH were the primary reactive species in the photocatalytic reaction.
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spelling doaj-art-eb9f3dfb839a4cd7acdc3d30382885582025-08-20T03:51:18ZengSociedade Brasileira de QuímicaQuímica Nova1678-70642025-07-0148710.21577/0100-4042.20250155Synthesis of the TiO2/g-C3N4 photocatalyst and its photocatalytic performance for selective oxidation of alcoholsShuangyan Menghttps://orcid.org/0009-0003-5431-4048Bin LiuMinglin XieChaoxin YunJin QiangKaizhou HeZhiwang YangXiangqian Wanghttps://orcid.org/0009-0009-1923-7538A composite photocatalyst, xTCN (xOTiO2/g-C3N4, where x represents the added quantity of graphite carbon nitride (g-C3N4)), was synthesized using a straightforward one-step hydrothermal method with H2O2 as an oxidant. The H2O2 incorporation into the xTCN composite facilitated the enrichment of oxygen (O) in titanium dioxide (TiO2). This synthesis process effectively reduced the bandgap energy, minimizing the recombination of photogenerated carriers. Concurrently, an O atom was integrated into the g-C3N4 molecule, which altered its bandgap structure and enhanced the photogenerated electron-hole separation efficiency. The dual modification effect was observed when 0.9TCN was used as the catalyst, which converted 77% of benzalcohol with a selectivity exceeding 99%. Additionally, five cycles of reuse only slightly decreased the benzalcohol conversion (by 16%) and selectivity (by 9%), indicating good reusability of the xTCN photocatalyst. The xTCN photocatalyst had an unchanged molecular structure before and after the photocatalytic reaction, demonstrating its superior light stability. The potential photocatalytic reaction mechanism was explored through an active species capture experiment and a Mott-Schottky (M-S) curve test. The results of these studies suggested that •O2- and •OH were the primary reactive species in the photocatalytic reaction.http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0100-40422025000700303&lng=en&tlng=enTiO2g-C3N4visible light catalysisselective oxidation of alcohol.
spellingShingle Shuangyan Meng
Bin Liu
Minglin Xie
Chaoxin Yun
Jin Qiang
Kaizhou He
Zhiwang Yang
Xiangqian Wang
Synthesis of the TiO2/g-C3N4 photocatalyst and its photocatalytic performance for selective oxidation of alcohols
Química Nova
TiO2
g-C3N4
visible light catalysis
selective oxidation of alcohol.
title Synthesis of the TiO2/g-C3N4 photocatalyst and its photocatalytic performance for selective oxidation of alcohols
title_full Synthesis of the TiO2/g-C3N4 photocatalyst and its photocatalytic performance for selective oxidation of alcohols
title_fullStr Synthesis of the TiO2/g-C3N4 photocatalyst and its photocatalytic performance for selective oxidation of alcohols
title_full_unstemmed Synthesis of the TiO2/g-C3N4 photocatalyst and its photocatalytic performance for selective oxidation of alcohols
title_short Synthesis of the TiO2/g-C3N4 photocatalyst and its photocatalytic performance for selective oxidation of alcohols
title_sort synthesis of the tio2 g c3n4 photocatalyst and its photocatalytic performance for selective oxidation of alcohols
topic TiO2
g-C3N4
visible light catalysis
selective oxidation of alcohol.
url http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0100-40422025000700303&lng=en&tlng=en
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