Embedding Thiophene-Amide into g-C<sub>3</sub>N<sub>4</sub> Skeleton with Induction and Delocalization Effects for High Photocatalytic H<sub>2</sub> Evolution

Molecular skeleton modification has become a recognized method that can effectively improve the photocatalytic performance of g-C<sub>3</sub>N<sub>4</sub> because it not only effectively promotes charge separation, but also tunes the conjugated system of g-C<sub>3</s...

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Main Authors: Shuang Tang, Yang-Sen Xu, Wei-De Zhang
Format: Article
Language:English
Published: MDPI AG 2022-09-01
Series:Catalysts
Subjects:
Online Access:https://www.mdpi.com/2073-4344/12/9/1043
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author Shuang Tang
Yang-Sen Xu
Wei-De Zhang
author_facet Shuang Tang
Yang-Sen Xu
Wei-De Zhang
author_sort Shuang Tang
collection DOAJ
description Molecular skeleton modification has become a recognized method that can effectively improve the photocatalytic performance of g-C<sub>3</sub>N<sub>4</sub> because it not only effectively promotes charge separation, but also tunes the conjugated system of g-C<sub>3</sub>N<sub>4</sub> to make it more conducive to photocatalytic reaction. Herein, thiophene-amide embedded g-C<sub>3</sub>N<sub>4</sub> (TA-CN-x) was successfully prepared by simple one-step thermal polycondensation using urea as a precursor and ethyl-2-amino-4-phenylthiophene-3-carboxylate (EAPC) as an additive. After embedding with thiophene-amide, the induction and delocalization effects are formed in TA-CN-x, which significantly improves the migration efficiency of photogenerated charge carriers. Meanwhile, the conjugate structure is changed due to structural modification, resulting in significant enhancement of visible light absorption compared to the pure g-C<sub>3</sub>N<sub>4</sub> (CN). Specifically, the optimized photocatalytic H<sub>2</sub> evolution rate of TA-CN-2 reaches 245.4 μmol·h<sup>−1</sup>, which is 8.4 times that of CN (with Pt nanoparticles as a co-catalyst), and the apparent quantum efficiency (AQY) at 450 nm is 13.6%. This work opens up a new modification process for fully tapping the photocatalytic hydrogen absorption potential of g-C<sub>3</sub>N<sub>4</sub>-based materials.
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spelling doaj.art-e5e10abb00f942d5a937e1e741e7a3e32023-11-23T15:31:26ZengMDPI AGCatalysts2073-43442022-09-01129104310.3390/catal12091043Embedding Thiophene-Amide into g-C<sub>3</sub>N<sub>4</sub> Skeleton with Induction and Delocalization Effects for High Photocatalytic H<sub>2</sub> EvolutionShuang Tang0Yang-Sen Xu1Wei-De Zhang2School of Chemistry and Chemical Engineering, South China University of Technology, 381 Wushan Road, Guangzhou 510640, ChinaInstitute of Information Technology, Shenzhen Institute of Information Technology, Shenzhen 518172, ChinaSchool of Chemistry and Chemical Engineering, South China University of Technology, 381 Wushan Road, Guangzhou 510640, ChinaMolecular skeleton modification has become a recognized method that can effectively improve the photocatalytic performance of g-C<sub>3</sub>N<sub>4</sub> because it not only effectively promotes charge separation, but also tunes the conjugated system of g-C<sub>3</sub>N<sub>4</sub> to make it more conducive to photocatalytic reaction. Herein, thiophene-amide embedded g-C<sub>3</sub>N<sub>4</sub> (TA-CN-x) was successfully prepared by simple one-step thermal polycondensation using urea as a precursor and ethyl-2-amino-4-phenylthiophene-3-carboxylate (EAPC) as an additive. After embedding with thiophene-amide, the induction and delocalization effects are formed in TA-CN-x, which significantly improves the migration efficiency of photogenerated charge carriers. Meanwhile, the conjugate structure is changed due to structural modification, resulting in significant enhancement of visible light absorption compared to the pure g-C<sub>3</sub>N<sub>4</sub> (CN). Specifically, the optimized photocatalytic H<sub>2</sub> evolution rate of TA-CN-2 reaches 245.4 μmol·h<sup>−1</sup>, which is 8.4 times that of CN (with Pt nanoparticles as a co-catalyst), and the apparent quantum efficiency (AQY) at 450 nm is 13.6%. This work opens up a new modification process for fully tapping the photocatalytic hydrogen absorption potential of g-C<sub>3</sub>N<sub>4</sub>-based materials.https://www.mdpi.com/2073-4344/12/9/1043photocatalystsg-C<sub>3</sub>N<sub>4</sub>thiophene-amideembeddinginduction effectdelocalization effect
spellingShingle Shuang Tang
Yang-Sen Xu
Wei-De Zhang
Embedding Thiophene-Amide into g-C<sub>3</sub>N<sub>4</sub> Skeleton with Induction and Delocalization Effects for High Photocatalytic H<sub>2</sub> Evolution
Catalysts
photocatalysts
g-C<sub>3</sub>N<sub>4</sub>
thiophene-amide
embedding
induction effect
delocalization effect
title Embedding Thiophene-Amide into g-C<sub>3</sub>N<sub>4</sub> Skeleton with Induction and Delocalization Effects for High Photocatalytic H<sub>2</sub> Evolution
title_full Embedding Thiophene-Amide into g-C<sub>3</sub>N<sub>4</sub> Skeleton with Induction and Delocalization Effects for High Photocatalytic H<sub>2</sub> Evolution
title_fullStr Embedding Thiophene-Amide into g-C<sub>3</sub>N<sub>4</sub> Skeleton with Induction and Delocalization Effects for High Photocatalytic H<sub>2</sub> Evolution
title_full_unstemmed Embedding Thiophene-Amide into g-C<sub>3</sub>N<sub>4</sub> Skeleton with Induction and Delocalization Effects for High Photocatalytic H<sub>2</sub> Evolution
title_short Embedding Thiophene-Amide into g-C<sub>3</sub>N<sub>4</sub> Skeleton with Induction and Delocalization Effects for High Photocatalytic H<sub>2</sub> Evolution
title_sort embedding thiophene amide into g c sub 3 sub n sub 4 sub skeleton with induction and delocalization effects for high photocatalytic h sub 2 sub evolution
topic photocatalysts
g-C<sub>3</sub>N<sub>4</sub>
thiophene-amide
embedding
induction effect
delocalization effect
url https://www.mdpi.com/2073-4344/12/9/1043
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