Preparation of CdS@TiO2/Ni2P photocatalyst for value-added organic transformation coupling with enhanced hydrogen evolution

In a dual-functional photocatalytic reaction system with coupled selective organic reductions and oxidation reaction, both the photogenerated electrons and holes can be simultaneously utilized to generate value-added products, make the overall process more valuable from a sustainability and economic...

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Autores principales: Yuangang Li, Shaosen Shi, Weike Shang, Huajing Li, Lihua Shen, Anning Zhou
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Lenguaje:EN
Publicado: Elsevier 2021
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spelling oai:doaj.org-article:afd69deed70c4478b2be6ed81872ed052021-12-04T04:36:28ZPreparation of CdS@TiO2/Ni2P photocatalyst for value-added organic transformation coupling with enhanced hydrogen evolution2666-934X10.1016/j.jciso.2021.100035https://doaj.org/article/afd69deed70c4478b2be6ed81872ed052021-12-01T00:00:00Zhttp://www.sciencedirect.com/science/article/pii/S2666934X21000349https://doaj.org/toc/2666-934XIn a dual-functional photocatalytic reaction system with coupled selective organic reductions and oxidation reaction, both the photogenerated electrons and holes can be simultaneously utilized to generate value-added products, make the overall process more valuable from a sustainability and economic perspective. Herein, CdS&P25–Ni2P (SPN) has been synthesized, which realized the selective transformation of organic compounds coupled with hydrogen evolution under visible light condition. The traditional sacrificial agent oxidation reaction is replaced by the dehydrogenation half reaction of aromatic alcohol with higher additional value, where high efficiency photocatalytic reaction can be realized. The effects of solvent, substituents, component of photocatalyst, co-catalyst loading and other factors on this reaction were explored. Under the optimal conditions, the substrate was almost completely transformed within 5 ​h, and the hydrogen production rate can reach 1.148 ​mmol·gcat−1·h−1. Through compare the research of different reaction systems, different possible reaction mechanisms and reaction paths have been proposed. This paper further explores the field of organic value-added transformation coupled with hydrogen production and provides a new strategy for the effective use of photogenerated electrons and holes, which will be inspirational for the future involving catalysis, materials and other fields.Yuangang LiShaosen ShiWeike ShangHuajing LiLihua ShenAnning ZhouElsevierarticleSelective organic transformationsValue-added chemicalsDual-functional photocatalytic systemsSolar fuelPhotocatalysisPhysical and theoretical chemistryQD450-801Chemical technologyTP1-1185ENJCIS Open, Vol 4, Iss , Pp 100035- (2021)
institution DOAJ
collection DOAJ
language EN
topic Selective organic transformations
Value-added chemicals
Dual-functional photocatalytic systems
Solar fuel
Photocatalysis
Physical and theoretical chemistry
QD450-801
Chemical technology
TP1-1185
spellingShingle Selective organic transformations
Value-added chemicals
Dual-functional photocatalytic systems
Solar fuel
Photocatalysis
Physical and theoretical chemistry
QD450-801
Chemical technology
TP1-1185
Yuangang Li
Shaosen Shi
Weike Shang
Huajing Li
Lihua Shen
Anning Zhou
Preparation of CdS@TiO2/Ni2P photocatalyst for value-added organic transformation coupling with enhanced hydrogen evolution
description In a dual-functional photocatalytic reaction system with coupled selective organic reductions and oxidation reaction, both the photogenerated electrons and holes can be simultaneously utilized to generate value-added products, make the overall process more valuable from a sustainability and economic perspective. Herein, CdS&P25–Ni2P (SPN) has been synthesized, which realized the selective transformation of organic compounds coupled with hydrogen evolution under visible light condition. The traditional sacrificial agent oxidation reaction is replaced by the dehydrogenation half reaction of aromatic alcohol with higher additional value, where high efficiency photocatalytic reaction can be realized. The effects of solvent, substituents, component of photocatalyst, co-catalyst loading and other factors on this reaction were explored. Under the optimal conditions, the substrate was almost completely transformed within 5 ​h, and the hydrogen production rate can reach 1.148 ​mmol·gcat−1·h−1. Through compare the research of different reaction systems, different possible reaction mechanisms and reaction paths have been proposed. This paper further explores the field of organic value-added transformation coupled with hydrogen production and provides a new strategy for the effective use of photogenerated electrons and holes, which will be inspirational for the future involving catalysis, materials and other fields.
format article
author Yuangang Li
Shaosen Shi
Weike Shang
Huajing Li
Lihua Shen
Anning Zhou
author_facet Yuangang Li
Shaosen Shi
Weike Shang
Huajing Li
Lihua Shen
Anning Zhou
author_sort Yuangang Li
title Preparation of CdS@TiO2/Ni2P photocatalyst for value-added organic transformation coupling with enhanced hydrogen evolution
title_short Preparation of CdS@TiO2/Ni2P photocatalyst for value-added organic transformation coupling with enhanced hydrogen evolution
title_full Preparation of CdS@TiO2/Ni2P photocatalyst for value-added organic transformation coupling with enhanced hydrogen evolution
title_fullStr Preparation of CdS@TiO2/Ni2P photocatalyst for value-added organic transformation coupling with enhanced hydrogen evolution
title_full_unstemmed Preparation of CdS@TiO2/Ni2P photocatalyst for value-added organic transformation coupling with enhanced hydrogen evolution
title_sort preparation of cds@tio2/ni2p photocatalyst for value-added organic transformation coupling with enhanced hydrogen evolution
publisher Elsevier
publishDate 2021
url https://doaj.org/article/afd69deed70c4478b2be6ed81872ed05
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