4.6 Article

Visible-Light-Driven Photocatalytic Oxidation of 5-Hydroxymethylfurfural to 2,5-Furandicarboxylic Acid over Plasmonic Au/ZnO Catalyst

期刊

ACS SUSTAINABLE CHEMISTRY & ENGINEERING
卷 10, 期 27, 页码 8778-8787

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acssuschemeng.2c01143

关键词

HMF; FDCA; photocatalysis; oxygen vacancy; H-2 treatment; Au; ZnO

资金

  1. Key Research & Development Program of Jiangsu Province [BE2020039]
  2. National Natural Science Foundation of China [32071723]

向作者/读者索取更多资源

This study fabricated Au/ZnO catalysts with different oxygen vacancies and used them for the photocatalytic oxidation of HMF to FDCA. The catalysts exhibited high selectivity and activity due to the localized surface plasmon resonance effect, oxygen vacancies, and the existence of the Schottky barrier. The Au/ZnODP-H catalyst treated by H2 showed the best performance, achieving high conversion of HMF and selectivity of FDCA.
Photocatalytic oxidation of 5-hydroxymethylfurfural (HMF) to 2,5-furandicarboxylic acid (FDCA) is an environmental friendly way to convert platform molecules into high-value chemicals. Here, Au/ZnO catalysts with different oxygen vacancies were fabricated by the deposition precipitation method and were used for the photocatalytic oxidation of HMF to FDCA under visible light irradiation. All of the Au/ZnO catalysts showed excellent photocatalytic oxidation selectivity to FDCA greater than 90% under mild conditions. The Au/ZnODP-H catalyst treated by H2 afforded the highest HMF conversion and the selectivities of FDCA up to 96.9%. The localized surface plasmon resonance effect of Au nanoparticles, oxygen vacancy, and the existence of the Schottky barrier enhance the separation and transfer efficiency of photogenerated electron-hole pairs of the catalyst, so as to enhance its photocatalytic activity. The active species trapping experiment and electron spin resonance analysis showed that center dot O2- and h+ were the active species responsible for the oxidation reaction. The recycle experiment also proved that the catalyst has good stability. This work provides a new strategy for the design of photocatalysts for converting biomass into high-value chemicals.

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