4.6 Article

High photocatalytic activity of Cu2O embedded in hierarchically hollow SiO2for efficient chemoselective hydrogenation of nitroarenes

Journal

JOURNAL OF MATERIALS SCIENCE
Volume 56, Issue 5, Pages 3874-3886

Publisher

SPRINGER
DOI: 10.1007/s10853-020-05449-x

Keywords

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Funding

  1. National Natural Science Foundation of China [21876069]
  2. Six Talent Peaks Project in Jiangsu [XCL-018]
  3. EPSRC [EP/P022863/1] Funding Source: UKRI

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A SiO2-Cu2O@SiO2 photocatalyst was constructed for efficient hydrogenation of nitroarenes in an aqueous system, successfully overcoming the strict hydrogenation conditions requirement. The confinement effect promotes the contact probability between hydrogen atoms and nitroarene molecules, ensuring high efficiency and selectivity of the reaction. This study demonstrates the promising industrial applications of visible-light catalytic hydrogenation of nitroarenes.
Photocatalytic organic conversion is a crucial process in the hydrogenation of nitroarenes, but harsh reaction conditions such as long reaction time, high hydrogen pressure, and organic medium still need to be considerably overcome under visible-light irradiation. Here, we have constructed a transition metal oxide photocatalyst by embedding low-cost Cu2O with strong visible-light absorption into hierarchically hollow SiO(2)sphere (SiO2-Cu2O@SiO2) that can suppress the escape of photogenerated atomic hydrogen and promote the contact probability between hydrogen atom and nitroarene molecules due to confinement effect. Remarkably, the SiO2-Cu2O@SiO(2)photocatalyst can exhibit efficient chemoselectivity toward the hydrogenation of various nitroarenes in an aqueous system at ambient conditions, successfully working out the requirement of strict hydrogenation conditions, especially for organic medium over almost all of the reported photocatalysts. Notably, quantitative aniline can be produced for the visible-light catalytic reduction of nitroarenes, suggesting a considerable potential for industrial applications. Graphic abstract

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