4.6 Article

Photocatalytic coupled redox cycle for two organic transformations over Pd/carbon nitride composites

Journal

CATALYSIS SCIENCE & TECHNOLOGY
Volume 9, Issue 18, Pages 5077-5089

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c9cy01382b

Keywords

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Funding

  1. National Natural Science Foundation of China [21872089, 21503127]
  2. Natural Science Basic Research Plan in Shaanxi Province of China [2017JM2008]
  3. Fundamental Research Funds for the Central Universities [GK201903038]
  4. 111 Project [B14041]

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Heterogeneous photocatalysis offers a means for green organic transformations. Generally, photogenerated electrons and holes are not utilized simultaneously and effectively. Here we report a coupling approach to promote simultaneously two organic transformations of the Ullmann C-C coupling reaction and the value-added aromatic alcohol oxidation reaction in inert solvent and under anaerobic conditions using a carbon nitride based composite (Pd/CN-450) prepared by loading Pd nanoparticles (NPs) on CN-450 (N defect and O dopant co-modified g-C3N4 with high crystallinity). Upon photo-excitation of the photocatalyst, the activation of carbon-halogen bonds of the adsorbed aryl halides can be promoted by the photogenerated electrons on Pd NPs and the aromatic alcohols undergo dissociation and dehydrogenation, and finally can be oxidized by the captured photogenerated holes from CN-450 in the presence of a Bronsted base. N defects, O doping, and improved crystallinity, controlled by changing the post-annealing temperature in molten salts, enhance the visible light absorption and improve charger carrier separation of the functionalized carbon nitride. The smaller size and high dispersity of Pd NPs give the higher surface area-to-volume ratio resulting in efficient adsorption and activation of reactant molecules on Pd NPs and allow for the effective interfacial interaction of CN-450 with Pd NPs for promoting electron transfer from CN-450 to Pd NPs. As a result, Pd/CN-450 displays a superior photocatalytic activity of the coupled reaction compared to Pd/g-C3N4 (Pd NP supported pristine g-C3N4). Moreover, the coupled reaction system has general applicability for various substrates and shows reusability.

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