| Authors | Maasoumeh Jafarpour, |
| Journal | Inorganic Chemistry |
| Page number | 9484-9495 |
| Serial number | 60 |
| Volume number | 13 |
| Paper Type | Full Paper |
| Published At | 2021 |
| Journal Grade | ISI |
| Journal Type | Typographic |
| Journal Country | Iran, Islamic Republic Of |
| Journal Index | JCR،Scopus |
Abstract
An unprecedented visible-light-driven photocatalytic
system consisting of Pd nanoparticles stabilized on g-C3N4-
imine-functionalized TiO2 nanoparticles was discovered for
photoassisted hydrogen generation followed by olefin hydrogenation
under mild conditions. The structural integrity of the assynthesized
photocatalyst was corroborated by Fourier transform
infrared spectroscopy, X-ray powder diffraction, energy-dispersive
X-ray spectroscopy, inductively coupled plasma atomic emission
spectroscopy, X-ray photoelectron spectroscopy, ultraviolet-diffuse
reflectance spectroscopy, Brunauer−Emmett−Teller measurements,
and thermogravimetric analysis (TGA). Transmission
electron microscopy and high-resolution scanning electron
microscopy revealed the nanoscopic nature of the catalyst. The
photocatalyst promoted several different transformations in a onepot
reaction sequence: hydrogen evolution through photocatalytic acceptorless formation of benzimidazoles as important
therapeutic agents followed by visible-light-driven photocatalytic reduction of olefins with a high hydrogen utilization efficiency of up
to 92% under mild conditions. A significant volume of H2 was produced under blue light-emitting diode (LED) irradiation during
the selective formation of benzimidazole, while the selectivity reduced significantly under a Xe lamp or in the dark. The in situgenerated
H2 could be activated by the as-prepared Pd-C3N4-imine/TiO2 photocatalyst to effectively hydrogenate olefins under mild
conditions at appropriate time exposed to blue LED irradiation. The light-dependent photocatalytic performance of the title catalyst
was assessed using action spectra by calculating the apparent quantum efficiency (AQE), which exhibited the maximum AQEs at 410
and 550 nm, at which the highest performance for styrene hydrogenation was obtained. The improved photoredox activity of the
title nanohybrid could be caused by the synergistic effects of the heterojunction of carbon nitride-Pd on TiO2 nanoparticles
evidenced by photoluminescence spectra and catalytic reactions. The catalyst proved to be air-stable, robust, recyclable, and very
active in the absence of any undesirable additives and reducing agents. Thus, this work presents a new protocol for improving the
photocatalytic properties of semiconducting materials for various photocatalytic applications under environmentally friendly
conditions.
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