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- Language
- English
- Conflict of Interest
- In relation to this article, we declare that there is no conflict of interest.
- Publication history
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Received January 29, 2024
Accepted May 8, 2024
- This is an Open-Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/bync/3.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
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Deposition of Ag@AgCl onto Flower-Like BiOCl for Promoting the Degradation of Methyl Orange: The Narrow Bandgap and Surface Plasmon Resonance Eff ect
Abstract
Photocatalysis technology is considered as a most promising method to decompose organic pollutant since the inexhaustible
solar energy and facile reaction condition. Herein, a series of fl ower-like Ag/AgCl/BiOCl photocatalysts are successfully
synthesized via hydrothermal and photochemical deposition method. All the samples are investigated and characterized by
X-Ray diff raction, Scanning electron microscopy, transmission electron microscope, ultraviolet–visible spectroscopy and
Photoluminescence to insight into the microstructures and optical properties. During the photocatalytic degradation of Methyl
orange experiments, the optimized Ag/AgCl/BiOCl sample prepared by photoreduction with 40 min exhibits the excellent
photocatalytic performance. Under visible-light irradiation for 60 min, degradation rate of Methyl orange reaches 97%, which
is 9.7, 6.1 and 4.6 times higher than that of AgCl, Ag/BiOCl and BiOCl, respectively. The UV–vis diff use refl ectance and
Photoluminescence spectra of the Ag/AgCl/BiOCl photocatalyst verify that the enhanced photocatalytic activity is ascribed
to its extended absorption range to visible-light region and the effi cient separation effi ciency of photogenerated carriers. In
addition, the radical trapping experiment demonstrates that photogenerated hole and superoxide radicals play critical roles
in the methyl orange degradation. The corresponding photocatalytic degradation mechanism is proposed that the excellent
photocatalytic activity is attributed to the surface plasmon resonance eff ect of metallic Ag and heterojunction structure of
Ag/AgCl/BiOCl photocatalysts.