TY - JOUR
T1 - Controlled Microwave-Assisted Synthesis of the 2D-BiOCl/2D-g-C 3 N 4 Heterostructure for the Degradation of Amine-Based Pharmaceuticals under Solar Light Illumination
AU - Al Marzouqi, Faisal
AU - Al Farsi, Basim
AU - Kuvarega, Alex T.
AU - Al Lawati, Haider A.J.
AU - Al Kindy, Salma M.Z.
AU - Kim, Younghun
AU - Selvaraj, Rengaraj
N1 - Funding Information:
R.S. wishes to thank the Sultan Qaboos University for providing financial support to carry out this work under SQU-SA joint collaborative research grant (CL/SQU-SA/18/ 07). Y.K. thanks the funding support by the National Research Foundation of Korea (NRF-2017R1A2B4001829). A.T.K. acknowledges support from the Nanotechnology and Water Sustainability Research Unit, UNISA.
Publisher Copyright:
© 2019 American Chemical Society.
PY - 2019/3/4
Y1 - 2019/3/4
N2 - Designing efficient 2D-bismuth oxychloride (BiOCl)/2D-g-C 3 N 4 heterojunction photocatalysts by the microwave-assisted method was studied in this work using different amounts of BiOCl plates coupled with g-C 3 N 4 nanosheets. The effects of coupling the 2D structure of g-C 3 N 4 with the 2D structure of BiOCl were systematically examined by scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy, X-ray diffraction, photoluminescence (PL), lifetime decay measurement, surface charges of the samples at various pH conditions, and UV-vis diffuse reflectance spectroscopy (UV-vis DRS). The prepared photocatalysts were used for the degradation of amine-based pharmaceuticals, and nizatidine was used as a model pollutant to evaluate the photocatalytic activity. The UV-vis DRS and other optical properties indicated the major effect of coupling of BiOCl with g-C 3 N 4 into a 2D/2D structure. The results showed a narrowing in the band gap energy of the composite form, whereas the PL and lifetime analysis showed greater inhibition of the electron-hole recombination process and slightly longer charge carrier lifetime. Accordingly, the BiOCl/g-C 3 N 4 composite samples exhibited an enhancement in the photocatalytic performance, specifically for the 10% BiOCl/g-C 3 N 4 sample. Moreover, the zeta potential of this sample at different pH values was evaluated to determine the isoelectric point of the synthesized composite material. Consequently, the pH was adjusted to match the isoelectric point of the complex materials, which further enhanced the activity. Further degradation of pharmaceuticals was studied under solar light irradiation, and 96% degradation was achieved within 30 min.
AB - Designing efficient 2D-bismuth oxychloride (BiOCl)/2D-g-C 3 N 4 heterojunction photocatalysts by the microwave-assisted method was studied in this work using different amounts of BiOCl plates coupled with g-C 3 N 4 nanosheets. The effects of coupling the 2D structure of g-C 3 N 4 with the 2D structure of BiOCl were systematically examined by scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy, X-ray diffraction, photoluminescence (PL), lifetime decay measurement, surface charges of the samples at various pH conditions, and UV-vis diffuse reflectance spectroscopy (UV-vis DRS). The prepared photocatalysts were used for the degradation of amine-based pharmaceuticals, and nizatidine was used as a model pollutant to evaluate the photocatalytic activity. The UV-vis DRS and other optical properties indicated the major effect of coupling of BiOCl with g-C 3 N 4 into a 2D/2D structure. The results showed a narrowing in the band gap energy of the composite form, whereas the PL and lifetime analysis showed greater inhibition of the electron-hole recombination process and slightly longer charge carrier lifetime. Accordingly, the BiOCl/g-C 3 N 4 composite samples exhibited an enhancement in the photocatalytic performance, specifically for the 10% BiOCl/g-C 3 N 4 sample. Moreover, the zeta potential of this sample at different pH values was evaluated to determine the isoelectric point of the synthesized composite material. Consequently, the pH was adjusted to match the isoelectric point of the complex materials, which further enhanced the activity. Further degradation of pharmaceuticals was studied under solar light irradiation, and 96% degradation was achieved within 30 min.
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U2 - 10.1021/acsomega.8b03665
DO - 10.1021/acsomega.8b03665
M3 - Article
C2 - 31459654
AN - SCOPUS:85062568873
SN - 2470-1343
VL - 4
SP - 4671
EP - 4678
JO - ACS Omega
JF - ACS Omega
IS - 3
ER -