Synthesis of Ce and Sm Co-Doped TiO2 Nanoparticles with Enhanced Photocatalytic Activity for Rhodamine B Dye Degradation

Author:

Slimani Yassine1ORCID,Almessiere Munirah A.12ORCID,Mohamed Mohamed J. S.3ORCID,Hannachi Essia4ORCID,Caliskan Serkan5ORCID,Akhtar Sultan1ORCID,Baykal Abdulhadi6,Gondal Mohammed A.37ORCID

Affiliation:

1. Department of Biophysics, Institute for Research and Medical Consultations (IRMC), Imam Abdulrahman Bin Faisal University, P.O. Box 1982, Dammam 31441, Saudi Arabia

2. Department of Physics, College of Science, Imam Abdulrahman Bin Faisal University, P.O. Box 1982, Dammam 31441, Saudi Arabia

3. Laser Research Group, Department of Physics, Interdisciplinary Research Center for Hydrogen and Energy Storage (IRC-HES), King Fahd University of Petroleum and Minerals (KFUPM), Dhahran 31261, Saudi Arabia

4. Department of Nuclear Medicine Research, Institute for Research and Medical Consultations (IRMC), Imam Abdulrahman Bin Faisal University, P.O. Box 1982, Dammam 31441, Saudi Arabia

5. Department of Physical and Applied Sciences, University of Houston-Clear Lake, Houston, TX 77058, USA

6. Department of Nanomedicine Research, Institute for Research and Medical Consultations (IRMC), Imam Abdulrahman Bin Faisal University, P.O. Box 1982, Dammam 31441, Saudi Arabia

7. K.A. CARE Energy Research and Innovation Center, King Fahd University of Petroleum & Minerals, Dhahran 31261, Saudi Arabia

Abstract

One of the major concerns that receive global attention is the presence of organic pollutants (dyes, pharmaceuticals, pesticides, phenolic compounds, heavy metals, and so on), originating from various industries, in wastewater and water resources. Rhodamine B is widely used in the dyeing of paints, plastics, textiles, and other fabrics, as well as biological products. It is highly persistent, toxic, and carcinogenic to organisms and humans when directly released into the water supply. To avoid this hazard, several studies have been conducted in an attempt to remove Rhodamine B from wastewater. Metal oxide semiconducting materials have gained great interest because of their ability to decompose organic pollutants from wastewater. TiO2 is one of the most effective photocatalysts with a broad range of applications. Several attempts have been made to improve its photocatalytic activity. Accordingly, we have prepared in this work a series of cerium (Ce) and samarium (Sm) co-doped TiO2 nanoparticles (x = 0.00, 0.25, 0.50, 1.00, and 2.00%) using a sol–gel auto-combustion approach. The influence of Ce–Sm concentrations on the structural, morphology, electronic, and optical properties, as well as the photocatalytic activity, was investigated. Structure and elemental mapping analyses proved the presence of Ce and Sm in the compositions as well as the development of the TiO2 anatase phase with a tetragonal structure and crystallite size of 15.1–17.8 nm. Morphological observations confirmed the creation of spherical nanoparticles (NPs). The examination of the electronic structure properties using density functional theory (DFT) calculations and of the optical properties using a UV/Vis diffuse spectrophotometer showed a reduction in the bandgap energy upon Ce–Sm co-doping. The photocatalytic activity of the synthesized products was assessed on the degradation of Rhodamine B dye, and it was found that all Ce–Sm co-doped TiO2 nanoparticles have better photocatalytic activities than pristine TiO2 nanoparticles. Among all of the prepared nanoparticles, the sample with x = 0.50% demonstrated the best photocatalytic activity, with a degradation efficiency of 98% within 30 min and a reaction rate constant of about 0.0616 min−1. h+ and •O2− were determined to be the most important active species in the photocatalytic degradation process. Besides the high photocatalytic degradation efficiency, these photocatalysts are highly stable and could be easily recovered and reused, which indicates their potential for practical applications in the future.

Publisher

MDPI AG

Subject

Physical and Theoretical Chemistry,Catalysis,General Environmental Science

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