Ce(3+)-ion, Surface Oxygen Vacancy, and Visible Light-induced Photocatalytic Dye Degradation and Photocapacitive Performance of CeO(2)-Graphene Nanostructures

Ce(3+)离子、表面氧空位、可见光诱导的光催化染料降解以及CeO(2)-石墨烯纳米结构的光电容性能

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Abstract

Cerium oxide nanoparticles (CeO(2) NPs) were fabricated and grown on graphene sheets using a facile, low cost hydrothermal approach and subsequently characterized using different standard characterization techniques. X-ray photoelectron spectroscopy and electron paramagnetic resonance revealed the changes in surface states, composition, changes in Ce(4+) to Ce(3+) ratio, and other defects. Transmission electron microscopy (TEM) and high resolution TEM revealed that the fabricated CeO(2) NPs to be spherical with particle size of ~10-12 nm. Combination of defects in CeO(2) NPs with optimal amount of two-dimensional graphene sheets had a significant effect on the properties of the resulting hybrid CeO(2)-Graphene nanostructures, such as improved optical, photocatalytic, and photocapacitive performance. The excellent photocatalytic degradation performances were examined by monitoring their ability to degrade Congo red ~94.5% and methylene blue dye ~98% under visible light irradiation. The photoelectrode performance had a maximum photocapacitance of 177.54 Fg(-1) and exhibited regular capacitive behavior. Therefore, the Ce(3+)-ion, surface-oxygen-vacancies, and defects-induced behavior can be attributed to the suppression of the recombination of photo-generated electron-hole pairs due to the rapid charge transfer between the CeO(2) NPs and graphene sheets. These findings will have a profound effect on the use of CeO(2)-Graphene nanostructures for future energy and environment-related applications.

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