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. 2022 Apr 19;12(9):1402.
doi: 10.3390/nano12091402.

Exploring the Influence of Synthesis Parameters on the Optical Properties for Various CeO2 NPs

Affiliations

Exploring the Influence of Synthesis Parameters on the Optical Properties for Various CeO2 NPs

Andreea L Chibac-Scutaru et al. Nanomaterials (Basel). .

Abstract

Cerium oxide (CeO2) nanoparticles were synthesized with a chemical precipitation method in different experimental conditions using cerium nitrate hexahydrate (Ce(NO3)3·6H2O) as a precursor, modifying the solution pH, the reaction time, and Co atoms as dopants, in order to tune the band gap energy values of the prepared samples. The physical characteristics of the synthesized ceria nanoparticles were evaluated by Fourier transform infrared (FT-IR) spectroscopy, X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), UV-Vis analyses and photoluminescence measurements. XRD data revealed a pure cubic fluorite structure of CeO2 NPs, the estimation of crystallite sizes by Scherrer's formula indicates the formation of crystals with dimensions between 11.24 and 21.65 nm. All samples contain nearly spherical CeO2 nanoparticles, as well as cubic, rhomboidal, triangular, or polyhedral nanoparticles that can be identified by TEM images. The optical investigation of CeO2 samples revealed that the band gap energy values are between 3.18 eV and 2.85 eV, and, after doping with Co atoms, the Eg of samples decreased to about 2.0 eV. In this study, we managed to obtain CeO2 NPs with Eg under 3.0 eV by only modifying the synthesis parameters. In addition, by doping with Co ions, the band gap energy value was lowered to 2.0 eV. This aspect leads to promising results that provide an encouraging approach for future photocatalytic investigations.

Keywords: CeO2 nanoparticles; Co-doping; band gap tuning; optical properties; pH variation.

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Conflict of interest statement

The authors declare no conflict of interest.

Figures

Figure 1
Figure 1
FTIR spectra of CeO2 nanoparticles prepared using various synthesis methods.
Figure 2
Figure 2
XRD patterns of CeO2/Co-doped CeO2 nanoparticles.
Figure 3
Figure 3
SEM images of V2 (a) and V2-Co (b) samples and EDX elemental analysis spectra of V2 (c) and V2-Co (d).
Figure 4
Figure 4
TEM images of CeO2 nanoparticles and the corresponding particle size distribution. Scale bar is 50 nm.
Figure 5
Figure 5
TEM images of Co-doped CeO2 nanoparticles and the corresponding particle size distribution. Scale bar is 50 nm.
Figure 6
Figure 6
UV–Vis absorption spectra of pristine CeO2 NPs: V1–V6 samples.
Figure 7
Figure 7
UV–Vis absorption spectra of V2 samples, pristine and Co-doped (a), and of V5 samples, pristine and Co-doped (b).
Figure 8
Figure 8
Reflectance spectra of pristine CeO2 NPs (V1–V6) (a) and of Co-doped CeO2 NPs (V2-Co, V5-Co) comparative to pristine V2 and V5 (b) (Inset: photo of V2 and V2-Co samples).
Figure 9
Figure 9
The Kubelka–Munk plots of different CeO2 NPs samples: V1–V6 (a), V2-Co comparative to V2 (b), and V5-Co relative to V5 (c).
Figure 10
Figure 10
Fluorescence spectra of pristine CeO2 NPs (V1–V6) at λex = 270 nm (a) and λex = 325 nm (b).
Figure 11
Figure 11
Fluorescence spectra of Co-doped CeO2 NPs (V2-Co, V5-Co) comparative to pristine V2 and V5 pristine CeO2 NPs at λex = 270 nm (a) and λex = 325 nm (b).

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