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. 2021 Aug 22;11(8):2143.
doi: 10.3390/nano11082143.

The Effect of Precursor Concentration on the Particle Size, Crystal Size, and Optical Energy Gap of CexSn1-xO2 Nanofabrication

Affiliations

The Effect of Precursor Concentration on the Particle Size, Crystal Size, and Optical Energy Gap of CexSn1-xO2 Nanofabrication

Naif Mohammed Al-Hada et al. Nanomaterials (Basel). .

Abstract

In the present work, a thermal treatment technique is applied for the synthesis of CexSn1-xO2 nanoparticles. Using this method has developed understanding of how lower and higher precursor values affect the morphology, structure, and optical properties of CexSn1-xO2 nanoparticles. CexSn1-xO2 nanoparticle synthesis involves a reaction between cerium and tin sources, namely, cerium nitrate hexahydrate and tin (II) chloride dihydrate, respectively, and the capping agent, polyvinylpyrrolidone (PVP). The findings indicate that lower x values yield smaller particle size with a higher energy band gap, while higher x values yield a larger particle size with a smaller energy band gap. Thus, products with lower x values may be suitable for antibacterial activity applications as smaller particles can diffuse through the cell wall faster, while products with higher x values may be suitable for solar cell energy applications as more electrons can be generated at larger particle sizes. The synthesized samples were profiled via a number of methods, such as scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray diffraction (XRD), and Fourier transform infrared spectroscopy (FT-IR). As revealed by the XRD pattern analysis, the CexSn1-xO2 nanoparticles formed after calcination reflect the cubic fluorite structure and cassiterite-type tetragonal structure of CexSn1-xO2 nanoparticles. Meanwhile, using FT-IR analysis, Ce-O and Sn-O were confirmed as the primary bonds of ready CexSn1-xO2 nanoparticle samples, whilst TEM analysis highlighted that the average particle size was in the range 6-21 nm as the precursor concentration (Ce(NO3)3·6H2O) increased from 0.00 to 1.00. Moreover, the diffuse UV-visible reflectance spectra used to determine the optical band gap based on the Kubelka-Munk equation showed that an increase in x value has caused a decrease in the energy band gap and vice versa.

Keywords: CexSn1−xO2 nanoparticles; energy band gap; polyvinylpyrrolidone; thermal treatment technique.

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Conflict of interest statement

The authors declare no conflict of interest.

Figures

Figure 1
Figure 1
(a) PVP chemical structure; (b) formation of the resonance structure of the pyrene ring of PVP.
Figure 2
Figure 2
Schematic illustration of the proposed mechanism of interaction between metal ions and PVP.
Figure 3
Figure 3
TEM images of (x0.00) Ce0.00Sn1.00O2, (x0.20) Ce0.20Sn0.80O2, (x0.40) Ce0.40Sn0.60O2, (x0.06) Ce0.60Sn0.40O2, (x0.08) Ce0.80Sn0.20O2 and (x1.00) Ce1.00Sn0.00O2) nanoparticles calcined at 650 °C.
Figure 4
Figure 4
Particle size distribution of (x/0.00) Ce0.00Sn1.00O2, (x/0.20) Ce0.20Sn0.80O2, (x/0.40) Ce0.40Sn0.60O2, (x/0.06) Ce0.60Sn0.40O2, (x/0.08) Ce0.80Sn0.20O2, and (x/1.00) Ce1.00Sn0.00O2) nanoparticles calcined at 650 °C.
Figure 5
Figure 5
SEM images of (x0.00) Ce0.00Sn1.00O2, (x0.20) Ce0.20Sn0.80O2, (x0.40) Ce0.40Sn0.60O2, (x0.06) Ce0.60Sn0.40O2, (x0.08) Ce0.80Sn0.20O2 and (x1.00), Ce1.00Sn0.00O2) nanoparticles calcined at 650 °C.
Figure 6
Figure 6
XRD patterns of (x0.00) Ce0.00Sn1.00O2, (x0.20) Ce0.20Sn0.80O2, (x0.40) Ce0.40Sn0.60O2, (x0.06) Ce0.60Sn0.40O2, (x0.08) Ce0.80Sn0.20O2 and (x1.00) Ce1.00Sn0.00O2) nanoparticles calcined at 650 °C.
Figure 6
Figure 6
XRD patterns of (x0.00) Ce0.00Sn1.00O2, (x0.20) Ce0.20Sn0.80O2, (x0.40) Ce0.40Sn0.60O2, (x0.06) Ce0.60Sn0.40O2, (x0.08) Ce0.80Sn0.20O2 and (x1.00) Ce1.00Sn0.00O2) nanoparticles calcined at 650 °C.
Figure 7
Figure 7
FTIR spectra of (a) the sample after drying at 80 °C ((b), x1.00) Ce1.00Sn0.00O2, ((c), x0.20) Ce0.20Sn0.80O2 ((d), x0.40) Ce0.40Sn0.60O2, ((e), x0.60) Ce0.60Sn0.40O2, ((f), x0.80) Ce0.80Sn0.20O2 and ((g), x0.00) Ce0.00Sn1.00O2 nanoparticles calcined at 650 °C.
Figure 8
Figure 8
The energy bandgap of (x0.00) Ce0.00Sn1.00O2, (x0.20) Ce0.20Sn0.80O2, (x0.40) Ce0.40Sn0.60O2, (x0.06) Ce0.60Sn0.40O2, (x0.08) Ce0.80Sn0.20O2, and (x1.00) Ce1.00Sn0.00O2) nanoparticles calcined at 650 °C.

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