Structural, morphological, and optical properties of SiC/PVP nanocomposite materials by changing the SiC concentration in PVP

Silicon carbide (SiC) nanotubes with a one-dimensional structure were successfully synthesized <i>via</i> the carbothermal method at 1800 °C. SEM results revealed a hollow interior and rough surface morphology. These SiC nanotubes were incorporated into a polyvinylpyrrolidone (PVP) matrix to produce SiC/PVP composite materials with different filler concentrations (1-5 wt%). XRD analysis confirmed the presence of the cubic 3C-SiC phase. SiC nanotubes were incorporated into a PVP polymer matrix at concentrations of 1, 2, 3, and 5 wt% SiC. Scanning electron microscopy (SEM) images revealed the morphology of the nanotubes of pure SiC. Energy-dispersive X-ray spectroscopy (EDS) and elemental mapping showed a non-uniform SiC distribution across the polymer, with the most uniform dispersion occurring at 3 wt%. X-ray diffraction (XRD) results indicated a decrease in crystallite size as SiC content increased, with the smallest crystallite size (11.86 nm) occurring at 3 wt% SiC/PVP. The microstrain and dislocation density also exhibited a similar trend, increasing from 1 wt% (0.00587) to 3 wt% (0.00698) and then decreasing at 5 wt% SiC/PVP (0.00271). Ultraviolet-Visible (UV-Vis) spectroscopy revealed a band gap reduction from 5.62 eV at 1 wt% to 5.51 eV at 3 wt% SiC/PVP, with a slight increase to 5.70 eV at 5 wt% SiC/PVP, indicating the most favorable optical properties at 3 wt% SiC/PVP composite materials. Fourier-transform infrared (FTIR) spectroscopy confirmed the physical interaction between SiC and PVP, characteristic Si-C stretching bands at 700-1000 cm<sup>-1</sup>, as well as the interaction of PVP carbonyl (C[double bond, length as m-dash]O) and C-N groups with Si-O/-OH groups on the SiC surface without any covalent bonding formation. The 3 wt% SiC/PVP composite demonstrated optimal dispersion, crystallite refinement, and optical properties, indicating its potential as the optimal loading concentration for electronics and semiconductors, optical devices, and energy storage and conversion, making it an ideal material for advanced technological uses.

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Publication Details

Journal
RSC Advances
Published
2025-01-01
DOI
https://doi.org/10.1039/d5ra08712k
Citations
1
Primary Topic
Polymer Nanocomposite Synthesis and Irradiation
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article
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article

Structural, morphological, and optical properties of SiC/PVP nanocomposite materials by changing the SiC concentration in PVP

Vusal Mammadov, Cristian Vacacela Gómez, Vitalii Yevdokymenko, Talía Tene et al.
1 citations
RSC Advances
Polymer Nanocomposite Synthesis and Irradiation
0.61
article

Structural, morphological, and optical properties of SiC/PVP nanocomposite materials by changing the SiC concentration in PVP

Vusal Mammadov, Cristian Vacacela Gómez, Vitalii Yevdokymenko, Talía Tene, Orkhan Gulahmadov, Lаla Gahramanli, M. A. Jafarov, D. S. Kamenskyh, Telkhanim Mahmudova, Christos Trapalis, Rana F. Khankishiyeva, Zeynab Addayeva, Mustafa Muradov, Shafiga Alakbarova
article en
1 citations

Abstract

Silicon carbide (SiC) nanotubes with a one-dimensional structure were successfully synthesized <i>via</i> the carbothermal method at 1800 °C. SEM results revealed a hollow interior and rough surface morphology. These SiC nanotubes were incorporated into a polyvinylpyrrolidone (PVP) matrix to produce SiC/PVP composite materials with different filler concentrations (1-5 wt%). XRD analysis confirmed the presence of the cubic 3C-SiC phase. SiC nanotubes were incorporated into a PVP polymer matrix at concentrations of 1, 2, 3, and 5 wt% SiC. Scanning electron microscopy (SEM) images revealed the morphology of the nanotubes of pure SiC. Energy-dispersive X-ray spectroscopy (EDS) and elemental mapping showed a non-uniform SiC distribution across the polymer, with the most uniform dispersion occurring at 3 wt%. X-ray diffraction (XRD) results indicated a decrease in crystallite size as SiC content increased, with the smallest crystallite size (11.86 nm) occurring at 3 wt% SiC/PVP. The microstrain and dislocation density also exhibited a similar trend, increasing from 1 wt% (0.00587) to 3 wt% (0.00698) and then decreasing at 5 wt% SiC/PVP (0.00271). Ultraviolet-Visible (UV-Vis) spectroscopy revealed a band gap reduction from 5.62 eV at 1 wt% to 5.51 eV at 3 wt% SiC/PVP, with a slight increase to 5.70 eV at 5 wt% SiC/PVP, indicating the most favorable optical properties at 3 wt% SiC/PVP composite materials. Fourier-transform infrared (FTIR) spectroscopy confirmed the physical interaction between SiC and PVP, characteristic Si-C stretching bands at 700-1000 cm<sup>-1</sup>, as well as the interaction of PVP carbonyl (C[double bond, length as m-dash]O) and C-N groups with Si-O/-OH groups on the SiC surface without any covalent bonding formation. The 3 wt% SiC/PVP composite demonstrated optimal dispersion, crystallite refinement, and optical properties, indicating its potential as the optimal loading concentration for electronics and semiconductors, optical devices, and energy storage and conversion, making it an ideal material for advanced technological uses.

RSC AdvancesVol. 15(58)
Universidad Técnica Particular de Loja (EC), Baku State University (AZ), National Centre of Scientific Research "Demokritos" (GR), Artsakh State University (AZ), Azerbaijan Scientific-Research & Design-Prospecting Power Engineering Institute (AZ), Ministry of Science and Education Republic of Azerbaijan (AZ), Institute of Bioorganic Chemistry and Petrochemistry V.P. Kukhar (UA), Azerbaijan University of Architecture and Construction (AZ), Universidad Ecotec (EC), University of Calabria (IT)
Openalex Percentile: Top 27%
Polymer Nanocomposite Synthesis and Irradiation
0.61
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