Graphene derivatives/Fe3O4/polymer nanocomposite films: Optical and electrical properties
Autor: | Mimouna Baitoul, Meryem Goumri, Rhizlane Hatel, Bernard Ratier |
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Rok vydání: | 2017 |
Předmět: |
Vinyl alcohol
Photoluminescence Materials science Nanocomposite Polymer nanocomposite Graphene 02 engineering and technology 010402 general chemistry 021001 nanoscience & nanotechnology Condensed Matter Physics 01 natural sciences 0104 chemical sciences law.invention symbols.namesake chemistry.chemical_compound Chemical engineering chemistry law symbols General Materials Science Composite material Fourier transform infrared spectroscopy 0210 nano-technology Absorption (electromagnetic radiation) Raman spectroscopy |
Zdroj: | Materials Chemistry and Physics. 193:156-163 |
ISSN: | 0254-0584 |
DOI: | 10.1016/j.matchemphys.2017.02.013 |
Popis: | This paper reports a simple solution casting method for the preparation of nanocomposite films in which graphene oxide (GO)/Fe 3 O 4 nanocomposites are incorporated into poly (vinyl alcohol) (PVA) matrix. The films obtained with different weight percent of GO/Fe 3 O 4 (0.5, 0.7 and 1 wt%) are subjected an in situ chemical and thermal reduction in order to explore the evolution and interactions between these components under different treatments and get an insight into on how this can affects the optical and electrical properties of these nanocomposites. Characterization was carried out using, UV–Vis absorption, Photoluminescence, electrical conductivity measurements, Fourier transform infrared spectroscopy (FT-IR) and Raman spectroscopy. Strong covalent functionalization occurs between the polymer and graphene derivatives (GD)/Fe 3 O 4 hybrids. The experimental results obtained for our nanocomposites films exhibit significant enhancement in properties highlighted the efficiency of the in situ thermal reduction. The high absorption with strong photoluminescence and electrical conductivity achieved might promote these nanocomposites for opto-electronic devices in near future. |
Databáze: | OpenAIRE |
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