Synthesis, photoluminescence and Magnetic properties of iron oxide (α-Fe2O3) nanoparticles through precipitation or hydrothermal methods
Creators
- 1. Laboratoire Structures, Propriétés et Modélisation des Solides CentraleSupélec, CNRS-UMR8580, Université Paris-Saclay 91190 Gif-sur-Yvette (France)
- 2. Unité de Recherche Electrochimie, Matériaux et Environnement UREME (UR17ES45), Faculté des Sciences de Gabès, Université de Gabès, Cité Erriadh, 6072 Gabès (Tunisia)
Description
Highlights: • Pure hematite nanoparticles were prepared through two different methods: precipitation and hydrothermal. • Synthesized nanoparticles were spherical shape with good crystallinity and phase purity. • Functional and compositional changes of nanoparticles were explored through FT-IR study. • The magnetic characteristic in the samples were carried out using the SQUID magnetometer. In this work the iron oxide (α-Fe2O3) nanoparticles are synthesized using two different methods: precipitation and hydrothermal. Size, structural, optical and magnetic properties were determined and compared using X-ray diffraction (XRD), Transmission Electron Microscopy (TEM), Scanning Electron Microscopy (SEM), Fourier Transform Infra-Red (FT-IR), Raman spectroscopy, Differential Thermal Analysis (DTA), Thermogravimetric Analysis (TGA), Ultraviolet–Visible (UV–Vis) analysis, Superconducting QUantum Interference Device (SQUID) magnetometer and Photoluminescence (PL). XRD data further revealed a rhombohedral (hexagonal) structure with the space group (R-3c) and showed an average size of 21 nm for hydrothermal samples and 33 nm for precipitation samples which concorded with TEM and SEM images. FT-IR confirms the phase purity of the nanoparticles synthesized. The Raman spectroscopy was used not only to prove that we have synthesized pure α-Fe2O3 but also to identify their phonon modes. The TGA showed three mass losses, whereas DTA resulted in three endothermic peaks. The decrease in the particle size of hematite of 33 nm for precipitation samples to 21 nm for hydrothermal samples is responsible for increasing the optical band gap of 1.94–2.10 eV where, the relation between them is inverse relationship. The products exhibited the attractive magnetic properties with good saturation magnetization, which were examined by a SQUID magnetometer. Photoluminescence measurements showed a strong emission band at 450 nm. Pure hematite prepared by hydrothermal method has smallest size, best crystallinity, highest band gap and best value of saturation magnetization compared to the hematite elaborated by the precipitation method.
Availability note (English)
Available from http://dx.doi.org/10.1016/j.physe.2018.04.009Additional details
Identifiers
- DOI
- 10.1016/j.physe.2018.04.009;
- PII
- S1386947718300110;
Publishing Information
- Journal Title
- Physica E. Low-Dimensional Systems and Nanostructures (Print)
- Journal Volume
- 101
- Journal Page Range
- p. 212-219
- ISSN
- 1386-9477
INIS
- Country of Publication
- Netherlands
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 53037032
- Subject category
- S77: NANOSCIENCE AND NANOTECHNOLOGY;
- Descriptors DEI
- DIFFERENTIAL THERMAL ANALYSIS; FOURIER TRANSFORM SPECTROMETERS; FOURIER TRANSFORMATION; HEMATITE; HYDROTHERMAL SYNTHESIS; INFRARED SPECTRA; MAGNETIC PROPERTIES; MAGNETOMETERS; NANOPARTICLES; PHOTOLUMINESCENCE; RAMAN SPECTROSCOPY; SCANNING ELECTRON MICROSCOPY; SQUID DEVICES; THERMAL GRAVIMETRIC ANALYSIS; TRANSMISSION ELECTRON MICROSCOPY; X-RAY DIFFRACTION
- Descriptors DEC
- CHEMICAL ANALYSIS; COHERENT SCATTERING; DIFFRACTION; ELECTRON MICROSCOPY; ELECTRONIC EQUIPMENT; EMISSION; EQUIPMENT; FLUXMETERS; GRAVIMETRIC ANALYSIS; INTEGRAL TRANSFORMATIONS; IRON ORES; LASER SPECTROSCOPY; LUMINESCENCE; MEASURING INSTRUMENTS; MICROSCOPY; MICROWAVE EQUIPMENT; MINERALS; ORES; OXIDE MINERALS; PARTICLES; PHOTON EMISSION; PHYSICAL PROPERTIES; QUANTITATIVE CHEMICAL ANALYSIS; SCATTERING; SPECTRA; SPECTROMETERS; SPECTROSCOPY; SUPERCONDUCTING DEVICES; SYNTHESIS; THERMAL ANALYSIS; TRANSFORMATIONS
Optional Information
- Copyright
- Copyright (c) 2018 Elsevier B.V. All rights reserved.