This paper presents the effect of Mn2+ substitution for Co2+, in CoFe2O4 embedded in SiO2 matrix, on the structural, surface, morphological and magnetic properties. X-ray diffraction (XRD) and Mossbauer spectroscopy indicate the presence of a nanocrystalline mixed cubic spinel. In all cases, for the nanocomposites (NCs) heat-treated at 200 degrees C, a single, low crystalline ferrite phase was remarked, while for the other heat-treatment temperatures up to 1200 degrees C and with increasing Mn content, the secondary phase of alpha-Fe2O3 appears, accompanied also by the secondary phase of SiO2 at 1200 degrees C. The Fourier transform infrared (FT-IR) spectroscopy confirms the consumption of starting metallic nitrates, the formation of Co-O, Mn-O, Fe-O bonds in ferrites@SiO2 matrix. The Mossbauer spectra show the characteristic magnetic patterns of Co and Mn spinels. According to the atomic force microscopy (AFM) analysis, the particle size increases from 15 to 80 nm with the increase of Mn content. The specific surface area varies in the range 150-450 m(2)/g due to the substitution of Co2+ ion with Mn2+ ion and decreases with increasing heat treatment temperature, reaching values below 1 m(2)/g at 1200 degrees C. All NCs have pores within the mesoporous range, with high dispersion of pores' sizes. Furthermore, the release of fine nanoparticles in aqueous environment is facilitated by the powders' mesoporous structure preserved at 200, 500 and 800 degrees C heat treatment temperatures. The porous network collapse after heat treatment at 1200 degrees C leads to releasing of bigger nanoparticles, in good agreement with AFM observation. Magnetization, coercivity and anisotropy evolve proportionally with the particle size for the NCs heat-treated at 800 degrees C (M-s = 18.9-36.3 emu/g; M-R = 3.05-14.1 emu/g, H-c = 31.83-53.2 kA/m, K= 0.378.10(-3) -1.21.10(-3) erg/cm(-1)) and inverse proportionally for those heat-treated at 1200 degrees C (M-s = 30.7-19.4 emu/g; M-R = 11.60 7.20 emu/g, H-c= 127.3-15.9 kA/m, K= 2.45.10(-3)-0.19.10(-3) erg/cm(-1)). The NCs with high Mn content heat-treated at 1200 degrees C show superparamagnetic behavior, while those with low Mn content display ferrimagnetic behavior. (C) 2021 Elsevier B.V. All rights reserved.

The influence of the CoFe2O4 nanoparticles concentration in silica matrix on the structural and magnetic properties of xCoFe(2)O(4)/(100-x)SiO2 nanocomposites with x=10, 30, 50, 70 and 90 was studied. Magnetic CoFe2O4 nanoparticles dispersed in silica matrix was obtained by sol-gel method, followed by annealing at 1100 degrees C. The X-ray diffraction pattern and FT-IR spectra revealed the single spinel ferrite structure for all samples. The FT-IR spectra also suggested the formation of the amorphous silica matrix. The results showed that the increase of cobalt ferrite concentration (x) in the silica matrix leads to high crystallinity, specific surface area and particle size. The magnetic CoFe2O4 nanoparticles have spherical shapes and size in the 6-35 nm range. The Mossbauer measurements were fitted with two Zeeman sextets, indicating that all the samples were completely magnetically ordered. The vibrating sample magnetometer studies showed that the saturation magnetization (Ms) and coercivity (Hc) of the CoFe2O4 nanocrystals embedded in silica matrix possessed a linear relationship with the mean crystallite size. Also, the saturation magnetization of the studied nanocomposites increases with the increase of cobalt ferrite concentration (x) in the silica matrix.

We have measured I-V and C-V characteristics, the temperature dependence of dark currents, and thermally stimulated depolarisation currents on fresh and stored samples of photoluminescent porous silicon, By storage in ambient, the low rectifying I-V curves become strong rectifying, and C-V curves become MIS-like. I-T characteristics for fresh samples have only one activation energy, in the 0.49-0.55 eV range. After storage, a slightly modified value, of about 0.50-0.60 eV is observed at low temperatures only. At about 280 K, the activation energy suddenly changes to 1.20-1.80 eV. Also, both the number and the positions of maxima in thermally stimulated depolarisation currents change by storage. The annealing at about 50 degrees C induces small reversible changes in I-T characteristics and strong irreversible ones in thermally stimulated depolarisation currents, both for fresh and stored samples. A simplified quantum confinement model is proposed to explain the main aspects of the electrical behaviour of porous silicon films. The surface and/or interface contributions are observed especially in thermally stimulated depolarisation currents. The changes induced by storage are attributed to the oxidation process of the internal surface of porous silicon films. (C) 1998 Elsevier Science S.A. All rights reserved.

The electrical transport of stabilised porous silicon layers was investigated. The samples were stored in ambient for 1,5-2 years, A MIS-like C-V characteristic, a strong rectifying I-V curve and I-T dependence with two activation energies were obtained, Thermally stimulated depolarization currents have an activation energy of 0.81-0.87 eV. The electrical properties are discussed in the frame of a quantum confinement model, keeping into account the surface component.