High-density polyethylene composites filled with micro- and nano-particles of nickel ferrite: magnetic, mechanical, and thermal properties.

With the increasing demand of new magnetic materials for modern technological application alternatives to conventional magnetic materials, the development of lightweight polymer magnetic composites has become a prominent research area. For this perspective, a new magnetic material was developed using 30 wt% nickel ferrite micro and nanoparticles as fillers for a high-density polyethylene matrix. The development process began with the synthesis of NF-micro and NF-nanoparticles using solid-state and co-precipitation techniques, respectively, followed by extrusion molding and injection molding. The success of the synthesis process and the purity of the spinel structure phase were confirmed. Additionally, using the extrusion process produced polymer magnetic composite materials with a good distribution of magnetic particles within the polymer matrix, resulting in good magnetic properties and enhanced mechanical properties of the polymer magnetic materials.

Exploring the Optical and Energetic Properties of a Co(II)-Based Mixed Ligand MOF.

Due to their remarkable properties, including remarkable porosity and extensive surface area, metal-organic frameworks (MOFs) are being investigated for various applications. Herein, we report the first Co(II)-based mixed ligand MOF, formulated Co4(HTrz)2(d-cam)2.5(µ-OH)3. Its 3D structure framework is composed of helical chains {[Co4(µ3-HTrz)4]8+}n connected by d-camphorate ligand building blocks and featured as an extended structure in an AB-AB fashion. The investigated compound displays a wide absorption range across the visible spectrum, characterized by an optical gap energy of 3.7 eV, indicating its semiconducting nature and efficient sunlight absorption capabilities across various wavelengths. The electrochemical performance demonstrated an excellent reversibility, cyclability, structural stability, as well as a specific capacity of up to 100 cycles at a scan rate of 0.1 mV·s-1 and a current density of 50 mA·g-1. Thus, it showcases its ability to retain the capacity over numerous charge-discharge cycles. Additionally, the investigated sample displayed an impressive rate capability during the Li-ion charge/discharge process. Therefore, the material's remarkable electrochemical properties can be ascribed to the synergistic effects of its large specific surface area of 348.294 m2·g-1 and well-defined pore size distribution of 20.448 Å, making it a promising candidate for high-performance Li-ion batteries.

Investigation of the Critical Behavior, Magnetocaloric Effect and Hyperfine Structure in the Fe72Nb8B20 Powders.

Microstructure as well as magnetic, thermal and magnetocaloric properties of the mechanically alloyed Fe72Nb8B20 powders have been investigated by means of Mössbauer spectrometry, differential scanning calorimetry (DSC), and magnetic measurements. The Mössbauer spectrometry results showed the formation of nanostructured Fe(B) and Fe(Nb) solid solutions, Fe2B boride, and an amorphous phase. The endothermic and exothermic peaks that are observed in the DSC curves might be related to the Curie temperature, and the crystallization of the amorphous phase, respectively. The critical exponent values around the magnetic phase transition of the amorphous phase (TC = 480 K), are deduced from the modified Arrott plots, Kouvel-Fisher curves and critical isotherm examination. The calculated values (ß = 0.457 ± 0.012, γ = 0.863 ± 0.136 and δ = 3.090 ± 0.004) are near to those of the mean field model, revealing a dominating role of magnetic order arising due to long-range ferromagnetic interactions, as the critical exponents are mean-field-like. The maximum entropy change and the refrigerant capacity values are 1.45 J/kg·K and 239 J/kg, respectively, under a magnetic field of 5 T.

Magnetic and spectroscopic properties of Ni-Zn-Al ferrite spinel: from the nanoscale to microscale.

This article presents the annealing effect on the structural, elastic, thermodynamic, optical, magnetic, and electric properties of Ni0.6Zn0.4Fe1.5Al0.5O4 (NZFAO) nanoparticles (NPs). The samples were successfully synthesized by the sol-gel method followed by annealing of the as-synthesized at 600, 800, 900, 1050, and 1200 °C. This approach yielded the formation of a highly crystalline structure with crystallite size ranging from 17 nm to 40 nm. X-ray diffraction (XRD), scanning electron microscopy (SEM) techniques, as well as energy disperse spectroscopy (EDS), Fourier transform infrared (FTIR) and Raman spectroscopy, were used in order to determine the structural and morphological properties of the prepared samples. Rietveld XRD refinement reveals that Ni-Zn-Al ferrite nanoparticles crystallize in inverse cubic (Fd3̄m) spinel structure. Using FTIR spectra, the elastic and thermodynamic properties were estimated. It was observed that the particle size had a pronounced effect on elastic and thermodynamic properties. Magnetic measurements were performed up to 700 K. The prepared ferrite samples present the highest Curie temperature, which decreases with increasing particle size and which is consistent with finite-size scaling. The thickness of the surface shell of about 1 nm was estimated from size-dependent magnetization measurements using the core-shell model. Besides, spin resonance, magnetostriction, temperature coefficient of resistance (TCR), and electrical resistivity properties have been scientifically studied and appear to be different according to their size. The optical properties of synthesized NZFAO nanoparticles were investigated, and the differences caused by the particle sizes are discussed on the basis of the phonon confinement effect. This effect was also inspected by the Raman analysis. Tuning of the physical properties suggests that the Ni-Zn-Al ferrite samples may be promising for multifunctional diverse applications.

Electronic structure and magnetic properties of Pr-Co intermetallics: ab initio FP-LAPW calculations and correlation with experiments.

First-principle calculations combining density functional theory and the full-potential linearized augmented plane wave (FP-LAPW) method are performed to investigate the electronic and magnetic structure of Pr2Co7 in its two polymorphic forms, (2:7 H) and (2:7 R), for the first time. This type of calculation was also performed for PrCo5 and PrCo2 intermetallics. We have computed the valence density of states separately for spin-up and spin-down states in order to investigate the electronic band structure. This is governed by the strong contribution of the partial DOS of 3d-Co bands compared to the partial DOS of the 4f-Pr bands. Such a high ferromagnetic state is discussed in terms of the strong spin polarization observed in the total DOS. The magnetic moments carried by the Co and Pr atoms located in several sites for all compounds are computed. These results mainly indicate that cobalt atoms make a dominant contribution to the magnetic moments. The notable difference in the atomic moments of Pr and Co atoms between different structural slabs is explained in terms of the magnetic characteristics of the PrCo2 and PrCo5 compounds and the local chemical environments of the Pr and Co atoms in different structural slabs of Pr2Co7. From spin-polarized calculations we have simulated the 3d and 4f band population to estimate the local magnetic moments. These results are in accordance with the magnetic moments calculated using the FP-LAPW method. In addition, the exchange interactions J ij are calculated and used as input for M(T) simulations. Involving the data obtained from the electronic structure calculations, the appropriate Padé Table is applied to simulate the magnetization M(T) and to estimate the mean-field Curie temperature. We report a fairly good agreement between the ab initio calculation of magnetization and Curie temperature with the experimental data.

Synthesis and Structural, Electrical, and Magnetic Properties of New Iron-Aluminum Alluaudite Phases ß-Na2Ni2M(PO4)3 (M = Fe and Al).

Herein we report the studies of different physical properties (structural, magnetic, thermal, morphologic, electrical, and electrochemical) of two new allotropic ß-Na2Ni2M(PO4)3 (NNMP) phosphates, with M = Fe and Al. Pure orthorhombic single-phase powders were prepared under air, using an autocombustion synthesis method. They crystallize in the orthorhombic Imma space group with similar unit cell parameters [a = 10.1592(2), b = 13.0321(3), c = 6.4864(2) Å] and [a = 10.3993(1), b = 13.1966(1), c = 6.4955(1) Å] for ß-Na2Ni2M(PO4)3 (NNAP) and ß-Na2Ni2Fe(PO4)3 (NNFP), respectively. Crystal structures of both compounds were determined using X-ray powder diffraction and Rietveld method refinements, which indicate the occurrence of Ni2+ in the 8g site, and of M3+ in the 4a site of the structure. The structure consists of a three-dimensional anionic framework obtained by the association on MO6, NiO6, and PO4 polyhedra, sharing edges and corners. The resulting three-dimensional structure creates monodimensional channels along the [100] and [010] directions formed by face-shared oxygen polyhedra and occupied by Na+ cations. This nondisordered cationic distribution is confirmed by a significant change of magnetic properties. Thus, both NNAP and NNFP samples show paramagnetic to ferromagnetic transition at 14 and 19 K, respectively. For the two compounds, thermal stability, electrical conductivity, and electrochemical properties have been also investigated. The intercalation/desintercalation properties of NNMP compounds as positive electrode were tested in sodium-ion batteries. The first cycling curves exhibit a significant polarization for both prepared samples.