Crystal Structure and Spectroscopic Characterization of a New Hybrid Compound, (C12H17N2)2[CdBr4], for Energy Storage Applications.

Organic-inorganic hybrid materials have recently found a vast variety of applications in the fields of energy storage and microelectronics due to their outstanding electric and dielectric characteristics, including high dielectric constant, low conductivity, and low dielectric loss. However, despite the promising properties of these materials, there remains a need to explore novel compounds with improved performance for practical applications. In this research paper, the focus is on addressing this scientific challenge by synthesizing and characterizing the new-centrosymmetric (C12H17N2)2[CdBr4] crystal. This compound offers potential advancements in energy storage technologies and microelectronics due to its unique structural and electronic properties. The chemical mentioned above crystallizes in the monoclinic system, and its protonated amine (C12H17N2)+ and isolated anion [CdBr4]2- are bound by C-H···π and N-H···Br hydrogen bonds to form its zero-dimensional structure. Through optical absorption analysis, the semiconductor nature of the material is verified, showcasing a band gap of around 2.9 eV. Furthermore, an in-depth examination of Nyquist plots reveals the material's electrical characteristics' sensitivity to frequency and temperature variations. By applying Jonscher's power law to analyze ac conductivity plots, it is observed that the variation in the exponent "s" accurately characterizes the conduction mechanism, aligning with CBH models. The compound exhibits low dielectric loss values and a high permittivity value (ε ∼ 105), making it a promising candidate for energy storage applications. By managing the scientific challenge of improving material performance for energy storage and microelectronics, this research contributes to advancing the field and opens avenues for further exploration and application of organic-inorganic hybrid materials.

A novel optical temperature sensor and energy transfer properties based on Tb3+/Sm3+ codoped SrY2(MoO4)4 phosphors.

A series of SrY2(MoO4)4 phosphors doped and co-doped with Tb3+/Sm3+ ions was synthesized to develop new optical temperature sensor materials. The structures, morphologies, and luminescent characteristics of these phosphors were thoroughly investigated. Luminescence spectra of mono-doped SrY2(MoO4)4 phosphors were measured under the excitation at 375 and 403 nm corresponding to direct excitation of Tb3+ and Sm3+, respectively. The characteristic luminescence bands corresponding to electronic transitions of terbium and samarium ions were detected and investigated for different dopant concentrations. The emission spectrum of the Tb3+/Sm3+ co-doped sample exhibited a total of five distinct emission peaks, indicating an energy transfer from Tb3+ to Sm3+ ions. The energy transfer efficiency from Tb3+ ions to Sm3+ ions was investigated in detail. At elevated temperatures, Tb3+ and Sm3+ exhibited distinct thermal sensitivities in their emission and excitation spectra, leading to evident thermochromic behavior. The fluorescence intensity ratio (FIR) was utilized with dual center to evaluate the temperature sensitivity of SrY2(MoO4)4:Tb3+/Sm3+ phosphors. The temperature sensing mechanism relied on the emission band intensity ratios of the 4G5/2 → 6H5/2, 4G5/2 → 6H9/2, and 4G5/2 → 6H7/2 transitions of Sm3+ in conjunction with the 5D5/2 → 7F5/2 transitions of Tb3+. This approach demonstrated high thermal sensitivity values, reaching up to 0.9% K-1. The studied nanoparticles exhibited sub-degree thermal resolution, making them suitable candidates for precise temperature-sensing applications.

Influence of Nd Substitution on the Phase Constitution in (Zr,Ce)Fe10Si2 Alloys with the ThMn12 Structure.

Iron-based compounds with a ThMn12-type structure have the potential to bridge the gap between ferrites and high performance Nd2Fe14B magnets. From the point of view of possible applications, the main advantage is their composition, with about 10 wt.% less rare earth elements in comparison with the 2:14:1 phase. On the other hand, the main issue delaying the development of Fe-rich alloys with a ThMn12-type structure is their structural stability. Therefore, various synthesis methods and stabilizing elements have been proposed to stabilize the structure. In this work, the influence of increasing Nd substitution on the phase constitution of Zr0.4-xNdxCe0.6Fe10Si2 (0 ≤ x ≤ 0.3) alloys was analyzed. X-ray diffraction and 57Fe Mössbauer spectrometry were used as the main methods to derive the stability range and destabilization routes of the 1:12 structure. For the arc-melted samples, an increase in the lattice parameters of the ThMn12-type structure was observed with the simultaneous growth of bcc-(Fe,Si) content with increasing Nd substitution. After isothermal annealing, the ThMn12-type structure (and the coexisting bcc-(Fe,Si)) were stable over the whole composition range. While the formation of a 1:12 phase was totally suppressed in the as-cast state for x = 0.3, further heat treatment resulted in the growth of about 45% of the ThMn12-type phase. The results confirmed that the stability range of ThMn12-type structure in the Nd-containing alloys was well improved by other substitutions and the heat treatment, which in turn, is also needed to homogenize the ThMn12-type phase. After further characterization of the magnetic properties and optimization of microstructure, such hard/soft magnetic composites can show their potential by exploiting the exchange spring mechanism.

Two-step single-reactor synthesis of oleic acid- or undecylenic acid-stabilized magnetic nanoparticles by thermal decomposition.

Different iron oxides (i.e., magnetite, maghemite, goethite, wüstite), particularly nanosized particles, show distinct effects on living organisms. Thus, it is of primary importance for their biomedical applications that the morphology and phase-structural state of these materials are investigated. The aim of this work was to obtain magnetic nanoparticles in a single reactor using Fe(III) acetylacetonate as the initial precursor for the synthesis of Fe(III) oleate or Fe(III) undecylate followed by their thermolysis in situ. We proposed a new approach, according to which the essential magnetite precursor (a complex salt of higher acids - Fe(III) alkanoates) is obtained in a solvent with a high boiling point via displacement reaction of acetylacetone with a higher acid from Fe(III) acetylacetonate during its elimination from the reaction mixture under vacuum conditions. Magnetic nanoparticles (NPM) were characterized in terms of morphology, hydrodynamic diameter, and composition via several techniques, such as transmission electron microscopy, dynamic light scattering, thermogravimetric analysis, Fourier-transform infrared spectroscopy/attenuated total reflectance, 57Fe Mössbauer spectroscopy, and X-ray diffraction. The effect of unsaturated oleic (OA) and undecylenic (UA) acids, which are both used as a reagent and as a nanoparticle stabilizer, as well as the influence of their ratio to Fe(III) acetylacetonate on the properties of particles were investigated. Stable dispersions of NPM were obtained in 1-octadecene within the OA or UA ratio from 3.3 mol to 1 mol of acetylacetonate and up to 5.5 mol/mol. Below the mentioned limit, NPM dispersions were colloidally unstable, and at higher ratios no NPM were formed which could be precipitated by an applied magnetic field. Monodisperse nanoparticles of iron oxides were synthesized with a diameter of 8-13 nm and 11-16 nm using OA and UA, respectively. The organic shell that enables the particle to be dispersed in organic media, in the case of oleic acid, covers their inorganic core only with a layer similar to the monomolecular layer, whereas the undecylenic acid forms a thicker layer, which is 65% of the particle mass. The result is a significantly different resistance to oxidation of the nanoparticle inorganic cores. The core of the particles synthesized using oleic acid is composed of more than 90% of maghemite. When undecylenic acid is used for the synthesis, the core is composed of 75% of magnetite.

The Effects of Various Parameters of the Microwave-Assisted Solvothermal Synthesis on the Specific Surface Area and Catalytic Performance of MgF2 Nanoparticles.

High-specific-surface-area MgF2 was prepared by microwave-assisted solvothermal synthesis. The influences of the solvent and the magnesium precursors, and the calcination atmospheres, on the nanoparticle sizes and specific surface areas, estimated by X-Ray Powder Diffraction, N2 sorption and TEM analyses, were investigated. Nanocrystallized (~7 nm) magnesium partially hydroxylated fluorides (MgF2-x(OH)x) with significant specific surface areas between 290 and 330 m2∙g-1 were obtained. After activation under gaseous HF, MgF2-x(OH)x catalysts underwent a large decrease of both their surface area and their hydroxide, rates as shown by their 19F and 1H solid-state NMR spectra. Expect for MgF2 prepared from the acetate precursor, an activity of 30-32 mmol/h∙g was obtained which was about 40% higher compared with that of MgF2 prepared using Trifluoroacetate method (21.6 mmol/h∙g).