Temperature Stable, High-Quality Factor Li2TiO3-Li4NbO4F Microwave Dielectric Ceramics

In this work, (1-x)Li2TiO3-xLi4NbO4F ceramics were prepared by the conventional solid-state ceramic route. With the increase of Li4NbO4F content, the phase structure transformed from ordered monoclinic to disordered cubic. By increasing Li3NbO4F content, the temperature coefficient of resonant frequency (τf) was successfully adjusted closer to zero, while the dielectric constant (εr) and microwave quality factor (Qf) decreased to some degree. Outstanding microwave dielectric properties with a εr = 18.7, Qf = 61,388 GHz (6.264 GHz), and τf = 0.9 ppm/°C were obtained for 0.9Li2TiO3-0.1Li4NbO4F ceramics sintered at 1050 °C for 2 h, which indicated that these ceramics are suitable for practical applications in the field of microwave substrates and components.

Ferroelectric and Dielectric Properties of BaZr0.2[Ti(1-x)Mgx/3Ta2x/3]0.8O3 Solid Solution

BaZr0.2[Ti(1-x)Mgx/3Ta2x/3]0.8O3 (x = 0.0, 0.05, 0.1, 0.2, 0.4, 0.6, 0.8, 1.0) (BZTMT) ceramics were prepared through conventional solid state ceramic route. The crystal structure and microstructure of the compounds were investigated respectively using XRD and SEM. The dielectric properties were measured in the frequency range of 100 Hz–1 MHz. The ferroelectric Curie temperature of BaZr0.2Ti0.8O3 (x = 0) shifted from 21°C to -10°C with the addition of minute amount of dopant (x = 0.025) and the paraelectric transition temperature is diffusive in nature. The relative permittivity and dielectric loss of BZTMT at 1 MHz varies from 5205 to 24 and 1.8 × 10–2 to 2.0 × 10–5 respectively, as the value of x increases from 0 to 1.

Structural and Magnetic Characterizations of Ruddlesden–Popper Family (Ca2-xNdxMnO4) Compound Synthesized by Ceramic Route

In this work, we were interested in the Ca2−xNdxMnO4 compounds when (0.1 ≤ x ≤ 0.4). These oxides are synthesized through the solid-state method. In this study, we investigated the evolution of the structure, the magnetic properties and the Mn3+/Mn4+ ratio with the Nd content. The morphological study shows a decrease in the size of the grain in relation to x. The X-ray diffraction reveals a transition from the tetragonal phase to the orthorhombic phase when x = 0.4. Magnetic measurements have been taken for all the compounds in the temperature range between 2 and 300 K. The temperature-dependent magnetic susceptibility shows the presence of three transitions TN, TC and TCO. A dramatic difference in magnetic susceptibility between ZFC and FC was observed below the Neel temperatures for Ca2-xNdxMnO4, which shows the onset of a ferromagnetic moment below these temperatures. This moment is caused by the Dzyaloshinskii–Moriya interaction.

A Comparative Study of Spinel ZnFe2O4 Ferrites Obtained via a Hydrothermal and a Ceramic Route: Structural and Magnetic Properties

The spinel ZnFe2O4 specimens were obtained via a hydrothermal and a ceramic method, respectively, and their structural and magnetic properties were comparatively studied. It was found that all the specimens exhibited a single-phase and mixed spinel structure. The magnetism of specimens synthesized via the hydrothermal method is obviously greater than that of specimen prepared via the ceramic method. This can be ascribed to the occupancy of Fe ions resulted from the loss of Zn during the hydrothermal process.

Sodium Alanate Dehydrogenation Properties Enhanced by MnTiO3 Nanoparticles

In this study, we investigated the influence of MnTiO3 nanoparticles additive on hydrogen released performance of NaAlH4 for the first time. The MnTiO3 nanoparticles were successfully synthesized using conventional solid-state ceramic route. It was found that the hydrogen released performance of NaAlH4 can be significantly improved by the addition of MnTiO3 nanoparticles. Meantime, the composite of NaAlH4 doped 5 wt% MnTiO3 possessed excellent dehydrogenation properties, the onset dehydrogenation temperature was only 70.6 °C, reduced by about 105 °C in comparison with the pristine NaAlH4, and approximately 5.01 wt% of hydrogen could be released from composite with temperature heated to 220 °C. The isothermal dehydrogenation test results indicated that the amount of hydrogen released by NaAlH4-5 wt% MnTiO3 composite could reach 4.4 wt% under 200 °C within 25 min. According to the analysis of X-ray diffraction, the presence of MnTiO3 nanoparticles did not alter the overall dehydrogenation pathway of NaAlH4, and the Al3 Ti phases formed after dehydrogenation, which enhanced hydrogen desorption performances of NaAlH4 .