Effects of Cu substitution on microstructures and microwave dielectric properties of Li2ZnSiO4 ceramics

Herein, the influence of Cu2+ substitution on the phase composition, bulk density, microstructures, and microwave dielectric properties of Li2CuxZn1−xSiO4 (0 ≤ x ≤ 0.06) ceramics prepared by a solid-state reaction were investigated. The results of XRD and mapping showed that Cu2+ substitution can avoid the influence of secondary phase on the properties of samples. According to the analysis of bulk density, microstructure and microwave dielectric properties, a proper amount of Cu substitution not only improved the sintering characteristics of Li2CuxZn1−xSiO4 ceramics, reduced the densification temperature from 1250 °C to 950 °C, but also increased the Q×f value. Furthermore, Cu2+ substitution also improved the temperature stability of the samples. Particularly, the Li2Cu0.04Zn0.96SiO4 ceramics sintered at 950 °C for 5 h possessed excellent microwave dielectric properties: εr = 5.624, Q×f = 12,764 GHz, and τf = −77 ppm/°C, exhibiting a potential for the low temperature co-fired ceramic applications.

Effect of Mn and Cu Substitution on the SrFeO3 Perovskite for Potential Thermochemical Energy Storage Applications

Perovskites are well-known oxides for thermochemical energy storage applications (TCES) since they show a great potential for spontaneous O2 release due to their non-stoichiometry. Transition-metal-based perovskites are particularly promising candidates for TCES owing to their different oxidation states. It is important to test the thermal behavior of the perovskites for TCES applications; however, the amount of sample that can be used in thermal analyses is limited. The use of redox cycles in fluidized bed tests can offer a more realistic approach, since a larger amount of sample can be used to test the cyclic behavior of the perovskites. In this study, the oxygen release/consumption behavior of Mn- or Cu-substituted SrFeO3 (SrFe0.5M0.5O3; M: Mn or Cu) under redox cycling was investigated via thermal analysis and fluidized bed tests. The reaction enthalpies of the perovskites were also calculated via differential scanning calorimetry (DSC). Cu substitution in SrFeO3 increased the performance significantly for both cyclic stability and oxygen release/uptake capacity. Mn substitution also increased the cyclic stability; however, the presence of Mn as a substitute for Fe did not improve the oxygen release/uptake performance of the perovskite.

Fabrication, characterization, and optimization of a novel copper-incorporated chitosan/gelatin-based scaffold for bone tissue engineering applications

Introduction: Fabricating composite scaffolds with improved physicochemical properties as artificial microenvironments are of great interest in bone tissue engineering. Given advantageous properties of nano-hydroxyapatite/chitosan/gelatin (nHA/Cs/Gel) scaffolds, the present study aimed to synthesize a modified nHA/Cs/Gel biomimetic scaffold with improved features. Methods: Pure and copper (Cu)-substituted nHA was synthesized using the chemical precipitation method under controlled pH and temperature. Pure and Cu-substituted nHA/Cs/Gel scaffolds were fabricated by salt-leaching/freeze-drying method. Physicochemical characteristics of nanoparticles and scaffolds were explored using XRD, FTIR, FE-SEM/EDX, and ICP. Besides, scaffold mechanical strength, degradation, porosity, swelling, biomineralization, and cytocompatibility were assessed. Results: Pure and Cu-substituted nHA were synthesized and characterized with appropriate Cu substitution and improved physical properties. All scaffolds were highly porous (porosity >98%) and Cu incorporation reduced porosity from 99.555 ± 0.394% to 98.69 ± 0.80% while enlarged the pore size to more than100 µm. Cu-substitution improved the scaffold mechanical strength and the best result was observed in nHA.Cu5%/Cs/Gel scaffolds by the compressive strength 88.869 ± 19.574 MPa. Furthermore, 3% and 5% Cu-substituted nHA enhanced the scaffold structural stability and supported osteoblast spread, adhesion, survival, mineralization, and proliferation. Moreover, long-term and sustainable Cu release from scaffolds was observed within 28 days. Conclusion: Cu-substituted nHA/Cs/Gel scaffolds mimic the porous structure and mechanical strength of cancellous bone, along with prolonged degradation and Cu release, osteoblast attachment, viability, calcium deposition, and proliferation. Taken together, our results indicate the upgraded properties of nHA.Cu5%/Cs/Gel scaffolds for future applications in bone tissue engineering.

Magnetic Properties and Morphology Copper-Substituted Barium Hexaferrites from Sol-Gel Auto-Combustion Synthesis

The copper (Cu) substitution in barium hexaferrite (BaFe12O19) crystals from the sol-gel auto-combustion synthesis is demonstrated as a cost-effective pathway to achieve alterable magnetic properties. Subsequent heat treatments at 450 °C and 1050 °C result in irregularly shaped nanoparticles characterized as the M-type BaFe12O19 with the secondary phase of hematite (α-Fe2O3). Despite the mixed phase, the substantial coercivity of 2626 Oe and magnetization as high as 74.8 emu/g are obtained in this undoped ferrite. The copper (Cu) doing strongly affects morphology and magnetic properties of BaFe12−xCuxO19 (x = 0.1, 0.3, and 0.5). The majority of particles become microrods for x = 0.1 and microplates in the case of x = 0.3 and 0.5. The coercivity and magnetization tend to reduce as Cu2+ increasingly substitutes Fe3+. From these findings, magnetic properties for various applications in microwave absorbers, recording media, electrodes, and permanent magnets can be tailored by the partial substitution in hexaferrite crystals.

Thermoelectric Power in Ce Systems with Unstable Valence

In this paper, we report on a few exemplary tests of the applicability of analysis based on the interconfiguration fluctuation model (ICF) for a description of the temperature dependence of the thermoelectric power, S(T). The examples include a series of alloys: CeNi2(Si1−yGey)2, Ce(Ni1−xCux)2Si2, and the fluctuating valence (FV) compound CeNi4Ga. The two series develop from CeNi2Si2 being the FV system, where the f states occupation increases progressively with the Ge or Cu substitution. We find here that the ICF model parameters are of similar magnitude both for the analysis of the temperature dependence of the magnetic susceptibility and thermoelectric power. The ICF-type model appears to be a powerful tool for the analysis of S(T) dependences in Ce-based FV compounds and alloys.

Effect of Cu Substitution on Magnetic Properties of Co0.6Ni0.4Fe2O4 Nanoferrites

This work is focusing on synthesizing the cobalt nanoferrite materials substituted by copper forming Co0.6Ni0.4-xCuxFe2O4 with x = 0.0, 0.1, and 0.3 using the sol-gel auto-combustion method. The phase analysis of XRD showed the spinel structure with the lattice parameter in the range 8.36-8.39 Å. FESEM image showed the grain size initially decreasing and then increasing with Cu concentration. The FTIR curve's two absorption bands in the specified range of frequency assured the spinel nano ferrite structure. The values of remanent ratios obtained from VSM showed their isotropic nature forming single domain ferrimagnetic particles.