Component Materials Research Articles

Cu1.3Mn1.7O4/LaNi0.6Fe0.4O3 composite with prospects for IT-SOFC/SOEC applications

Composite materials with the composition (100-x)Cu1.3Mn1.7O4/xLaNi0.6Fe0.4O3 (CMxLNF, where: x = 5, 10, 15, 20, 30, 40 and 50 wt%) were evaluated as possible coating materials for SOFC/SOEC metallic interconnects. The introduction of LaNi0.6Fe0.4O3 into spinel matrices improved electrical conductivity compared to pure Cu1.3Mn1.7O4. The measured Seebeck coefficient values indicate that carrier concentration increased with LaNi0.6Fe0.4O3 content, yet the activation energy of the carriers' mobility decreased. Extensive structural and microstructural studies of selected CM/LNF systems showed that composite material components exhibited high stability in relation to one another. Additionally, LaNi0.6Fe0.4O3 significantly improved the chemical stability of Cu1.3Mn1.7O4 in the presence of chromia, as tested after 150 h of exposure to air at 800 °C. Finally, coatings based on selected composite powders were deposited electrophoretically on the steel and were oxidized for 1500 h in air at 750 °C, confirming that CM10LNF can be applied as effective protective-conducting coatings on low-chromium ferritic steel.

Cross-sectional geometry effect on bending strength of gold micro-cantilever with trapezoidal cross-section

Gold is a promising material for movable components in MEMS devices by the high mass density, which allows reduction of the Brownian noise. Mechanical properties of metallic materials are known to be affected by the sample size effect. When bending test is utilized, the sample geometry effect is another factor. In this study, effects of the shape of the cross-section, or the cross-sectional geometry effect, are evaluated using micro-cantilevers with a trapezoidal cross-section. The yield stresses are ranged from 112 MPa to 185 MPa in micro-cantilevers composed of single crystalline gold, and the yield stresses varied from 372 MPa to 489 MPa in polycrystalline gold micro-cantilevers. The yield stress is found to be higher in the micro-cantilever having a smaller ratio of the top width over the bottom width, which demonstrates the cross-sectional geometry effect. Also, the cross-sectional geometry effect is more significant in the polycrystalline micro-cantilevers.

Biomedical Applications of Cold Atmospheric Plasma: Cancer Therapy and Virus Inactivation

Cold atmospheric plasma (CAP), known for its ability to generate Reactive Oxygen Species (ROS) and Reactive Nitrogen Species (RNS), has emerged as a promising tool in many biomedical applications, including cancer therapeutics and virus inactivation. In cancer therapy, ROS and RNS induced by plasma have been shown to selectively target cancer cells, triggering apoptosis and inhibiting tumor growth while sparing healthy cells. This selective cytotoxicity makes plasma an attractive option for localized cancer treatment with minimal side effects. Additionally, the antimicrobial properties of ROS and RNS make plasma an effective agent for virus inactivation. By connecting the dots between cancer therapy and virus disinfection, this review paper sheds light on the potential of plasma-generated ROS and RNS as versatile tools in medical applications, offering a dual benefit of targeted cancer treatment and effective virus control. Specifically, this review explores the effects of CAP treatment on B16 melanoma cells, assessing changes in cell viability, proliferation, apoptosis and oxidative stress response. Dichloroacetate (DCA), a mitochondrial modulator, has shown promise in inducing apoptosis in melanoma cells. However, its clinical use is limited by side effects related to its neurotoxicity and suspected carcinogenicity. The potential of CAP in enhancing the therapeutic efficacy of DCA on B16-F10 melanoma apoptosis is also explored. CAP therapeutics for other types of cancers are also explored in this review. Alongside its implications in oncology, CAP has gathered substantial attention for its extraordinary potential in neutralizing viruses. CAP’s exceptional precision in targeting viral envelopes, genetic material and structural components disrupts their integrity and vital functions. This orchestrated mechanism offers a swift and efficacious route to render viruses inactive, encompassing both enveloped and nonenveloped viral types. In parallel pursuit, this review examines CAP-generated reactive species’ proficiency in deactivating SARS-CoV-2 across various surfaces. The inquiry entails subjecting surfaces to CAP treatment, succeeded by quantifying viral load and scrutinizing viral integrity. The outcomes gleaned from these investigations provide pivotal insights into CAP’s potential as a robust surface disinfection strategy, poised to combat the propagation of viral transmission.

Finite element modeling simulation of oxygen evolution during charging in lithium-oxygen batteries

The quest for advanced energy storage solutions has intensified the focus on developing next-generation secondary batteries, with lithium-oxygen batteries (LOB) standing out for their superior theoretical gravimetric energy density. This study introduces a novel model-based approach to battery development, enabling the detailed analysis of charge–discharge cycles and oxygen evolution efficiency within a virtual environment. Our model distinctively simulates the oxidative decomposition of lithium peroxide (Li2O2) and differentiates between its formation through solution and surface pathways, addressing the complexities of the charging process and its multiple elementary steps. The developed model further categorizes the oxidative decomposition species into four distinct types, facilitating a comprehensive understanding of their interactions, voltage profile changes, and O2 evolution within the battery's porous cathode. This approach not only enhances the understanding of battery behavior but also aids in refining the design of component materials, thereby propelling forward the development of LOBs with improved energy density and cycle performance.

Advancements in printed components for proton exchange membrane fuel cells: A comprehensive review

Proton Exchange Membranes (PEM) are a promising technology for fuel cells and electrolyzer cells, in line with societal goals for clean and sustainable fuel conversion and generation, respectively, in a vast field of applications. PEM fuel cell (PEMFC) technology has an important advantage for energy conversion applications, because it requires a lower operating temperature and is lighter and more compact than other technologies, which makes it ideal for portable and transportation applications. However, open issues remain to be addressed for PEMFC that hinder their widespread adoption, both on the technical side, such as too high operational temperature range, cell efficiency, and long-term stability, as well as on the industrial side with implementation issues, material and device component availability, and cost. PEM technology research usually focuses on the synthesis of novel materials such as non-noble metal catalysts and non-halogenated membranes. In parallel, developing high-throughput and cost-effective manufacturing methods for components, in particular Membrane Electrode Assembly (MEA), can also lift an important barrier to their mass production, thus contributing to the same goals and securing industrial provision. From this perspective, printing technologies such as spray coating, inkjet printing, and screen printing have emerged as promising approaches with the required precision and scalability. This review covers recent advancements and developments in advanced PEMFC technology manufacturing, with a focus on 2D printing methodologies to fabricate some or all of the MEA components. Leveraging these techniques as simplified large-area manufacturing methods for PEM technology can become a more viable and industrially attractive solution. This work presents a comparison study addressing the key progress indicators both in process and in characterization to build a working framework in which both scientists, engineers and manufacturers can collaborate toward the industrial implementation of this emergent field.

Mechanical properties and thermal shock resistance of TiB2‒B4C composite ceramic tool materials at microscopic scale

AbstractA finite model incorporating microstructure was developed to investigate the thermal shock resistance of TiB2‒B4C composite ceramic cutting tool materials. Numerical simulations were conducted to analyze changes in the transient temperature field and thermal stress field during the thermal shock process. TiB2‒B4C composite ceramic tool materials were fabricated using discharge plasma sintering technology. With different B4C contents, different sintering temperatures and holding times as study variables, optimization of the sintering process parameters and ceramic material components was achieved through testing the mechanical and microscopic morphology of the ceramics. Thermal shock water quenching experiments were performed, and the strength‐decay method was employed to assess the thermal shock resistance of TiB2‒B4C ceramics. The findings indicate that the optimal sintering conditions are temperature of 1700°C and holding time of 5 min. The TiB2‒B4C ceramic material containing 20 vol% B4C exhibits superior comprehensive mechanical properties and thermal shock resistance, and its relative density, fracture toughness, hardness, and flexural strength were 99.3%, 6.8 MPa m1/2, 22.8 GPa, and 598 MPa, respectively. The critical thermal shock temperature difference falls within the range of 400°C‒500°C.

Tuning the thermo-mechanical synergies effect of solid oxide fuel cells with negative thermal expansion NdMnO3 in La0.6Sr0.4Co0.2Fe0.8O3-δ-based symmetric electrode

Solid oxide fuel cells (SOFCs) are efficient and clean energy conversion devices, but one of the major challenges for their marketization is the instability of different component materials under high temperature operating conditions. The existence of a certain internal stress gradient between materials with different thermal expansion characteristics in the process of SOFCs from low temperature assembly to high temperature use is the main reason of this instability, leading to the inability of SOFCs to repeat start-stop and the rapid decay of long-term stability performance. To improve these problems, a creative concept of fuel cell interface overall regulation is proposed, simplifying the complex interface between different components of SOFCs into a unified and adjustable quasi-zero difference thermal expansion interface. The composite of high catalytic activity electrode material and high stability negative thermal expansion material is used for electrolyte support structure symmetrical cell, which makes the whole cell “sandwich” structure thermally and mechanically compatible. As a concept verification, the classic high catalytic performance electrode material La0.6Sr0.4Co0.2Fe0.8O3-δ (LSCF), Gd0.2Ce0.8O2-δ (GDC) and NdMnO3 (NM) negative thermal expansion material with high chemical stability and mechanical stability were composited in equal proportions to form LSCF@GDC&NM electrode as the symmetrical electrode. After equal proportion compositing, the thermal expansion curve of LSCF@GDC&NM material can highly coincide with the thermal expansion curve of GDC, making the single cell with LSCF@GDC&NM electrode can withstand 25 power thermal cycles without significant performance decay, achieving 442 mW cm−2 at 800 °C and maintaining stably for 140 h without any degradation. These results show that using negative thermal expansion material to regulate electrode strategy is expected to make a whole zero difference thermal fuel cell configuration.

Impact of PCBM as a Third Component on Optical and Electrical Properties in Ternary Organic Blends.

This paper investigates the influence of constituent weight ratios on optical and electrical properties, with a particular focus on the intrinsic properties (such as electrical mobility) of ternary organic blends, highlighting the role of a third component. The study explores novel donor:acceptor1:acceptor2 (D:A1:A2) matrix blends with photovoltaic potential, systematically adjusting the ratio of the two acceptors in the mixtures, while keeping constant the donor:acceptor weight ratio (D:A = 1:1.4). Herein, depending on this adjustment, six different samples of 100-400 nm thickness are methodically characterized. Optical analysis demonstrates the spectral complementarity of the component materials and exposes the optimal weight ratio (D:A1:A2 = 1:1:0.4) for the highest optical absorption coefficient. Atomic force microscopy (AFM) analysis reveals improved and superior morphological attributes with the addition of the third component (fullerene). In terms of the electrical mobility of charge carriers, this study finds that the sample in which A1 = A2 has the greatest recorded value [μmax=1.41×10-4cm2/(Vs)]. This thorough study on ternary organic blends reveals the crucial relationship between acceptor ratios and the properties of the final blend, highlighting the critical function of the third component in influencing the intrinsic factors such as electrical mobility, offering valuable insights for the optimization of ternary organic solar cells.

Preparation of binder-free MoP/SnO2 carbon fiber composites with Cu-mediated surface modification for high-rate sodium ion storage

Nanofiber webs stacking with circular cross-section generally suffer from insufficient inter-fiber connection and thus poor electrical contact. Beyond regular 1D nanofibers, electrospinning is able to fabricate nanobelt webs with reinforced electron transfer for energy storage and conversion. Previously, we prepared quasi-2D belt-like fiber through electrospinning of PMo12-PPy-SnCl2-PVP-based solution (phosphomolybdic acid /polypyrrole /SnCl2 /polyvinylpyrrolidone) with freestanding property. Here, to boost the electrochemical performance, we proposed Cu-mediated surface engineering for construction of accessible active sites with balanced material components of MoP/SnO2 and carbon. As a result, thinner and porous belt-like fibers were obtained with high specific surface area (above 100 m2 g−1). The interfacial charge transfer was improved by superficial phosphides, as binder-free electrode the Cu-mediated MoP/SnO2 carbon fiber composite can deliver capacity above 200 mAh g−1 at 0.2 A g−1 under low mass loading (1.5–2.5 mg cm−2) and sustain capacity above 1.0 mAh cm−2 with loading around 5 mg cm−2 at 2 mA cm−2. Combined with ex-situ characterization, the sodiation process was probed.

Biomimetic artificial nacre-like microfiber of Co/C modified cellulose nanofiber/Ti3C2Tx MXene with efficient microwave absorption

Although considerable efforts have been made in the fabrication of MXene-based composites for microwave absorption (MA), there is a great challenge to assemble MXene into regularly arranged microfibers prepared by wet-spinning technique for application in the field of MA due to insufficient interlayer interactions between Ti3C2Tx flakes. Heterogeneous interface design by optimizing material components to construct ingenious microstructure is crucial for efficient microwave absorbers. Herein, artificial nacre-like supramolecular microfibers of Co/C modified cellulose nanofiber/Ti3C2Tx MXene (Co/C/CNF/Ti3C2Tx) with plenty of heterogeneous interfaces were prepared by a simple wet-spinning technology through a self-assembly process induced by hydrogen bonding interactions between CNF and Ti3C2Tx. The artificial nacre-like microfibers with layered structure possess abundant heterogeneous interfaces, which facilitate multiple reflections/scattering of electromagnetic waves (EMW) between these interfaces, and at the same time promote interfacial and dipole polarization. The introduction of magnetic Co/C nanoparticles not only offer additional magnetic loss ability and improved impedance matching, but also enhance conductivity loss and polarization loss. Benefiting from these advantages, Co/C/CNF/Ti3C2Tx (1:1:1) fiber exhibits superior MA performance with a minimum reflection loss (RLmin) of up to −62.32 dB (>99.9999 % energy absorption) and a broad effective absorption bandwidth (EAB) of 5.86 GHz. The work provides a promising method for the preparation of biomimetic artificial nacre-like MXene-based microfibers with efficient MA performance, which is expected to be applied in the field of flexible wearable electromagnetic protection.

Miniaturizing Hyperspectral Lidar System Employing Integrated Optical Filters

Hyperspectral LiDAR (HSL) has been utilized as an efficacious technique in object classification and recognition based on its unique capability to obtain ranges and spectra synchronously. Different kinds of HSL prototypes with varied structures have been promoted and measured its performance. However, almost all of these HSL prototypes employ complex and large spectroscopic devices, such as an Acousto-Optic Tunable Filter and Liquid-Crystal Tunable Filter, which makes this HSL system bulky and expensive, and then hinders its extensive application in many fields. In this paper, a smart and smaller spectroscopic component, an intergraded optical filter (IOF), is promoted to miniaturize these HSL systems. The system calibration, range precision, and spectral profile experiments were carried out to test the HSL prototype. Although the IOF employed here only covered a wavelength range of 699–758 nm with a six-channel passband and showed a transmittance of less than 50%, the HSL prototype showed excellent performance in ranging and spectral profile collecting. The spectral profiles collected are well in accordance with those acquired based on the AOTF. The spectral profiles of the fruits, vegetables, plants, and ore samples collected by the HSL based on an IOF can effectively reveal the status of the plants, the component materials, and ore species. Finally, we also showed the integrated design of the HSL based on a three-dimensional IOF and combined with a detector. The performance and designs of this HSL system based on an IOF show great potential for miniaturizing in some specific applications.

Tensile strength of particle reinforced composite with interfacial debonding

Strength prediction of a particle reinforced polymer composite (PRPC) is still challenging. Although a PRPC is overall isotropic, it is more difficult to predict its tensile strength accurately than a continuous fiber reinforced composite (CFRC). One reason for this difficulty is that the calculation of stress fields of the constituents in a PRPC are complicated. The other reason is that the strength of a PRPC is significantly affected by interfacial strength, which is hard to be measured directly. In our research, the discount of the composite strength after debonding is attributed to the intensifying stress concentration. Two stress concentration factors (SCFs) are derived respectively to characterize the stress fluctuations in the matrix caused by the embedded particle before and after debonding. Based on the micromechanics Bridging Model and the matrix true stress theory, these two SCFs can be applied to evaluate the interface strength and the ultimate tensile strength of the composite from the properties of its component materials. Illustrations are presented to verify the efficiency of our theory and analyze the main influencing factors on the strength of the PRPC, including mechanical properties of component materials, particle size and volume fraction.

Active-mixing printhead for on-the-fly composition adjustment of multi component materials in Direct Ink Writing

Multi-Material Additive Manufacturing (MMAM) enables the grading of material properties and the integration of functions within printed parts. While most MMAM methods are limited to process single-component or pre-mixed multi-component materials, the in-process mixing and extrusion of multi-component materials enables innovative material properties and use cases. When processing liquid multi-component materials, the individual component streams need to be homogenized in-process, but the required volume in conventional passive mixing hinders rapid transitions in material composition. In this paper, a two component printhead is presented which combines an active mixing approach with a continuous composition adjustment for a third additive. The approach to control the mixing composition is to influence the hydrodynamic equilibrium of individual material streams before merging them near the point of extrusion. The printhead’s functionality is verified in terms of mixing homogeneity and transition speed between material compositions.

Modeling of tungsten impurity transport and distribution in EAST based on multi-fluid and kinetic Monte Carlo simulations

In recent years, the materials of plasma facing components, such as divertor target plates, domes, and outer walls of tokamaks, such as ASDEX Upgrade, WEST, JET, EAST, and ITER, have been changed from carbon to tungsten because of its lower erosion and tritium retention rates. Impurities are produced by interactions between the plasma and the first wall. This study provides an investigation to simulate the transport and distribution of tungsten impurities in the edge plasma on EAST. The 2D multi-fluid edge plasma transport code SOLPS-ITER and 2D kinetic Monte Carlo impurity transport code DIVIMP were used in the simulations. The multi-fluid model in SOLPS-ITER and the kinetic Monte Carlo model in DIVIMP were employed to treat tungsten impurity ions. The 2D density contour distributions in the computational region and the 1D density radial profiles at the inner and outer midplanes of tungsten impurity particles with ionization states (W0–W+74) and the total tungsten particles with all charge states were obtained. With the heating power 1.5 MW and the line-averaged plasma density 2 × 1019 m−3, the results from SOLPS-ITER and DIVIMP show that the maximum density of tungsten ion with single ionization state is about 1014 m−3 and the total density of tungsten impurities with all charge states is about 1015 m−3 at the core boundary. To the best of our knowledge, the simulation results from SOLPS-ITER and DIVIMP are compared for the first time to benchmark SOLPS-ITER with the multi-fluid mode and DIVIMP with the kinetic model for tungsten impurity transport. The density distributions of tungsten impurities with different ionization states from SOLPS-ITER and DIVIMP are highly similar, and good agreement can be found under similar conditions involved in the calculation. From the comparison benchmark between SOLPS-ITER and DIVIMP for tungsten impurity transport, it can be concluded that the impurity transport approximation used by DIVIMP is good.

Assessment of different forecasting strategies for the breaking load resistance in notched specimens 3d-printed in PLA using additive manufacturing (FFF) technology

The introduction of fused deposition modelling in the industrial sector to produce functional components in thermoplastic materials, such as PLA, requires knowledge of the performance limits of such elements during the design phase. Predicting the breaking load resistance of notched specimens is essential to evaluate the mechanical performance of components manufactured using this technology. This study compares different methodologies based on the critical distance criterion (TCD) for predicting the static breaking strength of printed notched specimens made with Fused Filament Fabrication (FFF) technology using PLA material. Specimens with different topologies of V-notches were printed according to a standardized configuration. Various analysis techniques were applied to determine the breaking strength of each specimen. By comparing the results obtained with experimental data to assess their accuracy and reliability, it has been demonstrated that these methodologies, coupled with the concept of equivalent elastic material (EMC), can be useful for predicting static breaking load.

Catalyst residues severely impact the thermal stability and degradation mechanism of polycarbonates: How to turn a flaw into an opportunity

Three poly(cyclohexene carbonates) with molecular weights ranging from 4.9 to 9.4 kg/mol were synthesized from cyclohexene oxide and CO2 using macrocyclic phenolate dimetallic catalysts and purified by conventional purification procedure. A decrease in thermal stability of approximately 100 °C was observed in comparison to poly(cyclohexene carbonates) with similar molecular weights synthesized using salen metal catalysts. This decrease derives from the presence of traces of dimetallic catalyst which is able to promote the depolymerisation of poly(cyclohexene carbonate) to CO2 and cyclohexene oxide in contrast to the usual backbiting mechanism that leads to cyclic carbonate. The onset of the degradation can be precisely tuned by changing the amount of residual dimetallic catalyst or including species with functional groups that can reduce the availability of the catalytic centers. Therefore, the possibility of controlling the thermal stability of poly(cyclohexene carbonates) by varying the concentration of the catalyst and the surrounding chemical environment paves the way for the use of these polymers as components in self-sacrificial materials of interest for advanced applications.

Carbon Nanotubes Induce Mineralization of Human Cementoblasts

IntroductionCarbon nanotubes (CNT) are 1 of the allotropes of carbon with unique properties. CNT shows good bone-tissue compatibility and has been reported to induce osteogenesis; therefore, it is regarded as an ideal material in a wide range of applications. However, the therapeutic effect of CNT-containing materials in the healing of apical periodontal tissue is unknown. The purpose of this study was to clarify the effect of CNT on the proliferation and mineralization of the human cementoblast cell line (HCEM). MethodsThe proliferation of HCEM cells with CNT stimulation was assessed by 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide assay performed from 24–72 hours. Calcium deposition levels were evaluated by alizarin red S staining on days 7 and 10, and mineralization-related gene expression was examined by quantitative real-time polymerase chain reaction on days 3, 7, and 10. Scanning electron microscopy was used to observe the culture with CNT on day 14. ResultsCNT showed no cytotoxicity to HCEM cell proliferation. Treatment was performed with mineralization medium, CNT-induced HCEM mineralization on day 7, and increased calcium deposition on days 7 and 14. Messenger RNA expression of alkaline phosphatase was significantly increased throughout the experimental period, and bone sialoprotein was significantly increased on day 3 by CNT, whereas no effect was found on mRNA expression of type I collagen. CNT was observed in attachment to the cell surface on day 14. ConclusionsCNT promotes the mineralization of HCEM cells, indicating the potential as a new bioactive component for apical periodontal tissue regeneration materials through the regulation of cementoblast mineralization.

Compact cryogenic hydrogen test environment for small devices and material characterization

Currently, there is a great need for testing capabilities for material samples and components in LH2. This includes low temperature compatibility at 20 K, H2 compatibility and potential degradation or permeation effects. The test environment required for this is challenging and quite costly due to LH2 supply. Therefore, an alternative test concept was developed whereby the required amount of LH2 (typically 2–3 L) is generated directly on-site by simple condensation. This is achieved with a power-controlled cryocooler (115 W @ 80 K, 18 W @ 20 K). A cylindrical pressure vessel with an inner diameter of d = 109 mm and a length of approx. 500 mm designed for 2.1 MPa is used to hold the LH2 bath and the samples. The cryocooler and the sample chamber are installed in a common vacuum cryostat and are thermally coupled at the lower end. At the 20 K level, thermal coupling is achieved by a sophisticated thermosiphon arrangement. Hydrogen is taken from a pressure reservoir, pre-cooled at the cryocooler 80 K level, and then injected and liquefied within a couple of hours.

Thermal conductivity measurements for additively manufactured AlSi10Mg and Al6061-RAM2 Aluminum composites at cryogenic temperatures

Advances in 3D printing are disruptive opportunities for material selection and component design in cryogenics. However, thermophysical property measurements for these novel materials are generally unavailable at cryogenic temperatures. This experiment explores the variation in thermal conductivities due to print direction of two aluminium composites (AlSi10Mg and Al6061-RAM). The direct linear heat flow method was utilized to calculate thermal conductivities using a measured wattage input, temperature differential, and Fourier’s Law of Conduction. A multi-measurement linear regression was applied to determine thermal conductivities at fixed average temperatures over the range of 20-100K. The AlSi10Mg composite had a greater thermal conductivity than Al6061-T6 for both printing planes by approximately 230%. The XY-plane print direction resulted in a reduction in thermal conductivity compared with the Z-plane by approximately 30%. The AL6061-RAM composite had effective thermal conductivities smaller than the machined Al6061-T6 by approximately 70% for both print directions. The thermal conductivity in the Z-plane print direction was consistently greater than the thermal conductivity in the XY print direction. Validation studies were conducted utilizing Al6061-T6 and SS-304/304L. The calculated deviation for the validation samples depicted a 20% difference from the National Institute of Standards and Technologies (NIST) recommended reference values. The calculated uncertainty of the experimental system was 5-10%, increasing as temperature decreased. These preliminary measurements depict the need for further analysis on 3D printed composite materials and reverification of common materials due to improvements in current manufacturing methods since the classic experimental measurements were carried out for SS-304/304L and Al6061-T6.

Enhanced dielectric properties of co-substituted M-type Sr-La hexaferrite synthesized by citrate auto-combustion method

In this present research, comparative analysis of dielectric and electrical properties of M−type lanthanum-strontium (La-Sr) hexaferrites substituted with Co-Zr, Mn-Zr and Ni-Zr with chemical formulae: Sr0.85La0.15(CoZr)xFe12-2xO19, Sr0.85La0.15(MnZr)xFe12-2xO19 and Sr0.85La0.15(NiZr)xFe12-2xO19 (where x is 0.00 to 1.00 with ratio of 0.25) respectively have been investigated in 1 kHz to 1 MHz frequency range. The dielectric constant and loss tangent are generally shows decreasing trend with frequency and AC conductivity shows increasing trend with it. Dielectric constant, tangent loss and AC conductivity are increased with increase in substitution of Co-Zr and Mn-Zr doped La-Sr ferrites but shows opposite trend for Ni-Zr doped La-Sr hexaferrites. The higher electron exchange between ferrous cations (Fe2+) and ferric (Fe3+) cations are responsible for the higher polarization in ferrites. These newly synthesized ferrites have great potential for microwave absorbing material and microwave components