Excellent Dielectric Properties Research Articles

Microwave dielectric properties of Na2O–Ln2O3–MoO3–TiO2 (Ln = Nd, La and Ce) system with low‐sintering temperature

AbstractThis study examines the low‐loss and temperature‐stable Na2O–Ln2O3–MoO3–TiO2 (Ln = Nd, La and Ce) system, synthesized via a solid‐state process at low‐sintering temperatures ranging from 840°C to 900°C The structure, microstructure and microwave properties of the Na0.5Ln0.5MoO4–TiO2 (Ln = Nd, La and Ce) ceramics as a function of the sintering temperature were studied. The results of XRD patterns and microstructure characterization showed that the main phase in compositions belong to tetragonal scheelite and tetragonal structure. The ceramic composition Na0.5Ln0.5MoO4–TiO2 (Ln = Nd, La and Ce), sintered at 840°C–900°C for 2 hours, demonstrated excellent microwave dielectric properties, exhibiting relative dielectric constant (εr) of 13.9–14.4, Q × f value of about 31 100 (at 9.66 GHz) – 48 600 GHz (at 9.33 GHz), and temperature coefficient of –8.1 to –1 ppm/°C. Our work designs temperature‐stable microwave dielectric ceramics with low‐sintering temperature for LTCC technology applications.

Unlocking the Trade-off Between Intrinsic and Interfacial Thermal Transport of Boron Nitride Nanosheets by Surface Functionalization for Advanced Thermal Interface Materials.

The increasing computing power of AI presents a major challenge for high-power chip solution and heat dissipation. Boron nitride nanosheet-based thermal interface materials (BNNS-based TIMs) exhibit excellent electrical insulation property, ensuring the secure and stable operation of chips. However, the efficiency of micro/nano interfacial thermal transport is limited, impeding further enhancements in the thermal conductivity (TC) of BNNS-based TIMs. Here, a strategy of surface functionalization is reported to unlock the trade-off between the intrinsic and interfacial thermal transport of BNNS within TIMs. These results suggest that the surface functionalization maintains the intrinsic high TC of BNNS while significantly increasing binding energy between micro/nano interfaces in BNNS-based TIMs, effectively reducing interfacial thermal resistance of BNNS joint interfaces and interfaces between BNNSs and the matrix by 50% and 26.1%, respectively. The BNNS-based TIMs exhibit excellent TC (≈21-25W/(m·K)) and ultralow Young's modulus, which can promote the development of flexible high-performance chip cooling technology in the AI industry.

Exploration of microwave absorptivity and catalysis of CMF@Co-MoS2 for microwave-initiated depolymerization of lignin

Obtaining key platform chemicals from lignin is a sustainable refining concept of the non-petroleum route. Rapid pyrolysis is a potential refining technology, and microwave-assisted catalytic depolymerization with low energy consumption is preferred. Herein, we reported the strategy of microwave-initiated depolymerization using a self-designed dynamic vapor flow reaction system with a facilely prepared CMF@Co-MoS2-0.18 catalyst, achieving efficient conversion of lignin (Dealkalize) to monophenol. Under constant microwave irradiation (2.45 GHz), the CMF@Co-MoS2-0.18 catalyst had excellent dielectric properties (Dielectric loss factor: 0.56) and microwave heating properties (∼140 s rise to ∼ 600℃). Therefore, microwave-initiated depolymerization of lignin showed that the CMF@Co-MoS2-0.18 catalyst can improve the monophenol content (54.72 %) and phenol selectivity (35.84 %) under the synergistic effect of microwave absorptivity and catalysis. The reaction of the lignin model and kinetics analysis show that the CMF@Co-MoS2-0.18 catalyst increases the yield of monophenol by reducing depolymerization activation energy and selectively breaking the β-O-4 bond. The finite element analysis pointed out that under microwave irradiation, CMF@Co-MoS2-0.18 continuously conducted heat to lignin and the lignin vapor would have sufficient energy to collide with the catalyst active site at a high frequency, which led to an increase in the pre-exponential factor and initiated catalytic depolymerization lignin. In summary, we provide a potential pathway for the rapid conversion of lignin into key platform chemicals.

Performance of sandwich type fire-resistant flexible composite phase change material PEE@EBF for battery thermal management and runaway protection

To mitigate the risks of overheating and thermal runaway in lithium-ion batteries, this study proposes a novel sandwich-type fire-resistant flexible composite phase change material (CPCM), referred to as PEE@EBF. The core material (PEE) was created by melt-blending paraffin wax (PW), expanded graphite (EG), and ethylene–vinyl acetate copolymer (EVA). The outer layer, a fire-resistant coating (EBF), was applied to the surface of PEE and consists of epoxy resin (EP), boron nitride (BN), and the composite flame retardant (CFR). Test results demonstrated that PEE@EBF maintained structural integrity, exhibiting no significant deformation or leakage after being heated at 80 °C for 5 h. PEE@EBF also displayed a high latent heat of 166.6 J/g, thermal conductivity of 0.8 W/(m∙K), and excellent electrical insulation properties. Furthermore, it achieved a UL94 V-0 flame retardant rating, with notable reductions in peak heat release rate (PHRR) and peak smoke production rate (PSPR) by 67.8 % and 81.8 %, respectively. During long-term cycling at 4C, the peak temperature (PT) and maximum temperature difference (MTD) of batteries in the module incorporating PEE@EBF were reduced by 11.8 °C and 4 °C, respectively, compared to natural convection cooling. In addition, the heat generated during the battery thermal runaway was efficiently absorbed and transferred by PEE@EBF, delaying the irreversible thermal runaway process by 633 s. This indicated that the sandwich-type PEE@EBF was suitable for thermal management and fire protection in lithium-ion batteries or energy storage devices.

Preparation of Si3N4f/Si3N4 wave-transparent composites by vat photopolymerization combined with chemical vapor infiltration

The strategic combination of material selection, forming processes, and densification techniques is crucial for optimizing the performance of wave-transparent materials in extreme environments. This study is the first time to prepare Si3N4f/Si3N4 wave-transparent composites using a combination of vat photopolymerization (VPP) 3D printing and chemical vapor infiltration (CVI) processes. The effects of Si3N4f content on slurry preparation, green part printing, and final performance were systematically investigated. The addition of Si3N4f significantly enhanced the toughness of Si3N4 ceramics. Apart from their inherent toughening mechanisms, the "chimeric pinning" effect of the fibers contributes to increased interlayer bonding strength, thereby favorably impacting the mechanical properties. Combining VPP 3D printing and CVI processes resulted in Si3N4f/Si3N4 composites with a linear shrinkage rate within 1%, essentially achieving near-net shaping. Additionally, the composites exhibited excellent mechanical and dielectric properties, with a flexural strength of 76.2MPa, fracture toughness of 4.24MPa·m1/2, a dielectric constant of 4, and a dielectric loss tangent of 0.01. This study leverages the high strength and toughness advantages of Si3N4f and employs VPP 3D printing combined with CVI to achieve the objectives of lightweight, high transmittance, and near-net shaping. It provides theoretical support and experimental validation for designing and manufacturing wave-transparent materials.

Enhanced mechanical and dielectric properties of Si3N4−BN composite ceramics fabricated via reaction re-sinteirng process

Dense Si3N4−BN composite ceramics were synthesized using reaction re-sintering method which involved an in-situ reactive sintering followed by a re-sintering process, employing Si3N4 and SiB6 powders as raw materials. Initially, SiB6 underwent nitridation to form Si3N4 and BN during the in suit reactive sintering. Subsequently, the pores between the Si3N4 and BN grains were significantly removed during the re-sintering stage, facilitating the strong integration of Si3N4 and BN grains within the composite ceramics. The re-sintering process significantly enhanced both the density and mechanical properties of the composite ceramics. The generated BN grains were uniformly distributed throughout the Si3N4 matrix, thereby improving both the machinability and dielectric properties. The composite ceramics with 20 wt.% BN demonstrated excellent mechanical and dielectric properties, characterized by a low apparent porosity of 3.8%, a high flexural strength of 315.6 MPa, a Vickers hardness of 5.0 GPa, a low dielectric constant of 5.02, and a loss tangent ranging from 1× 10-3 to 2.5 × 10-3 at frequencies between 8.2 and 12.4 GHz.

High energy density and efficiency of laminated polymeric blend-based composites via introducing ultra-low content micrometer sheets

Polymeric blend-based composites are promising for dielectric capacitor due to the excellent dielectric and energy storage properties. However, the electric displacement difference (Dmax-Dr) and dielectric constant (εr) of the polymeric blend-based composites are incompatible, which further limits the improvement of the available energy densities (Ue). In this study, we propose the solution-processable laminated polymeric blend-based composites to address this challenge. The concurrent enhancement in Dmax-Dr, εr, Ue and charge-discharge efficiency (η) of designed composites is attributed to the synergistic interaction between macroscopic layered interfaces and microscopic interfaces. The laminated polymeric blend-based composites were fabricated by utilizing a blend of 50 wt% poly(vinylidene difluoride)-hexafluoropropylene (P(VDF-HFP)) and linear poly(methyl methacrylate) (PMMA) as the outer layer and P(VDF-HFP)/PMMA incorporated with an ultralow content alumina-modified strontium titanate plates (SrTiO3@Al2O3) the inner layer. As a result, laminated polymeric blend-based composite with the optimized content (0.5 vol%) delivers a maximum Ue of 14.36 J/cm3 due to highest Dmax-Dr of 7.96 μC/cm2, εr of 6.12 (1 kHz), Eb of 400 MV/m, and η of 76.6 %, outperforms those of representative polymer blend-based composites. Specially, laminated polymeric blend-based composite also exhibits the excellent energy storage reliability of different areas. Therefore, this contribution provides a viable approach to promote polymeric blend-based composites for capacitive energy storage.

Induced Electron Traps via the PCBM in P(VDF-HFP) Composites to Enhance Dielectric and Energy Storage Performance.

Polymer-based composites with excellent dielectric properties are essential for advanced energy storage applications. In this work, the [6,6]-phenyl-C61-butyric acid methyl ester (PCBM) as a filler was incorporated into the poly(vinylidene fluoride-co-hexafluoropropylene) (P(VDF-HFP)) composite to improve its dielectric performance. P(VDF-HFP) composite films with varying PCBM concentrations were prepared via solution casting and their dielectric, energy storage, and charge-discharge properties were characterized. It was found that the doped PCBM could introduce new charge traps with an energy level of 1.25 eV that modulate charge transport and energy storage characteristics of the polymer matrix. The dielectric constant of the composites was enhanced to the maximum of 10.87 as 0.2 vol% PCBM was added, while the breakdown strength reached 455 MV/m, achieving an energy density of 7.38 J/cm3, which is 33% higher than the pristine P(VDF-HFP) film. Furthermore, the charge-discharge efficiency of the composites was enhanced 66% under the electric field of 300 MV/m. These results demonstrate that PCBM significantly improves the dielectric and energy storage properties of P(VDF-HFP) composites, providing a promising approach for the development of high-performance dielectric materials in flexible energy storage devices.

Effect of binary ion substitution on the crystal structure and microwave dielectric properties of MgTa2O6 ceramics

AbstractMg1/3A11/3A21/3Ta2O6 ceramics (where A1 and A2 represent Co, Ni, or Zn) were prepared using the solid‐phase reaction route. The results of X‐ray diffraction and Raman tests showed that (Co1/2Ni1/2)2+, (Co1/ 2Zn1/2)2+, and (Ni1/2Zn1/2)2+ ions replaced Mg2+ ions in the lattice of MgTa2O6, resulting in the formation of a pure tri‐rutile structure. All three complex ions could significantly reduce the sintering temperature of the ceramics (by 150°C–200°C) and could broaden the sintering window. The large deviation (48.8%–69.2%) between the porosity corrected relative permittivity εr‐corr. and the theoretical relative permittivity εr‐theo. might be due to the overestimation of the ionic polarizability of Ta5+ by Shannon. (Co1/2Ni1/2)2+ has the most significant effect of increasing the bond energy of ceramic A–O bonds, reducing the τf value from 51 to 36 ppm/°C. In addition, the mechanisms affecting their dielectric properties are discussed based on bond ionicity (fi), full width at half maximum (FWHM) of Raman peak, and bond energy (E). Mg1/3Co1/3Ni1/3Ta2O6 ceramic sintered at 1350°C have the most excellent microwave dielectric properties: εr = 26.8, Q × f = 86,000 GHz, and τf = 36 ppm/°C.

Superhydrophobic Electrospun PI/PTFE Membranes with Ultralow Dielectric Constants for High-Frequency Telecommunication.

High-frequency, high-power, and high-speed telecommunication in a complex environment promotes the development of dielectric materials toward a low dielectric constant, low dielectric loss, good thermal properties, and long-term reliability. Here, polyimide/polytetrafluoroethylene (PI/PTFE) nanofiber membranes with an inherent super hydrophobicity, excellent dielectric properties, good thermal stability, and enhanced tensile strength were prepared via a simple electrospinning strategy and an imidization reaction. The obtained PI/PTFE membranes demonstrate a superlow average dielectric constant of 1.22-1.27 and a dielectric loss of 0.032-0.048 in high frequency, together with an enhanced tensile strength, benefiting from the special nanofiber-bead structure formed in the composite membrane. The mixing of polyamic acid (PAA) and PTFE in the electrospinning solution endows the obtained PI/PTFE nanofiber membrane with a uniform distribution of PTFE and thus an inherent superhydrophobicity with a water contact angle of 156.1 and 159.2° for PI/PTFE-30% and PI/PTFE-40%, respectively. Besides, the hydrophobicity could be kept even after standing more than 10,000 water drops, and the thermal properties exhibited promising results with Tmax = 587 °C and Td5% = 423 °C, rendering these PI/PTFE membranes favorable alternatives for prospective telecommunication.

Influence of casting-warm pressing process on the thermal conductivity of micro–nano-Al2O3 substrate

Alumina substrates are increasingly used for high-power integrated circuits due to their high thermal conductivity, low thermal expansion coefficient, and excellent insulation properties. However, pores in the green tape from the tape casting process reduce the thermal conductivity and permittivity of the sintered ceramic substrate. Researchers have attempted to minimize ceramic porosity with chemical additives or by sintering pure alumina at temperatures above 1650 °C, but these methods often degrade thermal conductivity or quality of substrate evenness. This study proposes a low-cost casting-warm pressing process to densify pure alumina ceramic substrates using micro–nano-mixed alumina powders and sintering at relatively low temperatures. The results indicate that the relative density of the pure alumina ceramic substrate prepared at 1500 °C is 93%, a 4.4% improvement over the tape casting process. Additionally, the thermal conductivity of the alumina substrate from the casting-warm pressing process reaches 15.89 W/(m K), which is 1.4 times higher than that of the tape casting process. Microstructure analysis shows that the casting-warm pressing process with micro- and nano-multi-scale mixed alumina powders forms a novel thermal conduction enhancement mechanism. Large particles in the green tape overlap, while small particles fill the spaces between the large particles. The connected micrometer-sized particle skeletons form high thermal conduction net channels in the substrate, improving the thermal conductivity for heat transfer.

Comprehensive Characterization of Bi1.34Fe0.66Nb1.34O6.35 Ceramics: Structural, Morphological, Electrical, and Magnetic Properties

Recent research in solid-state physics and materials engineering focuses on the development of new dielectric materials, with bismuth-based pyrochlores being already extensively applied in communications technology for their excellent dielectric properties and relatively low sintering temperatures. Herein, the structural, morphological, electrical, and magnetic properties of Bi1.34Fe0.66Nb1.34O6.35 ceramic, prepared by the sol–gel method and sintered at 500 °C, are investigated. The Rietveld refinement of the XRD pattern showed a cubic phase belonging to the space group Fd-3m and a crystallite size of 42 nm. Transmission electron microscopy further confirmed the crystallite size and the homogeneous distribution of Bi, Fe, Nb, and O elements, as evidenced by high-angle annular dark field imaging and STEM-EDX mapping. The morphology of the sample, assessed by scanning electron microscopy, is characterized by submicron-sized spherical particles. Dielectric spectroscopic studies revealed that the dielectric properties, strongly influenced by frequency and temperature, indicate the material’s potential for energy storage due to lower dielectric loss compared to the dielectric constant. The observed relaxation phenomena, confirmed through variations in dielectric loss and loss tangent, highlight the influence of grain boundaries and temperature on electron hopping and charge carrier dynamics. Using SQUID magnetometry, we identified two distinct magnetic phases. The primary phase, corresponding to the Bi1.34Fe0.66Nb1.34O6.35 ceramic, exhibits an antiferromagnetic behavior below its Néel temperature at around 8.8 K. A secondary high-Curie temperature ferrimagnetic phase, likely vestigial maghemite and/or magnetite, was also detected, indicating an estimated fraction below 0.02 wt.%.

Thermosetting boron-nitride-filled polybutadiene composites with enhanced thermal conductivity and good dielectric properties

Low dielectric materials with high heat dissipation, low dielectric constant (Dk), and dielectric loss (Df) are urgently needed to address the issues of signal cross-talk and heat accumulation arising from the rapid development of modern communication technology and the integration of microelectronics. Polyolefins, as hydrocarbon polymers, have shown significant potential due to their excellent low dielectric properties. However, their low polarity and flexible structures limit their thermal conductivity and thermomechanical properties. In this study, we developed a method to prepare thermosetting polybutadiene composites with enhanced thermal conductivity and good dielectric performance by modifying hexagonal boron nitride (h-BN) and hydroxyl-terminated polybutadiene (HTPB) with thermally cross-linkable benzocyclobutene (BCB) groups. The properties of the resulting composites were tailored by varying the filler content. With 30 wt% of the BCB-modified filler, the composite (HB-30) displayed excellent dielectric properties (Dk = 2.70; Df = 1.67 × 10−3 @10 GHz). Meanwhile, it exhibited a thermal conductivity of 0.615 W/mK at 35 °C, which was 7.1 times that of pristine HTPB. It also showed significantly enhanced mechanical properties and thermal stability with a storage modulus of 2.7 GPa and a glass transition temperature (Tg) of 208.5 °C. This method proved effective for preparing polymer composites with enhanced thermal conductivity, heat resistance, mechanical properties and good dielectric properties, making them suitable for high-frequency communication applications.

Zr4+ and Al3+ coordinated cross-linked conductive collagen fibers/solvent-free polyurethane foam with ultra-low reflective electromagnetic shielding properties

In recent years, electromagnetic shielding materials with low reflectance have developed rapidly. However, high material cost, poor bonding fastness, weak mechanical properties and other problems seriously limit its effect in practical use. In this work, flexible conductive collagen fibers (CLF-Zr4+/Al3+-CNTs) were prepared using chromium tanned waste leather as ingredient, carbon nanotubes (CNTs) as conductive filler and transition metal ions as coordination crosslinking agents, and their molecular dynamics were investigated by quantum chemical simulation software. On this basis, a flexible conductive foam with the double layer and double core-clad structure containing carbon nanotubes was constructed using the solvent-free polyurethane (SFPU) chemical foaming technology, and their electromagnetic shielding properties and reflectance were studied. The experiment results showed that when the ratio of CLF-Zr4+/Al3+-CNTs to SFPU polyol is 1:9 and the impregnation times of CNTs are 2, the loading capacity of CNTs in conductive foam is 0.14 mg/cm3, the electrical conductivity is 57.8 S/m, and the thermal conductivity is 0.061 W/(m·K). Meanwhile, when the thickness is 3 cm, the electromagnetic shielding performance is 42.09 dB, and the reflection efficiency is 0.66 %, the lowest reflection efficiency reaches 0.16 % in the experiment. The mechanism of electromagnetic shielding in conductive foams with the double layer and double core-clad structure has been further explored. The experiment results proved that the flexible conductive foam has excellent mechanical properties, stability, heat insulation and flame retardant properties, and has excellent electromagnetic shielding and low reflection characteristics due to its abundant holes, functional group, interface and hierarchical structure.

Exploring Structural and Optical Properties of Nanoparticles of Barium Titanate and Iron doped Barium Titanate and Their Potential Application in Antibacterial Activity

Background: Barium Titanate (BaTiO3) is a good candidate for a variety of applications due to its excellent dielectric, ferroelectric and piezoelectric properties. Methods: Pure and doped Barium Titanate (BTO) nanoparticles have been synthesized by the sol-gel method. Barium hydroxide octahydrate (Ba (OH)2.8H2O) and titanium (IV) iso-propoxide (Ti {OCH[CH3]2}4) were used as starting materials. Apart from pure Barium Titanate nanoparticles, Fe-doped BaTiO3 nanoparticles of three different concentrations: 0.1, 0.2 and 0.3 in mol% were prepared and characterized using X-ray diffraction (XRD), UV visible spectroscopy, Fourier Transform Infrared Spectroscopy (FTIR). Results: From the X-ray diffraction pattern, the particle size was found to be varied in a range of 17-25nm. By using UV visible spectroscopy it was observed that the band gap energy of pure BaTiO3 NP is 3.2eV. As the pure BaTiO3 nanoparticles are doped with 0.1% Fe, the band gap reduces to 3.175eV. For BaTiO3 doped with 0.2% and 0.3% Fe, the band gap energy values are 2.709 and 2.652 respectively. FTIR spectra were used to analyze the vibrational modes of BaTiO3. From the result obtained from FTIR, we can see that the absorption spectrum ranges from 450cm-1-4000cm-1. The prominent peak of pure BaTiO3 is at 500cm-1 which is due to the vibration of the Ti-O band in crystal lattice. For BaTiO3 doped with Fe2O3, the wave number of the absorption peak is shifted from 500cm-1 in pure BaTiO3. The antibacterial studies were conducted on Pseudomonas aeruginosa, Staphylococcus aureus and Escherichia coli. Conclusion: Both pure and iron-doped Barium Titanate showed significant antibacterial properties, confirming the antibacterial property of Barium Titanate nanoparticles.

Enhanced Oxidation Resistance and Interface Stability of Atomic-Layer-Deposited MoNx Electrodes via TiN Passivation for DRAM Cell Capacitor Applications.

The continuous miniaturization of dynamic random-access memory (DRAM) capacitors has amplified the demand for electrode materials featuring specific characteristics, such as low resistivity, high work function, chemical stability, excellent interface quality with high-k dielectrics, and superior mechanical properties. In this study, molybdenum nitride (MoNx) films were deposited using a plasma-enhanced atomic layer deposition (PEALD) employing bis(isopropylcyclopentadienyl)molybdenum(IV) dihydride and NH3 plasma for DRAM capacitor electrode applications. Depending on the deposition temperatures of the PEALD MoNx films ranging from 200 to 400 °C, the Mo/N ratio and crystal structure varied, transitioning from the cubic NaCl-B1-type MoN phase with Mo/N ratio of 1.4 to the cubic γ-Mo2N phase with Mo/N ratio of 1.9. Notably, MoNx films grown at 400 °C exhibited low resistivity (435 μΩ·cm), a high work function (5.28 eV), and superior mechanical hardness (11.3 GPa) compared to ALD TiN films. Despite these excellent properties, the PEALD MoNx electrode demonstrated insufficient chemical stability, particularly in terms of oxidation resistance and interface quality with ALD HfxZr1-xO2 (HZO) films. This resulted in poor morphology and the formation of significant oxygen-deficient HZO layers (such as HfO2-x), leading to considerable degradation in the electrical performance of metal-insulator-metal (MIM) capacitors. To mitigate this issue, a thin (2.5-14 nm) ALD TiN layer was introduced as a passivation layer between the MoNx bottom electrode and HZO dielectric. The TiN-passivated MoNx (TiN/MoNx) electrode showed substantially enhanced oxidation resistance and reduced interfacial reactions with the HZO dielectric. Consequently, MIM capacitors with TiN/MoNx bottom electrodes demonstrated outstanding electrical performance, including excellent dielectric properties, low leakage current density, and high mechanical strength. Hence, this study proposes a promising candidates for storage nodes in the next-generation DRAM capacitors.

Structural design and characterization of a new type of organic nonlinear optical flavanone crystal

Two new crystals were designed and obtained: the chalcone derivative HMMP (1-(2‑hydroxy-4-methoxyphenyl)-3-(4-(methylthio)phenyl)prop‑2-en-1-one) and the flavanone derivative 7M4MC (7‑methoxy-2-(4-(methylthio)phenyl)chroman-4-one). Yellow bulk 7M4MC single crystal with dimensions of 3 × 2 × 1 mm3 and orange-yellow needle-like HMMP single crystal were grown by solution evaporation. 7M4MC crystal belongs to the P21 space group of the monoclinic structure, which has a non-centrosymmetric structure. HMMP crystal monoclinic, belongs to the P21/m space group with a centrosymmetric structure. In the 7M4MC molecule, the methoxy and methylthio groups act as electron donors (D) and the carbonyl group acts as an electron acceptor (A), forming a d-π-A-π-D structure with an electron gradient. 7M4MC exhibits a high degree of second-harmonic generation intensity (11 × KDP), a broad transmission range (600–1600 nm, >88 %), an elevated optical energy bandgap (Eg = 2.57 eV), high thermal stability (Tm = 105 °C) and excellent dielectric properties (εr ≈ 2.1). This work not only provides two new crystals but also offers a viable molecular design option by changing the degree of intramolecular distortion by altering the backbone structure.

Effect of Diatomite on the Mechanical and Electrical Properties of Polyurethane/Epoxy Resin Composites

ABSTRACT Epoxy resin is widely utilized for the encapsulation of power semiconductor devices, necessitating excellent insulation properties, mechanical performance, and moisture resistance. In this study, hexadecyltrimethoxysilane was employed to modify diatomite, which was then combined with polyurethane-modified epoxy resin to fabricate a series of filled composites with varying diatomite content. The influence of diatomite content on the mechanical properties, thermal properties, and insulation performance of the polyurethane/epoxy resin composites was investigated. Experimental results showed that, under the synergistic effect of polyurethane and diatomite, the composite containing 4 wt.% diatomite exhibited improvements of 13.95% and 61.11% in tensile strength and flexural strength, respectively, compared to the epoxy resin. The elongation at break and flexural displacement also increased by 22.46% and 68.23%, respectively. Furthermore, the incorporation of diatomite effectively compensated for the thermal losses caused by polyurethane, enhancing thermal stability. Electrical property tests indicated that the addition of diatomite reduced the dielectric constant and conductivity of the epoxy resin while simultaneously improving its breakdown strength.

Structural characteristics, P-V-L theory, Raman spectra, and microwave dielectric properties of (La1-xNdx)2(Zr0.96Ti0.04)3(MoO4)9 ceramics for LTCC applications

This article explores the microwave dielectric properties of (La1-xNdx)2(Zr0.96Ti0.04)3(MoO4)9 (x=0.1,0.3,0.5, and 0.7) ceramics prepared by solid-state reaction. Utilizing the Rietveld refinement technique in XRD, the sample is identified as a trigonal crystal system belonging to the R3¯c space group. SEM analysis indicates that relative density has a significant impact on the εr and Q×f of ceramics. The Q×f values of ceramics are closely related to the FWHM of the Raman spectra. At 750℃, (La0.5Nd0.5)2(Zr0.96Ti0.04)3(MoO4)9 ceramic exhibited excellent dielectric properties: εr = 10.4 (±0.08), Q×f = 149,300 (±3211) GHz, τf = −34.8 (±0.7) ppm/℃. To gain a deeper understanding of the intrinsic mechanisms governing the microwave dielectric properties of ceramics, analysis based on the P-V-L theory reveals that the La(Nd)-O bond and Mo-O bond contribute significantly to εr and Q×f, respectively.

Mechanisms of enhanced performance in Zr4+/Ta5+ codoped rutile-TiO2 ceramics via broadband dielectric spectroscopy.

Aliovalent dopant codoped rutile-TiO2 materials have garnered attention due to their excellent performance properties, characterized by low loss tangent (tanδ), high dielectric permittivity (ε'), and stable ε' over a broad temperature range. This performance is primarily due to the electron-pinned defect-dipoles (EPDDs) of the complex defects [Formula: see text]Ti3+-[Formula: see text]Ti3+BTi. Notably, the excellent dielectric properties in ZrxTa2.5%Ti0.975-xO2 (Zr-TTO) ceramics can be achieved using the traditional mixed oxide method without the EPDDs, due to the absence of A3+ (acceptor doping ions). Instead, the existence of localized free electrons and oxygen vacancies ([Formula: see text]) in Zr-TTO structures, due to doping ions and the sintering process, was confirmed by X-ray photoelectron and Raman spectroscopies. These ceramics exhibited ε'~ 2 × 104 and tanδ < 0.03 at 1kHz and 25°C in the 2.5-10%Zr-TTO samples. Moreover, all ceramics demonstrated a maximum ε' change (∆ε') of less than ±15% over the temperature range suitable for X7R and X8R type ceramic capacitors. Significantly, the change in ε' related to relative humility was calculated to be less than ±0.5% over the range of 50-95% RH, indicating the environmental stability of the dielectric properties, which is essential for capacitor applications. Investigations suggested that at least four mechanisms contributed to this system: the intrinsic effect of ionic polarization, Ti4+ · e- -[Formula: see text]- Ti4+ · e- and Ti4+ · e- - [Formula: see text] defects, interfacial polarization at insulating grain boundaries, and non-Ohmic contact between the surface sample and the metal electrode.