Frequency dependence of dielectric properties of metallodielectric SrTiO3–Pt composites

The frequency dependence of dielectric properties of SrTiO₃–Pt (platinum) composites has been investigated. The SrTiO₃–Pt composites sintered at 1300 °C for 2 h was prepared by using conventional ceramic fabrication method. The dense metallodielectric composites without chemical reaction between SrTiO₃ and Pt during sintering process were obtained. The relative permittivity (ɛ_r) of SrTiO₃–Pt composites was increased with increase of amount of Pt. The maximum ɛ_r of 2150 at 1 MHz was obtained for the composite of SrTiO₃–27 vol.% Pt. Moreover, the SrTiO₃–Pt composites exhibited high values of ɛ_r at low frequencies than at high frequencies due to space charge polarization. The loss tangent (tan δ) of SrTiO₃–Pt composites increased with increasing amount of Pt, and decreased with increasing frequency up to 1 MHz. However, the tan δ of SrTiO₃–Pt composites was significantly increased at microwave frequency due to abrupt increase of ac conductivity of composite.     

Electrical and thermal properties of low permittivity Sr2Al2SiO7 ceramic filled HDPE composites

The feasibility of low permittivity Sr₂Al₂SiO₇ (SAS) ceramic filled high density polyethylene (HDPE) composites for substrate and packaging applications has been investigated in this paper. The composites were prepared by the melt mixing and hot pressing techniques. Scanning electron microscopic images of SAS filled HDPE showed the increased connectivity with filler loading. The composites showed excellent relative density (>98%) with low bulk density (<2.40 g cm^?3) and very low moisture absorption (<0.10 wt%). The relative permittivity (ε_r) and the dielectric loss (tan δ) at 1 MHz and at 5 GHz were found to be low and found to increase with filler volume fraction (V_f). The experimentally observed relative permittivity at 5 GHz was correlated with the values proposed by different theoretical models. Among them, effective medium theory (EMT) gave better fit with experimental values except at the highest filler loading (0.50 V_f). Improvement in the thermal properties was also observed with filler content. The coefficient of linear thermal expansion (CTE) was found to decrease with filler content. Thermal conductivity (TC) of the composite was greatly enhanced as a function of filler volume fraction. The composite with 0.50 filler volume fraction showed balanced thermal and dielectric properties with ε_r=4.2, tan δ=3.9×10^?3, TC=2.2 W m^?1 K^?1 and CTE=101 ppm/°C.     

Flexible and low cost lead free composites with high dielectric constant

Highly flexible lead free composite film having random distribution of ceramic filler was synthesized using Barium Titanate (BT) as a filler and inexpensive Thermoplastic Polyurethane (TPU) as a matrix. The results show that the 30 vol% BT-TPU composite has a dielectric constant of ~31 which is comparable to the expensive and difficult to produce PVDF based composites. With a breakdown field of 150 kV/mm, an energy density value of ~3 J/cm³ was estimated. These lead-free TPU based composites provide an alternative to PVDF based composites for energy storage applications.     

Enhanced thermal conductivity of low-temperature sintered borosilicate glass–AlN composites with β-Si3N4 whiskers

The effects of β-Si₃N₄ whiskers on the thermal conductivity of low-temperature sintered borosilicate glass–AlN composites were systematically investigated. The thermal conductivity of borosilicate glass–AlN ceramic composite was increased from 11.9 to 18.8 W/m K by incorporating 14 vol% β-Si₃N₄ whiskers, and high flexural strength up to 226 MPa were achieved along with low relative dielectric constant of 6.5 and dielectric loss of 0.16% at 1 MHz. Microstructure characterization and percolation model analysis indicated that thermal percolation network formation in the ceramic composites led to the high thermal conductivity. The crystallization of the borosilicate microcrystal glass also contributed to the enhancement of thermal conductivity. Such ceramic composites with low sintering temperature and high thermal conductivity might be a promising material for electronic packaging applications.     

Calcium copper titanate/polyurethane composite films with high dielectric constant,low dielectric loss and super flexibility

Calcium copper titanate(CCTO)/polyurethane composite films with high dielectric constant, low dielectric loss and super flexibility were fabricated by incorporating CCTO ceramic powders into millable polyurethane elastomer (MPU) matrix using a rubber milling combined with hot compression molding method. The composite films show uniform microstructures and the dielectric constant is as high as 35.2 while the dielectric loss is only 0.041 when CCTO content reaches 40 vol% at 100 Hz and room temperature (RT). Moreover, it is important to note that this film has stable dielectric constant and dielectric loss in a relatively wide temperature range (from 0 °C to 70 °C), which is significantly import to the practice use of electronic devices based on CCTO composites. In addition, the flexibility of the film could be retained even when the CCTO content is up to 40 vol% and the elongation at break of this composite film is as high as 159.1%. Theoretical analysis indicates that the experimental data are in good conformity to the effective medium theory (EMT) model with a derived n = 0.21, suggesting more close association of the dielectric constant with the CCTO filler size and shape.     

High permittivity ceramics loaded silicone elastomer composites for flexible electronics applications

The dielectric properties of silicone elastomer composites are important in designing flexible electronic devices. The recent explosive growth in wireless communication, automotive and biomedical applications increases the demand for flexible dielectric materials. However, it is very difficult to identify a homogeneous material which possesses these desired properties. Flexible silicone rubber- ceramic composites based BaTiO₃ (BT), SrTiO₃ (ST) and Ca_(1−x)Nd_(2x/3)TiO₃ (CNT) ceramic fillers have been prepared. The relative permittivity, thermal conductivity and water absorption increase whereas the coefficient of linear thermal expansion decrease as the volume fraction of filler increases. In the case of dielectric loss; a decreasing trend is shown by SR-ST and SR-CNT composites with filler volume fraction whereas SR-BT composites show a reverse trend since BT is a lossy material. The composites have εr in the range 3–14 in the microwave frequency range. The composites with high filler loading are suitable candidates for core of flexible dielectric waveguide and embedded capacitor applications and the composites with ST and CNT are suitable for cladding of flexible dielectric waveguide and also for microwave substrate applications     

Electrical properties of low-temperature-fired ferrite–dielectric composites

The effects of the BaO·(Nd_0.8Bi_0.2)₂O₃·4TiO₂ (BNBT) to NiCuZn ferrite ratio and addition of Bi₂O₃–B₂O₃–SiO₂–ZnO (BBSZ) glass on the sintering behavior, microstructure evolution, dielectric and magnetic properties of BNBT–NiCuZn ferrite composites were investigated in developing low-temperature-fired composites for high frequency electromagnetic interference (EMI) devices. The results indicate that these composites can be densified at 900 °C and exhibit superior dielectric and magnetic properties with the addition of BBSZ glass. The dielectric system used in the ferrite–dielectric composites reported in the previous studies mostly belong to the ferroelectricity group, which are not suitable for use in the high frequency range (>800 MHz) due to the selfresonance frequency limit. In this study, the dielectric constant remains nearly a constant over a wide range of frequencies (100 MHz to 1 GHz) and the magnetic resonance frequencies are larger than 100 MHz for the BNBT + BBSZ glass–NiCuZn ferrite composites. Therefore, the BNBT + BBSZ glass–NiCuZn ferrite composites can be a good candidate material for high frequency EMI device applications.     

Dielectric and ferroelectric hysteresis properties of 1–3 lead magnesium niobate–lead titanate ceramic/Portland cement composites

In this work, lead magnesium niobate–lead titanate (PMN–PT) ceramic was cut and filled with Portland cement (PC) to produce 1–3 connectivity PMN–PT/PC composites. Dielectric and ferroelectric hysteresis properties of these composites with PMN–PT ceramic volume content of 60% were investigated. Room temperature dielectric constant (?_r) at 1 kHz of the PMN–PT/PC composite was found to be ≈1500. At higher frequency (20 kHz), the dielectric constant was reduced to the value of ≈1300. Ferroelectric (polarization–electric field) hysteresis loops at 10–90 Hz and varying electric field were measured. The “instantaneous” remnant polarization (P_ir) at 50 Hz and at the electric field of 7 kV/cm of the PMN–PT/PC composite was found to be ≈10 μC/cm². These values of 1–3 composites therefore are promising when compared to previous results of composites at similar conditions.     

Elimination of parasitic effects due to measurement conditions of SrTiO3 thin films up to 40 GHz

Effective use of electromagnetic simulation software for evaluation of the microwave properties of dielectric thin films was demonstrated. The reliability of the high-frequency dielectric properties extracted from the measured S₁₁ reflection coefficients with the aid of the electromagnetic simulation software is mainly limited by how accurately the measured parasitics are simulated. The need to correct the parasitic differences between the simulation and measurement was shown by the significant dependence of probe contact position on the obtained dielectric properties. The parasitic differences were represented by series and parallel correction admittances connected to the measured admittance and were effectively eliminated. The high-frequency dielectric properties of a highly crystalline SrTiO₃ (STO) thin film were investigated up to 40 GHz by using the measurement techniques developed. The permittivity (relative dielectric constant) of the STO thin film remained substantially constant at 265 up to 40 GHz, and the dielectric loss value was about 0.03 at 40 GHz.     

Fabrication and properties of composites from BST and polypropylene-graft-poly(styrene-stat-divinylbenzene)

In this work, ceramic–polymer composites were fabricated from barium strontium titanate powder (BST) and polypropylene-graft-poly(styrene-stat-divinylbenzene) (ER) using a twin-screw extruder. The compounding process was characterized by rheological measurements. The effects of volume loading of BST on dielectric and mechanical properties were investigated. The dielectric properties were measured as a function of frequency and BST loading. For example, the relative permittivity and loss tangent (tan δ) of the BST–ER composites at 1 GHz were gradually increased from 2.4 and 0.0001 to 28.5 and 0.0085, respectively, as the loading was increased from 0 to 50.5 vol.%. Stearic acid (StA) was used as a surface-modifier of the BST. With an approximate surface coverage of 83%, an improvement in processability and a slight increase of the permittivity was observed, while tan δ remained low. The excellent dielectric characteristics of these composites, with high permittivity and low tan δ, make them attractive novel electronic materials for high frequency applications.     

Piezoelectric and dielectric properties of (K0.44Na0.52Li0.04)(Nb0.86Ta0.10Sb0.04)O3–PVDF composites

(Li, Ta, Sb) modified sodium potassium niobate/poly(vinylidene fluoride) [(K_0.44Na_0.52Li_0.04)(Nb_0.86Ta_0.10Sb_0.04)O₃–PVDF] 0-3 composites were prepared by a cold press technique, and their piezoelectric and dielectric properties were characterized. All composites exhibited good dispersion of ceramic particles in the polymer matrix. The piezoelectric and dielectric constants were found to be enhanced as the concentration of sodium potassium niobate increases. Even though the process is simple, the composite prepared in this study showed better piezoelectric and dielectric properties than PZT–polymer composites. At room temperature, a (K_0.44Na_0.52Li_0.04)(Nb_0.86Ta_0.10Sb_0.04)O₃–PVDF (7:3) composite revealed a relative dielectric constant, ?_r = 166, piezoelectric constant, d₃₃ = 33 pC/N and coercive field, E_c = 5 kV/cm.     

Preparation and characterization of lead-free (K0.47Na0.51Li0.02)(Nb0.8Ta0.2)O3 piezoceramic/epoxy composites with 0–3 connectivity

Lead-free (K_0.47Na_0.51Li_0.02)(Nb_0.8Ta_0.2)O₃ (KNLNT) piezoceramic/epoxy composites with 0–3 connectivity were prepared using cold-pressing. The dielectric and piezoelectric properties of the composites were examined as a function of mean particle size (D) within the range of 27–174 μm at a fixed ceramic content of 85 vol%. The dielectric constant increased with D by the combined effects of increased connectivity and decreased surface-to-volume ratio of ceramics. When D = 125 μm, the piezoelectric constant showed a highest value of 44 pC/N that is much greater than those of previous reports on lead-free piezoelectric 0–3 ceramic/polymer composites.     

Varistor and dielectric properties of SiO2 doped SnO2-Zn2SnO4 ceramic composites

In this work, SiO₂ doped SnO₂-Zn₂SnO₄ ceramic composites with excellent varistor and dielectric properties were prepared through traditional ceramic processing. The obtained nonlinear coefficient α was as high as 9.6, and the breakdown electrical field EB and leakage current density JL was as low as 5.9 V/mm and 62 μA/cm², respectively. At a low frequency of 40 Hz, the relative permittivity εr measured at room temperature was higher than 2.5×10⁴. The nonlinear decrease of the semicircle diameter in the complex impedance spectra with increasing DC bias voltage indicates that the grain boundary effect is an important origin of the varistor and giant permittivity properties. With an increase of temperature, the relaxor peak of the imaginary part M″ of the complex electric modulus shifted to high frequency and the activation energy E_a obtained from the M″ spectrum was about 0.31 eV, much lower than the grain boundary barrier height ϕ_b. The results suggest that other mechanisms may also be responsible for the giant permittivity property besides grain boundary barriers.     

Fabrication and origin of high-k carbon nanotube/epoxy composites with low dielectric loss through layer-by-layer casting technique

The distribution of polarized space charges and their relaxation behavior in high dielectric constant electric conductor/polymer composites are main factors that determine the frequency-dependent dielectric constant and dielectric loss. However, few reports focus on this motif. We present here the dielectric performance and mechanism of a unique kind of composites with multi-layers (coded as [MWCNT/EP]_x, where x refers to the number of layers), fabricated by using layer-by-layer casting technique. Each composite layer with same thickness was composed of multi-walled carbon nanotubes (MWCNTs) and epoxy (EP) resin. When the loading of MWCNTs is 0.5 wt%, the four-layer [MWCNT0.5/EP]₄ material shows the highest dielectric constant (465 at 1 Hz) and low dielectric loss tangent (0.7 at 1 Hz), about 4 and 2.1 × 10⁻² times the values of traditional MWCNT0.5/EP composite, respectively. By investigating the space charge polarization (SCP), Debye polarization and dielectric moduli in [MWCNT/EP]_x materials, the complex relationships and the origin among dielectric constant, dielectric loss, frequency and the content of filler were clearly elucidated. The SCP within each layer is different from that between layers. The greatly improved dielectric properties of [MWCNT/EP]_x materials are believed to be the reinforced SCP and blocked transport of carriers between every two layers.     

Microwave dielectric properties of Pb2MoO5 ceramic with ultra-low sintering temperature

Ultra-low firing microwave dielectric ceramic Pb₂MoO₅ with monoclinic structure was prepared via a conventional solid state reaction method. The sintering temperature ranged from 530 °C to 650 °C. The relative densities of the ceramic samples were about 97% when the sintering temperature was greater than 570 °C. The best microwave dielectric properties were obtained in the ceramic sintered at 610 °C for 2 h with a permittivity ∼19.1, a Q × f value about 21,960 GHz (at 7.461 GHz) and a temperature coefficient value of −60 ppm/°C. From the X-ray diffraction, backscattered electron image results of the co-fired samples with 30 wt% silver and aluminum additive, the Pb₂MoO₅ ceramics were found not to react with Ag and Al at 610 °C for 4 h. The microwave dielectric properties and ultra-low sintering temperature of Pb₂MoO₅ ceramic make it a promising candidate for low temperature co-fired ceramic applications.     

Magneto-dielectric laminated Ba(Fe0.5Nb0.5)O3-Bi0.2Y2.8Fe5O12 composites with high dielectric constant and high permeability

Magneto-dielectric laminated ceramic composites of xBa(Fe_0.5Nb_0.5)O₃-(1-x)Bi_0.2Y_2.8Fe₅O₁₂(BFN-BYIG) with high volume fractions of the giant dielectric constant material BFN (x=10, 30, 50, 70 wt%) were fabricated by the solid-state sintering method. Microstructure, dielectric and magnetic properties of the composites were investigated. The composites possess stable dielectric properties in the frequency range from 100 Hz to 1 MHz with high dielectric constant and low dielectric loss. The maximum permeability of the magneto-dielectric laminated composites reaches up to about 25. And the magnetic behaviors are strongly dependent on the mass ratio of BYIG. The results indicate that such multilayer structures of BFN/BYIG can enhance the permeability and decrease the dielectric and magnetic loss efficiently.     

Synthesis,characterization, and microwave dielectric properties of ZnTiTa2O8 ceramics with ixiolite structure obtained through the aqueous sol–gel process

Nano-sized ZnTiTa₂O₈ powders with ixiolite structure, with particle sizes ranging from 10 nm to 30 nm, were synthesized by thermal decomposition at 950 °C. The precursors were obtained by aqueous sol–gel and the compacted and sintered ceramics with nearly full density were obtained through subsequent heat treatment. The microstructure and electrical performance were characterized by field emission scanning electron microscopy, x-ray diffraction, and microwave dielectric measurements. All the samples prepared in the range 950–1150 °C exhibit single ixiolite phase and relative density between ~87% and ~94%. The variation of permittivity and Q·ƒ value agreed with that of the relative density. Pure ZnTiTa₂O₈ ceramic sintered at 1050 °C for 4 h exhibited good microwave dielectric properties with a permittivity of 35.7, Q·ƒ value of 57,550 GHz, and the temperature coefficient of resonant frequency of about −24.7 ppm/°C. The relatively low sintering temperature and excellent dielectric properties in the microwave range would make these ceramics promising for applications in electronics.     

Dielectric and electromagnetic wave absorption properties of reduced graphene oxide/barium aluminosilicate glass–ceramic composites

BaAl₂Si₂O₈ (BAS) glass–ceramic powders were prepared by sol–gel method. Graphene oxide (GO)/BAS mixture powders were prepared by a simple mixing process of GO and BAS. Dense and uniform reduced graphene oxide (RGO)/BAS composites were fabricated by the hot-pressing of GO/BAS, which was accompanied by the in-situ thermal reduction of GO. Microstructure, phase composition, dielectric and electromagnetic wave (EM) absorption properties of RGO/BAS were investigated. The results reveal that RGO can promote the hexacelsian-to-celsian phase transformation of BAS. In the frequency range from 8 GHz to 12 GHz, the complex permittivity of RGO/BAS increases with increasing RGO content. The composite with 1.5 wt% of RGO shows good EM absorbing ability. When the sample thickness is 2.1 mm, the minimum reflection coefficient (RC) reaches −33 dB, and the effective absorption bandwidth is more than 3.1 GHz.     

Dielectric properties of barium titanate–molybdenum composite

The barium titanate–molybdenum composites were prepared through solid state reaction method in argon atmosphere. The microstructure, resistivity, and dielectric properties of the composites were investigated. XRD results indicated that chemical reactions between barium titanate (BaTiO₃:BT) and molybdenum (Mo) have taken place during sintering, resulting in the formation of BaMoO₄ (BM) and BaTi₂O₅ (BT₂). The resistivity decreased with the increasing amount of Mo in the composites. The composites (when x = 5 and 20 wt.%) showed lower dielectric constant than pure BaTiO₃, especially, the dielectric constant (when x = 20 wt.%) reached a minimum value (<10⁴), while composites (when x = 10 and 15 wt.%) showed rather high dielectric constant at temperatures range from 25 °C to 160 °C. The dielectric constant of the composite gradually decreased with increase in frequency at the room temperature. The dielectric constant of composite (when x = 5 wt.%) comes up to 10⁴, and the T_c (Curie temperature) of the composite was relatively higher than that of BT (120 °C).     

Effect of the filler morphology on the crystallization behavior and dielectric properties of the polyvinylidene fluoride-based composite

Ceramic/polymer composites can be chemically stable, mechanically strong, and flexible, which make them candidates for electric devices, such as pressure or temperature sensors, energy storage or harvesting devices, actuators, and so forth. Depending on the application, various electrical properties are of importance. Polymers usually have low dielectric permittivity, but increased dielectric permittivity can be achieved by the addition of the ceramic fillers with high dielectric constant. With the aim to enhance dielectric properties of the composite without loss of flexibility, 5 wt% of BaTiO₃-Fe₂O₃ powder was added into a polyvinylidene fluoride matrix. The powder was prepared by different synthesis conditions to produce core/shell structures. The effect of the phase composition and morphology of the BaTiO₃-Fe₂O₃ core/shell filler on the structure and lattice dynamics of the polymer composites was investigated. Based on the results of the thermal analysis, various parameters of ceramic/polymer composites were determined. Differences in the phase composition and morphology of the filler have an influence on the formation of various polyvinylidene fluoride allomorphs and the degree of crystallinity. Furthermore, the dielectric performances of pure polyvinylidene fluoride and the polymer/ceramic composites were measured.