Defects and microstructure of highly conducting Al-doped ZnO ceramics obtained via spark plasma sintering

Al-doped ZnO ceramics were sintered by conventional sintering method and spark plasma sintering (SPS) respectively. Electrical properties and microstructure have been investigated by various measurements. The samples sintered via SPS exhibit a huge electrical conductivity, up to 3.0 × 10⁵ S/m at room temperature, which was much higher than that of the sample sintered via the conventional sintering. Structural and morphorlogical characterizations pointed out that the further incorporation of Al ions and the absence of a secondary phase, contribute to the increase of the carrier concentration. Raman spectroscopy revealed the occurrence of structural distortions and a disorder induced by Al doping. Photoluminescence spectra were interpreted by different electronic active defects such as the defect complexes (Al_Zn-Zn_i) which play a key for the high electrical conductivity. Thus, SPS and Al doping modified the microstructure and the concentration of the electronic active defects to ensure high electrical conductivities in doped ZnO-based ceramics.     

Fabrication and thermal conductivity of AlN/BN ceramics by spark plasma sintering

Aluminum nitride/boron nitride (AlN/BN) ceramics with 15–30 vol.% BN as secondary phase were fabricated by spark plasma sintering (SPS), using Yttrium oxide (Y₂O₃) as sintering aid. Effects of Y₂O₃ content and the SPS temperature on the density, phase composition, microstructure and thermal conductivity of the ceramics were investigated. The results revealed that with increasing the amount of starting Y₂O₃ in AlN/BN, Yttrium-contained compounds were significantly removed after SPS process, which caused decreasing of the residual grain boundary phase in the sintered samples. As a result, thermal conductivity of AlN/BN ceramics was remarkably improved. By addition of Y₂O₃ content from 3 wt.% to 8 wt.% into AlN/15 vol.% BN ceramics, the thermal conductivity increased from 110 W/m K to 141 W/m K.     

High-strength Ti2AlN ceramics prepared by pulse electric current sintering based on powders synthesized by molten salt method

Ti₂AlN powders were synthesized through molten salt method and re-calcination process using TiH₂, Al and TiN powders as raw materials at 1100 ℃. The composition of final composite was directly influenced by the initial Al and TiH₂ content in the starting mixture. The purity of the synthesized Ti₂AlN powder could reach 97.1 wt% when the Al molar ratio was 1.05. Then high strength Ti₂AlN ceramics were successfully prepared in different modes, including two forms of pulse electric current sintering (PECS/SPS) and hot-pressing sintering (HP). A record-high flexural strength of 719 MPa was obtained for the PECS/SPS with an electrical insulating die (PECS/SPS II) sintered sample, based on the synthesized powder in which the initial molar ratio of Al was 1.1. The sintering behaviors in various modes were analyzed, confirming the shrinkage of particles starting at lower temperature in PECS/SPS II. The density, microstructure, Vickers hardness and elastic modulus of sintered ceramics were also investigated. Therefore, the present work provided the new methods about powder preparation and ceramic sintering of Ti₂AlN, making it possible to be used as high strength structural ceramics.     

Effects of phase constitution and microstructure on energy storage properties of barium strontium titanate ceramics

Barium strontium titanate (Ba_0.3Sr_0.7TiO₃, BST) ceramics have been prepared by conventional sintering (CS) and spark plasma sintering (SPS). The effects of phase constitution and microstructure on dielectric properties, electrical breakdown process and energy storage properties of the BST ceramics were investigated. The X-ray diffraction analysis and dielectric properties measurements showed that the cubic and tetragonal phase coexisted in the SPS sample while the CS sample contained only tetragonal phase. Much smaller grain size, lower porosity, fewer defects and dislocation were observed in SPS samples, which greatly improved the electrical breakdown strength of the Ba_0.3Sr_0.7TiO₃ ceramics. The enhanced breakdown strength of the SPS samples resulted in an improved maximum electrical energy storage density of 1.13 J/cm³ which was twice as large as that of the CS sample (0.57 J/cm³). Meanwhile, the energy storage efficiency was improved from 69.3% to 86.8% by using spark plasma sintering.     

Sintering behavior and mechanical properties of spark plasma sintering SiO2-MgO ceramics

SiO₂-MgO ceramics containing different weight fractions (0, 0.5, 1, 2, and 4 wt%) of SiO₂ powder were prepared by mixing nano MgO powder, and the powder mixtures were densified by spark plasma sintering (SPS). The effect of SiO₂ addition and SPS method on the sintering behavior, microstructure and mechanical properties were investigated. Results were compared to specimens obtained by conventional hot pressing (HP) under a similar sintering schedule. The highest relative density, flexural strength and hardness of 2 wt% SiO₂-MgO ceramics reached 99.98%, 253.99 ± 7.47 MPa and 7.56 ± 0.21 GPa when sintered at 1400 °C by SPS, respectively. The observed improvement in the sintering behavior and mechanical properties are mainly attributed to grain boundary "strengthening" and intragranular "weakening" of the MgO matrix. Furthermore, the spark plasma sintering temperature could be decreased by more than 100 °C as compared with the HP method, SPS favouring enhanced grain boundary sliding, plastic deformation and diffusion in the sintering process.     

Comparison of hot pressing and spark plasma sintering in the densification behavior of indium tin oxide‐borosilicate glass composites

The goal of this study was to fabricate borosilicate glass matrix composites with high optical transmittance and high conductivity by forming percolated segregated networks of indium tin oxide (ITO) in the microstructure. ITO nanoparticles and borosilicate glass microspheres were mechanically mixed with ITO concentrations varying from 0 to 2.99 vol%. The mixes were then consolidated using either hot pressing (HP) or spark plasma sintering (SPS). The effects of changing sintering methods, along with varying other processing parameters such as heating rate, maximum temperature, and applied pressure, had surprising and unanticipated effects. Ac impedance spectroscopy (IS), SEM, and EDS results indicated the successful formation of a grain‐like microstructure of the sintered glass using both HP and SPS processing, with the ITO particles segregated to the boundary regions in all samples. IS results indicated percolation threshold values between 0.154 and 0.307 vol% ITO in the HP samples and between 0.307 and 0.764 vol% ITO in the SPS samples, with resistivities as low as 29 (Ω·cm) at 2.99 vol% ITO. Optical properties were dominated by impurities and light scattering at defects such as pores. Contrary to conventional belief, it was found that samples made using SPS required far higher temperatures to fully densify, with all other processing conditions being the same, compared with HP. This behavior was confirmed through repeat tests using different SPS equipment and a wide range of processing conditions.     

Effect of solid solution formation on densification of spark plasma sintered ZrC ceramics with TiC as sintering aid

The densification of ZrC ceramics doped with different contents of TiC prepared by spark plasma sintering at the temperatures between 1750 and 1850°C has been investigated. The microstructure and mechanical properties of the ceramics have been characterised. It was shown that TiC additions effectively promoted the densification process by forming (Zr,Ti)C solid solution. The relative densities and mechanical properties of ZrC samples increased with the increasing of TiC content or the sintering temperature. Ceramic with the content of TiC up to 10 vol.-% sintering at 1850°C showed an excellent combination of properties including a relative density of 98.7%, hardness of 20.8?GPa and flexural strength of 605?MPa.     

Processing of CaLa2S4 infrared transparent ceramics: A comparative study of HP and FAST/SPS techniques

The densification of CaLa₂S₄ (CLS) powders prepared by combustion method was investigated by the use of Field-Assisted Sintering Technique (FAST) and Hot Pressing (HP). CLS powders were sintered using FAST at 1000°C at different pressures and heating rates and sintered by HP under 120 MPa from 800°C to 1100°C for 6 hours with a heating rate of 10°C/min. Comparison of both techniques was further realized by use of the same conditions of pressure, dwell time, and heating rate. Complementary techniques (XRD, SEM-EDS, density measurements, FTIR spectroscopy) were employed to correlate the sintering processes/parameters to the microstructural/compositional developments and optical transmission of the ceramics. Both sintering techniques produce ceramics with submicrometer grain size and relative density of about 99%. Nevertheless, HP is more suitable to densify CLS ceramics without fragmentation and also reach higher transmission than FAST. Transmission of 40%–45% was measured out of a possible maximum of 69% based on the Fresnel losses in the 8-14 μm window when HP is applied at 1000°C for 6 hours under 120 MPa. In both techniques, ceramics undergo reduction issues that originate from graphitic sintering atmosphere.     

KNbTeO6 transparent ceramics prepared by the combination of pressure-less sintering and pseudo hot isostatic pressing

KNbTeO₆ transparent ceramics were prepared by combining pressure-less sintering and pseudo-hot isostatic pressing (PHIP) of the synthesized submicron single-phase powder. The PHIP was conducted by wrapping coarse magnesium aluminate powders around the pre-sintered body in the spark plasma sintering (SPS) furnace. With an average grain size of 412 ± 23 nm, the in-line transmittance of transparent KNbTeO₆ ceramics reaches 80.25% at 2677 nm. By contrast, the density of the samples prepared by conventional SPS with the same sintering procedure is only 98.73%, and the highest in-line transmittance 64.25% occurs at 4976 nm. In particular, by investigating the sintering mechanism of PHIP, the improvement of microstructure and optical transmittance could be attributed to the plastic deformation caused by shear stress. The obtained ceramics exhibited excellent mechanical and dielectric properties, which was benefited from the novel sintering technology.     

Preparation of dense La0.67Ca0.33MnO3 ceramics by plasma activated sintering and hot-pressing

Highly dense La_0.67Ca_0.33MnO₃ (LCMO) ceramics were prepared by plasma activated sintering (PAS) and hot-pressing (HP). The comparison of structural, magnetic, and electrical transport properties of the LCMO ceramics after PAS and HP were investigated. XRD and SEM analyses confirmed that both samples exhibited orthorhombic phase with highly dense microstructure. The differences of magnetic and electrical transport properties in PAS and HP LCMO ceramics could be attributed to the different grain sizes, which have an effect on grain boundaries, domain states, Mn–O–Mn bond angles and Mn–O bond lengths. On analyzing the fitting data with several empirical equations, the conduction mechanism of the samples was found to be electron-magnon scattering in the ferromagnetic low-temperature region and variable range hopping (VRH) in the paramagnetic high-temperature region.     

Effect of applied pressure on microstructure and properties of hot-pressed Ca-doped LaCrO3 ceramics

High-density chromium deficient calcium-doped lanthanum chromite-based ceramics (La_0.8Ca_0.2Cr_0.98O₃) were prepared by hot pressing (HP) at different sintering pressures, and the highest density can reach 98.8%. The effects of sintering pressure on the microstructure, mechanical properties, and electrical conductivity of La_0.8Ca_0.2Cr_0.98O₃ materials were studied. The experimental results show that HP can increase the density of lanthanum chromite-based ceramic materials and significantly inhibit the growth of grain size. As the sintering pressure increases, the strength and hardness gradually increase, but the fracture toughness decreases. When the sintering pressure is greater than 58 MPa, the presence of the second phase CaCr₂O₄ can be detected in the XRD results of the sintered ceramics. The SEM results showed that CaCr₂O₄ had two completely different morphologies in the sintered ceramics, and it was initially speculated that the possible causes were due to two different generation pathways. The electrical conductivity decreases with increasing sintering pressure, whereas the maximum electrical conductivity obtained is 18.61 S/cm in vacuum at 800°C for pressureless sintering ceramic.     

Spark Plasma Sintering of Bismuth Titanate Ceramics

Spark plasma sintering (SPS) was used to fabricate bismuth titanate (Bi₄Ti₃O₁₂) ceramics. The densification, microstructure development and dielectric properties were investigated. It was found that the densification process was greatly enhanced during SPS. The sintering temperature was 200°C lower and the microstructure was much finer than that of the pressureless sintered ceramics, and dense compacts with a high density of over 99% were obtained at a wide temperature range of 800°–1100°C. Dielectric property measurement indicated that the volatilization of Bi³⁺ was greatly restrained during SPS, resulting in an unprecedented low dielectric loss for pure Bi₄Ti₃O₁₂ ceramics.     

Spark plasma sintering and hot pressing of ZTA-NbC materials – A comparison of mechanical and electrical properties

Zirconia toughened alumina can be made electrically conductive and thus electric discharge machinable by addition of a percolating dispersion of niobium carbide. In order to boost the productivity of the sintering process spark plasma sintering was tested at identical temperature and pressure but shorter dwell than in hot pressing. SPS sintering parameters for ZTA-NbC are developed and spark plasma sintered ceramics are compared to the hot pressed benchmark.During SPS a percolating NbC backbone of niobium carbide grains is formed which enhances electrical conductivity but impedes densification. Identical strength at however higher sintering temperature is achieved by SPS but the fracture resistance and hardness were always superior in hot pressed samples. The monoclinic content of zirconia grains in as fired SPS samples is higher despite smaller average grain size and the transformation toughening effect is less pronounced. SPS promises economic benefits due to shorter dwell and cooling cycles.     

Thermal conductivity of spark plasma sintered SiC ceramics with Alumina and Yttria

In this study, dense SiC ceramics were fabricated at 1650?1750 °C for 10?60 min by spark plasma sintering (SPS) using 3?10 wt.% Al₂O₃-Y₂O₃ as sintering additives. Effects of sintering temperature, sintering additive content and holding time on microstructure as well as correlations between microstructure and thermal conductivity were investigated. An increase in the sintering temperature promotes grain growth. Extending holding time has little influence on grain size but results in formation of continuous network of sintering additive, which increases interfacial thermal resistance and thus decreases thermal conductivity. For SiC ceramics composed of continuous SiC matrix and discrete secondary phase (yttrium aluminum garnet, YAG), an increase in the sintering additive content results in smaller grain size and lower thermal conductivity. The lower thermal conductivity of the SiC ceramic with higher sintering additive content is mainly due to the smaller grain size rather than the low intrinsic thermal conductivity of YAG.     

Spark plasma sintering of SnO2 based varistors

In this research, for the first time, SnO₂-based varistors were fabricated via spark plasma sintering technique (SPS) and the microstructure and electrical properties of these varistors were investigated. Furthermore, the effect of post-annealing temperature in oxygen atmosphere on electrical properties of the SPSed samples was studied. The SPS process was performed at the sintering temperatures of 600, 650, and 700 ᵒC for 15 min with a maximum pressure of 90 MPa under vacuum condition. The SPSed sample which was sintered at 650 ᵒC possessed maximum density of 98% and the ultra-fine-grained microstructure with the mean grain size of 380 nm. Surprisingly, all SPSed samples exhibited Ohmic behavior with very low electric resistances. After post-annealing in oxygen atmosphere, Ohmic to non-Ohmic transition was observed in SPSed samples. The oxygen deficiency during the SPS process was responsible for the Ohmic characteristic of SPSed samples. Post-annealing of SPSed samples in the oxygen atmosphere resulted in Schottky barriers formation through oxygen adsorption at grain boundaries. The sample post-annealed at 1050 ᵒC presented the best non-Ohmic parameters including high breakdown electric field of 4500 V/cm and the nonlinear coefficient of 13. These electrical parameters are comparable with the conventional-sintered samples which was sintered at 1300 ᵒC and its breakdown electric field and nonlinear coefficient were equal to 900 V/cm and 8, respectfully.     

Effects of Preparation Conditions on the Structural and Optical Properties of Spark Plasma-Sintered PLZT (8/65/35) Ceramics

Transparent lanthanum-doped lead zirconate titanate (PLZT) ceramics with high density were fabricated using spark plasma sintering (SPS), a recently developed hot-pressing method. A wet–dry combination method was used to prepare the fine PLZT powders. The average grain size of the PLZT ceramics was less than 1 μm, because of a relatively low sintering temperature and a very short sintering time. The transmittance of PLZT ceramics increased with an increase of calcination temperature up to 700°C and then it slightly decreased with further increase of calcination temperature. The transmittance strongly depended on the SPS temperature and heat-treatment temperature. The pellet sintered at 900°C for 10 min and heat treated at 800°C for 1 h with a thickness of 0.5 mm showed a transmittance of 31% at a wavelength of 700 nm. The relationships between the transmittance and the microstructure were investigated.     

放电等离子烧结制备Ca3Co4O9陶瓷及其电学性能

采用化学共沉淀与放电等离子烧结相结合的方法制备了Ca3Co4O9陶瓷.通过X射线衍射,红外光谱仪,扫描电镜等表征手段,探讨了Ca3Co4O9的形成过程,研究了不同制备工艺对陶瓷的物相,显微结构和性能的影响.实验结果表明共沉淀前驱物800℃预烧6 h或8 h后,再经放电等离子850℃,压力30 MPa下烧结5 min,可以获得纯相Ca3Co4O9陶瓷;800℃预烧6 h的烧结体密度为4.53 g/cm3,800℃预烧8 h的烧结体密度为4.78 g/cm3;前驱物预烧8 h后再经放电等离子烧结的块体具有较好的电学性能.700℃时,电阻率为8.30×10-5 Ωm,Seebeck系数为182μV/K.电导率和Seebeck系数在目前Ca-Co-O材料中是较高的.     

In situ processing of electrically conducting graphene/SiC nanocomposites

The outstanding electronic and physico-chemical properties of graphene make it an ideal filler in the fabrication of conducting and robust ceramic composites. In this study, a novel single-step approach for processing electrically conducting and well dispersed graphene/SiC nanocomposites is shown. These materials were processed by growing epitaxial graphene with either α- or β-phase SiC ceramics during their densification via spark plasma sintering (SPS). About 4 vol.% of few-layer graphene domains were generated in situ during the SPS process, leading to a conducting graphene network that significantly enhanced the electrical performance of SiC. The in situ graphene SPS growth mechanism arose from the combined action of the electric current, high temperature and partial vacuum. This approach offers unprecedented opportunities for the fast manufacturing of graphene/SiC nanocomposites with superior electrical and mechanical properties, precluding the handling of potentially hazardous nanostructures. This method widens their possible applications, including micro-electromechanical systems, brakes, micro-turbines or micro-rotors.     

Role of synthesis method on microstructure and mechanical properties of graphene/carbon nanotube toughened Al2O3 nanocomposites

The effects of hot-pressing (HP) and spark plasma sintering (SPS) methods on the grain size, microstructural features, and mechanical behaviour of graphene nanoplatelet/carbon nanotubes (GNTs) reinforced Al₂O₃ nanocomposites were comprehensively studied. Different graphene nanoplatelet to carbon nanotube ratios were selected as the overall reinforcement content of composites prepared using HP and SPS. Highly densified samples (>98%) were obtained at 1650 °C under 40 MPa in Ar atmosphere, with dwell times of 1 h and 10 min for HP and SPS respectively. Both types of sample showed a mixture of inter- and transgranular fracture behaviour. A 50% grain size reduction was observed for samples prepared by HP compared to SPS samples. Both types of samples achieved a high flexural strength and fracture toughness of >400 MPa and 5.5 MPa m^1/2, whilst SPS samples peaked at relatively lower GNT contents than those for the HP samples. Based on analyses of the morphology, grain sizes and fracture mode, similar toughening mechanisms for both types of sample were observed, involving the complex characteristics of the combined GNT fillers.     

Dopant effects on high temperature mechanical properties of zirconium carbide ceramics

Combining theoretical and experimental methods, the effects of 5?vol.-% WC dopant on the microstructure evolution, sintering behaviour and mechanical properties of ZrC ceramics were investigated. WC dopant was found to improve the high temperature elastic modulus and bending strength of ZrC ceramics. Both calculations and experimental results showed that the formation of (Zr, W)C solid solution promote dissolution of the impurity oxygen from the starting powder into the lattice sites, resulting in less oxygen defects in grain boundaries. Internal friction curve can also conform that the ZrC ceramics doped with WC have cleaner grain boundaries, which improved higher elastic modulus and bending strength in WC doped ZrC ceramics at elevated temperature.