Reaction,densification, and mechanical properties of Ti2AlCx ceramics at low applied pressure and temperature

Ti₂AlC_x ceramic was produced by reactive hot pressing (RHP) of Ti:Al:C powder mixtures with a molar ratio of 2:1:1–.5 at 10–20 MPa, 1200–1300°C for 60 min. X-ray diffraction analysis confirmed the Ti₂AlC with TiC, Ti₃Al as minor phases in samples produced at 10–20 MPa, 1200°C. The samples RHPed at 10 MPa, 1300°C exhibited ≥95 vol.% Ti₂AlC with TiC as a minor phase. The density of samples increased from 3.69 to 4.04 g/cm³ at 10 MPa, 1200°C, whereas an increase of pressure to 20 MPa resulted from 3.84 to 4.07 g/cm³ (2:1:1 to 2:1:.5). The samples made at 10 MPa, 1300°C exhibited a density from 3.95 to 4.07 g/cm³. Reaction and densification were studied for 2Ti–Al–.67C composition at 10 MPa, 700–1300°C for 5 min showed the formation of Ti–Al intermetallic and TiC phases up to 900°C with Ti, Al, and carbon. The appearance of the Ti₂AlC phase was ≥1000°C; further, as the temperature increased, Ti₂AlC peak intensity was raised, and other phase intensities were reduced. The sample made at 700°C showed a density of 2.87 g/cm³, whereas at 1300°C it exhibited 3.98 g/cm³; further, soaking for 60 min resulted in a density of 4.07 g/cm³. Microhardness and flexural strength of Ti₂AlC_0.8 sample were 5.81 ± .21 GPa and 445 ± 35 MPa.     

Mechanical properties of hot-pressed transparent platelet alumina

The mechanical properties of transparent alumina densified by hot-pressing platelet-morphology powder were characterized and compared to samples using equiaxed (E) powder. The platelet alumina was prepared in two different starting orientations prior to hot-pressing. In the first, the platelets were poured into the die in a non-pre-aligned (NPA) state. In the second, the platelets were pre-aligned (PA) via a separate processing step. The characteristic strength of the NPA, PA, and E samples is 179, 206, and 207 MPA, respectively. The Weibull modulus of the NPA samples is m = 24, which is among the highest Weibull modulus reported for alumina. The Weibull modulus of the NPA samples is higher than the PA and E samples (m = 7 and m = 4, respectively) and is explained by a tighter grain size distribution. The Vickers hardness of the NPA, PA, and E samples were measured both parallel and perpendicular to the hot-pressing direction, with values on the order of 17 GPa, and minimal differences among different samples types. However, the pre-aligned samples exhibited hardness values nearly identical to sapphire in the corresponding crystallographic directions. This is due to the pre-alignment procedure resulting in significant crystallographic orientation in the final sintered parts.     

The influence of different SiC amounts on the microstructure,densification, and mechanical properties of hot-pressed Al2O3-SiC composites

The hot pressing process of monolithic Al₂O₃ and Al₂O₃-SiC composites with 0-25 wt% of submicrometer silicon carbide was done in this paper. The presence of SiC particles prohibited the grain growth of the Al₂O₃ matrix during sintering at the temperatures of 1450°C and 1550°C for 1 h and under the pressure of 30 MPa in vacuum. The effect of SiC reinforcement on the mechanical properties of composite specimens like fracture toughness, flexural strength, and hardness was discussed. The results showed that the maximum values of fracture toughness (5.9 ± 0.5 MPa.m^1/2) and hardness (20.8 ± 0.4 GPa) were obtained for the Al₂O₃-5 wt% SiC composite specimens. The significant improvement in fracture toughness of composite specimens in comparison with the monolithic alumina (3.1 ± 0.4 MPa.m^1/2) could be attributed to crack deflection as one of the toughening mechanisms with regard to the presence of SiC particles. In addition, the flexural strength was improved by increasing SiC value up to 25 wt% and reached 395 ± 1.4 MPa. The scanning electron microscopy (SEM) observations verified that the increasing of flexural strength was related to the fine-grained microstructure.     

Effects of doping by copper on electrical properties of LaCrO3 based perovskite

The use of nickel-yttria-stabilized zirconia (Ni/YSZ) as anode material for solid oxide fuel cell (SOFC) applications, presents some limitations such as poor stability in reduction/oxidation cycling, and poor sulphur tolerance which results in carbon deposition when utilizing hydrocarbon fuels. Even though lanthanum chromite (LaCrO₃ noted LCO) is an excellent alternative to Ni/YSZ, it is rarely used in SOFC applications due to its poor conductivity. In order to further progress in developing LCO materials, this work was conducted to improve the conductivity of LCO by copper doping. In particular, LaCr_1-xCu_xO₃ compounds with x = 0, 0.1, and 0.3 were synthesized via a solid-solid method. The followed preparation process allows obtaining a cubic structure with Pm-3m space group. The substitution of Cr with Cu resulted in a slight increase in lattice parameter a, but no change in structure or space group. Whereas, the band gap energy decreased from 3.68 eV for x = 0–3.06 eV for x = 0.3. The crystallite size increases with doping level. With regard to the obtained data from electrical measurements, a thermally activated and frequency depended conductivity was obtained for all samples. Furthermore, the correlated barrier hopping mechanism was proposed as a conduction mechanism, and an electrical transition from semiconductor to metallic behavior was observed. The conductivity increased also monotonously with Cu content and shows a maximum value of 4.5 S/m for x = 0.3. Besides, the tangent loss shows a maximum value of around 10⁴ for x = 0.1. The LaCr_0.7Cu_0.3O₃ compound could be a good candidate for SOFC applications, while LaCr_0.9 Cu_0.1O₃ can be used as a heating element.     

Effect of ZrB2 content on the densification,microstructure, and mechanical properties of ZrC-SiC ceramics

ZrC ceramics containing 30 vol% SiC-ZrB₂ were produced by high-energy ball milling and reactive hot pressing. The effects of ZrB₂ content on the densification, microstructure, and mechanical properties of ceramics were investigated. Fully dense ceramics were achieved as ZrB₂ content increased to 10 and 15 vol%. The addition of ZrB₂ suppressed grain growth and promoted dispersion of the SiC particles, resulting in fine and homogeneous microstructures. Vickers hardness increased from 23.0 ± 0.5 GPa to 23.9 ± 0.5 GPa and Young’s modulus increased from 430 ± 3 GPa to 455 ± 3 GPa as ZrB₂ content increased from 0 to 15 vol%. The increases were attributed to a combination of the higher relative density of ceramics with higher ZrB₂ content and the higher Young’s modulus and hardness of ZrB₂ compared to ZrC. Indentation fracture toughness increased from 2.6 ± 0.2 MPa⋅m^1/2 to 3.3 ± 0.1 MPa⋅m^1/2 as ZrB₂ content increased from 0 to 15 vol% due to the increase in crack deflection by the uniformly dispersed SiC particles. Compared to binary ZrC-SiC ceramics, ternary ZrC-SiC-ZrB₂ ceramics with finer microstructure and higher relative densities were achieved by the addition of ZrB₂ particles.     

The effects of microstructure on mechanical and electrical properties of W dispersed Al2O3 ceramics

This work aims to enhance the fracture toughness of brittle Al₂O₃ ceramics and apply insulated Al₂O₃ ceramics with electrical conductivity by dispersing second tungsten (W) metal particles. In order to investigate the effects of W dispersion on mechanical and electrical properties, Al₂O₃–W composites with various amounts of W (ranging from 5 vol% to 20 vol%) were fabricated by the hot-press sintering method at various sintering temperatures. Microstructure analysis revealed submicron Al₂O₃ matrix grains and W particles. The existence of three phases of Al₂O₃, W, and AlWO₄ was confirmed by X-ray diffraction patterns. All Al₂O₃–W composites showed higher fracture toughness than monolithic Al₂O₃. The toughening mechanism was attributed to crack deflection and crack bridging. Transgranular fracture was visible in all composites. Electrical resistivity dramatically lowered from 2.9 × 10¹² Ω cm of monolithic Al₂O₃ to 4.1 × 10² Ω cm of the composite with 20 vol% W addition. The percolation threshold is calculated as 18.5%. With the increase in sintering temperature, the amount of W particles was decreased and Al₂O₃ grains became large, leading to the reduced number of conductive pathways formed by the dispersed W particles. As a result, electrical conductivity was decreased.     

Effect of different contents of zirconia and yttrium oxide on microstructure and properties of high alumina ceramics

The effects of zirconia and yttrium oxide addition on microstructure, bulk density, microhardness, flexural strength, and wear resistance of high alumina ceramics (>97 wt% Al₂O₃, MSA ceramics) composed of MgO–SiO₂–Al₂O₃ system have been investigated. The results show that the addition of zirconia makes the mechanical properties and wear properties of ceramics composed of MgO–SiO₂–Al₂O₃–ZrO₂ (MSAZ ceramics) system have been greatly improved compared with MSA ceramics. In addition, the ceramics composed of MgO–SiO₂–Al₂O₃–ZrO₂–Y₂O₃ (MSAZY ceramics) system have better mechanical properties and wear properties than MSAZ ceramics. With the contents of zirconia and yttrium oxide increase, the bulk density, microhardness, and flexural strength of MSAZ and MSAZY ceramics increased at first and then decreased. However, the wear rate shows the opposite. When 0.4 wt% ZrO₂ and 0.6 wt% Y₂O₃ were added to the matrix, the wear rate of MSAZY ceramics reached a minimum of 0.042%, and the wear resistance was improved by about 73.8% compared with MSA ceramics with a wear rate of 0.16%. In addition, the optimum additions of zirconia and yttria are 0.4% and 0.6%, respectively.     

Processing,microstructure, and mechanical properties of hot-pressed ZrB2 ceramics with a complex Zr/Si/O-based additive

Densification behavior, microstructure, and mechanical properties of zirconium diboride (ZrB₂) ceramics modified with a complex Zr/Si/O-based additive were studied. ZrB₂ ceramics with 5–20 vol.% additions of Zr/Si/O-based additive were densified to >95% relative density at temperatures as low as 1400°C by hot-pressing. Improved densification behavior of ZrB₂ was observed with increasing additive content. The most effective additive amount for densification was 20 vol.%, hot-pressed at 1400°C (∼98% relative density). Microstructural analysis revealed up to 7 vol.% of residual second phases in the final ceramics. Improved densification behavior was attributed to ductility of the silicide phase, liquid phase formation at the hot-pressing temperatures, silicon wetting of ZrB₂ particles, and reactions of surface oxides. Room temperature strength ranged from 390 to 750 MPa and elastic modulus ranged from 440 to 490 GPa. Vickers hardness ranged from 15 to 16 GPa, and indentation fracture toughness was between 4.0 and 4.3 MPa·m^1/2. The most effective additive amount was 7.5 vol.%, which resulted in high relative density after hot-pressing at 1600°C and the best combination of mechanical properties.     

Effects of Gd2O3 and MgSiN2 sintering additives on the thermal conductivity and mechanical properties of Si3N4 ceramics

Si₃N₄ ceramics were prepared by gas pressure sintering at 1900°C for 12 h under a nitrogen pressure of 1 MPa using Gd₂O₃ and MgSiN₂ as sintering additives. The effects of the Gd₂O₃/MgSiN₂ ratio on the densification, microstructure, mechanical properties, and thermal conductivity of Si₃N₄ ceramics were systematically investigated. It was found that a low Gd₂O₃/MgSiN₂ ratio facilitated the thermal diffusivity of Si₃N₄ ceramics while a high Gd₂O₃/MgSiN₂ ratio benefited the densification and mechanical properties. When the Gd₂O₃/MgSiN₂ ratio was 1:1, Si₃N₄ ceramics obtained an obvious exaggerated bimodal microstructure and the optimal properties. The thermal conductivity, flexural strength, and fracture toughness were 124 W·m⁻¹·k⁻¹, 648 MPa, and 9.12 MPa·m^1/2, respectively. Comparing with the results in the literature, it was shown that Gd₂O₃-MgSiN₂ was an effective additives system for obtaining Si₃N₄ ceramics with high thermal conductivity and superior mechanical properties.     

Phase formation,microstructure development,and mechanical properties of kaolin-based mullite ceramics added with Fe2O3

The effects of Fe₂O₃ on phase evolution, density, microstructural development, and mechanical properties of mullite ceramics from kaolin and alumina were systematically studied. X-ray diffraction results suggested that the ceramics consisted of mullite, sillimanite, and corundum, in the sintering range of 1450°C–1580°C. However, as the sintering was raised to 1580°C, mullite is the main phase with a content of 94%, and the corundum phase content is 5.9%. Simultaneously, high-temperature sintering had a positive effect on the densification of the mullite ceramics, where both the bulk density and flexural strength could be optimized by adjusting the content of Fe₂O₃. It was found that 6 wt% Fe₂O₃ was optimal for the formation of rod-shaped mullite after sintering at 1550°C for 3 h. The sample's maximum bulk density was 2.84 g/cm³, with a flexural strength of 112 MPa. Meanwhile, rod-shaped mullite grains with an aspect ratio of ~9 were formed. As a result, a dense network structure was developed, thus leading to mullite ceramics with excellent mechanical properties. The effect of Fe₂O₃ on the properties might be attributed to the fact that Al³⁺ ions in the [AlO₆] octahedron were replaced by Fe³⁺ ions, resulting in lattice distortion.     

Rapid synthesis,electrical, and mechanical properties of polycrystalline Fe2AlB2 bulk from elemental powders

Polycrystalline Fe₂AlB₂ bulk including minor Al₂O₃ is synthesized by reactive hot pressing from Fe, Al, and B powders at 1200°C and 30 MPa for 30 minutes, with a relative density of 96%. The present approach enables a markedly reduced holding time compared with previous studies. The derived Fe₂AlB₂ shows an electrical resistivity of 2.27±0.01 μΩ·m, Vickers hardness of 10.2±0.2 GPa, flexural strength of 232±25 MPa, compressive strength of 2101±202 MPa, fracture toughness of 5.4±0.2 MPa·m^1/2 and work of fracture of 117±12 J/m². No dominant indentation cracks are observed, indicating that Fe₂AlB₂ may be quite damage tolerant. Interestingly, a noncatastrophic failure is present in the SENB test, with a high work of fracture. The energy‐absorbing mechanisms in inhibiting crack formation are delamination and pullout of Fe₂AlB₂ grains.     

Thermal and electrical properties of additive-free rapidly hot-pressed SiC ceramics

The thermal and electrical properties of newly developed additive free SiC ceramics processed at a temperature as low as 1850 °C (RHP0) and SiC ceramics with 0.79 vol.% Y₂O₃-Sc₂O₃ additives (RHP79) were investigated and compared with those of the chemically vapor-deposited SiC (CVD-SiC) reference material. The additive free RHP0 showed a very high thermal conductivity, as high as 164 Wm⁻¹ K⁻¹, and a low electrical resistivity of 1.2 × 10⁻¹ Ω cm at room temperature (RT), which are the highest thermal conductivity and the lowest electrical resistivity yet seen in sintered SiC ceramics processed at ≤1900 °C. The thermal conductivity and electrical resistivity values of RHP79 were 117 Wm⁻¹ K⁻¹ and 9.5 × 10⁻² Ω cm, respectively. The thermal and electrical conductivities of CVD-SiC parallel to the direction of growth were ∼324 Wm⁻¹ K⁻¹ and ∼5 × 10⁻⁴Ω⁻¹ cm⁻¹ at RT, respectively.     

Effect of ZrB2 content on phase assemblage and mechanical properties of Si3N4–ZrB2 ceramics prepared at low temperature

Based on the previous work on Si₃N₄–ZrB₂ [Wu et al. J Eur Ceram Soc;2017,37:4217], the influence of ZrB₂ addition on the phase and microstructure evolution of Si₃N₄–ZrB₂ composites was emphatically investigated, and the mechanical properties were compared with pure Si₃N₄ ceramics. It was revealed that the ratio of β‐ to (α+β)‐Si₃N₄ significantly increased from 14.3% in pure Si₃N₄ ceramics to 39.8% in Si₃N₄ with 15 vol% ZrB₂ addition, indicating that the introduction of ZrB₂ promoted α‐ to β‐Si₃N₄ phase transformation. As a consequence, the microstructure of the composite showed the bimodal distribution, containing both elongated and equiaxed Si₃N₄ grains. For the pure Si₃N₄, Vickers hardness, fracture toughness and flexural strength was 22.8 GPa, 7.6 MPa m^1/2, and 334.5 MPa, respectively. In contrast, the composite of Si₃N₄–30 vol% ZrB₂ simultaneously possessed an excellent combination of mechanical properties: 19.5 GPa in hardness, 9.8 MPa m^1/2 in toughness and 702.0 MPa in strength. Present study suggested that Si₃N₄‐based ceramics with high hardness, high toughness, and high strength could be obtained by the combination of appropriate ZrB₂ content and low hot‐pressing temperature.     

Fabrication,microstructure, mechanical and luminescence properties of transparent Yb3+-doped Sr5(PO4)3F nanostructured ceramics

The Sr₅(PO₄)₃F (S-FAP) crystal material is regarded as one of the most ideal optical materials for diode pumping owing to its huge absorption and emission cross sections and long fluorescence lifespan. In this investigation, S-FAP powders with varying Yb concentrations (0.1–5%) were produced using the coprecipitation method. Then a variety of S-FAP transparent ceramics with varying Yb content were fabricated using hot-pressing sintering. The crystalline phase structure of hexagonal Sr₅(PO₄)₃F was verified by XRD analysis of the precursor powder and the final ceramics. According to the powder SEM, the average grain size and the long axial-radial ratio of powders are decreasing as the Yb³⁺ concentration increases. Thermal-etched surface SEM reveals nanostructured S-FAP transparent ceramics with an average grain size of less than 200 nm were synthesized. The highest transmittances of the 3% ceramics at 500 and 1100 nm wavelengths are 51% and 79.78%, respectively. The ceramic cross-sectional SEM demonstrated that porosity is the primary scattering source influencing the enhancement of optical characteristics. The absorption, emission, and fluorescence lifetimes of S-FAP transparent ceramics with varying Yb concentrations were tested and discussed, and the absorption and emission cross sections corresponding to the major peak were reported. Some physical parameters of this set of ceramic samples were shown, including thermal diffusivity, specific heat capacity, and thermal diffusivity data, as well as micro-hardness.     

Effect of a new nonoxide additive,Y3Si2C2, on the thermal conductivity and mechanical properties of Si3N4 ceramics

Enhancement of the thermal conductivity of silicon nitride is usually achieved by sacrificing its mechanical properties (bending strength). In this study, β-Si₃N₄ ceramics were prepared using self-synthesized Y₃Si₂C₂ and MgO as sintering additives. It was found that the thermal conductivity of the Si₃N₄ ceramics was remarkably improved without sacrificing their mechanical properties. The microstructure and properties of the Si₃N₄ ceramics were analyzed and compared with those of the Y₂O₃-MgO additives. The addition of Y₃Si₂C₂ eliminated the inherent SiO₂ and introduced nitrogen to increase the N/O ratio of the grain-boundary phase, inducing Si₃N₄ grain growth, increasing Si₃N₄ grain contiguity, and reducing lattice oxygen content in Si₃N₄. Therefore, by replacing Y₂O₃ with Y₃Si₂C₂, the thermal conductivity of the Si₃N₄ ceramics was significantly increased by 31.5% from 85 to 111.8Wm⁻¹K⁻¹, but the bending strength only slightly decreased from 704 ± 63MPa to 669 ± 33MPa.     

Differences in microstructure and mechanical properties between Y-TZP and AL2O3-doped Y-TZP/bioglass ceramics

Y-TZP (YZ) and Al₂O₃-doped Y-TZP (AYZ) bioceramics with addition of different contents of a refractory bioglass were fabricated. The influence of the glass addition and sintering temperature on the densification behavior, microstructure, and mechanical properties of YZ and AYZ was studied. The developed ceramics contained small amounts of ZrSiO₄ and Ca₂P₂O₇ phases within the ZrO₂ matrix. The incorporation of glass to YZ promoted the ZrO₂ phase partitioning and enhanced the ZrO₂ grain growth at all the sintering temperatures, whereas the glass addition in AYZ prevented the Y₂O₃ redistribution between ZrO₂ grains and limited the ZrO₂ grain growth at 1300–1400°C. The hardness of the samples with glass was not significantly altered by using either YZ or AYZ. A slight increase in the fracture toughness with increasing glass content was found for YZ, while the fractured toughness of AYZ decreased by the glass addition. The more pronounced ZrO₂ phase partitioning of YZ with glass decreased the flexural strength, whereas AYZ maintained almost unaltered its flexural strength at a high level by the glass incorporation.     

Preparation and properties of dense ZrB2 composite reinforced by elongated SiC and Al3BC3 grains

Dense ZrB₂-SiC-Al₃BC₃ ultra-high temperature ceramic composite was fabricated by hot pressing sintering at 1900°C for 1 hour under a pressure of 20 MPa using Zirconium diboride (ZrB₂) as the raw material and a powder mixture of SiC, B₄C, Al, and carbon as the sintering additive. Al and B₄C underwent in situ reaction with carbon powder to produce Al₃BC₃, which promoted the densification of ZrB₂ ceramic. SiC grains were found to be elongated during sintering. The ZrB₂-SiC-Al₃BC₃ composite exhibited excellent mechanical properties, such as high flexural strength of 589 ± 147 MPa and fracture toughness of 7.81 ± 1.09 MPa m^1/2. Oxidation behavior of the ZrB₂-SiC-Al₃BC₃ composite was studied in air at 1500°C for 1 hour. A continuous layer of oxides consisting of a mixture of SiO₂, Al₂SiO₅, and Al₂O₃ was formed on the surface of the ZrB₂-SiC-Al₃BC₃ composite. This layer of oxides efficiently prevented oxygen from diffusing into the specimens during oxidation, which improved the oxidation resistance of the ZrB₂ ceramics.     

Effect of Y doping on microstructure and thermophysical properties of yttria stabilized hafnia ceramics

A series of Y₂O₃-doped HfO₂ ceramics (Hf_1-xY_xO_2-0.5×, x?=?0, 0.04, 0.08, 0.12, 0.16 and 0.2) were synthesized by solid-state reaction at 1600?°C. The microstructure, thermophysical properties and phase stability were investigated. Hf_1-xY_xO_2–0.5x ceramics were comprised of monoclinic (M) phase and cubic (C) phase when Y³⁺ ion concentration ranged from 0.04 to 0.16. The thermal conductivity of Hf_1-xY_xO_2–0.5x ceramic decreased as Y³⁺ ion concentration increased and Hf_0.8Y_0.2O_1.9 ceramic revealed the lowest thermal conductivity of ~?1.8?W/m*K at 1200?°C. The average thermal expansion coefficient (TEC) of Hf_1-xY_xO_2–0.5x between 200?°C and 1300?°C increased with the Y³⁺ ion concentration. Hf_0.8Y_0.2O_1.9 yielded the highest TEC of ~?10.4?×?10^?6 K^?1 while keeping good phase stability between room temperature and 1600?°C.     

Influence of sintering pressure on the microstructure and tribological properties of low temperature fast sintered hot-pressed Y-TZP

Contrarily to conventional sintering (CS) method where longer cycles and high temperature (1400–1500?°C) are applied to sinter yttria-stabilized tetragonal zirconia polycrystalline (Y-TZP) ceramics, this work presents a faster and low temperature (1175?°C) way through hot pressing (HP) to produce full densified zirconia with good mechanical and tribological properties. This work is concerned with the influence of sintering pressure on the microstructure and tribological properties of hot-pressed Y-TZP. For this purpose, four sintering pressures 5, 20, 60 and 100?MPa were tested. The wear tests were carried out by reciprocating ball-on-plate as a simplified test for tooth-to-restorative material contact under 37?°C using artificial saliva to mimic oral conditions. The results demonstrated that density, hardness and tribological properties are strongly influenced by the sintering pressure, namely an improvement with pressure increase was achieved. The highest density, hardness values and wear resistance were achieved for Y-TZP samples produced at P?=?100?MPa. Furthermore, it was revealed that a smaller grain size for Z100 samples (full densification condition) was achieved comparatively to conventional-sintered Y-TZP. This work proves that it is possible to produce dense Y-TZP materials under low sintering temperature and faster cycles with reduced grain size without compromise mechanical and tribological properties.     

Fabrication,microstructure, and optical properties of Yb:Y3ScAl4O12 transparent ceramics with different doping levels

Transparent Yb:Y₃ScAl₄O₁₂ (Yb:YSAG) ceramics with different ytterbium doping concentrations such as 5, 10, 15, 20 at.% have been successfully fabricated by solid-state reactive sintering. All the obtained ceramics are in dense and homogeneous structure after sintering at 1820°C for 30 hours and with a posttreatment by hot isostatic pressing at 1750°C for 3 hours with 200 MPa pressure. We systematically analyzed the influence of Yb³⁺ doping concentration on the microstructure and optical properties of the ceramics. The 10 at.% Yb:Y₃ScAl₄O₁₂ ceramics with a thickness of 3.2 mm show the best transparency as high as 80.9% at 1100 nm. The laser emission of the 10 at.% Yb:YSAG ceramics was tested, resulting in a maximum slope efficiency of 67.6% and a maximum output power of 11.3 W under quasi-continuous wave pump conditions. The tuning range spanned from 990 to 1071 nm.