Development of stabilized zirconia–alkali salts dual membranes for carbon dioxide capture

Molten Na₂CO₃–K₂CO₃ (NKC, 56–44 mol%) eutectic compositions were vacuum-impregnated, at the eutectic temperature, into two porous ZrO₂:8.6 mol% MgO (magnesium-partially stabilized zirconia, MgPSZ) and ZrO₂:8 mol% Y₂O₂ (yttria-fully stabilized zirconia, 8YSZ) ceramics. Thermogravimetric analyses were performed in mixtures of that composition with MgPSZ and 8YSZ ceramic powders. Before impregnation, porosity was achieved in the two compounds by addition and thermal removal of 30 vol.% NKC. To ascertain the carbonates had filled up through the ceramic body, both sides of the parallel and fracture surfaces of the disk-shaped impregnated compositions were observed in a scanning electron microscope and analyzed by energy-dispersive X-ray spectroscopy. The electrical conductivity of the two ceramics, before and after impregnation, was evaluated by electrochemical impedance spectroscopy in the 5 Hz–13 MHz frequency range from approximately 530 to 740°C. The permeation of the carbonate ions through the membranes via the eutectic composition was assessed by the threshold temperatures of the onset of the carbonate ion percolation. The objectives were to prepare dual-phase membranes for the separation of carbon dioxide and for the development of carbon dioxide sensors.     

Heat-treatment effect on the properties of a zirconia ceramic with a grainy structure

Conclusions The heat treatment at 2000°C of zirconia ceramic with a grainy structure causes the destabilization of the ZrO₂-CaO solid solutions but this is not complete after a 200-h dwell; the electrosmelted ZrO₂ ceramic stabilized with CaO is more stable under these conditions. The ZrO₂-Y₂O₃ solid solutions have greater stability on heating.When the grainy-structure zirconia ceramic is subjected to an isothermal dwell at 2000°C there is a consequent reduction in the strength properties caused either by the decomposition if the solid solutions (CaO-stabilized ceramic) or by the growth of crystals (Y₂O₃-stabilized ceramic).Deceased.Translated from Ogneupory, No, 7, pp. 51–55, July, 1979.     

Effects of TiO2 doping on the defect chemistry and thermo-physical properties of Yb2O3 stabilized ZrO2

Yb₂O₃ stabilized ZrO₂ (YbSZ) doped with different TiO₂ contents were produced, and their phase structure, thermal conductivities and thermal expansion coefficients were investigated. A new solid-solution model is proposed, i.e. Ti⁴⁺ would take the interstitial sites when its content is below a critical value (≤2.5 mol%) and then substitute for Zr⁴⁺. The abnormal lattice volume and thermo-physical properties of 2.5 mol% TiO₂ doped YbSZ, and the positive effects of TiO₂ doping on the thermal conductivity at moderate doping level are consistent with the new defect model. However, monoclinic phase is formed when the TiO₂ content reaches to 10 mol% and its content increases with doping content, which have negative influence on the thermo-physical properties. Considering the comprehensive properties, 10 mol% TiO₂ doped YbSZ is considered as a promising thermal barrier coating ceramic.     

Phase formation and lattice distortion of Lu2O3-doped ZrO2 in comparison with Y2O3-doped ZrO2

Lu₂O₃ and Y₂O₃ doping of 8, 11, and 18 mol% in ZrO₂ were prepared by solid solution reaction, aiming to study the phase stabilization of Lu₂O₃-doped ZrO₂ and Y₂O₃-doped ZrO₂ in terms of phase formation and lattice distortion. The Rietveld refinement results indicated that Lu₂O₃-doped ZrO₂ and Y₂O₃-doped ZrO₂ followed the same trend in terms of cubic phase fraction, increasing from 25%–30% (8 mol%) to 95%–100% (11 and 18 mol%). This phase formation was confirmed by observing the same diffraction ring pattern observed for the Lu₂O₃-doped ZrO₂ and Y₂O₃-doped ZrO₂. The Vickers hardness of the Lu₂O₃-doped ZrO₂ was 4.3% higher than that of Y₂O₃-doped ZrO₂ at 8 mol%, but 9.7% and 14.8% lower at 11 and 18 mol%, respectively. This was likely caused by the lattice distortion effect of Y₂O₃ doping overpowering the field strength difference between Lu³⁺ and Y³⁺.     

High-temperature compressive creep of novel fine-grained orthorhombic ZrO2 ceramics stabilized with 12 mol% Ta doping

A novel fine-grained orthorhombic ZrO₂ ceramic stabilized with 12?mol% Ta doping was fabricated by spark-plasma sintering from home-made powders, and its high-temperature mechanical properties evaluated for the first time by compressive creep tests in both Ar and air. It was found that the high-temperature plasticity of the ceramic deformed in Ar, under which the Ta-doped orthorhombic ZrO₂ is a black suboxide with abundant oxygen vacancies in its crystal structure, is controlled by grain boundary sliding (stress exponent ～2, and activation energy ～780–800?kJ/mol). However, the high-temperature plasticity of the ceramic deformed in air, under which the Ta-doped orthorhombic ZrO₂ is a white oxide due to the elimination in situ of oxygen vacancies, is controlled by recovery creep (stress exponent ～3, and activation energy ～750?kJ/mol). It was also observed that black Ta-doped orthorhombic ZrO₂ is more creep resistant than its white counterpart with the same grain size, and that the former deforms as the more conventional Y₂O₃-stabilized ZrO₂ does.     

Effect and mechanism of ZrO2 doping on the cracking behavior of melt-grown Al2O3 ceramics prepared by directed laser deposition

Directed laser deposition (DLD) is a new method for rapidly preparing melt-grown ceramics, but cracking problem greatly limited its application. In this study, cracking behavior of Al₂O₃ ceramics was suppressed by doping ZrO₂. Crack suppression mechanism of ZrO₂ doping in melt-grown ceramics was also analyzed. Process parameters which are prone to generating cracks were adopted in the experiments, and they contribute to showing the crack clearly. Results show that ZrO₂ doping has remarkable crack suppression effects. It is most obvious when ZrO₂ content is 37 mol%. Compared with those of pure Al₂O₃ ceramics, crack density reduces by 43.2%, and the number of longitudinal main cracks reduces by 63.2%. Doping of ZrO₂ forms dense composite microstructure with primary α-Al₂O₃ grains discretely distributing in eutectic continuous matrix. Therefore, initial crack sources are effectively reduced. Morphology of primary Al₂O₃ grains transforms from cellular to dendritic, which changes crack propagation mode from inter-granular to trans-granular. Mismatch of thermo-physical properties of different phase promotes the arrest, deflection, and bridging phenomena in crack propagation, contributing to crack suppression. On the basis of ZrO₂ doping, we have realized the preparation of crack-free eutectic ceramic (37 mol%ZrO₂) samples through further process optimization. The maximum size of the sample reaches 230 mm.     

Effects of manganese oxide addition and reductive atmosphere annealing on the phase stability and microstructure of yttria stabilized zirconia

The effects of Mn₃O₄ addition and reductive atmosphere (N₂:H₂ = 97:3) annealing on the microstructure and phase stability of yttria stabilized zirconia (YSZ) ceramics during sintering at 1500 °C for 3 h in air and subsequent annealing in a reductive atmosphere were investigated. Mn₃O₄ added 6 mol% YSZ (6YSZ) and 10 mol% YSZ (10YSZ) ceramics were prepared via the conventional solid-state reaction processes. The X-ray diffraction results showed that a single cubic phase of ZrO₂ was obtained in 1 mol% Mn₃O₄ added 6YSZ ceramic at a sintering temperature of 1500 °C for 3 h. A trace amount of monoclinic ZrO₂ phases were observed for 1 mol% Mn₃O₄ added 6YSZ ceramics after annealing at 1300 °C for 60 cycles in a reductive atmosphere by transmission electron microscopy. Furthermore, a single cubic ZrO₂ phase existed stably as Mn₃O₄ added 10YSZ ceramics was annealed at 1300 °C for 60 cycles in reductive atmosphere.     

Effects of ZrO2-La2O3 co-addition on the microstructural and optical properties of transparent Y2O3 ceramics

Commercial Y₂O₃ powder was used to fabricate Y₂O₃ ceramics sintered at 1600 °C and 1800 °C with concurrent addition of ZrO₂ and La₂O₃ as sintering aids. One group with different contents of La₂O₃ (0–10 mol%) with a fixed amount of 1 mol% ZrO₂ and another group with various contents of ZrO₂ (0–7 mol%) with a fixed amount of 10 mol% La₂O₃ were compared to investigate the effects of co-doping on the microstructural and optical properties of Y₂O₃ ceramics. At low sintering temperature of 1600 °C, the sample single doped with 10 mol% La₂O₃ exhibits much denser microstructure with a few small intragranular pores while the samples with ZrO₂ and La₂O₃ co-doping features a lot of large intergranular pores leading to lower density. When the sintering temperature increases to 1800 °C, samples using composite sintering aids exhibit finer microstructures and better optical properties than those of both ZrO₂ and La₂O₃ single-doped samples. It was proved that the grain growth suppression caused by ZrO₂ overwhelms the acceleration by La₂O₃. Meanwhile, 1 mol% ZrO₂ acts as a very important inflection point with regard to the influence of additive concentration on the transmittance, pore structure and grain size. The highest in-line transmittance of Y₂O₃ ceramic (1.2 mm in thickness) with 3 mol% of ZrO₂ and 10 mol% of La₂O₃ sintered at 1800 °C for 16 h is 81.9% at a wavelength of 1100 nm, with an average grain size of 11.2 µm.     

Heat-insulating properties of hollow Al2O3–ZrO2(CeO2)fibers fabricated using pampas grass as the template

Al₂O₃–ZrO₂(CeO₂) ceramic fibers have good heat insulation and high-temperature resistance. Pampas grass is a large perennial grass, or a natural fiber, with a hollow structure that can improve the heat insulation of the fiber by changing its heat transfer mode. This study introduces a method for the preparation of biomorphic Al₂O₃–ZrO₂(CeO₂) fibers with a hollow structure and a double-layer-tube structure using the pampas grass as thetemplate. Hollow ceramic fibers with good thermal insulation properties were prepared by soaking the pampas grass in ZrOCl₂, Ce(NO₃)₃, and AlCl₃ solutions before sintering them at high temperatures. When the zirconia doping ratio was 11 mol%, the biomorphic fiber with a double-layer-tube structure was prepared. The biomorphic fibers inherited the hollow structure of the pampas grass and retained the template fiber'scharacteristics of excellent continuity and a high degree of hollowness, whichdecreased the thermal conductivity of the fibers.     

Phase stability (at 1000°C) of hollow t-ZrO2 fibers costabilized by lanthana and yttria

Yttrium-stabilized ZrO₂ (YSZ) hollow fibers derived from a ceiba template present a 25%–53% reduction in thermal conductivity compared with traditional YSZ solid fibers. However, after prolonged preservation at 1000°C, tetragonal ZrO₂ (t-ZrO₂) can easily transform to monoclinic ZrO₂ (m-ZrO₂), which destroys the hollow structure of the YSZ fibers and results in loss of the structural advantages for heat insulation. To overcome this, in this study, biomorphic lanthana and yttrium costabilized zirconia (LaYSZ) fibers with a hollow structure are fabricated by doping appropriate amounts of lanthanum in the raw materials of YSZ fibers. X-ray diffraction, scanning electron microscopy, and thermal conductivity measurements are utilized to confirm the phase-stability superiority of LaYSZ fibers to that of YSZ fibers under harsh conditions. After preservation at 1000°C for 150 hours, the m-ZrO₂ content in the LaYSZ hollow fibers increases from 0 to 3.4 mol%, whereas that in the YSZ fibers increases from 0 to 10.25 mol%. Furthermore, owing to their better phase stability at 1000°C, the morphologies and heat-insulating properties of LaYSZ fibers are more improved in several aspects compared with YSZ fibers.     

Oxygen‐ion conduction in scandia‐stabilized zirconia‐ceria solid electrolyte (xSc2O3–1CeO2–(99−x)ZrO2, 5 ≤ x ≤ 11)

Solid oxide fuel cells (SOFCs) operating at intermediate temperature (500°C‐700°C) provide advantages of better durability, lower cost, and wider target application market. In this work, we have studied Sc₂O₃ (5‐11 mol%) stabilized ZrO₂–CeO₂ as a potential solid electrolyte for application in IT‐SOFCs. Lower Sc₂O₃ doping range than the traditional 11 mol% Sc₂O₃‐stabilized ZrO₂ is an interesting research topic as it could potentially lead to an electrolyte with reduced oxygen vacancy ordering, lower cost, and higher mechanical strength. XRD and Raman spectroscopy was used to study the phase equilibrium in ZrO₂–CeO₂–Sc₂O₃ system and impedance spectroscopy was done to estimate the grain, grain boundary, and total ionic conductivities. Maximum for the grain and grain‐boundary conductivities as well as the tetragonal‐cubic phase boundary was found at 8‐9 Sc₂O₃ mol% in ZrO₂‐1 mol% CeO₂ system. It is suggested that the addition of 1 mol% CeO₂ in the ZrO₂ host lattice has improved the phase stability of high‐conductivity cubic and tetragonal phases at the expense of low‐conductivity t′‐ and β‐phases.     

Effect of TiO2 and Ta2O5 co-doping on phase stability,fracture toughness,and sintering behavior of ZrO2 stabilized by 10mol%(Y0.4Gd0.3Yb0.3)2O3

The effect of TiO₂ and Ta₂O₅ co-doping on the phase structure, fracture toughness, and sintering behavior of 10mol%(Y_0.4Gd_0.3Yb_0.3)₂O₃-stabilized zirconia was investigated using X-ray diffraction, scanning electron microscopy, microindentation, and pressureless sintering. The results showed that 10mol%(Y_0.4Gd_0.3Yb_0.3)₂O₃–ZrO₂ had a single cubic phase structure, and an increase in the Ta₂O₅ (≥6 mol%) and TiO₂ doping concentrations resulted in a simultaneous increase in the content and stability of the tetragonal phase. The fracture toughness of TiO₂ and Ta₂O₅ co-doping 10mol%(Y_0.4Gd_0.3Yb_0.3)₂O₃–ZrO₂ decreased with an increase in the Ta₂O₅ content. On the other hand, the TiO₂ content had no significant effect on the fracture toughness of 10mol%(Y_0.4Gd_0.3Yb_0.3)₂O₃–ZrO₂. The sintering resistance of the specimens increased with an increasing in the Ta₂O₅ content; however, an increase in the TiO₂ content accelerated the densification of the specimens. When the Ta₂O₅ content was 10 mol% and the TiO₂ content was in the range of 4–8 mol%, a single non-transformable tetragonal phase structure with fracture toughness similar to that of 6–8 wt% Y₂O₃ stabilized ZrO₂ and excellent anti-sintering properties could be obtained. This structure can be explored as a thermal barrier coating material for high-temperature applications.     

A Novel Magnetodielectric Solid Solution Ceramic 0.4LiFe5O8–0.6Li2MgTi3O8 with Excellent Microwave Dielectric Properties

In this study, a novel spinel solid solution ceramic of 0.4LiFe₅O₈–0.6Li₂MgTi₃O₈ (0.4LFO–0.6LMT) has been developed and investigated. It is found that the 40 mol% LiFe₅O₈ and 60 mol% Li₂MgTi₃O₈ are fully soluble in each other and a disordered spinel phase is formed. The ceramic sample sintered at 1050°C/2 h exhibits both good magnetic and dielectric properties in the frequency range 1–10 MHz, with a permeability between 29.9~14.1 and magnetic loss tangent between 0.12~0.67, permittivity between 16.92~16.94 and dielectric loss tangent between 5.9 × 10^?3–2.3 × 10^?2. The sample also has good microwave dielectric properties with a relative permittivity of 16.1, a high quality factor (Q × f) ~28 500 GHz (at 7.8 GHz). Furthermore, 3 wt% H₃BO₃–CuO (BCu) addition can effectively lower the sintering temperature to 925°C and does not degrade the magnetodielectric properties. The chemical compatibility with silver electrode indicates that this kind of ceramics is a good candidate for the low‐temperature cofired ceramic (LTCC) application.     

Significantly improved dielectric properties of TiO2 ceramics through acceptor-doping and Ar/H2 annealing

The acceptor-doped rutile TiO₂ ceramics, x mol% M₂O₃-(1-x) mol% TiO₂ (M = Al³⁺, Ga³⁺, and In³⁺), were prepared by solid state reaction method. The influence of Ar/H₂ annealing on the structural and dielectric properties of the ceramics were systematically investigated. Our results reveal that the dielectric properties of the ceramics can be significantly improved by the Ar/H₂ annealing. Ga³⁺ is found to be the most suitable dopant with the best doping level of 5 mol%. Excellent dielectric properties of colossal and flat dielectric permittivity (~1.2 × 10⁵ (@1 kHz and 25 °C), low dielectric loss (~0.1), and good frequency stability were achieved over the temperature range of -70–150 °C in the Ar/H₂-annealed 5 mol% Ga₂O₃-95 mol% TiO₂ ceramic. This approach of acceptor-doping and Ar/H₂ annealing leads to two thermally activated relaxations in the sample. The low-temperature relaxation is argued to be a Maxwell-Wagner relaxation caused by frozen electrons, while the high-temperature relaxation is a glass-transition-like relaxation associated with the freezing process of the electrons. This work highlights that engineering low-temperature Maxwell-Wagner relaxation paves a new way other than the frequently used acceptor-donor dual doping to design superior dielectric properties in the TiO₂ system.     

High permittivity and excellent high-temperature energy storage properties of X9R BaTiO3–(Bi0.5Na0.5)TiO3 ceramics

We fabricated x(Bi_0.5Na_0.5)TiO₃–(1−x)[BaTiO₃–(Bi_0.5Na_0.5)TiO₃–Nb] (BNT-doped BTBNT-Nb) dielectric materials with high permittivity and excellent high-temperature energy storage properties. The initial powder of Nb-modified BTBNT was first calcined and then modified with different stoichiometric ratios of (Bi_0.5Na_0.5)TiO₃ (BNT). Variable-temperature X-ray diffraction (XRD) results showed that the ceramics with a small amount of BNT doping consisted of coexisting tetragonal and pseudocubic phases, which transformed into the pseudocubic phase as the test temperature increased. The results of transmission electron microscopy (TEM) showed that the ceramic grain was the core-shell structure. The permittivity of the 5 mol% BNT-doped BTBNT-Nb ceramic reached up to 2343, meeting the X9R specification. The discharge energy densities of all samples were 1.70-1.91 J/cm³ at room temperature. The discharge energy densities of all samples fluctuated by only ±5% over the wide temperature range from 25°C to 175°C and ±8% from 25°C to 200°C. The discharge energy density of the 50 mol% BNT-doped BTBNT-Nb ceramic was 2.01 J/cm³ at 210 kV/cm and 175°C. The maximum energy efficiencies of all ceramics were up to ~91% at high temperatures and were much better than those at room temperature. The stable dielectric properties within a wide temperature window and excellent high-temperature energy storage properties of this BNT-doped BTBNT-Nb system make it promising to provide candidate materials for multilayer ceramic capacitor applications.     

Development of ZrO2–WC composites by pulsed electric current sintering

ZrO₂–WC ceramic composites with 40 vol% WC were consolidated by pulsed electric current sintering (PECS) for 4 min at 1450 °C under a pressure of 60 MPa. The effect of ZrO₂ stabilizers and the source of WC powder on the densification, phase constitution, microstructure and mechanical properties of the ZrO₂–WC composites were investigated and analyzed. The experimental results revealed that the amount and type of ZrO₂ stabilizers played a primary role on the phase constitution and mechanical properties of the composites in comparison to the morphology and size of the WC powder. The 2 mol% Y₂O₃-stabilized composites exhibited much better mechanical properties than that of 1.75 mol% Y₂O₃-stabilized or 1 mol% Y₂O₃ + 6 or 8 mol% CeO₂ co-stabilized composites. A Vickers hardness of 16.2 GPa, fracture toughness of 6.9 MPa m^1/2, and flexural strength of 1982 MPa were obtained for the composites PECS from a mixture of nanometer sized WC and 2 mol% Y₂O₃-stabilized ZrO₂ powder.     

Observation of yttrium oxide segregation in a ZrO2-SiO2 glass-ceramic at nanometer dimensions

Dopant segregation at grain boundaries (GBs) in ceramics has been widely reported, while whether similar segregation behavior occurs in glass-ceramics remains unknown. The distribution of dopant in glass-ceramics may be totally different due to the existence of glass phase. This study examines the distribution of Y³⁺ ions in a ZrO₂-SiO₂ glass-ceramic. Two samples were prepared by hot pressing, yttrium oxide-doped, and undoped 65 mol% ZrO₂-35 mol% SiO₂ nanocrystalline glass-ceramics (NCGCs). The NCGCs had the same microstructure, that is, ZrO₂ nanoparticles (NPs) embedded in an amorphous SiO₂ matrix. XRD results showed that the undoped NCGC was composed of 20.9 wt% (weight percentage) monoclinic ZrO₂ (m-ZrO₂) and 79.1 wt% tetragonal ZrO₂ (t-ZrO₂), while the yttrium oxide-doped NCGC was composed of 9.6 wt% m-ZrO₂ and 90.4 wt% t-ZrO₂. X-ray energy-dispersive spectrometry (EDS) results in scanning electron transmission microscopy (STEM) mode demonstrated that Y³⁺ ions segregated both on the surface of ZrO₂ NPs and within the thin intergranular glass film (with a thickness of approximately 7 Å) between ZrO₂ NPs in the yttrium oxide-doped NCGC. Interestingly, no obvious Y signals were detected in the amorphous SiO₂ matrix. Density functional theory calculation results showed that Y³⁺ ions had a strong segregation tendency in the GB area and the segregation of Y³⁺ ions increased the work of separation of GB layer. These findings provide new understanding of the segregation behavior of dopant in glass-ceramics, which may offer useful guidance for other researchers to tailor the properties of glass-ceramics through GB engineering.     

Effect of High‐Temperature Aging on the Fracture Toughness of 40 mol% Ceria‐Stabilized Zirconia

The 40 mol% CeO₂‐stabilized ZrO₂ ceramic was synthesized by the sol‐spray pyrolysis method and aged at 1400°C–1600°C. The effects of high‐temperature aging on its fracture toughness were investigated after heat treatments at 1500°C for 6–150 h in air. Characterization results indicated that the activation energy for grain growth of 40 mol% CeO₂‐stabilized ZrO₂ was 593 ± 47 kJ/mol. The average grain size of this ceramic varied from 1.4 to 5.6 μm within the aging condition of 1500°C for 6–150 h. The Ce‐lean tetragonal phase has a constant tetragonality (ratio of the c‐axis to a‐axis of the crystal lattice) of 1.0178 during the aging process. It was found that the fracture toughness of 40 mol% CeO₂‐stabilized ZrO₂ was determined to be 2.0 ± 0.1 MPa·m^1/2, which did not vary significantly with prolonging aging time. Since no monoclinic zirconia was detected in the regions around the indentation crack‐middle and crack‐tip, the high fracture toughness maintained after high‐temperature aging can be attributed to the remarkable stability of the tetragonal phase in 40 mol% CeO₂‐stabilized ZrO₂ composition.     

Stability properties and microstructure properties of microwave-sintered CeO2 doped zirconia ceramics

Nanosized CeO₂–ZrO₂ powders prepared by atmospheric pressure pyrolysis were used as raw materials to prepare CeO₂–ZrO₂ ceramics using microwave sintering. The samples were characterised using bulk density measurements, X-ray diffraction (XRD), Fourier Transform Infrared Spectrometer (FT-IR), Raman, and scanning electron microscopy (SEM). The purpose was to determine the optimised microwave sintering process for CeO₂–ZrO₂ ceramics and reveal the corresponding mechanism. The results show that with a CeO₂ addition content above 5 mol%, the tetragonal phase peak appeared obviously in the sample. The results show that the tetragonal phase peak appears when the CeO₂ content is more than 5 mol%. The dopants, namely CeO₂, have reduced the solid solution's phase transformation temperature with the assistance of microwave heating. Additionally, the grain size of the CeO₂–ZrO₂ ceramics has shown a negative relationship with Ce content at a temperature of 900 °C. The reason is that the rapid sintering due to microwave sintering and the oxygen vacancies generated by CeO₂ can effectively inhibit grain growth. The regulation mechanism on microwave sintering of CeO₂–ZrO₂ ceramic was clarified, and the technical prototype of controlled prepared CeO₂–ZrO₂ ceramics by microwave sintering was constructed.     

Li2ZrO3 based Li-ion conductors doped with halide ions & sintered in oxygen-deficient atmosphere

All-solid-state batteries have recently attracted much attention for their high energy density and safety. Li₂ZrO₃-based Li-ion conductors with high electrochemical stability have potential applications for electrolytes in all-solid-state batteries. In this work, comparative investigations of Li₂ZrO₃ and halogen doped Li₂ZrO₃ ceramics were conducted by sintering at 700 °C in air or in oxygen-deficient atmosphere which was induced by a simple setup covering with corundum crucible. The analysis of phase composition reveals that the undoped Li₂ZrO₃ ceramic sintered in air contains pure monoclinic phase, while halogen-doped Li₂ZrO₃ sintered in air and all ceramics sintered in oxygen-deficient atmosphere are simultaneously composed of monoclinic and tetragonal phases. Li₂ZrO₃ ceramic with tetragonal phases has higher conductivity (0.28 mS cm⁻¹ for undoped Li₂ZrO₃) than the pure monoclinic Li₂ZrO₃ (0.07 mS cm⁻¹), and halogen doping can further enhance the conductivity of Li₂ZrO₃ ceramics higher than 0.5 mS cm⁻¹ at room temperature.