Luminescence properties of Eu3+- and Tb3+-doped δ-Bi2O3 stabilized by Th4+ substitution

The extent of incorporating Eu³⁺ and Tb³⁺ for bismuth in the oxygen-deficient fluorite structured Bi_0.50Th_0.50O_y has been examined together with the comprehension of their luminescence characteristics. The samples were synthesized by solution combustion method from which doping limits of Eu³⁺ and Tb³⁺, respectively, in the fluorite structure was determined. Uniform distribution of constituent elements was confirmed from elemental mapping. Doping Eu³⁺ and Tb³⁺-ions introduced compressive strain and oxygen vacancies in the system. Raman spectra of doped samples confirmed the fluorite structure and revealed the existence of oxygen vacancies in them. While Tb-doped samples showed a systematic decrease in band gap with increase in dopant concentration, such systematic variation was not observed for Eu-doped samples. Conclusions about the local site symmetry around Eu³⁺ and Tb³⁺ ions in the defect fluorite structure have been drawn from the photoluminescent spectral analysis of doped samples. Energy transfer from Bi³⁺ to Eu³⁺ and Tb³⁺-has been observed in these samples. The Judd-Ofelt analysis has been carried out to understand luminescence characteristics in these samples.     

Predicting properties of MgO·nAl2O3 by first-principles calculation combined with bond valence models

Spinel-type oxides have attracted tremendous attentions owing to their wide applications. However, the complicated composition and structure of spinel-type solid solution brought about challenge to explore the relationship among composition, structure, and properties. A new approach which combined first-principles calculation with bond valence models was developed to explore the composition dependence of structure and properties for spinel-type oxide solid solution. The first-principles calculation was used to simulate the structural parameters of spinel-type oxide solid solution. The mechanical and thermal properties of Mg_1-xAl_2(1+x/3)O₄ spinel-type solid solution were estimated by bond valence models based on the structure which was reconstructed from the structural parameters determined by the first-principles calculation. Besides, bond valence arguments were also used to assess the reliability of reconstructed structure. The results suggest that the extremely overbonded or underbonded atoms can be avoided in the reconstructed structure, which improves the stability of reconstructed structure. By comparing the results with experimental values, it can be seen that mechanical and thermal properties could be simulated exactly by the new approach and bulk modulus was used as an example to explore the relationship among composition, structure, and properties of Mg_1-xAl_2(1+x/3)O₄.     

Simultaneously enhanced electrical stability and nonlinearity in ZnO varistor ceramics: Role of Si-stabilized δ-Bi2O3 phase

In the present study, simultaneously enhanced electrical stability (low degradation rate of 8.0 × 10^?3 mA? h^1/2) and high nonlinear coefficient of 56 were obtained in ZnO varistors by doping SiO₂. To clarify the mechanism of enhanced properties, comprehensive microscopic analyses were studied. Particularly, the intrinsic point defects were quantitatively characterized for the first time. Results showed that the densities of zinc interstitials (Zn_i) and oxygen vacancies (V_o) were dramatically decreased, resulting in enhanced stability. Besides, reduced Zn_i and V_o decreased the total donor density, contributing to the improved barrier height and thus leading to enhanced nonlinearity. Combined with XRD and SEM results, it is deduced that such reduced Zn_i and V_o are attributed to the Si-stabilized high oxygen conducting δ-Bi₂O₃ phase. Furthermore, this elucidated mechanism, which has been long neglected in Si-doped varistors, may provide valuable insights into further developing high-performance ZnO varistors.     

Effect of CaO doping on the properties and crystallization behavior of Y2O3–Al2O3–SiO2 glass

Nowadays, Y₂O₃–Al₂O₃–SiO₂ (YAS) glass joining is considered to be a promising scheme for nuclear-grade continuous silicon carbide (SiC) fiber reinforced SiC matrix composites (SiC/SiC). CaO has great potential for nuclear applications since it has low reactivity and low decay rate under nuclear irradiation. In this paper, the effect of CaO doping on the structure, thermophysical properties, and crystallization behavior of YAS glass was systematically studied. As the CaO doping content increased, the number of bridge oxygens and the viscosity at high temperatures reduced gradually. After heat treatment at 1400 °C, the main phases in YAS glass were β-Y₂Si₂O₇, mullite, and SiO₂ (coexistence of crystalline and glass phases), while that with 3.0% CaO doping turned into a single glassy phase under the same treatment conditions. Moreover, a structural model and the modification mechanism were proposed, which provided a theoretical basis for the subsequent component design and optimization.     

Attenuation properties of epoxy-Ta2O5 and epoxy-Ta2O5-Bi2O3 composites at γ-ray energies 59.54 and 662 keV

Epoxy resin filled with suitable high Z elements can be a potential shield for X-rays and γ-rays. In this work, we present the γ-ray attenuation properties of epoxy composites filled with (0–30 wt%) Tantalum pentoxide (Ta₂O₅) and Ta₂O₅-Bi₂O_3, which were prepared by open mold cast technique. X-ray diffraction patterns showed crystalline peaks of Ta₂O₅ and bismuth oxide (Bi₂O₃) in the prepared epoxy-Ta₂O₅ and epoxy-Ta₂O₅-Bi₂O₃ composites. Homogeneity of the samples at higher filler wt% was revealed by SEM images. Mechanical characterization showed the enhanced mechanical strength of epoxy-Ta₂O₅-Bi₂O₃ composites compared to epoxy-Ta₂O₅. Higher storage modulus and glass transition temperature of the epoxy-Ta₂O₅-Bi₂O₃ composites showed enhanced stiffness and thermal stability when compared to neat and epoxy-Ta₂O₅. Decrease in the value of tan(δ) at higher content of filler loadings indicated the good adhesion between filler and matrix. Mass attenuation coefficients of epoxy-Ta₂O₅ (30 wt%) composites at γ-ray energies 59.54 and 662 keV were found to be 0.876 cm² g^–1 and 0.084 cm² g^–1, while that of epoxy-Ta₂O₅-Bi₂O₃ (30 wt% Bi₂O₃) composite were 1.271 cm² g^–1 and 0.088 cm² g^–1, respectively. The epoxy-5% Ta₂O₅-30% Bi₂O₃ composites with higher μ/ρ value and tensile strength may be a potential γ-ray shield in various radiation environments.     

Comprehensive study on corrosion protection properties of Al2O3, Cr2O3 and Al2O3–Cr2O3 ceramic coatings deposited by plasma spraying on carbon steel

In this study, individual Al₂O₃ and Cr₂O₃ coatings and Cr₂O₃-25, 50, 75 wt% Al₂O₃ composite coatings were applied on carbon steel by atmospheric plasma spraying method. Corrosion experiments were performed on as-sprayed and epoxy resin sealed coatings including potentiodynamic polarization, electrochemical impedance spectroscopy and long-term immersion in 3.5 wt% NaCl solution. Phase composition and microstructure of the coatings were investigated by x-ray diffraction, optical microscopy and scanning electron microscopy, before and after the corrosion experiment. The results showed that the Cr₂O₃ coating exhibited the best corrosion resistance, due to the densest microstructure and highest adhesion strength. The Cr₂O₃-25 wt% Al₂O₃ coating had the highest interconnected porosities and thus had the least corrosion resistance compared to other coatings. In general, the as-sprayed coatings induced a maximum increase of 3.93 times the polarization resistance (R_p) in the polarization experiment and a 3.5 times increase in the charge transfer resistance (R_ct) in the EIS experiment, which was not significant. Stresses caused by increased volume of corrosion products in the coating-substrate interface resulted in the spallation of Cr₂O₃-25, 50 wt% Al₂O₃ coatings from the substrate over long-term of immersion. The adhesion strength of the coatings was a determining criterion for the long-term durability of the coatings. The sealing treatment resulted in a significant increase in R_p and R_ct.     

Mechanical characteristics of FeAl2O4 and AlFe2O4 spinel phases in coatings – A study combining experimental evaluation and first-principles calculations

FeAl₂O₄ and AlFe₂O₄ have similar spinel structures but different atomic arrangements, leading to different properties. In this study, mechanical properties and structures of the two spinel phases in composite coatings prepared by reactive plasma spraying of Fe₂O₃-Al composite powder were investigated by means of multi-mode atomic force microscopy, X-ray diffraction, and scanning electron microscopy. It was demonstrated that AlFe₂O₄ was stronger than FeAl₂O₄ with a higher electron work function (EWF). First-principles calculations were conducted to understand the difference in mechanical properties between the two phases. It was shown that FeAl₂O₄ and AlFe₂O₄ have “normal” and “inverse” spinel structures with different configurations of valence electrons: Fe²⁺_tet(Al³⁺)₂O₄ and Fe³⁺_tet(Fe²⁺Al³⁺)_octO₄. Compared to Fe²⁺_tet(Al³⁺)₂O₄, Fe³⁺_tet(Fe²⁺Al³⁺)_octO₄ has its O and Fe atoms in the octahedral sites forming covalent bonds, which increase the stability and strength of the crystal, corresponding to higher EWF and larger bulk, shear and Young's moduli.     

Synthesis and properties of multiferroic 0.7BiFeO3−0.3BaTiO3 thin films by Mn doping

Multiferroic BiFeO₃?BaTiO₃ thin films that simultaneously exhibit ferroelectricity and ferromagnetism at room temperature were prepared by chemical solution deposition. Perovskite single-phase 0.7BiFeO₃?0.3BaTiO₃ thin films were successfully fabricated in the temperature range 600–700 °C on Pt/TiO_x/SiO₂/Si substrates. As the crystallization temperature was increased, grain growth proceeded, resulting in higher crystallinity at 700 °C. Although the 0.7BiFeO₃?0.3BaTiO₃ thin films exhibited poor polarization (P)?electric field (E) hysteresis loops owing to their low insulating resistance. The leakage current at high applied fields was effectively reduced by Mn doping at the Fe site of the 0.7BiFeO₃?0.3BaTiO₃ thin films, leading to improved ferroelectric properties. The 5 mol% Mn-doped 0.7BiFeO₃?0.3BaTiO₃ thin films simultaneously exhibited ferroelectric polarization and ferromagnetic magnetization hysteresis loops at room temperature.     

Pressure-less joining of SiCf/SiC composites by Y2O3–Al2O3–SiO2 glass: Microstructure and properties

In this study, Y₂O₃–Al₂O₃–SiO₂ (YAS) glass was prepared from Y₂O₃, Al₂O₃, and SiO₂ micron powders. Thermal expansion coefficient of as-obtained YAS glass was about 3.9 × 10⁻⁶, matching-well with that of SiC_f/SiC composites. SiC_f/SiC composites were then brazed under pressure-less state by YAS glass and effects of brazing temperature on microstructures and properties of resulting joints were investigated. The results showed that glass powder in brazed seam sintered and precipitated yttrium disilicate, cristobalite, and mullite crystals after heat treatment. With the increase in temperature, joint layer gradually densified and got tightly bonded to SiC_f/SiC composite. The optimal brazing parameter was recorded as 1400 °C/30 min and shear strength of the joint was 51.7 MPa. Formation mechanism of glass-ceramic joints was proposed based on combined analysis of microstructure and fracture morphology of joints brazed at different temperatures. Thermal shock resistance testing of joints was also carried out, which depicted decline in shear strength with the increase of thermal shock times. The strength of the joint after three successive thermal shock cycles at 1200 °C was 35.6 MPa, equivalent to 69% of that without thermal shock.     

Structure and surface properties of Al2O3–TiO2 ceramic coated AZ31 magnesium alloy

Magnesium and its alloys are the engineering materials which have the potential ability to be able to used widely particularly in the automotive, aerospace and in the biomedical sectors, especially thanks to their features such as lightness, specific strength that they have and biocompatibility. However, due to their poor wear resistance and corrosion resistance, the areas of usage are being restricted. This situation prevents Mg alloys to be used without any surface protection despite their good mechanical properties such as high strength/weight ratio. In this study, plasma spraying method is used to improve the poor corrosion resistance of AZ31 Mg alloy. Al₂O₃–13 wt% TiO₂ (AT13) and Al₂O₃–40 wt% TiO₂ (AT40) composite ceramic coatings were coated successfully on the surfaces of AZ31 Mg samples. The wear properties of the AT13 and AT40 coated samples were investigated for tribological applications. Surface morphology and microstructure of the duplex treated samples were analyzed by scanning electron microscopy (SEM) and X-ray diffraction (XRD). The microhardness value of the uncoated AZ31 Mg alloy is 40±3 HV_0.1, while the microhardness values of the AT40 and AT13 coatings are enhanced to 800±39 HV_0.1 and 1500±35 HV_0.1, respectively.     

Polymer nanocomposites containing β-Bi2O3 and silica nanoparticles: Thermal stability,surface topography and X-ray attenuation properties

Silicone polymer-based nanocomposites containing β-Bi₂O₃ nanoparticles with varying concentrations of silica nanoparticles are successfully prepared and characterized for thermal stability, surface topography, and X-ray attenuation property. Of all the samples studied here, silicone polymer of higher density (S1) containing β-Bi₂O₃ (50 wt%) and silica (0.025 wt%) nanoparticles is found to be thermally stable upto 424 and 375°C in argon and oxygen atmosphere, respectively. The atomic force microscopy image of top and cleaved surface of this nanocomposite exhibits an average roughness of 12 and 506 nm, respectively. It also exhibits the highest X-ray attenuation property, among the samples analyzed here, against X-rays of energies in the range of 30–66 keV. Therefore, S1 silicone polymer containing β-Bi₂O₃ and silica (0.025 wt%) nanoparticles is a potential material for the development of lead-free and X-ray opaque aprons, gloves, thyroid collar, gonad shield, and so on.     

Effects of TeO2/B2O3 substitution on synthesis,physical, optical and radiation shielding properties of ZnO–Li2O-GeO2-Bi2O3 glasses

Tellurite glass is a model material having superior features for several applications. It can be considered as a potential host matrix for different oxides, and this paper aims to study the effects of TeO₂/B₂O₃ substitution on synthesis, physical, optical and radiation shielding properties of ZnO–Li₂O-GeO₂-Bi₂O₃ glasses produced by melt quenching technique. The physical and optical features of the fabricated glasses were experimentally investigated by determining pivotal parameters such as density, XRD, tellurium ion concentration (N_i), linear refractive index (n_o), polaron radius (r_p) and inter nuclear distance (r_i). Moreover, the relative radiation deposition within the glasses was assessed via the attenuation coefficients (e.g. MAC), specific gamma ray constant (ᴦ), total stopping power (TSP), neutron cross sections, and dose rate (D). Our results suggest that both TeO₂ and B₂O₃ additives have a significant effect on the fundamental properties of the ZnO–Li₂O-GeO₂-Bi₂O₃ glasses. It also found that the lower thicknesses of the present glasses are required to provide the same level of shielding than ordinary, ilmenite, steel scrap, hematic-serpentine, ilmenite-limonite and basalt-magnetite concretes, RS253-G18 and RS360 glass shields. Therefore, presently investigated glasses are promising photon shields in different technological applications of gamma- and x-rays.     

Understanding δ-Bi2O3 fluorite degradation mechanism and related solutions for promising applications in distributed multigeneration

Oxygen selective membrane on the base of cermet δ-Bi₂O₃/Ag with an interpenetrating structure has the maximum potential efficiency of air separation. However, the degradation processes, including the phase degradation of fluorite δ-Bi₂O₃, do not make it possible to create a membrane with the required perfection and durability. In this work, the ordering of oxygen vacancies with the transformation of fluorite into the rhombohedral phase (S.G. R-3) was studied by powder HT XRD in situ at 600 °C on dense Bi_0.78Er_0.2Hf_0.02O_1.51 ceramics. Fast regeneration of disordered fluorite occurs at T = 640–700 °C. The phase degradation of fluorite due to the segregation of dopants at the second stage leads into stable phases - sillenite, tetragonal or rhombohedral phase (S.G. R-3m), depending on the composition of δ-Bi₂O₃. Fast regeneration of fluorite occurs when heated to 820 °C, which is unacceptable for membranes. Analysis of all available data allows us to propose approaches to optimize the composition of δ-Bi₂O₃ and technical solutions for creating durable oxygen selective membranes with promising use in distributed multigeneration. As a result of the analysis, a new solid electrolyte with better parameters was obtained.     

Preparation and photocatalytic antibacterial mechanism of porous metastable β-Bi2O3 nanosheets

Effective and safe application of antibacterials has always been an important aspect for their usage. High-efficiency photocatalytic technology driven by visible light for antibacterial action constitutes a practical solution for antibacterial agents and will not harm the human body or the environment. While most studies on β-Bi₂O₃ materials with good photocatalytic properties under visible light are conducted in the field of optoelectronics, their potential and mechanism as photocatalytic antibacterial agents have not yet been fully explored. Herein, we report the performance of sheet-like metastable β-Bi₂O₃ material with rich oxygen vacancies and high electron-hole separation efficiency in antibacterial processes, as well as a preliminary exploration of its antibacterial mechanism. The results revealed that the antibacterial activity of the product against E. coli greatly improved in comparison with commercially available α-Bi₂O₃ owing to its excellent structure and optical properties. In addition, gradient experiments and scavenger experiments have confirmed that the main antibacterial effect of β-Bi₂O₃ originates from reactive oxygen species (ROS), and the superoxide radical, ·O₂⁻, of generated ROS is the key reactive species in the antibacterial process. Through the detection of lipid peroxidation and bacterial respiratory-chain dehydrogenase activity, several pathways were identified for the excellent antibacterial activity of the product.     

Effect of yttria doping on the microstructure and mechanical properties of Al2O3–FeAl2O4 nanocomposites developed via solid state precipitation

We have recently reported the production of Al₂O₃-matrix nanocomposites via solid state precipitation of nanosized FeAl₂O₄ particles within the matrix grains during aging of Al₂O₃–10 wt.% Fe₂O₃ solid solutions in a reducing atmosphere (N₂ + 4% H₂). In addition to these nanoparticles, however, coarse micron-sized FeAl₂O₄ particles were present along the matrix grain boundaries. In the present work, we show that the addition of ～250 ppm yttria to the solid solutions suppressed the development of these intergranular particles, reducing their size by a factor of ～2 with optimum aging. A fracture toughness improvement by 45% and flexural strength improvement by 50% with respect to monolithic Al₂O₃ were recorded with the yttria-containing nanocomposite developed by aging for 20 h at 1450 °C. Aging also improved the hardness with respect to the solid solution. The change in fracture mode in the presence of the nanosized intragranular particles was believed to be the major contributing factor towards the improvement in toughness and therefore the strength. The higher strengths obtainable in the presence of yttria were attributed to the reduction of intergranular precipitate size relative to yttria-free nanocomposites.     

Preparation and study of the mechanical and optical properties of infrared transparent Y2O3–MgO composite ceramics

In this study, fine Y₂O₃–MgO composite nanopowders were synthesized via the sol–gel method. Dense Y₂O₃–MgO composite ceramics were fabricated by pre-sintering the green body in air at different temperatures for 1 h and then subjecting the sintered bodies to hot isostatic pressing at 1300°C for 1 h. The effects of pre-sintering temperature on the microstructural, mechanical, and optical properties of the resulting ceramics were studied. The average grain size of the ceramics was increased, whereas their hardness and fracture toughness were decreased with increasing pre-sintering temperature. A maximum fracture toughness of 1.42 MPa·m^1/2 and Vickers hardness of 10.4 GPa were obtained. The average flexural strength of the ceramics was 411 MPa at room temperature and reached 361 MPa at 600°C. A transmittance of 84% in the 3–5 µm region was obtained when the composite ceramics were sintered at 1400°C. Moreover, a transmittance of 76% in the 3–5 µm region was obtained at 500°C.     

On modelling of surface tension of CMC-α-Fe2O3 nanoparticles by fuzzy-hybrid approach: A comparison study

Surface tension is one of the most important rheological parameters of nanoliquids. It influences the thermophysical and mass transfer properties of nanostructures. Accurate estimation of the surface tension from operating variables is critical for determining optimal production processes. However, the challenges of producing nanoparticles and measuring their properties introduce experimental errors in the data used for mathematical modelling. Crisp regression approaches provide adequate representation of the data, but they do not provide information about the experimental uncertainty. In this study, a fuzzy-hybrid approach is proposed for mathematical modelling of surface tension of carboxymethyl cellulose/chitosan-α-Fe₂O₃ nanoparticles. Then, the proposed model is compared with a crisp model from a previous study. Error analysis is conducted to validate the constructed fuzzy model. It is observed that the fuzzy-hybrid modelling approach has yielded significantly lower error values (a 60%–90% improvement in all error metrics on average), and thus, it is superior to the crisp approach. This study contributes to the subject of modelling rheological properties. It is shown that the fuzzy-hybrid approach has impressive potential to be utilized for modelling the rheological properties of nanostructures.     

Fabrication and characterization of La2O3–Fe2O3–Bi2O3 nanopowders: Effects of La2O3 addition on structure,optical, and radiation-absorption properties

In this study, we fabricated and characterized six new nanopowders representing variations of La₂O₃–Fe₂O₃–Bi₂O₃, i.e., 100Bi₂O₃, 30Fe₂O₃–70Bi₂O₃, 3La₂O₃–27Fe₂O₃–70Bi₂O₃, 7La₂O₃–23Fe₂O₃–70Bi₂O₃, 10La₂O₃–20Fe₂O₃–70Bi₂O₃, and 20La₂O₃–10Fe₂O₃–70Bi₂O₃ (represented by 100B, 30F70B, 3L27F70B, 10L20F70B, and 20L10F70B, respectively). These nanopowders were prepared by the microwave-assisted hydrothermal synthesis method. Saponin extract from soapnuts was used as the nanoparticle capping agent. The structural, optical, and gamma radiation characteristics were measured, calculated, and analysed, respectively. The chemical structures of the nanocomposites influenced their optical and radiation shielding characteristics. The optical bandgaps of the 100B, 30F70B, 3L27F70B, 7L23F70B, 10L20F70B, and 20L10F70B nanopowders were 3.16, 3.13, 3.43, 3.45, 3.46, and 3.58 eV, respectively. The ranges of the mass attenuation coefficients of the nanopowders were computed, using XCOM, to be 0.0412–5.1624, 0.0401–4.5406, 0.0401–4.5285, 0.0401–4.5129, 0.0401–0.5015, and 0.0400–4.4156 cm²/g, respectively, and the ranges of mass energy absorption coefficients were found to be 0.0232–1.7525, 0.0228–1.5484, 0.0228–1.5598, 0.0288–1.5746, 0.0228–1.5853, and 0.0227–1.6192 cm²/g, respectively, for photon energies in the range of 0.1–10 MeV. The order of the dose rate trend was as follows: 30F70B < L27F70B < 7L23F70B < 10L20F70B < 20L10F70B. Analysis of the photon interaction parameters showed that the synthesized nanopowders could function well as fillers in radiation-shielding matrices.     

Effects of Al2O3–Y2O3/Yb2O3 additives on microstructures and mechanical properties of silicon nitride ceramics prepared by hot-pressing sintering

Silicon nitride (Si₃N₄) ceramics doped with two different sintering additive systems (Al₂O₃–Y₂O₃ and Al₂O₃–Yb₂O₃) were prepared by hot-pressing sintering at 1800℃ for 2 h and 30 MPa. The microstructures, nano-indentation test, and mechanical properties of the as-prepared Si₃N₄ ceramics were systematically investigated. The X-ray diffraction analyses of the as-prepared Si₃N₄ ceramics doped with the two sintering additives showed a large number of phase transformations of α-Si₃N₄ to β-Si₃N₄. Grain size distributions and aspect ratios as well as their effects on mechanical properties are presented in this study. The specimen doped with the Al₂O₃–Yb₂O₃ sintering additive has a larger aspect ratio and higher fracture toughness, while the Vickers hardness is relatively lower. It can be seen from the nano-indentation tests that the stronger the elastic deformation ability of the specimens, the higher the fracture toughness. At the same time, the mechanical properties are greatly enhanced by specific interlocking microstructures formed by the high aspect ratio β-Si₃N₄ grains. In addition, the density, relative density, and flexural strength of the as-prepared Si₃N₄ ceramics doped with Al₂O₃–Y₂O₃ were 3.25 g/cm³, 99.9%, and 1053 ± 53 MPa, respectively. When Al₂O₃–Yb₂O₃ additives were introduced, the above properties reached 3.33 g/cm³, 99.9%, and 1150 ± 106 MPa, respectively. It reveals that microstructure control and mechanical property optimization for Si₃N₄ ceramics are feasible by tailoring sintering additives.     

Sintering behavior and microwave dielectric properties of 0.67CaTiO3–0.33LaAlO3 ceramics modified by B2O3–Li2O–Al2O3 and CeO2

A low temperature sintering method was used to avoid the relatively high sintering temperatures typically required to prepare 0.67CaTiO₃–0.33LaAlO₃ (CTLA) ceramics. Additionally, CeO₂ was introduced into the CTLA ceramics as an oxygen-storage material to improve their microwave dielectric properties. 0.67CaTiO₃–0.33LaAlO₃ ceramics co-doped with B₂O₃–Li₂O–Al₂O₃ and CeO₂ were prepared by a conventional two-step solid-state reaction process. The sintering behavior, crystal structure, surface morphology, and microwave dielectric proprieties of the prepared ceramic samples were studied, and the reaction mechanism of CeO₂ was elucidated. CTLA+0.05 wt% BLA+3 wt% CeO₂ ceramics sintered at 1360 °C for 4 h exhibited the optimal microwave dielectric properties: dielectric constant (ε_r)=45.02, quality factor (Q×f)=43102 GHz, and temperature coefficient of resonant frequency (τ_f)=2.1 ppm/°C. The successful preparation of high-performance microwave dielectric ceramics provides a direction for the future development and commercialization of CTLA ceramics.