Showing papers in "Journal of Advanced Ceramics in 2021"
Nanjing University of Posts and Telecommunications1, Xi'an Jiaotong University2, Guilin University of Electronic Technology3, Donghua University4, Beijing Institute of Technology5, North China University of Science and Technology6, Shenzhen University7, Zhengzhou University8, Chinese Academy of Sciences9
TL;DR: High-entropy ceramics (HECs) as mentioned in this paper are solid solutions of inorganic compounds with one or more Wyckoff sites shared by equal or near-equal atomic ratios of multi-principal elements.
Abstract: High-entropy ceramics (HECs) are solid solutions of inorganic compounds with one or more Wyckoff sites shared by equal or near-equal atomic ratios of multi-principal elements. Although in the infant stage, the emerging of this new family of materials has brought new opportunities for material design and property tailoring. Distinct from metals, the diversity in crystal structure and electronic structure of ceramics provides huge space for properties tuning through band structure engineering and phonon engineering. Aside from strengthening, hardening, and low thermal conductivity that have already been found in high-entropy alloys, new properties like colossal dielectric constant, super ionic conductivity, severe anisotropic thermal expansion coefficient, strong electromagnetic wave absorption, etc., have been discovered in HECs. As a response to the rapid development in this nascent field, this article gives a comprehensive review on the structure features, theoretical methods for stability and property prediction, processing routes, novel properties, and prospective applications of HECs. The challenges on processing, characterization, and property predictions are also emphasized. Finally, future directions for new material exploration, novel processing, fundamental understanding, in-depth characterization, and database assessments are given.
346 citations
TL;DR: Ce2[Zr0.94(Mg1/3Sb2/3)0.06]3(MoO4)9 ceramics with excellent dielectric properties were sintered at 725 °C for 6 h as discussed by the authors.
Abstract: Ce2[Zr1−x(Mg1/3Sb2/3)x]3(MoO4)9 (0.02 ⩽ x ⩽ 0.10) ceramics were prepared by the traditional solid-state method. A single phase, belonging to the space group of $$R⩈erline 3 c$$
, was detected by using X-ray diffraction at the sintering temperatures ranging from 700 to 850 °C. The microstructures of samples were examined by applying scanning electron microscopy (SEM). The crystal structure refinement of these samples was investigated in detail by performing the Rietveld refinement method. The intrinsic properties were calculated and explored via far-infrared reflectivity spectroscopy. The correlations between the chemical bond parameters and microwave dielectric properties were calculated and analyzed by Phillips-van Vechten-Levine (P-V-L) theory. Ce2[Zr0.94(Mg1/3Sb2/3)0.06]3(MoO4)9 ceramics with excellent dielectric properties were sintered at 725 °C for 6 h (er = 10.37, Q×f = 71,748 GHz, and τf = −13.6 ppm/°C, er is the dielectric constant, Q×f is the quality factor, and τf is the temperature coefficient of resonant frequency).
122 citations
TL;DR: In this article, the authors investigated the energy storage performances of linear dielectric, relaxor ferroelectric, and antiferroelectric from the viewpoint of chemical modification, macro/microstructural design, and electrical property optimization.
Abstract: Dielectric ceramic capacitors, with the advantages of high power density, fast charge-discharge capability, excellent fatigue endurance, and good high temperature stability, have been acknowledged to be promising candidates for solid-state pulse power systems. This review investigates the energy storage performances of linear dielectric, relaxor ferroelectric, and antiferroelectric from the viewpoint of chemical modification, macro/microstructural design, and electrical property optimization. Research progress of ceramic bulks and films for Pb-based and/or Pb-free systems is summarized. Finally, we propose the perspectives on the development of energy storage ceramics for pulse power capacitors in the future.
109 citations
TL;DR: In this paper, the authors show the significance of material composition and printing processes in addressing these challenges and suggest the use of appropriate solid loading, solvent, and preceramic polymers in forming slurries.
Abstract: Conversion of inorganic-organic frameworks (ceramic precursors and ceramic-polymer mixtures) into solid mass ceramic structures based on photopolymerization process is currently receiving plentiful attention in the field of additive manufacturing (3D printing). Various techniques (e.g., stereolithography, digital light processing, and two-photon polymerization) that are compatible with this strategy have so far been widely investigated. This is due to their cost-viability, flexibility, and ability to design and manufacture complex geometric structures. Different platforms related to these techniques have been developed too, in order to meet up with modern technology demand. Most relevant to this review are the challenges faced by the researchers in using these 3D printing techniques for the fabrication of ceramic structures. These challenges often range from shape shrinkage, mass loss, poor densification, cracking, weak mechanical performance to undesirable surface roughness of the final ceramic structures. This is due to the brittle nature of ceramic materials. Based on the summary and discussion on the current progress of material-technique correlation available, here we show the significance of material composition and printing processes in addressing these challenges. The use of appropriate solid loading, solvent, and preceramic polymers in forming slurries is suggested as steps in the right direction. Techniques are indicated as another factor playing vital roles and their selection and development are suggested as plausible ways to remove these barriers.
104 citations
TL;DR: In this article, the authors systematically review the additive manufacturing technologies of SiC ceramic developed in recent years, including indirect additive manufacturing (Indirect AM) and direct AM (Direct AM) technologies.
Abstract: Silicon carbide (SiC) ceramic and related materials are widely used in various military and engineering fields. The emergence of additive manufacturing (AM) technologies provides a new approach for the fabrication of SiC ceramic products. This article systematically reviews the additive manufacturing technologies of SiC ceramic developed in recent years, including Indirect Additive Manufacturing (Indirect AM) and Direct Additive Manufacturing (Direct AM) technologies. This review also summarizes the key scientific and technological challenges for the additive manufacturing of SiC ceramic, and also forecasts its possible future opportunities. This paper aims to provide a helpful guidance for the additive manufacturing of SiC ceramic and other structural ceramics.
88 citations
TL;DR: In this article, the authors introduce the principles of the four 3D printing technologies and focus on the parameters of each technology that affect the densification of 3D printed ceramics, such as the performance of raw materials and the interaction between energy and materials.
Abstract: Three-dimensional (3D) printing technology is becoming a promising method for fabricating highly complex ceramics owing to the arbitrary design and the infinite combination of materials Insufficient density is one of the main problems with 3D printed ceramics, but concentrated descriptions of making dense ceramics are scarce This review specifically introduces the principles of the four 3D printing technologies and focuses on the parameters of each technology that affect the densification of 3D printed ceramics, such as the performance of raw materials and the interaction between energy and materials The technical challenges and suggestions about how to achieve higher ceramic density are presented subsequently The goal of the presented work is to comprehend the roles of critical parameters in the subsequent 3D printing process to prepare dense ceramics that can meet the practical applications
86 citations
TL;DR: In this paper, the influence of magnesium doping on the sintering behavior, crystal structure, and microwave dielectric properties of a melilite Ba2CuGe2O7 ceramic was investigated.
Abstract: A melilite Ba2CuGe2O7 ceramic was characterized by low sintering temperature and moderate microwave dielectric properties. Sintered at 960 °C, the Ba2CuGe2O7 ceramic had a high relative density 97%, a low relative permittivity (er) 9.43, a quality factor (Q×f) of 20,000 GHz, and a temperature coefficient of resonance frequency (τf) −76 ppm/°C. To get a deep understanding of the relationship between composition, structure, and dielectric performances, magnesium substitution for copper in Ba2CuGe2O7 was conducted. Influences of magnesium doping on the sintering behavior, crystal structure, and microwave dielectric properties were studied. Mg doping in Ba2CuGe2O7 caused negligible changes in the macroscopic crystal structure, grain morphology, and size distribution, while induced visible variation in the local structure as revealed by Raman analysis. Microwave dielectric properties exhibit a remarkable dependence on composition. On increasing the magnesium content, the relative permittivity featured a continuous decrease, while both the quality factor and the temperature coefficient of resonance frequency increased monotonously. Such variations in dielectric performances were clarified in terms of the polarizability, packing fraction, and band valence theory.
82 citations
TL;DR: In this article, a review of microwave dielectric ceramics (MWDCs) sintered higher than 1000 from 2010 up to now, °C is presented.
Abstract: The explosive process of 5G communication evokes the urgent demand of miniaturized and integrated dielectric ceramics filter. It is a pressing need to advance the development of dielectric ceramics utilization of emerging technology to design new materials and understand the polarization mechanism. This review provides the summary of the study of microwave dielectric ceramics (MWDCs) sintered higher than 1000 from 2010 up to now, °C with the purpose of taking a broad and historical view of these ceramics and illustrating research directions. To date, researchers endeavor to explain the structure-property relationship of ceramics with multitude of approaches and design a new formula or strategy to obtain excellent microwave dielectric properties. There are variety of factors that impact the permittivity, dielectric loss, and temperature stability of dielectric materials, covering intrinsic and extrinsic factors. Many of these factors are often intertwined, which can complicate new dielectric material discovery and the mechanism investigation. Because of the various ceramics systems, pseudo phase diagram was used to classify the dielectric materials based on the composition. In this review, the ceramics were firstly divided into ternary systems, and then brief description of the experimental probes and complementary theoretical methods that have been used to discern the intrinsic polarization mechanisms and the origin of intrinsic loss was mentioned. Finally, some perspectives on the future outlook for high-temperature MWDCs were offered based on the synthesis method, characterization techniques, and significant theory developments.
81 citations
TL;DR: In this paper, the effects of high entropy borates intermedia phases on the EM wave absorption properties were investigated, and five high entropy rare earth hexaborides (REB6) powders with coupling of dielectric and magnetic losses were designed and successfully synthesized through a facial one-step boron carbide reduction method.
Abstract: Considering the emergence of severe electromagnetic interference problems, it is vital to develop electromagnetic (EM) wave absorbing materials with high dielectric, magnetic loss and optimized impedance matching. However, realizing the synergistic dielectric and magnetic losses in a single phase material is still a challenge. Herein, high entropy (HE) rare earth hexaborides (REB6) powders with coupling of dielectric and magnetic losses were designed and successfully synthesized through a facial one-step boron carbide reduction method, and the effects of high entropy borates intermedia phases on the EM wave absorption properties were investigated. Five HE REB6 ceramics including (Ce0.2Y0.2Sm0.2Er0.2Yb0.2)B6, (Ce0.2Eu0.2Sm0.2Er0.2Yb0.2)B6, (Ce0.2Y0.2Eu0.2Er0.2Yb0.2)B6, (Ce0.2Y0.2Sm0.2 Eu0.2Yb0.2)B6, and (Nd0.2Y0.2Sm0.2Eu0.2 Yb0.2)B6 possess CsCl-type cubic crystal structure, and their theoretical densities range from 4.84 to 5.25 g/cm3. (Ce0.2Y0.2Sm0.2Er0.2 Yb0.2)B6 powders with the average particle size of 1.86 µm were found to possess the best EM wave absorption properties among these hexaborides. The RLmin value of (Ce0.2Y0.2Sm0.2Er0.2Yb0.2)B6 reaches −33.4 dB at 11.5 GHz at thickness of 2 mm; meanwhile, the optimized effective absorption bandwidth (EAB) is 3.9 GHz from 13.6 to 17.5 GHz with a thickness of 1.5 mm. The introduction of HE REBO3 (RE = Ce, Y, Sm, Eu, Er, Yb) as intermediate phase will give rise to the mismatching impedance, which will further lead to the reduction of reflection loss. Intriguingly, the HEREB6/HEREBO3 still possess wide effective absorption bandwidth of 4.1 GHz with the relative low thickness of 1.7 mm. Considering the better stability, low density, and good EM wave absorption properties, HE REB6 ceramics are promising as a new type of EM wave absorbing materials.
79 citations
TL;DR: In this article, the authors reviewed the milestones and the latest progress in the research of MAX phases and MXenes, from the perspective of ceramic science, focusing on the conversion from MAX phases to MXenes.
Abstract: MAX phases (Ti3SiC2, Ti3AlC2, V2AlC, Ti4AlN3, etc.) are layered ternary carbides/nitrides, which are generally processed and researched as structure ceramics. Selectively removing A layer from MAX phases, MXenes (Ti3C2, V2C, Mo2C, etc.) with two-dimensional (2D) structure can be prepared. The MXenes are electrically conductive and hydrophilic, which are promising as functional materials in many areas. This article reviews the milestones and the latest progress in the research of MAX phases and MXenes, from the perspective of ceramic science. Especially, this article focuses on the conversion from MAX phases to MXenes. First, we summarize the microstructure, preparation, properties, and applications of MAX phases. Among the various properties, the crack healing properties of MAX phase are highlighted. Thereafter, the critical issues on MXene research, including the preparation process, microstructure, MXene composites, and application of MXenes, are reviewed. Among the various applications, this review focuses on two selected applications: energy storage and electromagnetic interference shielding. Moreover, new research directions and future trends on MAX phases and MXenes are also discussed.
77 citations
TL;DR: In this article, the authors reported significantly suppressed thermal conductivity in SrTiO3-based thermoelectric ceramics via high-entropy strategy for the first time, and optimized electrical conductivity by defect engineering.
Abstract: Oxide-based ceramics could be promising thermoelectric materials because of their thermal and chemical stability at high temperature However, their mediocre electrical conductivity or high thermal conductivity is still a challenge for the use in commercial devices Here, we report significantly suppressed thermal conductivity in SrTiO3-based thermoelectric ceramics via high-entropy strategy for the first time, and optimized electrical conductivity by defect engineering In high-entropy (Ca02Sr02Ba02Pb02La02)TiO3 bulks, the minimum thermal conductivity can be 117 W/(m·K) at 923 K, which should be ascribed to the large lattice distortion and the huge mass fluctuation effect The power factor can reach about 295 μW/(m·K2) by inducing oxygen vacancies Finally, the ZT value of 02 can be realized at 873 K in this bulk sample This approach proposed a new concept of high entropy into thermoelectric oxides, which could be generalized for designing high-performance thermoelectric oxides with low thermal conductivity
TL;DR: In this paper, a one-pot hydrothermal method was used to construct a hierarchical structure of MoS2 nanosheets anchored on the surface and interlayer of Ti3C2Tx.
Abstract: In order to prevent the microwave leakage and mutual interference, more and more microwave absorbing devices are added into the design of electronic products to ensure its routine operation. In this work, we have successfully prepared MoS2/TiO2/Ti3C2Tx hierarchical composites by one-pot hydrothermal method and focused on the relationship between structures and electromagnetic absorbing properties. Supported by comprehensive characterizations, MoS2 nanosheets were proved to be anchored on the surface and interlayer of Ti3C2Tx through a hydrothermal process. Additionally, TiO2 nanoparticles were obtained in situ. Due to these hierarchical structures, the MoS2/TiO2/Ti3C2Tx composites showed greatly enhanced microwave absorbing performance. The MoS2/TiO2/Ti3C2Tx composites exhibit a maximum reflection loss value of −33.5 dB at 10.24 GHz and the effective absorption bandwidth covers 3.1 GHz (13.9–17 GHz) at the thickness of 1.0 mm, implying the features of wide frequency and light weight. This work in the hierarchical structure of MoS2/TiO2/Ti3C2Tx composites opens a promising door to the exploration of constructing extraordinary electromagnetic wave absorbents.
TL;DR: In this paper, a pyroelectric BiFeO3/g-C3N4 heterostructure was proposed for Rhodamine B (RhB) dye, which is fabricated via a simple mixing-calcining method.
Abstract: The BiFeO3/g-C3N4 heterostructure, which is fabricated via a simple mixing-calcining method, benefits the significant enhancement of the pyrocatalytic performance. With the growth of g-C3N4 content in the heterostructure pyrocatalysts from 0 to 25%, the decomposition ratio of Rhodamine B (RhB) dye after 18 cold-hot temperature fluctuation (25–65 °C) cycles increases at first and then decreases, reaching a maximum value of ∼94.2% at 10% while that of the pure BiFeO3 is ∼67.7%. The enhanced dye decomposition may be due to the generation of the internal electric field which strengthens the separation of the positive and negative carriers and further accelerates their migrations. The intermediate products in the pyrocatalytic reaction also have been detected and confirmed, which proves the key role of the pyroelectric effect in realizing the dye decomposition using BiFeO3/g-C3N4 heterostructure catalyst. The pyroelectric BiFeO3/g-C3N4 heterostructure shows the potential application in pyrocatalytically degrading dye wastewater.
TL;DR: In this paper, four cubic bixbyite structured high-entropy oxides RE2O3 were designed and synthesized, among which (Eu0.2Eu 0.2Yb0.3, (Sm0.1 and 4.6 W·m−1·K−1) are only 23.8% and 21.5% respectively of that of Y 2O3 (21.4 W·n−m− 1·k−1), while their thermal expansion coefficients are close to those of Y2O 3 and Al 2
Abstract: Y2O3 is regarded as one of the potential environmental barrier coating (EBC) materials for Al2O3f/Al2O3 ceramic matrix composites owing to its high melting point and close thermal expansion coefficient to Al2O3. However, the relatively high thermal conductivity and unsatisfactory calcium-magnesium-aluminosilicate (CMAS) resistance are the main obstacles for the practical application of Y2O3. In order to reduce the thermal conductivity and increase the CMAS resistance, four cubic bixbyite structured high-entropy oxides RE2O3, including (Eu0.2Er0.2Lu0.2Y0.2Yb0.2)2O3, (Sm0.2Er0.2Lu0.2Y0.2Yb0.2)2O3, (Sm0.2Eu0.2Er0.2Y0.2Yb0.2)2O3, and (Sm0.2Eu0.2Lu0.2Y0.2Yb0.2)2O3 were designed and synthesized, among which (Eu0.2Er0.2Lu0.2Y0.2Yb0.2)2O3 and (Sm0.2Er0.2Lu0.2Y0.2Yb0.2)2O3 bulks were prepared by spark plasma sintering (SPS) to investigate their mechanical and thermal properties as well as CMAS resistance. The mechanical properties of (Eu0.2Er0.2Lu0.2Y0.2Yb0.2)2O3 and (Sm0.2Er0.2Lu0.2Y0.2Yb0.2)2O3 are close to those of Y2O3 but become more brittle than Y2O3. The thermal conductivities of (Eu0.2Er0.2Lu0.2Y0.2Yb0.2)2O3 and (Sm0.2Er0.2Lu0.2Y0.2Yb0.2)2O3 (5.1 and 4.6 W·m−1·K−1) are only 23.8% and 21.5% respectively of that of Y2O3 (21.4 W·m−1·K−1), while their thermal expansion coefficients are close to those of Y2O3 and Al2O3. Most importantly, HE RE2O3 ceramics exhibit good CMAS resistance. After being attacked by CMAS at 1350 °C for 4 h, the HE RE2O3 ceramics maintain their original morphologies without forming pores or cracks, making them promising as EBC materials for Al2O3f/Al2O3 composites.
TL;DR: In this paper, the authors present perspectives and challenges for lead-free energy-storage multilayer ceramic capacitors (MLCCs) and discuss emerging applications of energy storage MLCCs in terms of advanced pulsed power sources and high-density power converters.
Abstract: The growing demand for high-power-density electric and electronic systems has encouraged the development of energy-storage capacitors with attributes such as high energy density, high capacitance density, high voltage and frequency, low weight, high-temperature operability, and environmental friendliness. Compared with their electrolytic and film counterparts, energy-storage multilayer ceramic capacitors (MLCCs) stand out for their extremely low equivalent series resistance
and equivalent series inductance, high current handling capability, and high-temperature stability. These characteristics are important for applications including fast-switching third-generation wide-bandgap semiconductors in electric vehicles, 5G base stations, clean energy generation, and smart grids. There have been numerous reports on state-of-the-art MLCC energy-storage solutions. However, lead-free capacitors generally have a low-energy density, and high-energy density
capacitors frequently contain lead, which is a key issue that hinders their broad application. In this review, we present perspectives and challenges for lead-free energy-storage MLCCs. Initially, the energy-storage mechanism and device characterization are introduced; then, dielectric ceramics for energy-storage applications with aspects of composition and structural optimization are summarized. Progress on state-of-the-art energy-storage MLCCs is discussed after elaboration of the fabrication process and structural design of the electrode. Emerging applications of energy-storage MLCCs are then discussed in terms of advanced pulsed power sources and high-density power converters from a theoretical and technological point of view. Finally, the challenges and future prospects for industrialization of lab-scale lead-free energy-storage MLCCs are discussed.
TL;DR: In this paper, the binary ZnO/NiCo2O4 nanoparticles were successfully synthesized via hydrothermal reaction and the electromagnetic wave absorption properties of the composites were investigated in detail.
Abstract: Nowadays, metal oxide-based electromagnetic wave absorbing materials have aroused widely attentions in the application of telecommunication and electronics due to their selectable mechanical and outstanding dielectric properties. Herein, the binary ZnO/NiCo2O4 nanoparticles were successfully synthesized via hydrothermal reaction and the electromagnetic wave absorption properties of the composites were investigated in detail. As a result, benefiting from the dielectric loss, the as-obtained ZnO/NiCo2O4-7 samples possessed a minimum reflection loss value of −33.49 dB at 18.0 GHz with the thickness of 4.99 mm. This work indicates that ZnO/NiCo2O4 composites have the promising candidate applications in electromagnetic wave absorption materials in the future.
TL;DR: In this article, a SiCnw-reinforced SiCNO (SiCnw/SiCNO) composite aerogels were fabricated through the in-situ growth of siCnw in polymer-derived SiC NO ceramic aerogel by using catalyst-assisted microwave heating at ultra-low temperature and in short time.
Abstract: Electromagnetic absorption (EMA) materials with light weight and harsh environmental robustness are highly desired and crucially important in the stealth of high-speed vehicles. However, meeting these two requirements is always a great challenge, which excluded the most attractive lightweight candidates, such as carbon-based materials. In this study, SiCnw-reinforced SiCNO (SiCnw/SiCNO) composite aerogels were fabricated through the in-situ growth of SiCnw in polymer-derived SiCNO ceramic aerogels by using catalyst-assisted microwave heating at ultra-low temperature and in short time. The phase composition, microstructure, and EMA property of the SiCnw/SiCNO composite aerogels were systematically investigated. The results indicated that the morphology and phase composition of SiCnw/SiCNO composite aerogels can be regulated easily by varying the microwave treatment temperature. The composite aerogels show excellent EMA property with minimum reflection loss of −23.9 dB@13.8 GHz, −26.5 dB@10.9 GHz, and −20.4 dB@14.5 GHz and the corresponding effective bandwidth of 5.2 GHz, 3.2 GHz, and 4.8 GHz at 2.0 mm thickness for microwave treatment at 600 °C, 800 °C, and 1000 °C, respectively, which is much better than that of SiCN ceramic aerogels. The superior EMA performance is mainly attributed to the improved impedance matching, multi-reflection, multi-interfacial polarization, and micro current caused by migration of hopping electrons.
TL;DR: In this paper, high performance hydroxyapatite (HA) ceramics with excellent densification and mechanical properties were successfully fabricated by digital light processing (DLP) three-dimensional (3D) printing technology.
Abstract: High performance hydroxyapatite (HA) ceramics with excellent densification and mechanical properties were successfully fabricated by digital light processing (DLP) three-dimensional (3D) printing technology. It was found that the sintering atmosphere of wet CO2 can dramatically improve the densification process and thus lead to better mechanical properties. HA ceramics with a relative density of 97.12% and a three-point bending strength of 92.4 MPa can be achieved at a sintering temperature of 1300 , which makes a solid foundation for application ℃ in bone engineering. Furthermore, a relatively high compressive strength of 4.09 MPa can be also achieved for a DLP-printed p-cell triply periodic minimum surface (TPMS) structure with a porosity of 74%, which meets the requirement of cancellous bone substitutes. A further cell proliferation test demonstrated that the sintering atmosphere of wet CO2 led to improve cell vitality after 7 days of cell culture Moreover, with the possible benefit from the bio-inspired structure, the 3D-printed TPMS structure significantly improved the cell vitality, which is crucial for early osteogenesis and osteointegration.
TL;DR: In this article, gold nanoparticles (AuNPs) decorated Ti3C2Tx nanosheets were fabricated through a self-reduction reaction of Ti3c2Tx with HAuCl4 aqueous solution.
Abstract: In this work, gold nanoparticles (AuNPs) decorated Ti3C2Tx nanosheets (MXene/AuNPs composite) are fabricated through a self-reduction reaction of Ti3C2Tx nanosheets with HAuCl4 aqueous solution. The obtained composite is characterized as AuNPs with the diameter of about 23 nm uniformly dispersing on Ti3C2Tx nanosheets without aggregation. The composite (MXene decorated on 4.8 wt% AuNPs) is further employed to construct supercapacitor for the first time with a higher specific capacitance of 278 F·g−1 at 5 mV·s−1 than that of pure Ti3C2Tx and 95% of cyclic stability after 10,000 cycles. Furthermore, MXene/AuNPs composite symmetric supercapacitor with filter paper as separator and H2SO4 as electrolyte, is assembled. The supercapacitor exhibits a high volumetric energy density of 8.82 Wh·L−1 at a power density of 264.6 W·L−1 and ultrafast-charging/discharging performance. It exhibits as a promising candidate applied in integrated and flexible supercapacitors.
TL;DR: In this article, the authors investigated the evolution process of TBC prepared by suspension plasma spraying (SPS) under CMAS attack and proposed a corrosion model to describe the generation and evolution of the reaction layer and bending of thermal barrier coating (TBC).
Abstract: Calcium-magnesium-alumino-silicate (CMAS) corrosion is a critical factor which causes the failure of thermal barrier coating (TBC). CMAS attack significantly alters the temperature and stress fields in TBC, resulting in their delamination or spallation. In this work, the evolution process of TBC prepared by suspension plasma spraying (SPS) under CMAS attack is investigated. The CMAS corrosion leads to the formation of the reaction layer and subsequent bending of TBC. Based on the observations, a corrosion model is proposed to describe the generation and evolution of the reaction layer and bending of TBC. Then, numerical simulations are performed to investigate the corrosion process of free-standing TBC and the complete TBC system under CMAS attack. The corrosion model constructs a bridge for connecting two numerical models. The results show that the CMAS corrosion has a significant influence on the stress field, such as the peak stress, whereas it has little influence on the steady-state temperature field. The peak of stress increases with holding time, which increases the risk of the rupture of TBC. The Mises stress increases nonlinearly along the thick direction of the reaction layer. Furthermore, in the traditional failure zone, such as the interface of the top coat and bond coat, the stress obviously changes during CMAS corrosion.
TL;DR: In this paper, a two-layer Ruddlesden-Popper (RP) oxide La0.25Sr2.75FeNiO7−δ (LSFN) was successfully synthesized and studied as the potential active single-phase and composite cathode for protonic ceramics fuel cells (PCFCs).
Abstract: New two-layer Ruddlesden—Popper (RP) oxide La0.25Sr2.75FeNiO7−δ (LSFN) in the combination of Sr3Fe2O7−δ and La3Ni2O7−δ was successfully synthesized and studied as the potential active single-phase and composite cathode for protonic ceramics fuel cells (PCFCs). LSFN with the tetragonal symmetrical structure (I4/mmm) is confirmed, and the co-existence of Fe3+/Fe4+ and Ni3+/Ni2+ couples is demonstrated by X-ray photoelectron spectrometer (XPS) analysis. The LSFN conductivity is apparently enhanced after Ni doping in Fe-site, and nearly three times those of Sr3Fe2O7−δ, which is directly related to the carrier concentration and conductor mechanism. Importantly, anode supported PCFCs using LSFN-BaZr0.1Ce0.7Y0.2O3−δ (LSFN-BZCY) composite cathode achieved high power density (426 mW·cm−2 at 650 °C) and low electrode interface polarization resistance (0.26 Ω·cm2). Besides, distribution of relaxation time (DRT) function technology was further used to analyse the electrode polarization processes. The observed three peaks (P1, P2, and P3) separated by DRT shifted to the high frequency region with the decreasing temperature, suggesting that the charge transfer at the electrode-electrolyte interfaces becomes more difficult at reduced temperatures. Preliminary results demonstrate that new two-layer RP phase LSFN can be a promising cathode candidate for PCFCs.
TL;DR: In this paper, a simple solvothermal process was developed to synthesize Bi2WO6 microspheres constructed by aggregated nanoflakes, which possess the photocatalytic memory effect through the trapping and release of photogenerated electrons by the reversible chemical state change of W component in the (WO4)2− layers.
Abstract: Photocatalysts with the photocatalytic “memory” effect could resolve the intrinsic activity loss of traditional photocatalysts when the light illumination is turned off Due to the dual requirements of light absorption and energy storage/release functions, most previously reported photocatalysts with the photocatalytic “memory” effect were composite photocatalysts of two phase components, which may lose their performance due to gradually deteriorated interface conditions during their applications In this work, a simple solvothermal process was developed to synthesize Bi2WO6 microspheres constructed by aggregated nanoflakes The pure phase Bi2WO6 was found to possess the photocatalytic “memory” effect through the trapping and release of photogenerated electrons by the reversible chemical state change of W component in the (WO4)2− layers When the illumination was switched off, Bi2WO6 microspheres continuously produced H2O2 in the dark as those trapped photogenerated electrons were gradually released to react with O2 through the two-electron O2 reduction process, resulting in the continuous disinfection of Escherichia coli bacteria in the dark through the photocatalytic “memory” effect No deterioration of their cycling H2O2 production performance in the dark was observed, which verified their stable photocatalytic “memory” effect
TL;DR: In this paper, the authors present the fundamentals of garnet-type solid electrolytes, preparation methods, air stability, some strategies for improving the conductivity based on experimental and computational results, interfacial issues, and finally applications and challenges for future developments of LLZO solid electrolyte for all-solid-state lithium batteries.
Abstract: All-solid-state lithium batteries (ASSLBs), which use solid electrolytes instead of liquid ones, have become a hot research topic due to their high energy and power density, ability to solve battery safety issues, and capabilities to fulfill the increasing demand for energy storage in electric vehicles and smart grid applications. Garnet-type solid electrolytes have attracted considerable interest as they meet all the properties of an ideal solid electrolyte for ASSLBs. The garnet-type Li7La3Zr2O12 (LLZO) has excellent environmental stability; experiments and computational analyses showed that this solid electrolyte has a high lithium (Li) ionic conductivity (10−4–10−3 S·cm−1), an electrochemical window as wide as 6 V, stability against Li metal anode, and compatibility with most of the cathode materials. In this review, we present the fundamentals of garnet-type solid electrolytes, preparation methods, air stability, some strategies for improving the conductivity based on experimental and computational results, interfacial issues, and finally applications and challenges for future developments of LLZO solid electrolytes for ASSLBs.
TL;DR: In this article, a three-layered phosphor structure was designed and prepared by the spin coating of BaSi2N2O2:Eu (cyan-emitting) and (Sr,Ca)AlSiN3:EU (red-emiting) phosphor films on the Y3Al5O12:Ce (YAG: Ce) ceramic synthesized by the solid-state reaction under vacuum sintering.
Abstract: A three-layered phosphor structure was designed and prepared by the spin coating of BaSi2N2O2:Eu (cyan-emitting) and (Sr,Ca)AlSiN3:Eu (red-emitting) phosphor films on the yellow-emitting Y3Al5O12:Ce (YAG:Ce) phosphor ceramic synthesized by the solid-state reaction under vacuum sintering. In order to achieve high color rendering lighting, the influence of the composition and structure of the three-layered phosphors on the optical, thermal, and electrical properties of the chip-on-board (COB) packaged white-light-emitting diodes (WLEDs) was studied systematically. The WLED with the structure of “red+cyan+yellow” (R+C+Y) three-layered phosphor generated neutral white light and had a luminous efficacy of 75 lm/W, the fidelity index (Rf) of 93, the gamut index (Rg) of 97, and the correlated color temperature (CCT) of 3852 K. Under the excitation of laser diode (LD), the layer-structured phosphor yielded the white light with a luminous efficacy of 120 lm/W, color rendering index (CRI) of 90, and CCT of 5988 K. The result indicates that the three-layered phosphor structure is a promising candidate to achieve high color rendering and high luminous efficacy lighting.
TL;DR: In this paper, some thermal barrier coating materials including YSZ (yttria partially stabilized zirconia), GdPO4, and LaPO4 were prepared into bulks and the effects of their surface roughness on wettability and spreading characteristics of molten CMAS were investigated.
Abstract: Calcium-magnesium-alumina-silicate (CMAS) corrosion is an important cause for thermal barrier coating (TBC) failure, which has attracted increased attentions. In this study, some thermal barrier coating (TBC) materials including YSZ (yttria partially stabilized zirconia), GdPO4, and LaPO4 were prepared into bulks, and the effects of their surface roughness on wettability and spreading characteristics of molten CMAS were investigated. As-fabricated and polished bulks with different surface roughness were exposed to CMAS corrosion at 1250 °C for 1 and 4 h, following by macro and micro observations. Results revealed that compared with the as-fabricated bulks, molten CMAS on the polished samples had lower wettability and a smaller spreading area, mainly attributable to the reduced capillary force to drive the melt spreading. Meanwhile, GdPO4 and LaPO4 bulks exhibited lower CMAS wettability than YSZ bulk. It is thus considered that reducing the surface roughness is beneficial to CMAS corrosion resistance of TBCs.
TL;DR: In this article, the authors showed that self-charge compensation occurs between these two dopant ions when co-doped into Ti4+ sites, which can improve the electrical properties of the grain boundary (GB).
Abstract: The giant dielectric behavior of CaCu3Ti4O12 (CCTO) has been widely investigated owing to its potential applications in electronics; however, the loss tangent (tanδ) of this material is too large for many applications. A partial substitution of CCTO ceramics with either Al3+ or Ta5+ ions generally results in poorer nonlinear properties and an associated increase in tanδ (to ∼0.29–1.15). However, first-principles calculations showed that self-charge compensation occurs between these two dopant ions when co-doped into Ti4+ sites, which can improve the electrical properties of the grain boundary (GB). Surprisingly, in this study, a greatly enhanced breakdown electric field (∼200–6588 V/cm) and nonlinear coefficient (∼4.8–15.2) with a significantly reduced tanδ (∼0.010–0.036) were obtained by simultaneous partial substitution of CCTO with acceptor-donor (Al3+, Ta5+) dopants to produce (Al3+, Ta5+)-CCTO ceramics. The reduced tanδ and improved nonlinear properties were attributed to the synergistic effects of the co-dopants in the doped CCTO structure. The significant reduction in the mean grain size of the (Al3+, Ta5+)-CCTO ceramics compared to pure CCTO was mainly because of the Ta5+ ions. Accordingly, the increased GB density due to the reduced grain size and the larger Schottky barrier height (Φb) at the GBs of the co-doped CCTO ceramics were the main reasons for the greatly increased GB resistance, improved nonlinear properties, and reduced tanδ values compared to pure and single-doped CCTO. In addition, high dielectric constant values (e′ ≈ (0.52–2.7) × 104) were obtained. A fine-grained microstructure with highly insulating GBs was obtained by Ta5+ doping, while co-doping with Ta5+ and Al3+ resulted in a high Φb. The obtained results are expected to provide useful guidelines for developing new giant dielectric ceramics with excellent dielectric properties.
TL;DR: In this article, a new class of high-entropy M3B4 borides of the orthorhombic structure has been synthesized in the bulk form for the first time.
Abstract: A new class of high-entropy M3B4 borides of the Ta3B4-prototyped orthorhombic structure has been synthesized in the bulk form for the first time. Specimens with compositions of (V0.2Cr0.2Nb0.2Mo0.2Ta0.2)3B4 and (V0.2Cr0.2Nb0.2Ta0.2W0.2)3B4 were fabricated via reactive spark plasma sintering of high-energy-ball-milled elemental boron and metal precursors. The sintered specimens were ∼98.7% in relative densities with virtually no oxide contamination, albeit the presence of minor (4–5 vol%) secondary high-entropy M5B6 phases. Despite that Mo3B4 or W3B4 are not stable phase, 20% of Mo3B4 and W3B4 can be stabilized into the high-entropy M3B4 borides. Vickers hardness was measured to be 18.6 and 19.8 GPa at a standard load of 9.8 N. This work has further expanded the family of different structures of high-entropy ceramics reported to date.
TL;DR: In this article, a bifunctional oxygen electrode material for reversible solid oxide cells (RSOCs) was proposed and compared with the pure LNO, the optimum composition of LNO-30LDC exhibited the lowest polarization resistance (Rp) of 0.53 and 0.12 Ω·cm2 in air at 650 and 750 °C.
Abstract: In this work, La2NiO4+δ-xCe0.55La0.45O2−δ (denoted as LNO-xLDC) with various LDC contents (x = 0, 10, 20, 30, and 40 wt%) were prepared and evaluated as bifunctional oxygen electrodes for reversible solid oxide cells (RSOCs). Compared with the pure LNO, the optimum composition of LNO-30LDC exhibited the lowest polarization resistance (Rp) of 0.53 and 0.12 Ω·cm2 in air at 650 and 750 °C, respectively. The enhanced electrochemical performance of LNO-30LDC oxygen electrode was mainly attributed to the extended triple phase boundary and more oxygen ionic transfer channels. The hydrogen electrode supported single cell with LNO-30LDC oxygen electrode displayed peak power densities of 276, 401, and 521 mW·cm−2 at 700, 750, and 800 °C, respectively. Moreover, the electrolysis current density of the single cell demonstrated 526.39 mA·cm−2 under 1.5 V at 800 °C, and the corresponding hydrogen production rate was 220.03 mL·cm−2·h−1. The encouraging results indicated that LNO-30LDC was a promising bifunctional oxygen electrode material for RSOCs.
TL;DR: In this paper, the effects of dispersant and surfactant contents on the rheological properties of alumina slurries, stability of wet foams, and microstructure and mechanical properties of sintered ceramics were investigated.
Abstract: Porous ceramics have been widely used in heat insulation, filtration, and as a catalyst carrier. Ceramics with high porosity and high strength are desired; however, this high porosity commonly results in low strength materials. In this study, porous alumina with high porosity and high strength was prepared by a popular direct foaming method based on particle-stabilized wet foam that used ammonium polyacrylate (PAA) and dodecyl trimethyl ammonium chloride (DTAC) as the dispersant and hydrophobic modifier, respectively. The effects of the dispersant and surfactant contents on the rheological properties of alumina slurries, stability of wet foams, and microstructure and mechanical properties of sintered ceramics were investigated. The microstructure of porous ceramics was regulated using wet foams to achieve high strength. For a given PAA content, the wet foams exhibited increasing stability with increasing DTAC content. The most stable wet foam was successfully obtained with 0.40 wt% PAA and 0.02 wt% DTAC. The corresponding porous alumina ceramics had a porosity of 82%, an average grain size of 0.7 µm, and a compressive strength of 39 MPa. However, for a given DTAC content, the wet foams had decreasing stability with increasing PAA content. A possible mechanism to explain these results is analyzed.
TL;DR: In this paper, the effects of the sintering temperature on densification processes, microstructure, and optical properties of Y2O3:Yb3+ 5 at% ceramics have been studied.
Abstract: Y2O3:Yb3+ 5 at% ceramics have been synthesized by the reactive sintering method using different commercial yttria powders (Alfa-Micro, Alfa-Nano, and ITO-V) as raw materials. It has been shown that all Y2O3 starting powders consist from agglomerates up to 5–7 µm in size which are formed from 25–60 nm primary particles. High-energy ball milling allows to significantly decreasing the median particle size D50 below 500 nm regardless of the commercial powders used. Sintering experiments indicate that powder mixtures fabricated from Alfa-Nano yttria powders have the highest sintering activity, while (Y0.86La0.09Yb0.05)2O3 ceramics sintered at 1750 °C for 10 h are characterized by the highest transmittance of about 45%. Y2O3:Yb3+ ceramics have been obtained by the reactive sintering at 1750–1825°C using Alfa-Nano Y2O3 powders and La2O3+ZrO2 as a complex sintering aid. The effects of the sintering temperature on densification processes, microstructure, and optical properties of Y2O3:Yb3+ 5 at% ceramics have been studied. It has been shown that Zr4+ ions decrease the grain growth of Y2O3:Yb3+ ceramics for sintering temperatures 1750–1775 °C. Further increasing the sintering temperature was accompanied by a sharp increase of the average grain size of ceramics referred to changes of structure and chemical composition of grain boundaries, as well as their mobility. It has been determined that the optimal sintering temperature to produce high-dense yttria ceramics with transmittance of 79%–83% and average grain size of 8 µm is 1800 °C. Finally, laser emission at ∼1030.7 nm with a slope efficiency of 10% was obtained with the most transparent Y2O3:Yb3+ 5 at% ceramics sintered.