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Effect of Al2O3 coating on the properties of Si3N4 ceramics prepared by vat photopolymerization Al2O3 涂层对罐槽光聚合制备的 Si3N4 陶瓷性能的影响
IF 5.1 2区 材料科学 Q1 MATERIALS SCIENCE, CERAMICS Pub Date : 2024-09-19 DOI: 10.1016/j.ceramint.2024.09.245
Qi-Wen Wang , Zhang-Ao Shi , Lin Guo , Wei-Hao Cai , Jia-Min Wu , Chong Tian , Xin Lin , Hai-Sheng Xu , Fen Wang , Yu-Sheng Shi
The preparation of Si3N4 ceramics by vat photopolymerization (VPP) has motivated increasing research interest. However, it is challenging to prepare Si3N4 ceramics by VPP due to the high UV-light absorbance and refractive index of powder. In this paper, a method for Al2O3-coated Si3N4 powder was proposed. Combined with the boehmite-coated and high-temperature treatment, Al2O3 was successfully coated on the surface of Si3N4 powder. The effect of Al2O3 content on the properties of Si3N4 powders, slurry and the sintered Si3N4 samples were investigated. The Al2O3 coating layer not only improves the curing forming ability of Si3N4 slurries, but also can directly act as one of the sintering aids of Si3N4 ceramics. The bulk density of the samples decreases from 3.04 ± 0.02 g/cm3 to 2.97 ± 0.01 g/cm3 with the increase of coating content, while the porosity increases from 5.38 ± 0.89 % to 7.54 ± 0.63 %. The sample of 5 wt % Al2O3 coating content has the maximum flexural strength of 474.28 ± 16.38 MPa and the highest relative density of 94.62 ± 0.89 %. This work can not only obtain a great modification effect, but also promote the dense sintering of Si3N4 ceramics during subsequent stages, which provides a constructive method for modifying Si3N4 powders to achieve photopolymerization.
通过大桶光聚合(VPP)制备 Si3N4 陶瓷的研究兴趣日益浓厚。然而,由于粉末具有较高的紫外光吸收率和折射率,用 VPP 法制备 Si3N4 陶瓷具有很大的挑战性。本文提出了一种 Al2O3 包覆 Si3N4 粉末的方法。结合沸石包覆和高温处理,成功地在 Si3N4 粉末表面包覆了 Al2O3。研究了 Al2O3 含量对 Si3N4 粉末、浆料和烧结 Si3N4 样品性能的影响。Al2O3 涂层不仅能提高 Si3N4 泥浆的固化成型能力,还能直接作为 Si3N4 陶瓷的烧结助剂之一。随着涂层含量的增加,样品的体积密度从 3.04 ± 0.02 g/cm3 降至 2.97 ± 0.01 g/cm3,而孔隙率则从 5.38 ± 0.89 % 增至 7.54 ± 0.63 %。Al2O3 涂层含量为 5 wt % 的样品的抗折强度最大,为 474.28 ± 16.38 MPa,相对密度最高,为 94.62 ± 0.89 %。这项工作不仅能获得很好的改性效果,还能在后续阶段促进 Si3N4 陶瓷的致密烧结,为改性 Si3N4 粉末实现光聚合提供了一种建设性方法。
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引用次数: 0
Study on performance regulation of electro-mechanical properties 3D printed BaTiO3/HA porous structure composite ceramic 3D 打印 BaTiO3/HA 多孔结构复合陶瓷的机电性能调控研究
IF 5.1 2区 材料科学 Q1 MATERIALS SCIENCE, CERAMICS Pub Date : 2024-09-19 DOI: 10.1016/j.ceramint.2024.09.243
Xin Zhao , Jimin Chen , Yong Zeng
BaTiO3/Ca10(PO4)6(OH)2 composite ceramic is an outstanding representative of piezoelectric biomaterials, with excellent biocompatibility and piezoelectric effect, and has potential applications in the field of bone tissue repair. In this work, vat photopolymerization 3D printing technology was used to fabricate triply periodic minimal surface structure BaTiO3/Ca10(PO4)6(OH)2 composite ceramic bone tissue scaffolds with different pore sizes and porosity, and their mechanical and electrical properties were studied. First, the ceramic slurry configuration process was optimized to obtain a ceramic slurry with high solid content (45 vol%) and excellent rheological properties. Then the effect of sintering temperature on microstructure, relative density, mechanical properties, and electrical properties is discussed. The results show that when sintering at 1300 °C, the BaTiO3/Ca10(PO4)6(OH)2 composite ceramic has the highest relative density (99.18 %), the highest compressive strength (44 MPa), large relative dielectric constant (379–389), and low dielectric loss. The polarization electric field strength of the BaTiO3/Ca10(PO4)6(OH)2 composite ceramic was set to 15 kV/cm through the test of the hysteresis loop. Finally, based on multi-physics coupled finite element simulation, the effects of different porosity and different pore sizes on stress distribution and piezoelectric potential were analyzed, and the relationship between them was explored through experiments. The results show that as the porosity increases and the pore size decreases, the mechanical properties of the scaffold decrease significantly, and its compressive strength ranges between 1.67 and 4.26 MPa; as the porosity increases and the pore size increases, the piezoelectric coefficient (d33) of the scaffold showed a decreasing trend, and its d33 ranged between 2 and 9 pC/N. The mechanical and electrical properties of the scaffold meet the performance requirements of cancellous bone. In summary, this work provides a strategy for the application of customized BaTiO3/Ca10(PO4)6(OH)2 composite ceramic scaffolds in new-generation orthopedic implants.
BaTiO3/Ca10(PO4)6(OH)2 复合陶瓷是压电生物材料的杰出代表,具有优异的生物相容性和压电效应,在骨组织修复领域具有潜在的应用前景。本研究采用大桶光聚合3D打印技术制备了具有不同孔径和孔隙率的三周期最小表面结构BaTiO3/Ca10(PO4)6(OH)2复合陶瓷骨组织支架,并对其力学性能和电学性能进行了研究。首先,对陶瓷浆料配置工艺进行了优化,以获得固含量高(45 vol%)、流变性能优异的陶瓷浆料。然后讨论了烧结温度对微观结构、相对密度、机械性能和电气性能的影响。结果表明,在 1300 ℃ 烧结时,BaTiO3/Ca10(PO4)6(OH)2 复合陶瓷具有最高的相对密度(99.18%)、最高的抗压强度(44 兆帕)、较大的相对介电常数(379-389)和较低的介电损耗。通过磁滞环测试,BaTiO3/Ca10(PO4)6(OH)2 复合陶瓷的极化电场强度被设定为 15 kV/cm。最后,基于多物理场耦合有限元模拟,分析了不同孔隙率和不同孔径对应力分布和压电势的影响,并通过实验探讨了两者之间的关系。结果表明,随着孔隙率的增加和孔径的减小,支架的力学性能明显下降,其抗压强度在 1.67-4.26 MPa 之间;随着孔隙率的增加和孔径的增大,支架的压电系数(d33)呈下降趋势,其 d33 在 2-9 pC/N 之间。该支架的机械性能和电性能符合松质骨的性能要求。总之,这项研究为定制的 BaTiO3/Ca10(PO4)6(OH)2 复合陶瓷支架在新一代骨科植入物中的应用提供了一种策略。
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引用次数: 0
The effect of carbon addition on the synthesis process and the physical/electrocatalytic properties of FeTiO3 nanopowder produced by solution combustion synthesis method 加碳对溶液燃烧合成法制备的 FeTiO3 纳米粉体的合成过程及物理/电催化性能的影响
IF 5.1 2区 材料科学 Q1 MATERIALS SCIENCE, CERAMICS Pub Date : 2024-09-19 DOI: 10.1016/j.ceramint.2024.09.153
Saman Soltani Alasvand, Sahar Mollazadeh Beidokhti, Jalil Vahdati Khaki, Erfan Hassanizadeh
The FeTiO3 nanopowder is a vital engineering material known for its exceptional performance in energy generation, storage, electrochemical sensors, and catalysis. However, synthesizing FeTiO3 nanopowder with high crystallinity and phase purity typically requires specialized equipment and controlled heat treatment due to the instability of Fe2+ ions. Using the one-step solution combustion synthesis (SCS) method, FeTiO3 nanopowder withe high crystallinity were successfully produced utilizing basic equipment. Additionally, the influence of carbon additives on phase transitions, as well as the physical and physicochemical properties of the synthesized powder, was examined. XRD results indicate that increasing the amount of fuel, particularly glycine, creates a stable environment for the crystallization of FeTiO3 nanoparticles. Moreover, enhancing the carbon content in precursor solutions with urea enhances reduction conditions and boosts the stability of FeTiO3 in the final product. The presence of carbon additives in glycine-fuel samples leads to unfavorable outcomes by increasing the levels of TiO2 and Fe3O4 undesirable phases. Incorporating additive carbon into the urea-synthesized precursor solution resulted in a particle size increase exceeding 50 nm and raised the combustion temperature by a minimum of 230 °C. Furthermore, the presence of 15 wt% additive carbon in the sample synthesized with glycine improved the specific surface area of particles from 2.44 m2/g to 18.41 m2/g. Obtained results have shown that achieving high crystallinity of FeTiO3 nanopowder is feasible through a one-step solution combustion synthesis process. This can be accomplished by carefully choosing the synthesis conditions, such as the type and quantity of fuel, along with the carbon additive.
FeTiO3 纳米粉体是一种重要的工程材料,因其在能源生成、存储、电化学传感器和催化方面的卓越性能而闻名。然而,由于 Fe2+ 离子的不稳定性,合成具有高结晶度和相纯度的 FeTiO3 纳米粉体通常需要专业设备和受控热处理。采用一步溶液燃烧合成(SCS)法,利用基本设备成功制备出了高结晶度的 FeTiO3 纳米粉体。此外,还考察了碳添加剂对相变的影响以及合成粉末的物理和理化性质。XRD 结果表明,增加燃料(尤其是甘氨酸)的用量可为 FeTiO3 纳米粒子的结晶创造稳定的环境。此外,用尿素提高前驱体溶液中的碳含量可改善还原条件,提高最终产品中 FeTiO3 的稳定性。甘氨酸燃料样品中碳添加剂的存在会增加 TiO2 和 Fe3O4 等不良相的含量,从而导致不利的结果。在尿素合成的前驱体溶液中加入添加剂碳会导致粒度增加 50 纳米以上,并使燃烧温度升高 230 °C。此外,在使用甘氨酸合成的样品中加入 15 重量%的添加剂碳,可将颗粒的比表面积从 2.44 m2/g 提高到 18.41 m2/g。所得结果表明,通过一步溶液燃烧合成工艺获得高结晶度的 FeTiO3 纳米粉体是可行的。通过精心选择合成条件,如燃料的种类和数量以及碳添加剂,可以实现这一目标。
{"title":"The effect of carbon addition on the synthesis process and the physical/electrocatalytic properties of FeTiO3 nanopowder produced by solution combustion synthesis method","authors":"Saman Soltani Alasvand,&nbsp;Sahar Mollazadeh Beidokhti,&nbsp;Jalil Vahdati Khaki,&nbsp;Erfan Hassanizadeh","doi":"10.1016/j.ceramint.2024.09.153","DOIUrl":"10.1016/j.ceramint.2024.09.153","url":null,"abstract":"<div><div>The FeTiO<sub>3</sub> nanopowder is a vital engineering material known for its exceptional performance in energy generation, storage, electrochemical sensors, and catalysis. However, synthesizing FeTiO<sub>3</sub> nanopowder with high crystallinity and phase purity typically requires specialized equipment and controlled heat treatment due to the instability of Fe<sup>2+</sup> ions. Using the one-step solution combustion synthesis (SCS) method, FeTiO<sub>3</sub> nanopowder withe high crystallinity were successfully produced utilizing basic equipment. Additionally, the influence of carbon additives on phase transitions, as well as the physical and physicochemical properties of the synthesized powder, was examined. XRD results indicate that increasing the amount of fuel, particularly glycine, creates a stable environment for the crystallization of FeTiO<sub>3</sub> nanoparticles. Moreover, enhancing the carbon content in precursor solutions with urea enhances reduction conditions and boosts the stability of FeTiO<sub>3</sub> in the final product. The presence of carbon additives in glycine-fuel samples leads to unfavorable outcomes by increasing the levels of TiO<sub>2</sub> and Fe<sub>3</sub>O<sub>4</sub> undesirable phases. Incorporating additive carbon into the urea-synthesized precursor solution resulted in a particle size increase exceeding 50 nm and raised the combustion temperature by a minimum of 230 °C. Furthermore, the presence of 15 wt% additive carbon in the sample synthesized with glycine improved the specific surface area of particles from 2.44 m<sup>2</sup>/g to 18.41 m<sup>2</sup>/g. Obtained results have shown that achieving high crystallinity of FeTiO<sub>3</sub> nanopowder is feasible through a one-step solution combustion synthesis process. This can be accomplished by carefully choosing the synthesis conditions, such as the type and quantity of fuel, along with the carbon additive.</div></div>","PeriodicalId":267,"journal":{"name":"Ceramics International","volume":"50 22","pages":"Pages 48041-48063"},"PeriodicalIF":5.1,"publicationDate":"2024-09-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142262657","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Microstructure and wear property of (TiN + NbC) double ceramic phase-reinforced in FeCrNiCoAl high-entropy alloy coating fabricated by laser cladding 激光熔覆制造的(TiN + NbC)双陶瓷相增强铁铬镍钴铝高熵合金涂层的显微结构和磨损性能
IF 5.1 2区 材料科学 Q1 MATERIALS SCIENCE, CERAMICS Pub Date : 2024-09-19 DOI: 10.1016/j.ceramint.2024.09.248
Jitai Han , Sida Tang , Jiahui Guan , Yuyi Mao , Kui Zhu , Yin Li , Peng Li
This study delves into the influence of TiN and NbC ceramic particles on the phase structure, grain organization, microhardness, and wear resistance of FeCoNiCrAl High-Entropy Alloy (HEA) composite coatings produced through laser cladding. The integration of ceramic particles induced a dual BCC solid-solution phase structure (B2+BCC), with the formation of a TiNb phase upon the melting and interaction of TiN and NbC in the melt pool. The ceramic particles significantly modified the grain structure of the HEA coatings, disrupting the Columnar-to-Equiaxed Transition (CET) and favoring the emergence of equiaxed grains. The TiN particles induced a substantial refinement of grain size, albeit unevenly, while NbC had a milder effect. The combined presence of TiN and NbC particles resulted in a more uniform grain refinement, enhancing the mechanical properties of the coatings. Notably, the (TiN + NbC)/HEAs composite coating demonstrated superior mechanical performance under the synergistic effect of both ceramic particles. The average microhardness value increased by 55.80 % compared to 17-4Ph stainless steel, and the wear rate was reduced by 88.38 %, with the wear mechanism primarily involving abrasive and oxidative wear.
本研究深入探讨了 TiN 和 NbC 陶瓷颗粒对通过激光熔覆生产的 FeCoNiCrAl 高熵合金 (HEA) 复合涂层的相结构、晶粒组织、显微硬度和耐磨性的影响。陶瓷颗粒的加入诱导了双 BCC 固溶相结构(B2+BCC),熔池中的 TiN 和 NbC 熔化和相互作用后形成了 TiNb 相。陶瓷颗粒极大地改变了 HEA 涂层的晶粒结构,破坏了柱状到等轴状转变 (CET),有利于等轴晶粒的出现。TiN 颗粒导致了晶粒尺寸的大幅细化,尽管细化不均匀,而 NbC 的影响则较为温和。TiN 和 NbC 颗粒的共同存在使晶粒细化更加均匀,从而提高了涂层的机械性能。值得注意的是,在两种陶瓷颗粒的协同作用下,(TiN+NbC)/HEAs 复合涂层表现出了卓越的机械性能。与 17-4Ph 不锈钢相比,平均显微硬度值提高了 55.80%,磨损率降低了 88.38%,磨损机制主要包括磨料磨损和氧化磨损。
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引用次数: 0
Biomass-based perovskite/graphene oxide composite for the removal of organic pollutants from wastewater 基于生物质的 Perovskite/Graphene Oxide 复合材料用于去除废水中的有机污染物
IF 5.1 2区 材料科学 Q1 MATERIALS SCIENCE, CERAMICS Pub Date : 2024-09-19 DOI: 10.1016/j.ceramint.2024.09.249
Shimaa M. Ali , Basma Ashour , Mohamed G. Farahat , Rabab M. El-Sherif
Water pollution is a critical issue that affects both human health and the environment. Biomass-based LaFeO3 is prepared by the microwave-assisted method using rice straw as a cellulose source. Then LaFeO3/graphene oxide (GO) composite is prepared by ultrasonication to facilitate the perovskite-GO binding. Raman and FTIR spectra of the prepared composite identify the presence of the perovskite, biochar, cellulose and GO oxide phases and proves the surface functional groups interactions. Transmission electron microscope image shows that the GO sheets are homogeneous covered with the perovskite nanoparticles. The adsorption performance of the LaFeO3/GO composite for the removal of methylene blue (MB) and congo red (CR) dyes from aqueous solution is optimized. Adsorption follows pseudo 2nd order kinetic model and Freundlich isotherm, with maximum adsorption capacities of 319.5 and 416.7 mg/g for MB and CR, respectively. These values are higher than those reported for magnetic GO composites, indicating the excellent adsorption ability of the proposed perovskite/GO composite. A thermodynamic study shows that the adsorption of MB is exothermic, while it is endothermic for CR and combines physisorption and chemisorption characteristics for both dyes. The proposed adsorbent shows a good performance in the presence of NaCl interferent, with the possibility of regeneration and efficient successive reuse.
水污染是影响人类健康和环境的一个关键问题。以水稻秸秆为纤维素源,采用微波辅助法制备生物质基 LaFeO3。然后通过超声波处理制备出 LaFeO3/氧化石墨烯(GO)复合材料,以促进包晶石-GO 的结合。所制备复合材料的拉曼光谱和傅立叶变换红外光谱显示了包晶、生物炭、纤维素和 GO 氧化物相的存在,并证明了表面官能团之间的相互作用。透射电子显微镜图像显示,GO 片均匀地覆盖着包晶纳米颗粒。对 LaFeO3/GO 复合材料从水溶液中去除亚甲基蓝(MB)和刚果红(CR)染料的吸附性能进行了优化。吸附遵循伪二阶动力学模型和 Freundlich 等温线,对 MB 和 CR 的最大吸附容量分别为 319.5 和 416.7 mg/g。这些数值高于磁性 GO 复合材料的相关报道,表明所提出的包晶石/GO 复合材料具有出色的吸附能力。热力学研究表明,对 MB 的吸附是放热的,而对 CR 的吸附是内热的,并且两种染料都具有物理吸附和化学吸附特性。所提出的吸附剂在氯化钠干扰物的存在下表现出良好的性能,并有可能再生和有效地连续重复使用。
{"title":"Biomass-based perovskite/graphene oxide composite for the removal of organic pollutants from wastewater","authors":"Shimaa M. Ali ,&nbsp;Basma Ashour ,&nbsp;Mohamed G. Farahat ,&nbsp;Rabab M. El-Sherif","doi":"10.1016/j.ceramint.2024.09.249","DOIUrl":"10.1016/j.ceramint.2024.09.249","url":null,"abstract":"<div><div>Water pollution is a critical issue that affects both human health and the environment. Biomass-based LaFeO<sub>3</sub> is prepared by the microwave-assisted method using rice straw as a cellulose source. Then LaFeO<sub>3</sub>/graphene oxide (GO) composite is prepared by ultrasonication to facilitate the perovskite-GO binding. Raman and FTIR spectra of the prepared composite identify the presence of the perovskite, biochar, cellulose and GO oxide phases and proves the surface functional groups interactions. Transmission electron microscope image shows that the GO sheets are homogeneous covered with the perovskite nanoparticles. The adsorption performance of the LaFeO<sub>3</sub>/GO composite for the removal of methylene blue (MB) and congo red (CR) dyes from aqueous solution is optimized. Adsorption follows pseudo 2nd order kinetic model and Freundlich isotherm, with maximum adsorption capacities of 319.5 and 416.7 mg/g for MB and CR, respectively. These values are higher than those reported for magnetic GO composites, indicating the excellent adsorption ability of the proposed perovskite/GO composite. A thermodynamic study shows that the adsorption of MB is exothermic, while it is endothermic for CR and combines physisorption and chemisorption characteristics for both dyes. The proposed adsorbent shows a good performance in the presence of NaCl interferent, with the possibility of regeneration and efficient successive reuse.</div></div>","PeriodicalId":267,"journal":{"name":"Ceramics International","volume":"50 23","pages":"Pages 49085-49094"},"PeriodicalIF":5.1,"publicationDate":"2024-09-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142262653","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Insight into insulation degradation mechanism of Al2O3 involved with positive and negative defects 与正负缺陷有关的 Al2O3 绝缘降解机制透视
IF 5.1 2区 材料科学 Q1 MATERIALS SCIENCE, CERAMICS Pub Date : 2024-09-19 DOI: 10.1016/j.ceramint.2024.09.241
Jiawen Pan , Jiaqi Geng , Qunwei Guo , Lu Zou , Bo Chi , Jian Pu
Al2O3 with the desired electrical insulating properties and thermal shock resistivity has been extensively applied in the field of solid oxide fuel cells and oxygen sensors. However, degradation of the insulating Al2O3 layer is an intractable issue in practical applications. In this study, different point defect structures of Al2O3 were realized with the substitutional doping effect of ZrO2 and MgO. The MgO dopant provides positively charged oxygen vacancies, whereas the ZrO2 dopant tends to trigger negatively charged vacancy formation at Al3+ sites. The oxygen vacancy concentration of Al2O3 exhibits the following trend: MgO-doped Al2O3 > Al2O3 > ZrO2-doped Al2O3. Furthermore, the densification morphology, insulating properties, and oxygen vacancy migration of Al2O3 have been confirmed to be largely affected by the extrinsic factors. This study indicates that oxygen vacancy migration depends on the applied electric field at high temperatures. As the voltage and temperature increase, oxygen vacancy migration shows obvious electric-field-dependent characteristics, and its aggregation macroscopically shows hole defects. The defect position of Al2O3 is nonstoichiometric Al2O3-x with poor crystallinity. Therefore, it is believed that the oxygen vacancy migration triggered by the second phase directly determines the insulation performance and causes the degradation of Al2O3 materials.
具有理想电绝缘性能和抗热震性的 Al2O3 已被广泛应用于固体氧化物燃料电池和氧传感器领域。然而,在实际应用中,绝缘 Al2O3 层的降解是一个棘手的问题。本研究利用 ZrO2 和 MgO 的置换掺杂效应实现了 Al2O3 的不同点缺陷结构。氧化镁掺杂剂提供了带正电荷的氧空位,而 ZrO2 掺杂剂则倾向于在 Al3+ 位点引发带负电荷的空位形成。Al2O3 的氧空位浓度呈现以下趋势:掺杂 MgO 的 Al2O3 > 掺杂 Al2O3 > 掺杂 ZrO2 的 Al2O3。此外,研究还证实 Al2O3 的致密化形态、绝缘性能和氧空位迁移在很大程度上受到外在因素的影响。这项研究表明,氧空位迁移取决于高温下的外加电场。随着电压和温度的升高,氧空位迁移表现出明显的电场依赖性特征,其聚集宏观上表现出空洞缺陷。Al2O3 的缺陷位置是结晶度较差的非全度Al2O3-x。因此,第二相引发的氧空位迁移直接决定了 Al2O3 材料的绝缘性能,并导致其降解。
{"title":"Insight into insulation degradation mechanism of Al2O3 involved with positive and negative defects","authors":"Jiawen Pan ,&nbsp;Jiaqi Geng ,&nbsp;Qunwei Guo ,&nbsp;Lu Zou ,&nbsp;Bo Chi ,&nbsp;Jian Pu","doi":"10.1016/j.ceramint.2024.09.241","DOIUrl":"10.1016/j.ceramint.2024.09.241","url":null,"abstract":"<div><div>Al<sub>2</sub>O<sub>3</sub> with the desired electrical insulating properties and thermal shock resistivity has been extensively applied in the field of solid oxide fuel cells and oxygen sensors. However, degradation of the insulating Al<sub>2</sub>O<sub>3</sub> layer is an intractable issue in practical applications. In this study, different point defect structures of Al<sub>2</sub>O<sub>3</sub> were realized with the substitutional doping effect of ZrO<sub>2</sub> and MgO. The MgO dopant provides positively charged oxygen vacancies, whereas the ZrO<sub>2</sub> dopant tends to trigger negatively charged vacancy formation at Al<sup>3+</sup> sites. The oxygen vacancy concentration of Al<sub>2</sub>O<sub>3</sub> exhibits the following trend: MgO-doped Al<sub>2</sub>O<sub>3</sub> &gt; Al<sub>2</sub>O<sub>3</sub> &gt; ZrO<sub>2</sub>-doped Al<sub>2</sub>O<sub>3</sub>. Furthermore, the densification morphology, insulating properties, and oxygen vacancy migration of Al<sub>2</sub>O<sub>3</sub> have been confirmed to be largely affected by the extrinsic factors. This study indicates that oxygen vacancy migration depends on the applied electric field at high temperatures. As the voltage and temperature increase, oxygen vacancy migration shows obvious electric-field-dependent characteristics, and its aggregation macroscopically shows hole defects. The defect position of Al<sub>2</sub>O<sub>3</sub> is nonstoichiometric Al<sub>2</sub>O<sub>3-x</sub> with poor crystallinity. Therefore, it is believed that the oxygen vacancy migration triggered by the second phase directly determines the insulation performance and causes the degradation of Al<sub>2</sub>O<sub>3</sub> materials.</div></div>","PeriodicalId":267,"journal":{"name":"Ceramics International","volume":"50 23","pages":"Pages 49003-49010"},"PeriodicalIF":5.1,"publicationDate":"2024-09-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142262655","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Improved mechanical properties of porous Si3N4 ceramics strengthened by β-Si3N4 seeds fabricated by vat photopolymerization 通过大桶光聚合法制造的 β-Si3N4 种子强化的多孔 Si3N4 陶瓷的机械性能得到改善
IF 5.1 2区 材料科学 Q1 MATERIALS SCIENCE, CERAMICS Pub Date : 2024-09-19 DOI: 10.1016/j.ceramint.2024.09.247
Guang-Xin Mao , Jia-Min Wu , Chong Tian , Chun-Lei Liu , Xin Lin , Fen Wang , Hai-Sheng Xu , Yu-Sheng Shi
Porous Si3N4 ceramics are widely applied in aerospace and mechanical fields owing to their excellent properties. Furthermore, vat photopolymerization (VPP) technology can fabricate Si3N4 components with complicated structures and high precision, but its layer-by-layer printing method leads to poor mechanical properties of ceramics. In this study, porous Si3N4 ceramics with a porosity of 28.41 % strengthened by directional β-Si3N4 were fabricated by combining VPP technology and seeding method. Rheological behavior and curing properties of the slurry were explored, and the influence of β-Si3N4 content on the mechanical properties of printed Si3N4 ceramics was investigated systematically. With the increase of β-Si3N4 content, the orientation degree of β-Si3N4 grains increased gradually, while fracture toughness and flexural strength of the ceramics exhibited a trend of increased first and then decreased and Vickers hardness gradually decreased. As β-Si3N4 content increased to 5 wt%, the fracture toughness and flexural strength of porous Si3N4 ceramics were improved from 4.23 MPa m1/2 and 214.7 MPa–5.65 MPa m1/2 and 272.0 MPa, respectively. Therefore, this work indicates that vat photopolymerization combined with seeding method is a promising approach for the fabrication of porous Si3N4 ceramics with high performance and complex structures.
多孔 Si3N4 陶瓷因其优异的性能被广泛应用于航空航天和机械领域。此外,大桶光聚合(VPP)技术可以制造结构复杂、精度高的 Si3N4 元件,但其逐层印刷的方法导致陶瓷的机械性能较差。本研究结合 VPP 技术和播种方法,制备了孔隙率为 28.41% 的多孔 Si3N4 陶瓷,该陶瓷由定向 β-Si3N4 增强。探讨了浆料的流变行为和固化性能,并系统研究了β-Si3N4含量对印刷Si3N4陶瓷力学性能的影响。随着β-Si3N4含量的增加,β-Si3N4晶粒的取向度逐渐增大,陶瓷的断裂韧性和抗弯强度呈先增大后减小的趋势,维氏硬度逐渐减小。当β-Si3N4含量增加到5 wt%时,多孔Si3N4陶瓷的断裂韧性和抗弯强度分别从4.23 MPa-m1/2和214.7 MPa提高到5.65 MPa-m1/2和272.0 MPa。因此,这项工作表明,大桶光聚合与播种方法相结合是制造高性能复杂结构多孔 Si3N4 陶瓷的一种可行方法。
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引用次数: 0
Effects of the SmFeN content on the electromagnetic wave absorbing properties of sandwich-structured YSZ/SmFeN/YSZ composites SmFeN 含量对三明治结构 YSZ/SmFeN/YSZ 复合材料电磁波吸收特性的影响
IF 5.1 2区 材料科学 Q1 MATERIALS SCIENCE, CERAMICS Pub Date : 2024-09-19 DOI: 10.1016/j.ceramint.2024.09.246
Hongning Zhang, Tianni Lu, Qianxi Zhang, Zhenwei Huang, Na Li, Jinman Zhang, Chunzhong Liu
In this study, the thermal barrier material Yttria Stabilized Zirconia (YSZ) and the electromagnetic wave (EMW) absorbing agent samarium iron nitrogen (SmFeN) were used to prepare a YSZ/SmFeN/YSZ sandwich-structured composite. The YSZ/SmFeN interface was prepared perpendicular to the directions of EMWs. The EMW attenuation of the composites with different SmFeN contents and their mechanisms were studied using electromagnetic parameters, impedance matching, Cole–Cole circles, and minimum reflection loss (RLmin value). Dielectric loss was the dominant mechanism behind EMW attenuation for the composites. In addition, the dipole orientation of SmFeN and the presence of phase interface induced the dielectric loss. The mechanism of dipole orientation polarization was influenced by SmFeN content; the lesser the SmFeN content in the composite, the higher the ε (real part of dielectric coefficient). The frequency at which ε peaked shifted decreased with increasing SmFeN content. Higher dielectric losses were observed in the frequency band of 4.0–8.0 GHz. The EMW absorption rate showed that the optimum EMW absorption effect was achieved when the thickness ratio of YSZ:SmFeN:YSZ was 1:4:1 and the thickness is 3.325 mm. The corresponding RLmin was −35.3 dB and effective absorption bandwidth was 9.5 GHz (8.3–17.9 GHz).
本研究使用热障材料钇稳定氧化锆(YSZ)和电磁波吸收剂钐铁氮(SmFeN)制备了一种 YSZ/SmFeN/YSZ 夹层结构复合材料。制备的 YSZ/SmFeN 界面垂直于电磁波的方向。利用电磁参数、阻抗匹配、科尔-科尔圆和最小反射损耗(RLmin 值)研究了不同 SmFeN 含量复合材料的电磁波衰减及其机理。介电损耗是复合材料电磁波衰减的主要机制。此外,SmFeN 的偶极取向和相界面的存在也诱发了介电损耗。偶极取向极化机制受 SmFeN 含量的影响;复合材料中 SmFeN 含量越低,ε(介电常数的实部)越高。ε达到峰值的频率随 SmFeN 含量的增加而降低。在 4.0-8.0 GHz 频段观察到较高的介电损耗。电磁波吸收率表明,当 YSZ:SmFeN:YSZ 的厚度比为 1:4:1、厚度为 3.325 mm 时,电磁波吸收效果最佳。相应的 RLmin 为 -35.3 dB,有效吸收带宽为 9.5 GHz(8.3-17.9 GHz)。
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引用次数: 0
Phase selectivity upon flash-lamp annealing of sputter deposited amorphous titanium oxide films 溅射沉积非晶氧化钛薄膜闪灯退火时的相选择性
IF 5.1 2区 材料科学 Q1 MATERIALS SCIENCE, CERAMICS Pub Date : 2024-09-19 DOI: 10.1016/j.ceramint.2024.09.252
R. Gago , S. Prucnal , J. Azpeitia , I. Jiménez , L. Álvarez-Fraga
We report the impact of flash-lamp-annealing (FLA) on the structural evolution of amorphous titania (TiO2) films produced by DC reactive magnetron sputtering. TiO2 films were grown at room-temperature at different oxygen partial pressure (PO2) and subsequently annealed as a function of the FLA energy density. X-ray diffraction confirms that FLA induces phase formation from the initial amorphous state with a general transition from anatase to rutile by increasing the FLA energy density (temperature). Interestingly, the transformation onset of anatase to rutile is achieved at lower energy densities for higher PO2. On the contrary, films with a highly resilient anatase phase can be produced at relatively low PO2. A detailed analysis of the pristine amorphous structure carried out by X-ray absorption near-edge structure indicates the role of oxygen sites in the observed phase transformation. In particular, oxygen vacancies seem to stabilize the anatase phase at high temperatures. The results show the relevance of subtle changes in the initial amorphous structure for phase selectivity in TiO2 films upon FLA.
我们报告了闪光灯退火(FLA)对直流反应磁控溅射法生产的无定形二氧化钛(TiO2)薄膜结构演变的影响。二氧化钛薄膜在室温、不同氧分压(PO2)条件下生长,随后随 FLA 能量密度的变化而退火。X 射线衍射证实,随着 FLA 能量密度(温度)的增加,FLA 会诱导从最初的无定形态形成相,并从锐钛矿转变为金红石型。有趣的是,PO2 越高,锐钛型向金红石型转变的起始能量密度越低。相反,在相对较低的 PO2 条件下,可以生产出具有高弹性锐钛矿相的薄膜。通过 X 射线吸收近边结构对原始无定形结构进行的详细分析表明,氧位点在观察到的相变中发挥了作用。特别是,氧空位似乎能在高温下稳定锐钛矿相。结果表明,初始无定形结构的微妙变化与二氧化钛薄膜在 FLA 时的相选择性有关。
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引用次数: 0
Gamma radiation-induced changes in the structural and optical properties of CsPbBr3 thin films for space applications 伽马辐射诱导的用于太空应用的铯硼铍 3 薄膜的结构和光学特性变化
IF 5.1 2区 材料科学 Q1 MATERIALS SCIENCE, CERAMICS Pub Date : 2024-09-19 DOI: 10.1016/j.ceramint.2024.09.239
Zhuan Zhao , Muhammad Amin Padhiar , Shaolin Zhang , Teng Ma , Noor Zamin Khan , Yongqiang Ji , Zubair Maroof , Shusheng Pan
Perovskite nanocrystals (NCs) are emerging as a next generation display technology. In this regard, exploring the structural and optical stability when subjected to radiation is crucial for expanding their application in aerospace and radiation detection technologies. In this study, we investigated the effects of gamma radiation on CsPbBr3 heterojunction thin films through a comprehensive analysis of their structural and optical characteristics. The thin films of CsPbBr3 were subjected to varying doses of gamma radiation, ranging from 100 krad to 1 Mrad, followed by thorough examination using X-ray diffraction (XRD) and optical spectroscopy techniques. Our findings unveil significant changes in the crystal structure of CsPbBr3 thin films when exposed to gamma radiation, including shifts in diffraction peak positions from cubic to monoclinic phases, broadening of peaks, and variations in peak intensities due to induced surface defects. The optical properties, such electroluminescence (EL) and photoluminescence (PL) intensity slightly drops at the moderate irradiation dose of 300 krad, while at an irradiation dose of 1 Mrad deteriorated severely. Notably, 300 krad is equivalent to the radiation dose accumulated by satellites in low-Earth orbit over 10 years. The findings in this work suggest the fabricated CsPbBr3 thin film has the potential to be used in space applications.
透镜纳米晶体(NCs)正在成为下一代显示技术。因此,探索其在辐射作用下的结构和光学稳定性对于扩大其在航空航天和辐射探测技术中的应用至关重要。在这项研究中,我们通过全面分析 CsPbBr3 异质结薄膜的结构和光学特性,研究了伽马辐射对其的影响。我们对 CsPbBr3 薄膜进行了从 100krad 到 1 Mrad 的不同剂量的伽马辐射,然后使用 X 射线衍射 (XRD) 和光学光谱技术对其进行了全面检查。我们的研究结果揭示了铯铋硼薄膜在伽马射线照射下晶体结构的显著变化,包括衍射峰位置从立方相向单斜相移动、峰值变宽,以及由于表面缺陷引起的峰值强度变化。在中等辐照剂量(300krad)下,电致发光(EL)和光致发光(PL)强度等光学特性略有下降,而在辐照剂量(1 Mrad)下则严重恶化。值得注意的是,300krad 相当于卫星在低地球轨道上 10 年积累的辐射剂量。这项研究结果表明,所制造的铯硼铍薄膜具有在太空应用中使用的潜力。
{"title":"Gamma radiation-induced changes in the structural and optical properties of CsPbBr3 thin films for space applications","authors":"Zhuan Zhao ,&nbsp;Muhammad Amin Padhiar ,&nbsp;Shaolin Zhang ,&nbsp;Teng Ma ,&nbsp;Noor Zamin Khan ,&nbsp;Yongqiang Ji ,&nbsp;Zubair Maroof ,&nbsp;Shusheng Pan","doi":"10.1016/j.ceramint.2024.09.239","DOIUrl":"10.1016/j.ceramint.2024.09.239","url":null,"abstract":"<div><div>Perovskite nanocrystals (NCs) are emerging as a next generation display technology. In this regard, exploring the structural and optical stability when subjected to radiation is crucial for expanding their application in aerospace and radiation detection technologies. In this study, we investigated the effects of gamma radiation on CsPbBr<sub>3</sub> heterojunction thin films through a comprehensive analysis of their structural and optical characteristics. The thin films of CsPbBr<sub>3</sub> were subjected to varying doses of gamma radiation, ranging from 100 krad to 1 Mrad, followed by thorough examination using X-ray diffraction (XRD) and optical spectroscopy techniques. Our findings unveil significant changes in the crystal structure of CsPbBr<sub>3</sub> thin films when exposed to gamma radiation, including shifts in diffraction peak positions from cubic to monoclinic phases, broadening of peaks, and variations in peak intensities due to induced surface defects. The optical properties, such electroluminescence (EL) and photoluminescence (PL) intensity slightly drops at the moderate irradiation dose of 300 krad, while at an irradiation dose of 1 Mrad deteriorated severely. Notably, 300 krad is equivalent to the radiation dose accumulated by satellites in low-Earth orbit over 10 years. The findings in this work suggest the fabricated CsPbBr<sub>3</sub> thin film has the potential to be used in space applications.</div></div>","PeriodicalId":267,"journal":{"name":"Ceramics International","volume":"50 23","pages":"Pages 48995-49002"},"PeriodicalIF":5.1,"publicationDate":"2024-09-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142262660","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
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Ceramics International
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