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Hydrolysis mechanisms of titanium precursors in hydrothermal synthesis of barium titanate: A combined computational and experimental study 水热合成钛酸钡过程中钛前驱体的水解机理:计算与实验相结合的研究
IF 5.6 2区 材料科学 Q1 MATERIALS SCIENCE, CERAMICS Pub Date : 2026-01-01 DOI: 10.1016/j.ceramint.2025.12.180
Hanze Mu , Jie Yu , Saiwei Luan , Tong Wu , Yuanyuan Xiong , Lei Zhang
The nature of the titanium source can play a crucial role in the hydrothermal synthesis of BaTiO3, particularly in the hydrolysis of the titanium source. In this study, combining Density functional theory (DFT) calculations with X-ray diffraction, scanning electron microscopy and Fourier-transform infrared spectroscopy, the influence of different titanium sources (TiCl4, H2TiO3, TiO2, and C16H36O4Ti) hydrolysis rate on the crystal structure, morphology of BaTiO3 powders and the dielectric properties of the sintered ceramics were investigated. Both computational and experimental results demonstrate that the hydrolysis rate of the titanium source affects the supply of Ti during the reaction, which in turn influences the nucleation and growth of BaTiO3. While the hydrolysis rates of TiCl4 and TiO2 meet the requirements of Ti supply during the synthesis of BaTiO3, a slower hydrolysis rate of TiO2 could result in smaller and more uniform particle sizes for its low energy barrier (0.12eV). The BaTiO3 powder synthesized with the TiO2 source exhibited the smallest average particle size (120 nm) and the highest tetragonality (c/a = 1.0082). Correspondingly, the ceramic sintered from this powder showed the lowest dielectric loss and a high dielectric constant (2300).
钛源的性质在水热合成BaTiO3中起着至关重要的作用,特别是在钛源的水解过程中。本研究将密度泛函理论(DFT)计算与x射线衍射、扫描电镜和傅里叶变换红外光谱相结合,研究了不同钛源(TiCl4、H2TiO3、TiO2和C16H36O4Ti)水解速率对烧结陶瓷BaTiO3粉末的晶体结构、形貌和介电性能的影响。计算和实验结果均表明,钛源的水解速率影响反应过程中Ti的供给,进而影响BaTiO3的成核和生长。而TiCl4和TiO2的水解速率可以满足BaTiO3合成过程中Ti的供给要求,而TiO2的水解速率越慢,由于其低能垒(0.12eV),可以得到更小更均匀的粒径。用该TiO2源合成的BaTiO3粉体平均粒径最小(120 nm),四方性最高(c/a = 1.0082)。相应地,由该粉末烧结而成的陶瓷具有最低的介电损耗和较高的介电常数(2300)。
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引用次数: 0
Ablation resistance and heat insulation performance of integrated Cf/SiBCN ceramic-polymer gradient composites in arc wind tunnel 集成Cf/SiBCN陶瓷-聚合物梯度复合材料在电弧风洞中的抗烧蚀和隔热性能
IF 5.6 2区 材料科学 Q1 MATERIALS SCIENCE, CERAMICS Pub Date : 2026-01-01 DOI: 10.1016/j.ceramint.2025.12.025
Chunlei Xia , Weihua Xie , Songhe Meng , Fajun Yi , Fan Yang , Dong Yu , Bo Gao , Tongxiang Deng
The advancement of future hypersonic vehicles poses tangible challenges to the innovation of thermal protection materials. Herein, we prepared a novel integrated Cf/SiBCN amorphous ceramic-polymer continuous gradient thermal protection composite. Ablation tests were conducted on the integrated gradient material specimens using an arc-heated wind tunnel under heat flux conditions of 1.85 MW/m2 and 2.15 MW/m2, respectively. Although the ablation surface temperature of the material reached 1915 °C, its back temperature remained much lower than 105 °C within 300 s. The mass ablation rate and linear ablation rate were 3.42 × 10−6 g/(mm2·s) and −0.0028 mm/s, respectively. No obvious ablation cracks or holes were observed on the material surface. Notably, an in-situ molten protective layer formed on the specimen surface during the ablation process. Composed of silicides and borides, this dense molten layer covering the surface not only enables self-repair of damage but also enhances the ablation resistance and oxidation resistance of the material further. This material exhibits excellent ablation resistance, thermal insulation performance, and ablation deformation resistance. This study contributes to advancing the innovation of functionally and structurally integrated gradient thermal protection materials and has practical application potential in the field of hypersonic vehicles.
未来高超声速飞行器的发展对热防护材料的创新提出了切实的挑战。本文制备了一种新型的集成Cf/SiBCN非晶陶瓷-聚合物连续梯度热防护复合材料。在热流密度为1.85 MW/m2和2.15 MW/m2的条件下,采用电弧加热风洞对一体化梯度材料试样进行了烧蚀试验。虽然材料的烧蚀表面温度达到1915℃,但在300 s内其背温仍远低于105℃。质量消融速率和线性消融速率分别为3.42 × 10−6 g/(mm2·s)和−0.0028 mm/s。材料表面未观察到明显的烧蚀裂纹和孔洞。值得注意的是,在烧蚀过程中,试样表面形成了原位熔融保护层。由硅化物和硼化物组成的致密熔融层覆盖在材料表面,不仅可以自我修复损伤,还可以进一步提高材料的抗烧蚀性和抗氧化性。该材料具有优异的抗烧蚀性能、保温性能和抗烧蚀变形性能。该研究有助于推进功能和结构一体化梯度热防护材料的创新,在高超声速飞行器领域具有实际应用潜力。
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引用次数: 0
Gas sensitivity in SnO2-SnWO4 composite nanostructures SnO2-SnWO4复合纳米结构的气敏性
IF 5.6 2区 材料科学 Q1 MATERIALS SCIENCE, CERAMICS Pub Date : 2026-01-01 DOI: 10.1016/j.ceramint.2025.12.174
NiNa Ma, ShuYi Ma, Ping Ni, YinYue Wang, Heng Wang, JiaMin Zhu, GeGe Fan, JiaYun Guo, HaiYan Wang
As the economy surges forward at a brisk pace, people's living standards are concurrently improving. However, they are increasingly besieged by the detrimental effects of environmental pollution. Triethylamine, a significant volatile organic compound pollutant, is crucial to detect effectively. In this paper, the SnO2/SnWO4 sensor was synthesized using a singular hydrothermal technique predicated on the concept of composite modification. As gas-sensitive materials, the diminutive SnO2/SnWO4 nanosheets demonstrate remarkable sensitivity (181.63) to 200 ppm of triethylamine gas at a modest operating temperature of 130 °C. Additionally, they feature swift desorption rates (8 s) along with superb repeatability and enduring stability. Furthermore, the sensitization mechanism of this composite structure stems from several factors: the reduction in grain size, an increase in specific surface area, the formation of n-n heterojunctions, and the influence of electron concentration. This study verifies that fabricating n-n heterojunctions through composite modification represents a significant method for enhancing the gas sensitivity of sensors.
在经济快速发展的同时,人民的生活水平也在不断提高。然而,他们越来越受到环境污染的不利影响。三乙胺是一种重要的挥发性有机化合物污染物,对其进行有效检测至关重要。本文采用基于复合改性概念的单一水热技术合成了SnO2/SnWO4传感器。作为气敏材料,小型SnO2/SnWO4纳米片在130°C的适度工作温度下对200ppm的三乙胺气体具有显著的灵敏度(181.63)。此外,它们具有快速的解吸速率(8秒)以及极好的可重复性和持久的稳定性。此外,该复合结构的敏化机制源于几个因素:晶粒尺寸的减小、比表面积的增加、n-n异质结的形成以及电子浓度的影响。该研究验证了通过复合改性制备n-n异质结是提高传感器气体灵敏度的重要方法。
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引用次数: 0
Tribology and mechanical performance of gradient Si:DLC and (Si,N):DLC layers on Ti6Al7Nb alloy Ti6Al7Nb合金上梯度Si:DLC和(Si,N):DLC层的摩擦学和力学性能
IF 5.6 2区 材料科学 Q1 MATERIALS SCIENCE, CERAMICS Pub Date : 2026-01-01 DOI: 10.1016/j.ceramint.2025.12.090
Kamil Kleszcz , Witold Szymański , Łukasz Kaczmarek , Daniel Kottfer , Patrik Kľučiar , Mateusz Marzec , Anna Adamczyk , Krzysztof Mars , Karol Kyzioł
The bearing surfaces of joint implants created the need for a specific class of materials that are resistant to wear and corrosion in the environment of the human body, all the while staying biocompatible. Diamond-like carbon (DLC) layers are one of the most prominent solutions, proposed in scientific literature to fill this niche. The ability to dope amorphous DLC structures with atoms that enhance desirable properties or display biological activity further justifies high interest in the topic. This work explores and compares gradient and non-gradient doping with silicon and nitrogen in the case of DLC layers deposited by PECVD (Plasma Enhanced Chemical Vapor Deposition). The scope of this article entails a comparison of morphologies and topographies investigated by SEM and AFM, differences and similarities in chemistry are emphasized with the help of FTIR, Raman and XPS spectroscopy. Relevant mechanical (Young's modulus, hardness) and tribological (coefficient of friction, wear) properties are measured and paralleled in the case of gradient and non-gradient Si:DLC/(Si,N):DLC layers. Superior hardness of gradient DLC layers was proven with (Si,N):DLC layer showing the best result (17.9 GPa), compared to non-gradient equivalent (13.6 GPa). Additionally, gradient Si:DLC layer and silicon gradient (Si,N):DLC layer showed lower coefficient of friction (down to 0.14) and wear (down to 5.37·10−6 mm3/N·m), in comparison to non-gradient equivalents.
关节植入物的承载表面产生了对一种特殊材料的需求,这种材料在人体环境中耐磨损和腐蚀,同时保持生物相容性。类金刚石碳(DLC)层是科学文献中提出的最突出的解决方案之一,以填补这一空缺。用原子掺杂非晶态DLC结构以增强理想性能或显示生物活性的能力进一步证明了对该主题的高度兴趣。本研究探索并比较了在PECVD(等离子体增强化学气相沉积)沉积DLC层的情况下,硅和氮的梯度和非梯度掺杂。本文的范围是通过SEM和AFM研究的形貌和地形进行比较,并借助FTIR,拉曼和XPS光谱强调化学上的差异和相似之处。在梯度和非梯度Si:DLC/(Si,N):DLC层的情况下,测量并平行了相关的力学(杨氏模量,硬度)和摩擦学(摩擦系数,磨损)性能。梯度DLC层具有优异的硬度,(Si,N):DLC层的硬度最高(17.9 GPa),优于非梯度DLC层(13.6 GPa)。此外,与非梯度层相比,梯度Si:DLC层和硅梯度(Si,N):DLC层的摩擦系数低至0.14,磨损系数低至5.37·10−6 mm3/N·m。
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引用次数: 0
Influence of Dy-doped copper–zinc ferrite ceramics for energy storage applications 掺镝铜锌铁氧体陶瓷对储能应用的影响
IF 5.6 2区 材料科学 Q1 MATERIALS SCIENCE, CERAMICS Pub Date : 2026-01-01 DOI: 10.1016/j.ceramint.2025.12.103
Zhengyou Li , Jagadeesha Angadi V , Kiran Shinde , Abdullah M. Al-Enizi , Mohd Ubaidullah , Enas S. Radwan
In this study, Cu0.5Zn0.5DyxFe2-xO4 (ZCDF; x = 0.0, 0.005, 0.01, 0.015, 0.02) spinel ferrite nanoparticles were synthesized using the solution combustion method and investigated for their structural, morphological, and electrochemical properties, with a focus on hydrogen evolution reaction (HER) performance. X-ray diffraction (XRD) confirmed the formation of a single-phase cubic structure with the Fd-3m space group across all doping levels. FTIR spectra validated the retention of characteristic metal–oxygen vibrations, while XRF and elemental mapping confirmed the homogeneous incorporation and spatial distribution of Dy3+ ions without forming secondary phases. Optical microscopy revealed a progressive enhancement in surface homogeneity with increasing Dy content. Electrochemical analyses demonstrated a significant improvement in HER activity for the x = 0.005 sample, which exhibited the lowest overpotential and charge transfer resistance, attributed to enhanced conductivity and optimal catalytic site availability. Tafel slope and EIS analyses corroborated the improved charge transfer kinetics. Cyclic voltammetry (CV) showed excellent capacitive behavior, with x = 0.02 displaying the highest areal capacitance (16.08 mF/cm2), indicating dual electrochemical functionality. These findings suggest that Dy-doped Cu-Zn ferrites are promising multifunctional materials for energy storage and electrocatalytic hydrogen production applications.
本研究采用溶液燃烧法合成了Cu0.5Zn0.5DyxFe2-xO4 (ZCDF; x = 0.0, 0.005, 0.01, 0.015, 0.02)尖晶石铁素体纳米颗粒,并对其结构、形态和电化学性能进行了研究,重点研究了析氢反应(HER)性能。x射线衍射(XRD)证实,在所有掺杂水平上都形成了具有Fd-3m空间群的单相立方结构。FTIR光谱证实了特征金属氧振动的保留,而XRF和元素映射证实了Dy3+离子的均匀结合和空间分布,没有形成二次相。光学显微镜显示,随着Dy含量的增加,表面均匀性逐渐增强。电化学分析表明,x = 0.005样品的HER活性显著提高,由于电导率增强和最佳催化位点可用性,该样品表现出最低的过电位和电荷转移电阻。Tafel斜率和EIS分析证实了电荷传递动力学的改善。循环伏安法(CV)显示出优异的电容性能,当x = 0.02时显示出最高的面电容(16.08 mF/cm2),表明具有双重电化学功能。这些发现表明,镝掺杂Cu-Zn铁氧体是一种很有前途的多功能储能材料和电催化制氢材料。
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引用次数: 0
Cu-carbon hollow and solid sphere modified triphasic TiO2 for efficient H2 generation in deionized water and river water 铜碳空心实心球改性三相TiO2在去离子水和河水中高效产氢
IF 5.6 2区 材料科学 Q1 MATERIALS SCIENCE, CERAMICS Pub Date : 2026-01-01 DOI: 10.1016/j.ceramint.2025.12.100
Junfeng Yang , Jingfeng Wu , Jun Xiong , Yu Wen , Shengyan Yin , Qin Zhang
Herein, utilizing cheap carbonated beverage (Fanta) as the carbon source, the multiphasic TiO2/Cu-C composites are successfully designed and prepared for efficient photocatalytic H2 generation. Excitingly, the controllable preparation of triphasic, biphasic and rutile phase TiO2 can be achieved by adjusting the reaction temperature. As expected, under ultraviolet–visible light irradiation, the triphasic TiO2/Cu-C-5 exhibited the best photocatalytic H2 evolution rate (HER, 28.53 mmol g−1 h−1), which is about 21.45 and 1.65 times as high as than that of triphasic TiO2 and P25/Cu-C-5, respectively. In addition, the HER reached 7.67, 12.47 and 3.46 mmol g−1 h−1 in Tianyi lake water, Ganjing river water and Bohai seawater, respectively. Furthermore, the experiment of inorganic salt ions effect on HPR shows that NO3 and SO42- ions have great negative influence. This transient photocurrent response, photoluminescence and photoluminescence lifetime experiments indicate that the carrier Cu-C and the construction of heterophase junctions are conducive to the separation of photogenerated charges and reducing their recombination efficiency, resulting in the improvement of the photocatalytic hydrogen evolution performance. Meanwhile, the Cu-C sample contains hollow spheres, which facilitate the refraction of light and enhance its absorption. These advantages strongly prove that the triphasic TiO2/Cu-C photocatalyst has potential application prospects in the field of catalytic hydrogen evolution in deionized water and natural water.
本文以廉价碳酸饮料(芬达)为碳源,成功设计并制备了多相TiO2/Cu-C复合材料,用于高效光催化制氢。令人兴奋的是,通过调节反应温度,可以实现三相、双相和金红石相TiO2的可控制备。结果表明,在紫外-可见光照射下,TiO2/Cu-C-5的光催化析氢速率最高,为28.53 mmol g−1 h−1,分别是TiO2/ P25/Cu-C-5的21.45倍和1.65倍。此外,天宜湖水体、赣江水体和渤海海水的HER分别达到7.67、12.47和3.46 mmol g−1 h−1。此外,无机盐离子对HPR的影响实验表明,NO3 -和SO42-离子对HPR有较大的负面影响。这种瞬态光电流响应、光致发光和光致发光寿命实验表明,载流子Cu-C和异相结的构建有利于光生电荷的分离,降低其复合效率,从而提高光催化析氢性能。同时,Cu-C样品中含有空心球体,有利于光的折射,增强了光的吸收。这些优点有力地证明了TiO2/Cu-C三相光催化剂在去离子水和天然水催化析氢领域具有潜在的应用前景。
{"title":"Cu-carbon hollow and solid sphere modified triphasic TiO2 for efficient H2 generation in deionized water and river water","authors":"Junfeng Yang ,&nbsp;Jingfeng Wu ,&nbsp;Jun Xiong ,&nbsp;Yu Wen ,&nbsp;Shengyan Yin ,&nbsp;Qin Zhang","doi":"10.1016/j.ceramint.2025.12.100","DOIUrl":"10.1016/j.ceramint.2025.12.100","url":null,"abstract":"<div><div>Herein, utilizing cheap carbonated beverage (Fanta) as the carbon source, the multiphasic TiO<sub>2</sub>/Cu-C composites are successfully designed and prepared for efficient photocatalytic H<sub>2</sub> generation. Excitingly, the controllable preparation of triphasic, biphasic and rutile phase TiO<sub>2</sub> can be achieved by adjusting the reaction temperature. As expected, under ultraviolet–visible light irradiation, the triphasic TiO<sub>2</sub>/Cu-C-5 exhibited the best photocatalytic H<sub>2</sub> evolution rate (HER, 28.53 mmol g<sup>−1</sup> h<sup>−1</sup>), which is about 21.45 and 1.65 times as high as than that of triphasic TiO<sub>2</sub> and P25/Cu-C-5, respectively. In addition, the HER reached 7.67, 12.47 and 3.46 mmol g<sup>−1</sup> h<sup>−1</sup> in Tianyi lake water, Ganjing river water and Bohai seawater, respectively. Furthermore, the experiment of inorganic salt ions effect on HPR shows that NO<sub>3</sub><sup>−</sup> and SO<sub>4</sub><sup>2</sup><sup>-</sup> ions have great negative influence. This transient photocurrent response, photoluminescence and photoluminescence lifetime experiments indicate that the carrier Cu-C and the construction of heterophase junctions are conducive to the separation of photogenerated charges and reducing their recombination efficiency, resulting in the improvement of the photocatalytic hydrogen evolution performance. Meanwhile, the Cu-C sample contains hollow spheres, which facilitate the refraction of light and enhance its absorption. These advantages strongly prove that the triphasic TiO<sub>2</sub>/Cu-C photocatalyst has potential application prospects in the field of catalytic hydrogen evolution in deionized water and natural water.</div></div>","PeriodicalId":267,"journal":{"name":"Ceramics International","volume":"52 3","pages":"Pages 3049-3059"},"PeriodicalIF":5.6,"publicationDate":"2026-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145996353","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
Effect of number of layers on the synergistic enhancement of in vitro cytocompatibility, tribo-mechanical and chemical properties of functionally graded Ti6Al4V-YSZ composites by spark plasma sintering 层数对放电等离子烧结功能梯度Ti6Al4V-YSZ复合材料体外细胞相容性、摩擦力学和化学性能协同增强的影响
IF 5.6 2区 材料科学 Q1 MATERIALS SCIENCE, CERAMICS Pub Date : 2026-01-01 DOI: 10.1016/j.ceramint.2025.12.113
R. Jayasree , S.N. Sahoo , Mangal Roy , D. Chakravarty
The interface plays a vital role in determining the performance of a functionally graded material (FGM). In the present work, the difference in compositional gradation at the interfaces of a three-layered (3L) Ti6Al4V-yttria stabilized zirconia (YSZ) FGM was reduced by increasing the number of layers to five (5L). The FGM samples were prepared by spark plasma sintering (SPS) and the effects of the number of layers on hardness, compressive and bending strength, wear, corrosion, and in vitro cytocompatibility were investigated. Due to lower compositional variation among layers the 5L FGM yielded better bulk density (99.4 %) compared to the 3L FGM (96.3 %) and also yielded strong interfacial bonding devoid of microcracks, porosity or reaction layers leading to 12 % and 26 % improvement in compressive and flexural strength, respectively. A gradual increase in hardness with YSZ content (10–90 %) was observed in 5L compared to the 3L samples with maximum hardness reaching 1490 ± 10 HV0.3 for the 5L sample containing 90 % YSZ. The increased hardness resulted in a concomitant 1.5-fold improvement in wear resistance in the sample. The 5L sample also exhibited 58 % and 30 % higher corrosion resistance on the YSZ-rich and Ti6Al4V-rich sides respectively, which can be attributed to the formation of a stable passive film in the matrix along with its superior density. The improved corrosion resistance of the FGMs promoted cell viability and enhanced alkaline phosphatase activity. The present investigation demonstrates the benefits of increasing the number of layers in the Ti6Al4V-YSZ FGMs fabricated by SPS on the tribo-mechanical, corrosion and biological properties enhancing their potential as promising dental implant materials.
界面对功能梯度材料(FGM)的性能起着至关重要的作用。在本研究中,将三层(3L) ti6al4v - ytria稳定氧化锆(YSZ) FGM的层数增加到5层(5L),减少了界面上的成分级配差异。采用火花等离子烧结(SPS)法制备了FGM材料,考察了层数对FGM材料硬度、抗压强度、抗弯强度、耐磨性、耐腐蚀性和体外细胞相容性的影响。由于层间成分变化较小,5L FGM的体积密度(99.4%)优于3L FGM(96.3%),并且界面结合强,没有微裂纹、孔隙或反应层,抗压和抗弯强度分别提高了12%和26%。与3L样品相比,5L样品的硬度随YSZ含量(10 ~ 90%)的增加而逐渐升高,当YSZ含量为90%时,5L样品的最大硬度达到1490±10hv0.3。硬度的增加使样品的耐磨性提高了1.5倍。5L样品在富ysz和富ti6al4v侧的耐蚀性也分别提高了58%和30%,这可归因于在基体中形成了稳定的钝化膜以及其优越的密度。增强的抗腐蚀性能促进了细胞活力,增强了碱性磷酸酶活性。本研究表明,增加SPS制备的Ti6Al4V-YSZ FGMs的层数,在摩擦力学、腐蚀和生物性能方面都有很大的好处,从而增强了其作为牙科种植材料的潜力。
{"title":"Effect of number of layers on the synergistic enhancement of in vitro cytocompatibility, tribo-mechanical and chemical properties of functionally graded Ti6Al4V-YSZ composites by spark plasma sintering","authors":"R. Jayasree ,&nbsp;S.N. Sahoo ,&nbsp;Mangal Roy ,&nbsp;D. Chakravarty","doi":"10.1016/j.ceramint.2025.12.113","DOIUrl":"10.1016/j.ceramint.2025.12.113","url":null,"abstract":"<div><div>The interface plays a vital role in determining the performance of a functionally graded material (FGM). In the present work, the difference in compositional gradation at the interfaces of a three-layered (3L) Ti6Al4V-yttria stabilized zirconia (YSZ) FGM was reduced by increasing the number of layers to five (5L). The FGM samples were prepared by spark plasma sintering (SPS) and the effects of the number of layers on hardness, compressive and bending strength, wear, corrosion, and in vitro cytocompatibility were investigated. Due to lower compositional variation among layers the 5L FGM yielded better bulk density (99.4 %) compared to the 3L FGM (96.3 %) and also yielded strong interfacial bonding devoid of microcracks, porosity or reaction layers leading to 12 % and 26 % improvement in compressive and flexural strength, respectively. A gradual increase in hardness with YSZ content (10–90 %) was observed in 5L compared to the 3L samples with maximum hardness reaching 1490 ± 10 HV<sub>0.3</sub> for the 5L sample containing 90 % YSZ. The increased hardness resulted in a concomitant 1.5-fold improvement in wear resistance in the sample. The 5L sample also exhibited 58 % and 30 % higher corrosion resistance on the YSZ-rich and Ti6Al4V-rich sides respectively, which can be attributed to the formation of a stable passive film in the matrix along with its superior density. The improved corrosion resistance of the FGMs promoted cell viability and enhanced alkaline phosphatase activity. The present investigation demonstrates the benefits of increasing the number of layers in the Ti6Al4V-YSZ FGMs fabricated by SPS on the tribo-mechanical, corrosion and biological properties enhancing their potential as promising dental implant materials.</div></div>","PeriodicalId":267,"journal":{"name":"Ceramics International","volume":"52 3","pages":"Pages 3208-3221"},"PeriodicalIF":5.6,"publicationDate":"2026-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145996421","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
Wetting and reactivity of molten AlCoCrFeNi high-entropy alloy on ceramic substrates: A comparative study of Al2O3 and ZrO2 Al2O3和ZrO2对高熵合金在陶瓷基体上的润湿性和反应性的影响
IF 5.6 2区 材料科学 Q1 MATERIALS SCIENCE, CERAMICS Pub Date : 2026-01-01 DOI: 10.1016/j.ceramint.2025.12.114
S. Terlicka , S. Gambaro , M. Janusz-Skuza , L. Fenocchio , F. Valenza
The interfacial behavior between molten AlCoCrFeNi high-entropy alloy (HEA) and oxide ceramics was systematically studied to evaluate, for the first time, how ceramic composition and stoichiometry affect wetting and reactivity. Understanding these interactions is crucial for designing next-generation ceramic-metal composites, high-temperature joining methods, and HEA manufacturing processes, where controlled wetting is vital. Sessile-drop experiments were performed at 1450 °C under vacuum on polycrystalline alumina (Al2O3) and yttria-stabilized zirconia (YSZ) substrates, both in stoichiometric (ZrO2) and oxygen-deficient (ZrO2-x) forms. SEM/TEM analysis of HEA/oxide ceramic interfaces, supported by CALPHAD thermodynamic calculations using an in-house GHEA database, showed that wetting behavior strongly depends on substrate stoichiometry. The HEA partially wet Al2O3 (θf(HEA/Al2O3) ∼ 88°) but did not wet stoichiometric ZrO2 (θf(HEA/ZrO2) ∼ 101°), with no evidence of chemical bonding in either case, indicating that these substrates could be suitable as a possible casting mold for HEA production. In contrast, the non-stoichiometric ZrO2-x substrate promoted reactive wetting (θf(HEA/ZrO2x) ∼ 77°), accompanied by interfacial dissolution and formation of a stable metallurgical bond. This behavior emphasizes the important role of oxygen deficiency in activating interfacial reactions and changing wetting dynamics. Overall, this study offers the first insight into the molten HEA/oxide ceramic interface, demonstrating how ceramic stoichiometry governs the transition from inert to reactive wetting. These results provide a scientific basis for adapting HEA/oxide ceramic interfaces in advanced joining, coating, and composite technologies operating at high temperatures, as well as in HEA production.
系统研究了高熵合金(HEA)与氧化物陶瓷之间的界面行为,首次评价了陶瓷成分和化学计量对润湿性和反应性的影响。了解这些相互作用对于设计下一代陶瓷-金属复合材料、高温连接方法和HEA制造工艺至关重要,其中控制润湿至关重要。在1450°C的真空条件下,在多晶氧化铝(Al2O3)和钇稳定氧化锆(YSZ)衬底上进行了化学计量(ZrO2)和缺氧(ZrO2-x)两种形式的无基滴实验。HEA/氧化物陶瓷界面的SEM/TEM分析,以及CALPHAD使用内部HEA数据库进行的热力学计算,表明润湿行为强烈依赖于衬底化学计量。HEA部分湿润了Al2O3 (θf(HEA/Al2O3) ~ 88°),但没有湿润化学测量的ZrO2 (θf(HEA/ZrO2) ~ 101°),在两种情况下都没有化学结合的证据,表明这些衬底可能适合作为HEA生产的可能的铸造模具。相反,非化学测量的ZrO2-x衬底促进了反应性润湿(θf(HEA/ZrO2−x) ~ 77°),伴随着界面溶解和形成稳定的冶金键。这种行为强调了缺氧在激活界面反应和改变润湿动力学中的重要作用。总的来说,这项研究首次深入了解了熔融HEA/氧化物陶瓷界面,展示了陶瓷化学计量学如何控制从惰性润湿到反应性润湿的转变。这些结果为在高温下的高级连接、涂层和复合技术以及HEA生产中采用HEA/氧化物陶瓷界面提供了科学依据。
{"title":"Wetting and reactivity of molten AlCoCrFeNi high-entropy alloy on ceramic substrates: A comparative study of Al2O3 and ZrO2","authors":"S. Terlicka ,&nbsp;S. Gambaro ,&nbsp;M. Janusz-Skuza ,&nbsp;L. Fenocchio ,&nbsp;F. Valenza","doi":"10.1016/j.ceramint.2025.12.114","DOIUrl":"10.1016/j.ceramint.2025.12.114","url":null,"abstract":"<div><div>The interfacial behavior between molten AlCoCrFeNi high-entropy alloy (HEA) and oxide ceramics was systematically studied to evaluate, for the first time, how ceramic composition and stoichiometry affect wetting and reactivity. Understanding these interactions is crucial for designing next-generation ceramic-metal composites, high-temperature joining methods, and HEA manufacturing processes, where controlled wetting is vital. Sessile-drop experiments were performed at 1450 °C under vacuum on polycrystalline alumina (Al<sub>2</sub>O<sub>3</sub>) and yttria-stabilized zirconia (YSZ) substrates, both in stoichiometric (ZrO<sub>2</sub>) and oxygen-deficient (ZrO<sub>2-x</sub>) forms. SEM/TEM analysis of HEA/oxide ceramic interfaces, supported by CALPHAD thermodynamic calculations using an in-house GHEA database, showed that wetting behavior strongly depends on substrate stoichiometry. The HEA partially wet Al<sub>2</sub>O<sub>3</sub> (<span><math><mrow><msub><mi>θ</mi><msub><mi>f</mi><mrow><mo>(</mo><mrow><mi>H</mi><mi>E</mi><mi>A</mi><mo>/</mo><msub><mrow><mi>A</mi><mi>l</mi></mrow><mn>2</mn></msub><msub><mi>O</mi><mrow><mn>3</mn><mspace></mspace></mrow></msub></mrow><mo>)</mo></mrow></msub></msub></mrow></math></span> ∼ 88°) but did not wet stoichiometric ZrO<sub>2</sub> (<span><math><mrow><msub><msub><mi>θ</mi><mi>f</mi></msub><mrow><mo>(</mo><mrow><mi>H</mi><mi>E</mi><mi>A</mi><mo>/</mo><mi>Z</mi><mi>r</mi><msub><mi>O</mi><mn>2</mn></msub></mrow><mo>)</mo></mrow></msub></mrow></math></span> ∼ 101°), with no evidence of chemical bonding in either case, indicating that these substrates could be suitable as a possible casting mold for HEA production. In contrast, the non-stoichiometric ZrO<sub>2-x</sub> substrate promoted reactive wetting (<span><math><mrow><msub><mi>θ</mi><msub><mi>f</mi><mrow><mo>(</mo><mrow><mi>H</mi><mi>E</mi><mi>A</mi><mo>/</mo><mi>Z</mi><mi>r</mi><msub><mi>O</mi><mrow><mn>2</mn><mo>−</mo><mi>x</mi></mrow></msub></mrow><mo>)</mo></mrow></msub></msub></mrow></math></span> ∼ 77°), accompanied by interfacial dissolution and formation of a stable metallurgical bond. This behavior emphasizes the important role of oxygen deficiency in activating interfacial reactions and changing wetting dynamics. Overall, this study offers the first insight into the molten HEA/oxide ceramic interface, demonstrating how ceramic stoichiometry governs the transition from inert to reactive wetting. These results provide a scientific basis for adapting HEA/oxide ceramic interfaces in advanced joining, coating, and composite technologies operating at high temperatures, as well as in HEA production.</div></div>","PeriodicalId":267,"journal":{"name":"Ceramics International","volume":"52 3","pages":"Pages 3222-3236"},"PeriodicalIF":5.6,"publicationDate":"2026-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145996426","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
Structure-property relationships of AWO4 (A = Na, Li, Ca, Sr, Bi, Sm) microwave dielectric ceramics with different entropy designs 不同熵设计下AWO4 (A = Na, Li, Ca, Sr, Bi, Sm)微波介质陶瓷的结构-性能关系
IF 5.6 2区 材料科学 Q1 MATERIALS SCIENCE, CERAMICS Pub Date : 2026-01-01 DOI: 10.1016/j.ceramint.2025.12.131
Weichen Xu , Xiaomeng Li , Hong Wang , Fuliang Wang , Shouqiang Han , Jing Guo
Microwave dielectric ceramics are critical components in wireless communications. However, it is still a challenge to develop microwave dielectric ceramics with reduced sintering temperatures, high thermal stabilities and good dielectric properties at the same time. Herein, the entropy value, which is able to modulate the grain boundary energy and adjust the inherent sintering temperature, is engineered to develop high-performance microwave dielectric ceramics with low sintering temperatures. The structure-property relationships of AWO4 ceramics, including (NaCaBi)1/3WO4, (NaCaSrBi)1/4WO4, (NaLiCaBiSm)1/5WO4 and (NaLiCaSrBiSm)1/6WO4 with increased entropy values are investigated systematically. X-ray diffraction and high-resolution TEM analyses confirm the formation of single-phase solid solutions with the tetragonal scheelite structure in AWO4 ceramics. As the number of elements in the A-site varies, the relative permittivities, Q × f values and TCF values shift in the range of 12.2–16.5, 8,000–25,000 GHz and −32.3–31.6 ppm/°C, respectively. Simultaneously, the high-entropy samples demonstrate the lowest sintering temperature of 750 °C among the four formulations. Phillips-Van Vechten-Levine (PVL) complex chemical bond theory reveals that the covalency, lattice energy and bond energy affect the relative permittivity, Q × f value and TCF value, respectively. Raman spectra suggest that high entropy value leads to increased disorder, and infrared reflectivity spectra illustrate that the dielectric response is dominated by polarized optical phonons of [WO4] tetrahedron. It is anticipated that entropy design will facilitate the development of microwave dielectric ceramics in low temperature co-fired ceramic applications.
微波介质陶瓷是无线通信中的关键器件。然而,如何同时开发出烧结温度低、热稳定性高、介电性能好的微波介质陶瓷仍是一个挑战。利用能够调制晶界能和调节固有烧结温度的熵值,开发出具有低烧结温度的高性能微波介质陶瓷。系统地研究了(NaCaBi)1/3WO4、(NaCaSrBi)1/4WO4、(NaLiCaBiSm)1/5WO4和(NaLiCaSrBiSm)1/6WO4等AWO4陶瓷在熵值增大时的结构-性能关系。x射线衍射和高分辨率透射电镜分析证实了AWO4陶瓷中形成了具有四方白钨矿结构的单相固溶体。随着a位元素数量的变化,相对介电常数、Q × f值和TCF值分别在12.2 ~ 16.5 GHz、8000 ~ 25000 GHz和- 32.3 ~ 31.6 ppm/°C范围内发生变化。同时,高熵样品的烧结温度最低,为750℃。philips - van veechten - levine (PVL)复合化学键理论揭示共价、晶格能和键能分别影响相对介电常数、Q × f值和TCF值。拉曼光谱表明高熵值导致无序性增加,红外反射率光谱表明介质响应由[WO4]四面体的偏振光学声子主导。预计熵设计将促进微波介质陶瓷在低温共烧陶瓷中的应用。
{"title":"Structure-property relationships of AWO4 (A = Na, Li, Ca, Sr, Bi, Sm) microwave dielectric ceramics with different entropy designs","authors":"Weichen Xu ,&nbsp;Xiaomeng Li ,&nbsp;Hong Wang ,&nbsp;Fuliang Wang ,&nbsp;Shouqiang Han ,&nbsp;Jing Guo","doi":"10.1016/j.ceramint.2025.12.131","DOIUrl":"10.1016/j.ceramint.2025.12.131","url":null,"abstract":"<div><div>Microwave dielectric ceramics are critical components in wireless communications. However, it is still a challenge to develop microwave dielectric ceramics with reduced sintering temperatures, high thermal stabilities and good dielectric properties at the same time. Herein, the entropy value, which is able to modulate the grain boundary energy and adjust the inherent sintering temperature, is engineered to develop high-performance microwave dielectric ceramics with low sintering temperatures. The structure-property relationships of AWO<sub>4</sub> ceramics, including (NaCaBi)<sub>1/3</sub>WO<sub>4</sub>, (NaCaSrBi)<sub>1/4</sub>WO<sub>4</sub>, (NaLiCaBiSm)<sub>1/5</sub>WO<sub>4</sub> and (NaLiCaSrBiSm)<sub>1/6</sub>WO<sub>4</sub> with increased entropy values are investigated systematically. X-ray diffraction and high-resolution TEM analyses confirm the formation of single-phase solid solutions with the tetragonal scheelite structure in AWO<sub>4</sub> ceramics. As the number of elements in the A-site varies, the relative permittivities, <em>Q</em> × <em>f</em> values and <em>TCF</em> values shift in the range of 12.2–16.5, 8,000–25,000 GHz and −32.3–31.6 ppm/°C, respectively. Simultaneously, the high-entropy samples demonstrate the lowest sintering temperature of 750 °C among the four formulations. Phillips-Van Vechten-Levine (PVL) complex chemical bond theory reveals that the covalency, lattice energy and bond energy affect the relative permittivity, <em>Q</em> × <em>f</em> value and <em>TCF</em> value, respectively. Raman spectra suggest that high entropy value leads to increased disorder, and infrared reflectivity spectra illustrate that the dielectric response is dominated by polarized optical phonons of [WO<sub>4</sub>] tetrahedron. It is anticipated that entropy design will facilitate the development of microwave dielectric ceramics in low temperature co-fired ceramic applications.</div></div>","PeriodicalId":267,"journal":{"name":"Ceramics International","volume":"52 3","pages":"Pages 3389-3398"},"PeriodicalIF":5.6,"publicationDate":"2026-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145996472","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
Space environment properties of Al2O3f/Al2O3 composites Al2O3f/Al2O3复合材料的空间环境性能
IF 5.6 2区 材料科学 Q1 MATERIALS SCIENCE, CERAMICS Pub Date : 2026-01-01 DOI: 10.1016/j.ceramint.2025.12.138
Jiang Bin-zhi , Xiang Yang , Mo Chen , Peng Zhi-hang , Wen Jin , Cao Jian-ping , Li Hai-long
Continuous alumina fiber-reinforced alumina matrix composites (Al2O3f/Al2O3 composites) were fabricated via a precursor infiltration and pyrolysis (PIP) route. The effects of simulated space environments— thermal vacuum, thermal cycling, and total-dose irradiation— on the microstructure and mechanical properties were systematically evaluated. After exposure, the composite flexural strength dropped by 75 %, 76 %, and 86 %, respectively, while the tensile strength of individual alumina fibers decreased by 36.3 %, 27.0 %, and 21.6 %. XRD, SEM, and XPS analyses suggest increased crystallinity, surface cracking, and matrix fragmentation that weaken fiber/matrix interfacial integrity, thereby degrading flexural performance.
采用前驱体渗透热解(PIP)法制备了连续氧化铝纤维增强氧化铝基复合材料(Al2O3f/Al2O3复合材料)。系统评估了模拟空间环境(热真空、热循环和总剂量辐照)对微结构和力学性能的影响。暴露后,复合材料的抗弯强度分别下降了75%、76%和86%,而单个氧化铝纤维的抗拉强度分别下降了36.3%、27.0%和21.6%。XRD、SEM和XPS分析表明,结晶度增加、表面开裂和基体碎裂削弱了纤维/基体界面的完整性,从而降低了抗弯性能。
{"title":"Space environment properties of Al2O3f/Al2O3 composites","authors":"Jiang Bin-zhi ,&nbsp;Xiang Yang ,&nbsp;Mo Chen ,&nbsp;Peng Zhi-hang ,&nbsp;Wen Jin ,&nbsp;Cao Jian-ping ,&nbsp;Li Hai-long","doi":"10.1016/j.ceramint.2025.12.138","DOIUrl":"10.1016/j.ceramint.2025.12.138","url":null,"abstract":"<div><div>Continuous alumina fiber-reinforced alumina matrix composites (Al<sub>2</sub>O<sub>3f</sub>/Al<sub>2</sub>O<sub>3</sub> composites) were fabricated via a precursor infiltration and pyrolysis (PIP) route. The effects of simulated space environments— thermal vacuum, thermal cycling, and total-dose irradiation— on the microstructure and mechanical properties were systematically evaluated. After exposure, the composite flexural strength dropped by 75 %, 76 %, and 86 %, respectively, while the tensile strength of individual alumina fibers decreased by 36.3 %, 27.0 %, and 21.6 %. XRD, SEM, and XPS analyses suggest increased crystallinity, surface cracking, and matrix fragmentation that weaken fiber/matrix interfacial integrity, thereby degrading flexural performance.</div></div>","PeriodicalId":267,"journal":{"name":"Ceramics International","volume":"52 3","pages":"Pages 3470-3480"},"PeriodicalIF":5.6,"publicationDate":"2026-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145996510","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
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Ceramics International
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