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Dual strategy to enhance the nitridation resistance of MoSi2-based ceramics for high-temperature applications 提高高温mosi2基陶瓷耐氮化性能的双重策略
IF 6.2 2区 材料科学 Q1 MATERIALS SCIENCE, CERAMICS Pub Date : 2026-01-18 DOI: 10.1016/j.jeurceramsoc.2026.118155
Lu Zhu , Nana Zhu , Pengju Tang , Baojing Zhang , Shengyuan Lei , Xiaohong Wang , Peizhong Feng
MoSi2‑based ceramics with superior high‑temperature nitridation resistance were developed through a dual strategy combining Al alloying and pre‑oxidation. A two-step route, self-propagating high-temperature synthesis followed by spark plasma sintering, was employed to prepare MoSi2 and Al-alloyed Mo(Si0.95Al0.05)2. Al incorporation and pre‑oxidation at 1500 °C produced dense Al–Si–O composite scales that merged the impermeability of SiO2 with the thermal stability of Al2O3. During direct nitridation at 1200 °C, the nitrogen diffusion coefficients of Mo(Si0.95Al0.05)2 decreased by 76% and 82% in the rapid (0–16 h) and slow (16–64 h) stages, and its overall mass change was much lower than that of MoSi2. Pre‑oxidation further enhanced protection, reducing diffusion coefficients to 0.005 and 0.001 mg/cm2·h0.5 compared with MoSi2 (0.007 and 0.004 mg/cm2·h0.5), due to the formation of stable Al–Si–O scales. Therefore, the pioneering dual strategy demonstrates a novel approach for developing advanced MoSi2-based ceramics with outstanding high-temperature nitridation resistance.
采用Al合金化和预氧化相结合的双重策略制备了具有优异耐高温氮化性能的MoSi2基陶瓷。采用自蔓延高温合成-火花等离子烧结两步法制备了MoSi2和Mo(Si0.95Al0.05)2铝合金。在1500℃下,Al掺入和预氧化产生了致密的Al - si - o复合鳞片,将SiO2的不渗透性与Al2O3的热稳定性结合在一起。在1200℃直接硝化过程中,Mo(Si0.95Al0.05)2的氮扩散系数在快速(0 ~ 16 h)和慢速(16 ~ 64 h)阶段分别下降了76%和82%,其总体质量变化量远低于MoSi2。预氧化进一步增强了保护作用,与MoSi2(0.007和0.004 mg/cm2·h0.5)相比,扩散系数降低到0.005和0.001 mg/cm2·h0.5,这是由于形成了稳定的Al-Si-O鳞片。因此,开创性的双重策略为开发具有优异耐高温氮化性能的先进mosi2基陶瓷提供了一种新方法。
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引用次数: 0
Giant piezoelectric properties in hard-type PMNN-PZT ceramics via templated grain growth using BZT templates 利用BZT模板在硬型PMNN-PZT陶瓷中模板化晶粒生长制备巨压电特性
IF 6.2 2区 材料科学 Q1 MATERIALS SCIENCE, CERAMICS Pub Date : 2026-01-17 DOI: 10.1016/j.jeurceramsoc.2026.118143
Jae-Min Cha , Cheol-Woo Ahn , Hyun-Ae Cha , Byung-Dong Hahn , Woon-Ha Yoon , Young Kook Moon , Seog-Young Yoon , Jong-Jin Choi
Textured Pb[(Mg0.5Ni0.5)1/3Nb2/3]O3-PbZrTiO3 (PMNN–PZT) piezoelectric ceramics were fabricated by the templated grain growth (TGG) method. Plate-like Ba(Zr0.1Ti0.9)O3 (BZT) templates were synthesized by topochemical molten salt synthesis (TMSS) and employed to promote grain orientation. Compared with conventional BaTiO3 (BT) templates, BZT templates exhibited lower reactivity with the matrix, resulting in a reduced tetragonal phase shift and a higher Lotgering factor after texturing. The phase composition of PMNN–PZT was further optimized to the morphotropic phase boundary (MPB) region by adjusting the Zr/Ti ratio. The textured ceramics thus obtained exhibited both a high piezoelectric charge coefficient (d₃₃ ∼ 610 pC/N) and a high mechanical quality factor (Qm ∼1145), overcoming the typical trade-off between these properties. These findings demonstrate that BZT templating is an effective strategy for tailoring phase composition and enhancing the electromechanical performance of textured piezoelectric ceramics.
采用模板晶粒生长(TGG)法制备了Pb[(Mg0.5Ni0.5)1/3Nb2/3]O3-PbZrTiO3 (PMNN-PZT)织构压电陶瓷。采用拓扑化学熔盐合成法(TMSS)合成了Ba(Zr0.1Ti0.9)O3 (BZT)板状模板,并利用其促进晶粒取向。与传统的BaTiO3 (BT)模板相比,BZT模板与基体的反应性较低,导致织构后四方相移减少,Lotgering因子更高。通过调整Zr/Ti比,进一步将PMNN-PZT的相组成优化到嗜形相边界(MPB)区域。由此获得的织构陶瓷具有高压电电荷系数(d₃₃~ 610 pC/N)和高机械质量因子(Qm ~ 1145),克服了这些特性之间的典型权衡。这些结果表明,BZT模板是一种有效的策略,以定制相组成和提高机电性能的织构压电陶瓷。
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引用次数: 0
Enhancing the spectral selectivity of MgTiO3 via Mn doping for high temperature solar thermal conversion Mn掺杂提高MgTiO3在高温太阳热转换中的光谱选择性
IF 6.2 2区 材料科学 Q1 MATERIALS SCIENCE, CERAMICS Pub Date : 2026-01-17 DOI: 10.1016/j.jeurceramsoc.2026.118152
Ziqin Lin , Tianxia Xie , Zhuolin Xie , Anqi Dai , Yang Yuan , Peng Sun , Yanqi Song , Zhenggang Fang , Chunhua Lu
Solar absorbers are vital for concentrated solar power (CSP) systems, yet spectral selectivity solar absorbers (SSAs) struggle with high-temperature stability in air. This study introduced Mn ions into MgTiO3 (MTO) via a high temperature solid-phase synthesis technique to optimize the spectral selectivity. Unlike conventional doping that increased both absorptance and emittance, MgTi0.4Mn0.6O3 (MTMO-0.6) boosted solar absorptance (α = 0.85) while maintaining low emittance (ε = 0.39, 1073.15 K) in the 2.5–15 μm wavelength range. Besides, the material retained high spectral selectivity (α/ε = 0.84/0.41) after heat treatment at 800 °C in air atmosphere for 90 h in total (9 h cycles−1, 10 cycles), showing excellent thermal stability. Moreover, under concentrated solar irradiation of 10.83 W·cm−2, MTMO-0.6 sample reached an equilibrium temperature of 848 ℃, surpassing that of MTO and SiC. The proposed Mn-doped MgTiO3 has the potential as a solar absorber for high temperature solar thermal conversion.
太阳能吸收体对于聚光太阳能发电(CSP)系统至关重要,但光谱选择性太阳能吸收体在空气中的高温稳定性方面存在问题。本研究通过高温固相合成技术将Mn离子引入到MgTiO3 (MTO)中,以优化其光谱选择性。与常规掺杂提高吸收度和发射度不同,MgTi0.4Mn0.6O3 (MTMO-0.6)在2.5 ~ 15 μm波长范围内提高了太阳吸收率(α = 0.85),同时保持了较低的发射度(ε = 0.39, 1073.15 K)。此外,材料在800℃空气中热处理90 h(9 h循环- 1,10循环)后,仍保持较高的光谱选择性(α/ε = 0.84/0.41),表现出优异的热稳定性。此外,在10.83 W·cm−2的太阳辐照下,MTMO-0.6样品达到了848℃的平衡温度,超过了MTO和SiC。所提出的mn掺杂MgTiO3具有作为高温太阳能热转换的太阳能吸收剂的潜力。
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引用次数: 0
Environmental-friendly gray glaze with photonic micro-nanostructure 具有光子微纳米结构的环保型灰色釉料
IF 6.2 2区 材料科学 Q1 MATERIALS SCIENCE, CERAMICS Pub Date : 2026-01-17 DOI: 10.1016/j.jeurceramsoc.2026.118153
Haiyong Li , Hongquan Zhan , Pan Liu , Xuewen Han , Mengjun Liu , Rongting Pan , Chang-an Wang
This paper aims to address the preparation and structural coloring mechanism of an environmental-friendly gray glaze with photonic micro-nanostructure. Based on the results of XRD, SEM, TEM and EDS, it can be concluded that the special separated network structure with a FeZnTiO4-rich crystal phase and a Si-/Ca-rich glassy phase can be formed in glaze layer. Due to the introduction of Fe2O3, the separated crystal phase displays an urchin-like microstructure. Therefore, under the action of this photonic structure, the desirable gray glaze can be obtained. In addition, the gray glaze exhibits excellent optical property of angle-independency, overcoming the disadvantage of angular dependency of ordered photonic crystals. The more performances about stain resistance and corrosion resistance show its great potential application in daily use. This study provides a new idea for the development of environmental-friendly glazes by the design of photonic structures.
本文旨在研究一种具有光子微纳结构的环保型灰色釉的制备及其结构着色机理。XRD、SEM、TEM和EDS分析结果表明,釉层形成了富fezntio4晶相和富Si / ca玻璃相的特殊分离网络结构。由于Fe2O3的引入,分离的晶相呈现出海胆状的微观结构。因此,在这种光子结构的作用下,可以得到理想的灰釉。此外,该灰釉具有良好的不依赖角度的光学特性,克服了有序光子晶体依赖角度的缺点。其耐污、耐腐蚀性能显示出其在日常应用中的巨大潜力。本研究为利用光子结构设计开发环境友好型釉料提供了新的思路。
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引用次数: 0
FORC applications in BaTiO₃-based ferroelectric materials and related capacitors FORC在BaTiO₃基铁电材料及相关电容器中的应用
IF 6.2 2区 材料科学 Q1 MATERIALS SCIENCE, CERAMICS Pub Date : 2026-01-16 DOI: 10.1016/j.jeurceramsoc.2026.118149
Tian Wang , Jingyi Hao , Lei Zhang , Min Chen , Yanna Cheng , Feng Yu , Jianfeng Li , Yiting Guo , Haixia Liu
BaTiO₃(BT)-based ferroelectric materials are pivotal for high-energy-density capacitors, However, their performance is limited by high remanent polarization and associated hysteresis losses. Traditional characterization methods often fail to resolve local polarization behaviors, which hinders the rational design of materials with enhanced energy storage properties. This review highlights the necessity and advancement of the First-Order Reversal Curve (FORC) technique. Based on the Preisach model, FORC analysis is effective in disentangling reversible and irreversible polarization contributions at the microstructural level. We systematically summarize its recent applications in BT-based ceramics, thin films, and multilayer ceramic capacitors (MLCCs), focusing on composition design, grain and domain engineering, defect control, and interface optimization. The FORC method offers insights into the relationships between dynamic domain switching and energy storage properties, thereby enabling targeted improvements in energy density and efficiency. This review underscores the critical role of FORC in guiding the development of next-generation ferroelectric energy storage devices.
BaTiO₃(BT)基铁电材料是高能量密度电容器的关键,然而,它们的性能受到高剩余极化和相关滞后损失的限制。传统的表征方法往往不能解决局部极化行为,这阻碍了增强储能性能材料的合理设计。本文综述了一阶反转曲线(FORC)技术的必要性和进展。基于Preisach模型,FORC分析在微观结构水平上可以有效地分离可逆和不可逆极化贡献。我们系统地总结了其在bt基陶瓷、薄膜和多层陶瓷电容器(mlcc)中的最新应用,重点是成分设计、晶粒和畴工程、缺陷控制和界面优化。FORC方法提供了动态域切换和能量存储特性之间关系的见解,从而能够有针对性地提高能量密度和效率。这篇综述强调了FORC在指导下一代铁电储能装置发展中的关键作用。
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引用次数: 0
Controlling sinterability and phase evolution in pyrochlore glass-ceramics via cationic radius ratio (rA/rB) for nuclear waste forms 利用放射性废物形态的阳离子半径比(rA/rB)控制焦绿石微晶玻璃的烧结性和相演化
IF 6.2 2区 材料科学 Q1 MATERIALS SCIENCE, CERAMICS Pub Date : 2026-01-16 DOI: 10.1016/j.jeurceramsoc.2026.118151
Hongru Jin, Ce Zheng, Yichun Bi, Zili Liu, Shengkai Wang, Xiaoqiang Li
Pyrochlore glass-ceramics are promising materials for nuclear waste immobilization, in which Zr⁴⁺ substitution for Ti⁴⁺ is known to enhance radiation resistance. However, high levels of Zr4 + substitution increase cation disorder, elevating the energy barrier for crystallization and posing synthesis challenge. In this study, the cation disorder in the pyrochlore structure was controlled by tuning the rA/rB ratio in Gd2-xLnxTi2-yZryO7 (LnNd, Dy, and Y) glass-ceramics. The results indicate that B-site Zr⁴⁺ substitution decreases the rA/rB ratio, leading to higher activation energy and impairing sinterability. In contrast, A-site Nd³⁺ substitution increases the rA/rB ratio, effectively mitigating these adverse effects and enabling sintering at lower temperatures. The phase composition was precisely regulated by the rA/rB ratio, progressing through four distinct stages: monoclinic, pyrochlore, coexisting pyrochlore/defect-fluorite, and defect-fluorite, showing a linear correlation between pyrochlore content and rA/rB. This work successfully demonstrates rA/rB regulation for fabricating advanced Zr4+-substituted glass-ceramic waste forms.
焦绿石微晶玻璃是很有前途的核废料固定化材料,其中Zr⁴⁺取代Ti⁴⁺已知可以增强抗辐射性。然而,高水平的Zr4 +取代增加了阳离子的无序性,提高了结晶的能量势垒,给合成带来了挑战。在本研究中,通过调节Gd2-xLnxTi2-yZryO7 (LnNd, Dy, Y)玻璃陶瓷中的rA/rB比,控制了焦绿石结构中的阳离子无序性。结果表明,b位Zr⁴⁺的取代降低了rA/rB比,导致活化能升高,降低了烧结性能。相比之下,a位Nd³取代增加了rA/rB比,有效地减轻了这些不利影响,并使烧结能在更低的温度下进行。相组成受rA/rB比值的精确调控,经历单斜、焦绿石、焦绿石/缺陷萤石共存、缺陷萤石4个阶段,焦绿石含量与rA/rB呈线性相关。这项工作成功地证明了rA/rB调控用于制造先进的Zr4+取代玻璃陶瓷废料。
{"title":"Controlling sinterability and phase evolution in pyrochlore glass-ceramics via cationic radius ratio (rA/rB) for nuclear waste forms","authors":"Hongru Jin,&nbsp;Ce Zheng,&nbsp;Yichun Bi,&nbsp;Zili Liu,&nbsp;Shengkai Wang,&nbsp;Xiaoqiang Li","doi":"10.1016/j.jeurceramsoc.2026.118151","DOIUrl":"10.1016/j.jeurceramsoc.2026.118151","url":null,"abstract":"<div><div>Pyrochlore glass-ceramics are promising materials for nuclear waste immobilization, in which Zr⁴⁺ substitution for Ti⁴⁺ is known to enhance radiation resistance. However, high levels of Zr<sup>4 +</sup> substitution increase cation disorder, elevating the energy barrier for crystallization and posing synthesis challenge. In this study, the cation disorder in the pyrochlore structure was controlled by tuning the r<sub>A</sub>/r<sub>B</sub> ratio in Gd<sub>2-x</sub>Ln<sub>x</sub>Ti<sub>2-y</sub>Zr<sub>y</sub>O<sub>7</sub> (Ln<img>Nd, Dy, and Y) glass-ceramics. The results indicate that B-site Zr⁴⁺ substitution decreases the r<sub>A</sub>/r<sub>B</sub> ratio, leading to higher activation energy and impairing sinterability. In contrast, A-site Nd³⁺ substitution increases the r<sub>A</sub>/r<sub>B</sub> ratio, effectively mitigating these adverse effects and enabling sintering at lower temperatures. The phase composition was precisely regulated by the r<sub>A</sub>/r<sub>B</sub> ratio, progressing through four distinct stages: monoclinic, pyrochlore, coexisting pyrochlore/defect-fluorite, and defect-fluorite, showing a linear correlation between pyrochlore content and r<sub>A</sub>/r<sub>B</sub>. This work successfully demonstrates r<sub>A</sub>/r<sub>B</sub> regulation for fabricating advanced Zr<sup>4+</sup>-substituted glass-ceramic waste forms.</div></div>","PeriodicalId":17408,"journal":{"name":"Journal of The European Ceramic Society","volume":"46 8","pages":"Article 118151"},"PeriodicalIF":6.2,"publicationDate":"2026-01-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146036912","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
Scalable single-step fabrication of high-entropy oxide coatings by axial solution precursor plasma spray 轴向溶液前驱体等离子喷涂可扩展单步制备高熵氧化物涂层
IF 6.2 2区 材料科学 Q1 MATERIALS SCIENCE, CERAMICS Pub Date : 2026-01-16 DOI: 10.1016/j.jeurceramsoc.2026.118150
Gidla Vinay , Stefan Björklund , Ilari Angervo , Ashish Ganvir , Shrikant Joshi
High-entropy oxides (HEOs) are promising for energy and structural applications, yet conventional synthesis routes yield powders that require multiple post-processing steps before use. This study demonstrates single-step fabrication of a transition-metal HEO coating via axial-fed solution precursor plasma spraying (SPPS) using equimolar Co-Cu-Mg-Ni-Zn nitrate hydrates. The resulting coatings are dense, adherent, and phase-pure, exhibiting a rock-salt structure confirmed by XRD, uniform cation distribution by SEM/EDS, and oxidized cations with oxygen-vacancy signatures by XPS. Comparative analysis of different spray conditions shows that phase purity and microstructure are governed by atomization and in-flight residence time, rather than plasma energy alone. The findings establish that suitable parameter control enables complete cation mixing and rapid in-flight phase formation without post-processing. This single-step route from solution to functional coatings provides a scalable pathway for HEO manufacture, with potential applications ranging from battery electrodes to high-temperature thermal and environmental barrier coatings (TBCs/EBCs) across different HEO families.
高熵氧化物(HEOs)在能源和结构应用方面前景广阔,但传统的合成路线产生的粉末在使用前需要多个后处理步骤。本研究利用等摩尔的Co-Cu-Mg-Ni-Zn硝酸盐水合物,通过轴向供给溶液前驱体等离子喷涂(SPPS)一步制备过渡金属HEO涂层。结果表明,该涂层具有致密、黏附、相纯的特点,XRD证实其为岩盐结构,SEM/EDS证实其阳离子分布均匀,XPS证实其为具有氧空位特征的氧化阳离子。对不同喷射条件的对比分析表明,相纯度和微观结构受雾化和飞行停留时间的影响,而不仅仅受等离子体能量的影响。研究结果表明,适当的参数控制可以实现完全的阳离子混合和快速的飞行相形成,而无需后处理。这种从溶液到功能涂层的单步路线为HEO制造提供了一种可扩展的途径,其潜在应用范围从电池电极到不同HEO家族的高温热障和环境屏障涂层(tbc / ebc)。
{"title":"Scalable single-step fabrication of high-entropy oxide coatings by axial solution precursor plasma spray","authors":"Gidla Vinay ,&nbsp;Stefan Björklund ,&nbsp;Ilari Angervo ,&nbsp;Ashish Ganvir ,&nbsp;Shrikant Joshi","doi":"10.1016/j.jeurceramsoc.2026.118150","DOIUrl":"10.1016/j.jeurceramsoc.2026.118150","url":null,"abstract":"<div><div>High-entropy oxides (HEOs) are promising for energy and structural applications, yet conventional synthesis routes yield powders that require multiple post-processing steps before use. This study demonstrates single-step fabrication of a transition-metal HEO coating via axial-fed solution precursor plasma spraying (SPPS) using equimolar Co-Cu-Mg-Ni-Zn nitrate hydrates. The resulting coatings are dense, adherent, and phase-pure, exhibiting a rock-salt structure confirmed by XRD, uniform cation distribution by SEM/EDS, and oxidized cations with oxygen-vacancy signatures by XPS. Comparative analysis of different spray conditions shows that phase purity and microstructure are governed by atomization and in-flight residence time, rather than plasma energy alone. The findings establish that suitable parameter control enables complete cation mixing and rapid in-flight phase formation without post-processing. This single-step route from solution to functional coatings provides a scalable pathway for HEO manufacture, with potential applications ranging from battery electrodes to high-temperature thermal and environmental barrier coatings (TBCs/EBCs) across different HEO families.</div></div>","PeriodicalId":17408,"journal":{"name":"Journal of The European Ceramic Society","volume":"46 8","pages":"Article 118150"},"PeriodicalIF":6.2,"publicationDate":"2026-01-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145986745","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
Giant strain vanishes in multilayer ceramics: The limitation of defect-dipole engineering 大应变在多层陶瓷中消失:缺陷偶极子工程的局限性
IF 6.2 2区 材料科学 Q1 MATERIALS SCIENCE, CERAMICS Pub Date : 2026-01-15 DOI: 10.1016/j.jeurceramsoc.2026.118147
Chengming Li , Lang Bian , Jianhui Jia , Shangpeng Yang , Kai Li , Pengrong Ren
The introduction of oxygen vacancies and defect dipoles to induce giant bending strain is a cutting-edge strategy to improve the performance of piezoelectric ceramics. However, its feasibility in a more widely used multi-layer structure is still unknown. In this study, it is found that the giant strain successfully achieved in single-layer ceramics almost disappeared in multi-layer ceramics based on the same material system. The system analysis shows that the internal mechanical clamping effect introduced by the multi-layer structure and the opposite bending direction between adjacent layers are the root causes of large strain failure. The conclusion of this study clearly points out that the excellent piezoelectric properties in unconstrained single-layer samples cannot be directly converted into the actual advantages of multi-layer devices. This finding provides a crucial application perspective correction for the current popular defect engineering research.
引入氧空位和缺陷偶极子诱导巨大弯曲应变是提高压电陶瓷性能的前沿策略。然而,它在更广泛应用的多层结构中的可行性仍然是未知的。本研究发现,基于相同材料体系的多层陶瓷中,单层陶瓷中成功实现的巨应变几乎消失。系统分析表明,多层结构引入的内部机械夹紧效应和相邻层间相反的弯曲方向是造成大应变破坏的根本原因。本研究的结论清楚地指出,无约束单层样品优异的压电性能并不能直接转化为多层器件的实际优势。这一发现为当前流行的缺陷工程研究提供了重要的应用视角修正。
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引用次数: 0
Porous alumina ceramics with integrated open and closed pores synthesized from thermal-oxidation of colloidal assembled aluminum particles via freeze casting 由胶体组装铝颗粒通过冷冻铸造热氧化合成具有开孔和闭孔集成的多孔氧化铝陶瓷
IF 6.2 2区 材料科学 Q1 MATERIALS SCIENCE, CERAMICS Pub Date : 2026-01-13 DOI: 10.1016/j.jeurceramsoc.2026.118146
Wenhao Li , Renhong Gan , Jiuhao You , Zhuoran Li , Xiaoyan Zhang
Hierarchically porous ceramics featuring aligned pores and pore walls assembled from hollow microspheres were fabricated via a novel processing route. Initially, pre-oxidized metallic aluminum solid microspheres were dispersed in a tert-butanol-based suspension, which was subsequently subjected to freeze casting and thermal treatment. This process resulted in the formation of oriented pores together with in situ generated hollow microspheres. The hierarchical pore structure consists of aligned channels (14.5 μm in diameter) produced by solvent sublimation, and closed pores (around 2.2 μm in diameter) formed through a Kirkendall-effect-driven hollowing transformation. The obtained porous ceramics exhibit favorable characteristics, including a sintering expansion of 2.80 %, high porosity, and enhanced compressive strength. By optimizing the sintering temperature and heating rate, porous alumina ceramics with a porosity of 67.8 % and a compressive strength of 64.75 MPa were achieved. These materials show promising potential for applications requiring lightweight structures without compromising mechanical performance.
通过一种新的工艺路线制备了由空心微球组装而成的具有排列孔和孔壁的分层多孔陶瓷。首先,将预氧化金属铝固体微球分散在基于叔丁醇的悬浮液中,随后进行冷冻铸造和热处理。这一过程导致了定向孔的形成以及原位生成的空心微球的形成。层次化孔隙结构由溶剂升华形成的排列通道(直径14.5 μm)和kirkendall效应驱动的中空转化形成的封闭孔隙(直径约2.2 μm)组成。制备的多孔陶瓷具有良好的烧结膨胀率为2.80 %,孔隙率高,抗压强度增强等特点。通过优化烧结温度和升温速率,可制得孔隙率为67.8% %、抗压强度为64.75 MPa的多孔氧化铝陶瓷。这些材料在不影响机械性能的轻型结构应用中显示出很大的潜力。
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引用次数: 0
Tailoring the Hf/(Ti+Ta) ratio to achieve synergistic oxide-induced ablation resistance in C/C-(Hf, Ti, Ta)C-SiC composites 调整Hf/(Ti+Ta)比例,在C/C-(Hf, Ti, Ta)C- sic复合材料中实现协同抗氧化烧蚀
IF 6.2 2区 材料科学 Q1 MATERIALS SCIENCE, CERAMICS Pub Date : 2026-01-12 DOI: 10.1016/j.jeurceramsoc.2026.118145
Qianqian Fan , Yanqin Fu , Fan Zhou , Junhao Zhao , Xue Li , Yuxin Li , Qingzhe Cui , Pei Wang , Yulei Zhang
Despite the improved ablation resistance offered by Hf-based ultra-high temperature ceramics (UHTCs) in carbon/carbon (C/C) composites, the porous oxide scales formed during ablation limits their long-term thermal stability, hindering advanced application. Herein, this work proposed the incorporation of Hf/Ti+Ta with varying molar ratios into C/C composites via reactive melt infiltration, and the resulting multi-component oxides after ablation promoted the formation of a dense oxide layer, thereby improving long-term ablation performance. The finding reveals that all samples were relatively dense and exhibited an identical layered structure around carbon fibers. Notably, the composites with a Hf/Ti/Ta molar ratio of 8:2:1 (8-HTT) exhibited superior ablation resistance, owing to the formation of a dense, adherent surface oxide layer, consisting of (Hf, Ti, Ta)O2 and HfTiO4. As the ablation duration increased to 240 s, the linear ablation rate for 8-HTT decreased to 0.7 μm/s, which was attributed to the self-healing effect enabled by low-melting-point oxide Hf6Ta2O17. This work establishes a theoretical foundation and optimization strategy for designing high-performance ablation-resistant C/C composites for extreme thermal environments.
尽管高频基超高温陶瓷(UHTCs)在碳/碳(C/C)复合材料中提供了更好的抗烧蚀性能,但烧蚀过程中形成的多孔氧化层限制了其长期热稳定性,阻碍了其进一步应用。本文提出通过反应熔融渗透将不同摩尔比的Hf/Ti+Ta掺入C/C复合材料中,烧蚀后形成的多组分氧化物促进了致密氧化物层的形成,从而提高了长期烧蚀性能。这一发现表明,所有的样品都相对致密,并且在碳纤维周围呈现出相同的层状结构。值得注意的是,Hf/Ti/Ta摩尔比为8:2:1 (8-HTT)的复合材料具有优异的抗烧蚀性能,这是由于表面形成了致密的氧化层,由(Hf, Ti, Ta)O2和HfTiO4组成。当烧蚀时间增加到240 s时,8-HTT的线性烧蚀速率降低到0.7 μm/s,这是由于低熔点氧化物Hf6Ta2O17的自愈作用。本研究为设计高性能抗烧蚀C/C复合材料在极端热环境中的应用奠定了理论基础和优化策略。
{"title":"Tailoring the Hf/(Ti+Ta) ratio to achieve synergistic oxide-induced ablation resistance in C/C-(Hf, Ti, Ta)C-SiC composites","authors":"Qianqian Fan ,&nbsp;Yanqin Fu ,&nbsp;Fan Zhou ,&nbsp;Junhao Zhao ,&nbsp;Xue Li ,&nbsp;Yuxin Li ,&nbsp;Qingzhe Cui ,&nbsp;Pei Wang ,&nbsp;Yulei Zhang","doi":"10.1016/j.jeurceramsoc.2026.118145","DOIUrl":"10.1016/j.jeurceramsoc.2026.118145","url":null,"abstract":"<div><div>Despite the improved ablation resistance offered by Hf-based ultra-high temperature ceramics (UHTCs) in carbon/carbon (C/C) composites, the porous oxide scales formed during ablation limits their long-term thermal stability, hindering advanced application. Herein, this work proposed the incorporation of Hf/Ti+Ta with varying molar ratios into C/C composites via reactive melt infiltration, and the resulting multi-component oxides after ablation promoted the formation of a dense oxide layer, thereby improving long-term ablation performance. The finding reveals that all samples were relatively dense and exhibited an identical layered structure around carbon fibers. Notably, the composites with a Hf/Ti/Ta molar ratio of 8:2:1 (8-HTT) exhibited superior ablation resistance, owing to the formation of a dense, adherent surface oxide layer, consisting of (Hf, Ti, Ta)O<sub>2</sub> and HfTiO<sub>4</sub>. As the ablation duration increased to 240 s, the linear ablation rate for 8-HTT decreased to 0.7 μm/s, which was attributed to the self-healing effect enabled by low-melting-point oxide Hf<sub>6</sub>Ta<sub>2</sub>O<sub>17</sub>. This work establishes a theoretical foundation and optimization strategy for designing high-performance ablation-resistant C/C composites for extreme thermal environments.</div></div>","PeriodicalId":17408,"journal":{"name":"Journal of The European Ceramic Society","volume":"46 8","pages":"Article 118145"},"PeriodicalIF":6.2,"publicationDate":"2026-01-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146036563","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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Journal of The European Ceramic Society
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