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Synergistic enhancement of thermoelectric performance in n-type Sb2Te3 alloyed PbTe via I/Ge co-doping I/Ge共掺杂对n型Sb2Te3合金PbTe热电性能的协同增强
IF 6.2 2区 材料科学 Q1 MATERIALS SCIENCE, CERAMICS Pub Date : 2026-02-04 DOI: 10.1016/j.jeurceramsoc.2026.118212
Xinyu Wang , Ruipeng Wang , Jianli Jiang , Haining Meng , Haigang Hou , Jian Yang , Guiwu Liu , Guanjun Qiao
PbTe-based thermoelectric materials are promising for mid-temperature waste heat recovery, yet n-type PbTe underperforms its p-type counterpart. Herein, high-performance n-type PbTe is achieved through I/Ge co-doping and in-situ composite engineering with Sb2Te3 prepared by melting combined spark plasma sintering. Sb2Te3 alloying introduce in-situ formed Sb/Sb2Te3 precipitates. Furthermore, iodine doping optimizes the carrier concentration to ∼3.4 × 1019 cm–3, boosting the room-temperature electrical conductivity to ∼1404 S cm−1 and yielding a high power factor of ∼17.4 μW cm−1 K−2 for the PbTe-Sb2Te3 sample. Meanwhile, lattice thermal conductivity is synergistically suppressed to ∼0.37 W m–1 K–1 at 673 K through Ge-induced point defects/off-center anharmonicity and Sb/Sb2Te3 precipitates. This synergistic strategy results in a peak ZT of ∼1.30 at 823 K and a high average ZT of ∼0.91 at 323–823 K. This work demonstrates that synergistic I/Ge co-doping and composite precipitation effectively enhance thermoelectric performance in n-type PbTe.
基于PbTe的热电材料有望用于中温废热回收,但n型PbTe的性能不如p型。本文通过I/Ge共掺杂和原位复合工程,以熔融组合火花等离子烧结法制备Sb2Te3,实现了高性能n型PbTe。Sb2Te3合金引入原位形成的Sb/Sb2Te3相。此外,碘掺杂将载流子浓度优化到~ 3.4 × 1019 cm - 3,将PbTe-Sb2Te3样品的室温电导率提高到~ 1404 S cm - 1,并产生了~ 17.4 μW cm - 1 K - 2的高功率因数。同时,通过锗诱导的点缺陷/偏心不谐性和Sb/Sb2Te3析出,晶格热导率协同抑制到~ 0.37 W m-1 K - 1(673 K)。这种协同策略导致在823 K处ZT峰值为~ 1.30,在323-823 K处ZT峰值为~ 0.91。本工作证明了协同I/Ge共掺杂和复合沉淀有效地提高了n型PbTe的热电性能。
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引用次数: 0
Corrosion resistance of Yb-silicate materials to molten slag for protective coating applications 用于保护涂层的yb -硅酸盐材料对熔渣的耐腐蚀性
IF 6.2 2区 材料科学 Q1 MATERIALS SCIENCE, CERAMICS Pub Date : 2026-02-03 DOI: 10.1016/j.jeurceramsoc.2026.118207
Min-Soo Nam , Jin-Kwon Kim , Sahn Nahm , Seongwon Kim
Integrated Gasification Combined Cycle (IGCC) technology offers efficient and cleaner coal-based power generation but introduces corrosion challenges associated with high temperatures and molten slag. This study examines the corrosion behavior of ytterbium monosilicate (Yb₂SiO₅) and its composites containing 5 and 10 wt% Al₂O₃ under IGCC slag conditions. The addition of Al₂O₃ promotes the formation of garnet phases with higher thermal expansion, improving compatibility with the substrate. Samples exposed to molten slag were evaluated for microstructural evolution, thermal expansion, conductivity, and slag resistance. Yb₂SiO₅ exhibited high thermal stability and formed dense protective layers that limited slag infiltration. The composites enhanced thermal compatibility with carbon steel, increasing the coefficient of thermal expansion (CTE) to 9.8 × 10⁻⁶ and 10.9 × 10⁻⁶ K⁻¹ , respectively. The formation of a protective Yb₂Si₂O₇ layer underscores the potential of ytterbium silicates as effective high-temperature coatings for IGCC applications.
综合气化联合循环(IGCC)技术提供了高效、清洁的煤基发电,但也带来了与高温和熔渣相关的腐蚀挑战。本研究研究了单硅酸钇(Yb₂SiO₅)及其含有5和10 wt% Al₂O₃的复合材料在IGCC渣条件下的腐蚀行为。Al₂O₃的加入促进了热膨胀率更高的石榴石相的形成,提高了与基体的相容性。样品暴露于熔渣中,评估其微观结构演变、热膨胀、电导率和抗渣性。Yb₂SiO₅表现出高热稳定性,并形成了致密的保护层,限制了渣的渗透。复合材料增强了与碳钢的热相容性,将热膨胀系数(CTE)分别提高到9.8 × 10⁻⁶和10.9 × 10⁻⁶K⁻¹ 。Yb₂Si₂O₇保护层的形成强调了硅酸钇作为IGCC应用的有效高温涂层的潜力。
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引用次数: 0
Mechanistic elucidation of cold sintering behavior in SrFe12O19 ceramics: Role of transient solvent, temperature, and particle morphology SrFe12O19陶瓷冷烧结行为的机理研究:瞬态溶剂、温度和颗粒形貌的作用
IF 6.2 2区 材料科学 Q1 MATERIALS SCIENCE, CERAMICS Pub Date : 2026-02-02 DOI: 10.1016/j.jeurceramsoc.2026.118204
Siyuan Wang , Wei Cai , WenJin Wu , Huasong Liu , Jianwei Zheng , Liang Qiao , Yao Ying , Juan Li , Jing Yu , Naoki Wakiya , Jingwu Zheng , Shenglei Che
Cold sintering, characterized by low temperature, low energy consumption, and environmental friendliness, offers a promising route for sintering SrFe12O19. This study systematically investigates the effects of transient solvent composition, sintering temperature, and powder morphology on the densification mechanism of SrFe12O19. In the acetic acid–ethanol transient solvent system, Fe3 + ions preferentially dissolved and reacted with acetate and hydroxyl groups to form iron–carboxylate species, which facilitated particle bonding and densification. However, increased solvent concentration and cold sintering temperature cause its decomposition into Fe2O3, and gas release; trapped gas forms pores that impede densification, leading to reduced densification at higher temperatures. Meanwhile, irregular powders promote the “dissolution–precipitation” process more effectively than spherical ones. Under optimized conditions, 16 mol/L transient solvent concentration, 40 wt% addition, 250 °C sintering temperature, 1 GPa pressure, and 3 h holding time, the ball-milled powder achieved a optimal combined magnetic properties (Hcj = 5.31 kOe, Ms = 60.39 emu/g).
冷烧结具有低温、低能耗、环保等特点,为SrFe12O19的烧结提供了一条很有前途的途径。本研究系统地研究了瞬态溶剂组成、烧结温度和粉末形貌对SrFe12O19致密化机理的影响。在醋酸-乙醇瞬态溶剂体系中,Fe3 +离子优先溶解并与乙酸和羟基反应形成羧酸铁,有利于颗粒键合和致密化。但随着溶剂浓度和冷烧结温度的升高,其分解为Fe2O3,并有气体释放;被困气体形成孔隙,阻碍致密化,导致在较高温度下致密化程度降低。同时,不规则粉末比球形粉末更能促进“溶解-沉淀”过程。在最佳条件下,瞬时溶剂浓度为16 mol/L,添加量为40 wt%,烧结温度为250℃,压力为1 GPa,保温时间为3 h,球磨粉获得了最佳的复合磁性能(Hcj = 5.31 kOe, Ms = 60.39 emu/g)。
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引用次数: 0
Searching the limits of compositionally complex AlB2-type diboride solid solutions for hypersonic applications 寻找复合alb2型二硼化物固溶体在高超声速应用中的极限
IF 6.2 2区 材料科学 Q1 MATERIALS SCIENCE, CERAMICS Pub Date : 2026-02-02 DOI: 10.1016/j.jeurceramsoc.2026.118206
F. Monteverde , S. Cassese , D. De Prisco , S. Mungiguerra , R. Savino
Compositionally complex (CC) AlB2-type diboride solid solutions (DSSs) containing IV-V-VI group metals were investigated as candidate materials for hypersonic applications using a ground entry simulator. Each CCDSS was composed of Ti and three other transition metals among Zr-Hf-Nb-Ta. Single phase CCDSS dense discs were spark plasma sintered and then exposed to a supersonic dissociated airflow (nominal Mach 3). The overall degradation of the discs was highly dependent on the combination of starting metals, and massive preferential oxidation occurred. The coexistence of Nb and Ta was detrimental. A thermal study was devised and implemented in a numerical model to validate the experimental set-up. The experimental results also showed good agreement with predictions based on a thermodynamic assessment.
利用地面进入模拟器,研究了含有IV-V-VI族金属的组成复合物(CC) alb2型二硼化物固溶体(DSSs)作为高超声速应用的候选材料。每个CCDSS由Ti和Zr-Hf-Nb-Ta中的其他三种过渡金属组成。用火花等离子体烧结单相CCDSS致密圆盘,然后暴露在超音速分离气流(名义马赫3)中。圆盘的整体降解高度依赖于起始金属的组合,并发生了大量的优先氧化。Nb和Ta的共存是有害的。设计了一个热研究,并在数值模型中实施,以验证实验设置。实验结果也与基于热力学评估的预测结果非常吻合。
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引用次数: 0
Entropy-driven design of ultra-low loss olivine CaY1–x(Nd0.25Sm0.25Eu0.25Yb0.25)xGaO4 microwave dielectric ceramics for 5 G dielectric resonator antennas 5 G介质谐振器天线用超低损耗绿石CaY1-x (Nd0.25Sm0.25Eu0.25Yb0.25) x高4微波介质陶瓷的熵驱动设计
IF 6.2 2区 材料科学 Q1 MATERIALS SCIENCE, CERAMICS Pub Date : 2026-02-02 DOI: 10.1016/j.jeurceramsoc.2026.118205
Yang Zhou , Yanling Huang , Qiumei Huang , Ning Guan , Ning Zhang , Huaicheng Xiang , Ying Tang , Liang Fang
Next-generation wireless communication demands microwave dielectric ceramics that effectively achieve ultra-low loss, a stable resonant frequency, and a low permittivity. Here we demonstrate an entropy-engineering strategy that selectively disorders the [A(2)O6] octahedral site while preserving the rigid [GaO4] tetrahedral backbone in gallium-based olivine A2GaO4. A series of CaY1–x(Nd0.25Sm0.25Eu0.25Yb0.25)xGaO4 ceramics was synthesized by solid-state reaction at 1260–1420 °C. Systematic increases in configurational entropy (ΔSconfig) and ionic-size disorder (δR) drive a reversible PnmaPmnb symmetry switch, suppress phase separation, and expand the lattice. At x = 0.8, the high-entropy single-phase olivine exhibits εr = 9.2 ± 0.2, Q×f = 151,025 ± 400 GHz, and τf = -39.8 ± 2.0 ppm/°C, while Vickers hardness rises to 5.79 ± 0.2 GPa. Ultra-low loss is synergistically influenced by ΔSconfig, δR, and packing fraction. A C-band dielectric resonator antenna fabricated from the x = 0.8 composition achieves 92.63 % radiation efficiency and 6.39 dBi gain, validating the entropy-design paradigm for high-frequency applications.
下一代无线通信要求微波介质陶瓷能够有效地实现超低损耗、稳定的谐振频率和低介电常数。在这里,我们展示了一种熵工程策略,该策略选择性地破坏了镓基橄榄石A2GaO4中的[A(2)O6]八面体位点,同时保留了刚性的[高4]四面体骨架。采用固相反应在1260 ~ 1420℃下合成了一系列CaY1-x (Nd0.25Sm0.25Eu0.25Yb0.25) x高四陶瓷。构型熵(ΔSconfig)和离子尺寸无序(δR)的系统增加驱动了可逆的Pnma→Pmnb对称开关,抑制了相分离,并扩展了晶格。0.8 x = ,熵值单相橄榄石展览εr = 9.2  ±0.2 ,问151025×f =  ± 400 GHz,和τf = -39.8  ± 2.0 ppm /°C,而维氏硬度上升到5.79 ±0.2  GPa。超低损失受ΔSconfig、δR和填料分数的协同影响。由x = 0.8组成的c波段介电谐振器天线实现了92.63 %的辐射效率和6.39 dBi增益,验证了高频应用的熵设计范式。
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引用次数: 0
Effect of temperature on bending mechanical behavior of 3D angle-interlock woven Al₂O₃/mullite ceramic matrix composites 温度对三维角互锁编织Al₂O₃/莫来石陶瓷基复合材料弯曲力学行为的影响
IF 6.2 2区 材料科学 Q1 MATERIALS SCIENCE, CERAMICS Pub Date : 2026-01-31 DOI: 10.1016/j.jeurceramsoc.2026.118203
Yueying Yin , Zemin Liu , Diansen Li , Lei Jiang , Stepan V. Lomov , Frederik Desplentere
This study systematically investigates the evolution of bending properties and damage mechanisms of three-dimensional angle-interlock woven alumina/mullite ceramic matrix composites (3DAW Al₂O₃-CMCs) under room-temperature (RT) and various high-temperature environments. The experimental temperature range was set from RT to 1200°C. The results indicate that the bending properties of 3DAW Al₂O₃-CMCs exhibit a non-monotonic temperature dependence, initially increasing before decreasing, with optimal performance observed at 1000°C where the maximum bending strength and bending modulus reach 128 MPa and 15.20 GPa, respectively. The damage mechanism shifts with increasing temperature: from localized fiber fracture and matrix cracking, to ductile fracture characterized by matrix softening and enhanced interfacial bonding, and finally to the state of matrix degradation coupled with fiber bundles collapse.
本研究系统地研究了三维角互锁编织氧化铝/莫来石陶瓷基复合材料(3DAW Al₂O₃-CMCs)在室温和各种高温环境下弯曲性能的演变和损伤机理。实验温度范围为RT ~ 1200℃。结果表明:3DAW Al₂O₃- cmc的抗弯性能表现出非单调的温度依赖性,先升高后降低,在1000℃时抗弯强度和抗弯模量分别达到128 MPa和15.20 GPa,抗弯性能最佳。随着温度的升高,损伤机制由局部纤维断裂和基体开裂转变为基体软化和界面结合增强的韧性断裂,最后转变为基体降解和纤维束坍塌的状态。
{"title":"Effect of temperature on bending mechanical behavior of 3D angle-interlock woven Al₂O₃/mullite ceramic matrix composites","authors":"Yueying Yin ,&nbsp;Zemin Liu ,&nbsp;Diansen Li ,&nbsp;Lei Jiang ,&nbsp;Stepan V. Lomov ,&nbsp;Frederik Desplentere","doi":"10.1016/j.jeurceramsoc.2026.118203","DOIUrl":"10.1016/j.jeurceramsoc.2026.118203","url":null,"abstract":"<div><div>This study systematically investigates the evolution of bending properties and damage mechanisms of three-dimensional angle-interlock woven alumina/mullite ceramic matrix composites (3DAW Al₂O₃-CMCs) under room-temperature (RT) and various high-temperature environments. The experimental temperature range was set from RT to 1200°C. The results indicate that the bending properties of 3DAW Al₂O₃-CMCs exhibit a non-monotonic temperature dependence, initially increasing before decreasing, with optimal performance observed at 1000°C where the maximum bending strength and bending modulus reach 128 MPa and 15.20 GPa, respectively. The damage mechanism shifts with increasing temperature: from localized fiber fracture and matrix cracking, to ductile fracture characterized by matrix softening and enhanced interfacial bonding, and finally to the state of matrix degradation coupled with fiber bundles collapse.</div></div>","PeriodicalId":17408,"journal":{"name":"Journal of The European Ceramic Society","volume":"46 9","pages":"Article 118203"},"PeriodicalIF":6.2,"publicationDate":"2026-01-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146098817","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
Reaction-controlled effects of (YbxSc1-x)2Si2O7 solid solution against molten calcia-magnesia-aluminosilicate (CMAS) corrosion for environmental barrier coating application (YbxSc1-x)2Si2O7固溶体对环境屏障涂层中熔融钙镁铝硅酸盐(CMAS)腐蚀的反应控制效应
IF 6.2 2区 材料科学 Q1 MATERIALS SCIENCE, CERAMICS Pub Date : 2026-01-31 DOI: 10.1016/j.jeurceramsoc.2026.118182
Min-Soo Nam , Sahn Nahm , Seongwon Kim
Environmental barrier coatings (EBCs) are essential for protecting SiCf/SiC ceramic matrix composites from water vapor recession and calcia-magnesia-aluminosilicate (CMAS) corrosion in gas turbines. In this study, (YbxSc1−x)2Si2O7 solid solutions with varying Yb/Sc ratios are evaluated as CMAS-resistant EBC topcoat candidates. Five compositions are synthesized and tested at 1500 °C. Corrosion resistance improves as the optical basicity of the disilicate matches that of CMAS, minimizing chemical reactions and apatite formation; Sc-containing compositions exhibit the best performance. Increasing Sc content decreases the ionic radius and lattice parameters, further inhibiting Ca2+ –to–RE3+ substitution. Microstructural analysis shows Yb-rich samples retain surface CMAS, whereas Sc-rich samples experience rapid grain-boundary infiltration with less reaction. Thermophysical measurements confirm low, stable thermal conductivity and coefficient of thermal expansion compatibility with SiCf/SiC substrates. These results indicate that (YbxSc1−x)2Si2O7 solid solutions offer a balanced combination of CMAS corrosion resistance, thermal compatibility, and low thermal conductivity for robust EBCs.
环境屏障涂层(EBCs)是保护SiCf/SiC陶瓷基复合材料免受水蒸气衰退和钙镁铝硅酸盐(CMAS)腐蚀的关键。在这项研究中,具有不同Yb/Sc比率的(YbxSc1−x)2Si2O7固溶体被评估为抗cmas的EBC面漆候选者。合成了五种组合物,并在1500℃下进行了测试。当二硅酸盐的光学碱度与CMAS的光学碱度相匹配时,耐腐蚀性提高,减少了化学反应和磷灰石的形成;含sc的组合物表现出最好的性能。Sc含量的增加降低了离子半径和晶格参数,进一步抑制了Ca2+到re3 +的取代。微观结构分析表明,富钇样品保留了表面CMAS,而富钪样品则经历了快速的晶界渗透,反应较少。热物理测量证实了低,稳定的导热系数和热膨胀系数与SiCf/SiC衬底的相容性。这些结果表明,(YbxSc1−x)2Si2O7固溶体为坚固的EBCs提供了CMAS耐腐蚀性,热相容性和低导热性的平衡组合。
{"title":"Reaction-controlled effects of (YbxSc1-x)2Si2O7 solid solution against molten calcia-magnesia-aluminosilicate (CMAS) corrosion for environmental barrier coating application","authors":"Min-Soo Nam ,&nbsp;Sahn Nahm ,&nbsp;Seongwon Kim","doi":"10.1016/j.jeurceramsoc.2026.118182","DOIUrl":"10.1016/j.jeurceramsoc.2026.118182","url":null,"abstract":"<div><div>Environmental barrier coatings (EBCs) are essential for protecting SiC<sub>f</sub>/SiC ceramic matrix composites from water vapor recession and calcia-magnesia-aluminosilicate (CMAS) corrosion in gas turbines. In this study, (Yb<sub>x</sub>Sc<sub>1−x</sub>)<sub>2</sub>Si<sub>2</sub>O<sub>7</sub> solid solutions with varying Yb/Sc ratios are evaluated as CMAS-resistant EBC topcoat candidates. Five compositions are synthesized and tested at 1500 °C. Corrosion resistance improves as the optical basicity of the disilicate matches that of CMAS, minimizing chemical reactions and apatite formation; Sc-containing compositions exhibit the best performance. Increasing Sc content decreases the ionic radius and lattice parameters, further inhibiting Ca<sup>2</sup><sup>+</sup> –to–RE<sup>3+</sup> substitution. Microstructural analysis shows Yb-rich samples retain surface CMAS, whereas Sc-rich samples experience rapid grain-boundary infiltration with less reaction. Thermophysical measurements confirm low, stable thermal conductivity and coefficient of thermal expansion compatibility with SiC<sub>f</sub>/SiC substrates. These results indicate that (Yb<sub>x</sub>Sc<sub>1−x</sub>)<sub>2</sub>Si<sub>2</sub>O<sub>7</sub> solid solutions offer a balanced combination of CMAS corrosion resistance, thermal compatibility, and low thermal conductivity for robust EBCs.</div></div>","PeriodicalId":17408,"journal":{"name":"Journal of The European Ceramic Society","volume":"46 9","pages":"Article 118182"},"PeriodicalIF":6.2,"publicationDate":"2026-01-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146191682","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
First-principles guided design and high-pressure sintering of polymer-derived high-entropy carbides with superior hardness and modulus 第一性原理指导设计和高压烧结聚合物衍生的高熵碳化物具有优异的硬度和模量
IF 6.2 2区 材料科学 Q1 MATERIALS SCIENCE, CERAMICS Pub Date : 2026-01-30 DOI: 10.1016/j.jeurceramsoc.2026.118191
Yimin Ouyang , Saidi Wang , Linwei Guo , Tao Zhang , Mengdong Ma , Bin Du
Linking atomic-scale modeling with experimental processes, first-principles calculations were combined with polymer-derived ceramic (PDC) route and high-pressure sintering to design and fabricate (Ta0.25Nb0.25Hf0.25Zr0.25)C high-entropy carbides (HECs) with exceptional hardness and modulus. The calculations show that increasing applied pressure enhances the elastic constants, bulk modulus, and theoretical hardness, guiding powder densification at 6 GPa and 1600°C (HEC1) or 1800°C (HEC2). Dense bulk ceramics with relative densities of 95.19 % and 96.33 %, were obtained without phase decomposition. Compared with HEC1, HEC2 exhibits improved crystallinity, reduced porosity, and enhanced mechanical properties, including a Vickers hardness of 28.3 GPa, nanoindentation hardness of 33.2 GPa, elastic modulus of 440.7 GPa, and fracture toughness of 4.0 MPa·m1/2. These findings highlight that integrating the PDC route with high-pressure sintering facilitates the fabrication of dense, high-performance HECs, offering a promising pathway for structural applications in extreme environments.
将原子尺度模型与实验过程相结合,将第一性原理计算与聚合物衍生陶瓷(PDC)路线和高压烧结相结合,设计并制备了具有优异硬度和模量的(Ta0.25Nb0.25Hf0.25Zr0.25)C高熵碳化物(HECs)。计算结果表明,施加压力增大可提高弹性常数、体积模量和理论硬度,在6 GPa和1600°C (HEC1)或1800°C (HEC2)下引导粉末致密化。在不进行相分解的情况下,得到了相对密度为95.19 %和96.33 %的致密体陶瓷。与HEC1相比,HEC2的结晶度提高,孔隙率降低,力学性能增强,维氏硬度为28.3 GPa,纳米压痕硬度为33.2 GPa,弹性模量为440.7 GPa,断裂韧性为4.0 MPa·m1/2。这些发现表明,将PDC路线与高压烧结相结合,有助于制造致密、高性能的hec,为极端环境下的结构应用提供了一条有前景的途径。
{"title":"First-principles guided design and high-pressure sintering of polymer-derived high-entropy carbides with superior hardness and modulus","authors":"Yimin Ouyang ,&nbsp;Saidi Wang ,&nbsp;Linwei Guo ,&nbsp;Tao Zhang ,&nbsp;Mengdong Ma ,&nbsp;Bin Du","doi":"10.1016/j.jeurceramsoc.2026.118191","DOIUrl":"10.1016/j.jeurceramsoc.2026.118191","url":null,"abstract":"<div><div>Linking atomic-scale modeling with experimental processes, first-principles calculations were combined with polymer-derived ceramic (PDC) route and high-pressure sintering to design and fabricate (Ta<sub>0.25</sub>Nb<sub>0.25</sub>Hf<sub>0.25</sub>Zr<sub>0.25</sub>)C high-entropy carbides (HECs) with exceptional hardness and modulus. The calculations show that increasing applied pressure enhances the elastic constants, bulk modulus, and theoretical hardness, guiding powder densification at 6 GPa and 1600°C (HEC1) or 1800°C (HEC2). Dense bulk ceramics with relative densities of 95.19 % and 96.33 %, were obtained without phase decomposition. Compared with HEC1, HEC2 exhibits improved crystallinity, reduced porosity, and enhanced mechanical properties, including a Vickers hardness of 28.3 GPa, nanoindentation hardness of 33.2 GPa, elastic modulus of 440.7 GPa, and fracture toughness of 4.0 MPa·m<sup>1/2</sup>. These findings highlight that integrating the PDC route with high-pressure sintering facilitates the fabrication of dense, high-performance HECs, offering a promising pathway for structural applications in extreme environments.</div></div>","PeriodicalId":17408,"journal":{"name":"Journal of The European Ceramic Society","volume":"46 8","pages":"Article 118191"},"PeriodicalIF":6.2,"publicationDate":"2026-01-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146080441","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
Reducing heat treatment time and temperature for dense crystalline ytterbium disilicate environmental barrier coatings 减少致密结晶二硅酸镱环境屏障涂层的热处理时间和温度
IF 6.2 2区 材料科学 Q1 MATERIALS SCIENCE, CERAMICS Pub Date : 2026-01-29 DOI: 10.1016/j.jeurceramsoc.2026.118190
P. Khamsepour , P. Bansal , D. Guay , A.C. Tavares , B. Guerreiro , R.S. Lima , K.R. Beyerlein
Ytterbium disilicate (YbDS) environmental barrier coatings (EBCs) are deposited by atmospheric plasma spray (APS) to protect aeroengine components made of SiCfiber(f)/SiC ceramic matrix composites. During deposition, rapid solidification of molten YbDS particles upon impact creates an amorphous structure which needs to be crystallized. This study optimized crystallization heat treatment for dense (∼2 % porosity) EBCs with as-sprayed crystallinity between 10 % and 50 %. Stable ytterbium silicate phases (YbDS and Yb₂SiO₅ (YbMS)) are formed above 1200 °C, regardless of initial crystallinity. EBCs with crystallinity of 15 % produced metastable phases at 1100 °C, requiring at least 10 h to transform them into stable phases, while coatings with 50 % crystallinity formed stable phase after only 4 h. The morphology and hardness of EBCs after crystallization are shown to be comparable irrespective of the heat treatment temperature. This demonstrates that partially crystalline as-sprayed YbDS can be crystallized faster and at lower temperatures, potentially reducing production costs.
采用常压等离子喷涂(APS)技术制备了二硅酸钇(YbDS)环境屏障涂层,以保护由SiCfiber(f)/SiC陶瓷基复合材料制成的航空发动机部件。在沉积过程中,熔融的YbDS颗粒在撞击后迅速凝固,形成需要结晶的非晶结构。该研究优化了致密(~ 2 %孔隙率)EBCs的结晶热处理,其喷射结晶度在10 %至50 %之间。稳定的硅酸钇相(YbDS和yb2 SiO₅(YbMS))在1200°C以上形成,无论初始结晶度如何。结晶度为15% %的EBCs在1100℃时产生亚稳相,至少需要10 h才能转变为稳定相,而结晶度为50% %的涂层仅需要4 h即可形成稳定相。结果表明,EBCs结晶后的形貌和硬度与热处理温度无关。这表明,部分结晶的YbDS可以在更低的温度下更快地结晶,从而潜在地降低生产成本。
{"title":"Reducing heat treatment time and temperature for dense crystalline ytterbium disilicate environmental barrier coatings","authors":"P. Khamsepour ,&nbsp;P. Bansal ,&nbsp;D. Guay ,&nbsp;A.C. Tavares ,&nbsp;B. Guerreiro ,&nbsp;R.S. Lima ,&nbsp;K.R. Beyerlein","doi":"10.1016/j.jeurceramsoc.2026.118190","DOIUrl":"10.1016/j.jeurceramsoc.2026.118190","url":null,"abstract":"<div><div>Ytterbium disilicate (YbDS) environmental barrier coatings (EBCs) are deposited by atmospheric plasma spray (APS) to protect aeroengine components made of SiC<sub>fiber(f)</sub>/SiC ceramic matrix composites. During deposition, rapid solidification of molten YbDS particles upon impact creates an amorphous structure which needs to be crystallized. This study optimized crystallization heat treatment for dense (∼2 % porosity) EBCs with as-sprayed crystallinity between 10 % and 50 %. Stable ytterbium silicate phases (YbDS and Yb₂SiO₅ (YbMS)) are formed above 1200 °C, regardless of initial crystallinity. EBCs with crystallinity of 15 % produced metastable phases at 1100 °C, requiring at least 10 h to transform them into stable phases, while coatings with 50 % crystallinity formed stable phase after only 4 h. The morphology and hardness of EBCs after crystallization are shown to be comparable irrespective of the heat treatment temperature. This demonstrates that partially crystalline as-sprayed YbDS can be crystallized faster and at lower temperatures, potentially reducing production costs.</div></div>","PeriodicalId":17408,"journal":{"name":"Journal of The European Ceramic Society","volume":"46 8","pages":"Article 118190"},"PeriodicalIF":6.2,"publicationDate":"2026-01-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146079967","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
Processing of porous SiC/cordierite composites with enhanced thermal shock resistance and negative thermal expansion 增强抗热震和负热膨胀的多孔碳化硅/堇青石复合材料的加工
IF 6.2 2区 材料科学 Q1 MATERIALS SCIENCE, CERAMICS Pub Date : 2026-01-29 DOI: 10.1016/j.jeurceramsoc.2026.118183
M. Sayed , N.A. Ajiba , S.B. Hanna, S.M. Naga
The present study aims to fabricate porous SiC/cordierite composites using the direct foaming technique followed by a sintering process, targeting enhanced thermal shock resistance and thermal expansion behavior. For this purpose, SiC was added in varying contents (20, 40, and 60 wt%) to the prepared pure stoichiometric cordierite matrix to evaluate their effects on porosity, phase composition, microstructure, mechanical, and thermal properties of the produced composites. The results showed that the porosity of the fabricated composites increased from 55.34 % to 68.49 % with the addition of SiC. The X-ray analysis (XRD) indicated that the addition of 20–40 wt% SiC induced a transformation from hexagonal to orthorhombic cordierite, whereas a higher SiC content of 60 wt% resulted in the coexistence of both α- and β-cordierite phases. The coefficient of thermal expansion (CTE) decreased with the addition of SiC into the cordierite matrix, while the compressive strength exhibited a maximum value for the 20 wt% SiC composite with a negative coefficient of thermal expansion. The SiC/cordierite composites demonstrated significantly improved thermal shock resistance compared to pure cordierite, allowing the SiC/cordierite composites to withstand over 40 thermal cycles without failure. The results suggest that the fabricated SiC/cordierite composites are promising candidates for high-temperature applications, offering a favorable combination of thermal stability, mechanical strength, and enhanced thermal shock resistance.
本研究旨在利用直接发泡技术和烧结工艺制备多孔碳化硅/堇青石复合材料,以增强其抗热震性和热膨胀性能。为此,将不同含量(20、40和60 wt%)的SiC添加到制备的纯化学计量堇青石基体中,以评估其对制备的复合材料的孔隙率、相组成、微观结构、力学和热性能的影响。结果表明:SiC的加入使复合材料的孔隙率由55.34 %提高到68.49 %;x射线分析(XRD)表明,添加20 ~ 40 wt% SiC时,堇青石由六方晶向正方晶转变,而添加60 wt% SiC时,α-和β-堇青石相共存。随着SiC的加入,堇青石基体的热膨胀系数(CTE)降低,而抗压强度在20% wt% SiC时达到最大值,热膨胀系数为负。与纯堇青石相比,SiC/堇青石复合材料的抗热冲击性能显著提高,使SiC/堇青石复合材料能够承受超过40次的热循环而不会失效。结果表明,制备的SiC/堇青石复合材料具有良好的热稳定性、机械强度和增强的抗热震性,是高温应用的理想候选者。
{"title":"Processing of porous SiC/cordierite composites with enhanced thermal shock resistance and negative thermal expansion","authors":"M. Sayed ,&nbsp;N.A. Ajiba ,&nbsp;S.B. Hanna,&nbsp;S.M. Naga","doi":"10.1016/j.jeurceramsoc.2026.118183","DOIUrl":"10.1016/j.jeurceramsoc.2026.118183","url":null,"abstract":"<div><div>The present study aims to fabricate porous SiC/cordierite composites using the direct foaming technique followed by a sintering process, targeting enhanced thermal shock resistance and thermal expansion behavior. For this purpose, SiC was added in varying contents (20, 40, and 60 wt%) to the prepared pure stoichiometric cordierite matrix to evaluate their effects on porosity, phase composition, microstructure, mechanical, and thermal properties of the produced composites. The results showed that the porosity of the fabricated composites increased from 55.34 % to 68.49 % with the addition of SiC. The X-ray analysis (XRD) indicated that the addition of 20–40 wt% SiC induced a transformation from hexagonal to orthorhombic cordierite, whereas a higher SiC content of 60 wt% resulted in the coexistence of both α- and β-cordierite phases. The coefficient of thermal expansion (CTE) decreased with the addition of SiC into the cordierite matrix, while the compressive strength exhibited a maximum value for the 20 wt% SiC composite with a negative coefficient of thermal expansion. The SiC/cordierite composites demonstrated significantly improved thermal shock resistance compared to pure cordierite, allowing the SiC/cordierite composites to withstand over 40 thermal cycles without failure. The results suggest that the fabricated SiC/cordierite composites are promising candidates for high-temperature applications, offering a favorable combination of thermal stability, mechanical strength, and enhanced thermal shock resistance.</div></div>","PeriodicalId":17408,"journal":{"name":"Journal of The European Ceramic Society","volume":"46 8","pages":"Article 118183"},"PeriodicalIF":6.2,"publicationDate":"2026-01-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146079973","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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