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Rare earth-doped ZrB2-MoSi2 ceramics: Densification and oxidation behavior 掺稀土的 ZrB2-MoSi2 陶瓷:致密化和氧化行为
IF 5.8 2区 材料科学 Q1 MATERIALS SCIENCE, CERAMICS Pub Date : 2024-10-15 DOI: 10.1016/j.jeurceramsoc.2024.116992
Laura Silvestroni , Hai-Tao Liu , Diletta Sciti , Xin-Gang Wang , Guo-Jun Zhang
The effect of rare earth oxides (REO), Nd2O3 and Eu2O3, on the densification and oxidation behavior of pressureless sintered ZrB2-MoSi2 ceramic composites was investigated. Addition of REO results in the formation of REO-silicates which are liquid at the sintering temperature and contribute to matter transfer mechanisms. Oxidation studies at 1500 °C for 0.5–4 h evidenced that Eu2O3 can improve oxidation resistance in the ZrB2-MoSi2 system, especially after prolonged exposition, whilst Nd2O3 induces faster degradation of the ceramic. It was found that the Eu dispersed both in silica and in zirconia modifies the rheological properties of the glassy phase thus playing an important role in hindering oxygen inward from the atmosphere to the subsurface, resulting in a noticeable improvement of the oxidation resistance.
研究了稀土氧化物(REO)(Nd2O3 和 Eu2O3)对无压烧结 ZrB2-MoSi2 陶瓷复合材料的致密化和氧化行为的影响。加入 REO 后形成的 REO 硅酸盐在烧结温度下呈液态,有助于物质转移机制。在 1500 °C 下进行 0.5-4 小时的氧化研究表明,Eu2O3 可以提高 ZrB2-MoSi2 系统的抗氧化性,尤其是在长时间暴露后,而 Nd2O3 则会导致陶瓷加速降解。研究发现,分散在二氧化硅和氧化锆中的 Eu 改变了玻璃相的流变特性,从而在阻止氧气从大气进入次表层方面发挥了重要作用,从而显著提高了抗氧化性。
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引用次数: 0
Novel Co and Cr free, high-temperature black ceramic pigment based on (Ni, Mn) co-doping (CuFe)Fe4O8 基于(镍、锰)共掺杂 (CuFe)Fe4O8 的新型无钴、无铬高温黑色陶瓷颜料
IF 5.8 2区 材料科学 Q1 MATERIALS SCIENCE, CERAMICS Pub Date : 2024-10-15 DOI: 10.1016/j.jeurceramsoc.2024.116987
Guo Feng , Tiantian Liu , Feng Jiang , Zhiqi Guo , Liangliang Xiao , Qian Wu , Xiaojun Zhang , Qing Hu , Jianmin Liu , Jian Liang
Novel Co and Cr free, high-temperature (Ni, Mn) co-doping (CuFe)Fe4O8 black ceramic pigment was synthesized. The results indicate that the brightness (L*) values of the synthesized pigments decrease first, then reach an optimal value, and then increase with the doping amounts increasing of both Ni2O3 and MnO2. The optimized Ni2O3 and MnO2 doping amounts are 0.20 (molar ratio to (CuFe)Fe4O8) and 0.75 (molar ratio to (CuFe)Fe4O8), respectively. L*, a* and b* values of the optimized pigment (0.20Ni, 0.75Mn) co-doping (CuFe)Fe4O8 are 21.36, 1.10 and −0.24, respectively. The crystal phase of the optimized pigment is (CuFe)Fe4O8 (JCPDS73–2314). The crystal size of the pigment is 0.8–1.5μm with excellent dispersivity. The glazing temperatures have little effect on the coloration of the pigment when used at 1000℃, 1150℃ and 1300℃. The results show that the pigments have excellent high-temperature resistance and are expected to be widely used in high-temperature glazing coloration.
合成了新型无钴、无铬高温(镍、锰)共掺杂(CuFe)Fe4O8 黑色陶瓷颜料。结果表明,随着 Ni2O3 和 MnO2 掺杂量的增加,合成颜料的亮度(L*)值先减小,然后达到一个最佳值,再增大。最佳的 Ni2O3 和 MnO2 掺杂量分别为 0.20(与(CuFe)Fe4O8 的摩尔比)和 0.75(与(CuFe)Fe4O8 的摩尔比)。优化颜料(0.20Ni、0.75Mn)共掺杂(CuFe)Fe4O8 的 L*、a* 和 b* 值分别为 21.36、1.10 和 -0.24。优化颜料的晶相为 (CuFe)Fe4O8 (JCPDS73-2314)。颜料的晶体尺寸为 0.8-1.5μm,分散性极佳。上釉温度在 1000℃、1150℃ 和 1300℃时对颜料的着色影响不大。结果表明,该颜料具有优异的耐高温性能,有望广泛应用于高温上釉着色。
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引用次数: 0
Hot zone electrical resistance measurement for health monitoring of SiC and Si-based materials 热区电阻测量用于监控碳化硅和硅基材料的健康状况
IF 5.8 2区 材料科学 Q1 MATERIALS SCIENCE, CERAMICS Pub Date : 2024-10-15 DOI: 10.1016/j.jeurceramsoc.2024.116985
A. Bident, J. Roger, A. Ebel, F. Rebillat
SiC-based materials are good candidates for structural applications at high temperature. However, due to their limited damage tolerance, in-service health monitoring using electrical conductivity measurements would be beneficial. Still, electrical measurements in hot zones on these materials remain a major challenge and require the design of a specific contact material that ensure adhesion of the measurement wires to the material while limiting chemical reactivity with the substrate. TiSi2-Si eutectic compound was found to be a good candidate for this application. An electrical conductivity (EC) measurement was carried out up successfully to 1300 °C in vacuum on a sintered SiC sample using this contact material. Post-measurement analysis of the contact was carried out, and cracks and SiC growth were observed, but without any impact on the electrical resistance measurement.
碳化硅基材料是高温下结构应用的良好候选材料。然而,由于其损坏耐受性有限,使用电导率测量进行在役健康监测将大有裨益。不过,在这些材料的热区进行电气测量仍然是一项重大挑战,需要设计一种特定的接触材料,以确保测量导线与材料的粘附性,同时限制与基材的化学反应。研究发现,TiSi2-Si 共晶化合物是这一应用的理想候选材料。使用这种接触材料对烧结的碳化硅样品进行了电导率(EC)测量,测量温度在真空中达到 1300 °C。测量后对触点进行了分析,观察到裂纹和碳化硅生长,但对电阻测量没有任何影响。
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引用次数: 0
Microstructure evolution and mechanical properties of SiCf/BN/SiBCN composite after high temperature thermal exposure 高温热暴露后 SiCf/BN/SiBCN 复合材料的微观结构演变和力学性能
IF 5.8 2区 材料科学 Q1 MATERIALS SCIENCE, CERAMICS Pub Date : 2024-10-15 DOI: 10.1016/j.jeurceramsoc.2024.116988
Zhongmin Li , Xun Zhang , Han Liu , Philip J. Withers , Ping Xiao
The present study investigates the microstructure evolution and subsequent mechanical properties of SiCfiber/BN/SiBCNmatrix composites after high temperature exposure. These composites display a tough failure response under three-point bending retaining 80 % of the as-processed strength, even after elevated temperature exposure up to 1350 °C for 10 h. This is due to crack deflection accompanied by extensive fiber pull-out. In addition, both thermodynamic modelling and phase analysis by XRD show higher matrix degradation in vacuum than in N2 atmosphere due to the lower N2 partial pressure. After thermally exposure at 1500°C, carbothermal reaction in the matrix leads to the formation of a porous composite, and the composites retains a tough failure response. Meanwhile, SiBCN matrix degradation and SiC fiber strength degradation occurs, which results in a significant decrement in composite strength. Modest increases in the fiber/matrix interfacial shear strength occur upon exposure at temperatures up to 1350°C, and then significantly reduce upon exposure to 1500 °C in N2.
本研究探讨了高温暴露后碳化硅纤维/氮化硼/碳化硅基复合材料的微观结构演变及其机械性能。这些复合材料在三点弯曲条件下表现出了坚韧的失效响应,即使在高达 1350 °C 的高温下暴露 10 小时,仍能保持加工时 80% 的强度。这是由于裂纹挠度伴随着大量纤维拉出所致。此外,通过 XRD 进行的热力学建模和相分析表明,由于 N2 分压较低,真空中的基体降解程度高于 N2 大气中的基体降解程度。在 1500°C 的热暴露条件下,基体中的碳热反应导致多孔复合材料的形成,复合材料保持了坚韧的失效响应。同时,SiBCN 基体发生降解,SiC 纤维强度发生降解,导致复合材料强度显著下降。在温度高达 1350°C 时,纤维/基体界面剪切强度略有增加,而在氮气中温度达到 1500°C 时,纤维/基体界面剪切强度又显著降低。
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引用次数: 0
W6+ doped CuMoO4 ceramics with low dielectric permittivity and near-zero temperature coefficient of resonant frequency for ULTCC application 掺杂 W6+ 的 CuMoO4 陶瓷具有低介电常数和近零温度系数的谐振频率,适用于超短波无损陶瓷电路(ULTCC)应用
IF 5.8 2区 材料科学 Q1 MATERIALS SCIENCE, CERAMICS Pub Date : 2024-10-12 DOI: 10.1016/j.jeurceramsoc.2024.116986
Ruihang Li , Luchao Ren , Le Xin , Pengchao Shao , Jia Wang , Zengli Gao , Panpan Lyu , Cuncheng Li , Hui Peng , Mingwei Zhang
This study optimizes the temperature coefficient of resonant frequency (τf) in CuMoO4 ceramics from −36 to −8.82 ppm/°C through W6+ B-site substitution. XRD analysis confirms the single-phase structure of CuMo1-xWxO4 ceramics, while Rietveld refinements reveal an expansion in lattice parameters. W6+ substitution slightly reduces the relative permittivity (εr) due to the changes in sintering density and ion polarizability. Moreover, the internal effects of W6+ substitution on the Q×f value are systematically investigated by analyzing the Raman peak's full width at half maximum (FWHM) and conducting packing fraction calculations. Additionally, lattice distortion and bond valence analyses elucidate the intrinsic mechanism behind τf improvement. Consequently, when x = 0.08, CuMo1-xWxO4 sintered at 625°C exhibits superior overall performance: εr = 5.13, Q×f = 65,506 GHz, τf = −8.82 ppm/°C. Furthermore, it demonstrates good chemical compatibility with Al electrodes making the material more suitable for ULTCC practical applications.
本研究通过 W6+ B 位取代,优化了 CuMoO4 陶瓷谐振频率 (τf) 的温度系数,从 -36 ppm/°C 降至 -8.82 ppm/°C。XRD 分析证实了 CuMo1-xWxO4 陶瓷的单相结构,而 Rietveld 精炼则揭示了晶格参数的扩展。由于烧结密度和离子极化性的变化,W6+ 的替代略微降低了相对介电常数 (εr)。此外,通过分析拉曼峰的半最大全宽(FWHM)和进行堆积分数计算,系统地研究了 W6+ 替代对 Q×f 值的内部影响。此外,晶格畸变和键价分析还阐明了 τf 改善背后的内在机制。因此,当 x = 0.08 时,在 625°C 下烧结的 CuMo1-xWxO4 表现出卓越的整体性能:εr = 5.13,Q×f = 65,506 GHz,τf = -8.82 ppm/°C。此外,该材料与铝电极具有良好的化学兼容性,因此更适合 ULTCC 实际应用。
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引用次数: 0
Effects of limiting current density and current step rate on microstructure and hardness of flash sintered MgAl2O4 ceramics 极限电流密度和电流阶跃率对闪速烧结 MgAl2O4 陶瓷微观结构和硬度的影响
IF 5.8 2区 材料科学 Q1 MATERIALS SCIENCE, CERAMICS Pub Date : 2024-10-11 DOI: 10.1016/j.jeurceramsoc.2024.116982
Ning Han , Shoulei Yang , Shuyue Chen , Zhiyi Wang , Mengjie Yang , Lei Fan , Xiaoqing Guo , Yujin Dai , Yidan Wang , Shuangqing Chen , Zhengkai Zhang , Yun Zhang
This study investigates the effects of limiting current density and current step rate on the microstructure and hardness of current-step flash-sintered (CS-FS) disc-shaped MgAl2O4 ceramics. The results indicated that, unlike conventional flash sintering, the temperature of the sample during the current-step flash started at a lower initial value and subsequently increased gradually. Furthermore, the differences in oxygen vacancies between the positive and negative sides of the CS-FS-ed MgAl2O4 ceramics were significantly reduced. This led to the CS-FS samples exhibiting higher relative density, finer grain size, a more uniform microstructure, and increased hardness. The homogeneous microstructure resulted in consistent hardness across both sides of each CS-FS-ed sample. Additionally, as the limiting current density increased, the grain sizes near the positive and negative sides gradually enlarged, while the relative density initially increased before decreasing. A similar trend was observed when the current step rate decreased.
本研究探讨了限制电流密度和电流阶跃率对电流阶跃闪蒸烧结(CS-FS)盘形 MgAl2O4 陶瓷微观结构和硬度的影响。结果表明,与传统的闪蒸烧结不同,电流步进闪蒸过程中样品的温度从较低的初始值开始,随后逐渐升高。此外,CS-FS-ed MgAl2O4 陶瓷正负极之间的氧空位差异显著减小。这使得 CS-FS 样品表现出更高的相对密度、更细的晶粒尺寸、更均匀的微观结构和更高的硬度。均匀的微观结构使每个 CS-FS 样品的两面都具有一致的硬度。此外,随着极限电流密度的增加,正负极附近的晶粒尺寸逐渐增大,而相对密度则先增加后减小。当电流阶跃率降低时,也观察到类似的趋势。
{"title":"Effects of limiting current density and current step rate on microstructure and hardness of flash sintered MgAl2O4 ceramics","authors":"Ning Han ,&nbsp;Shoulei Yang ,&nbsp;Shuyue Chen ,&nbsp;Zhiyi Wang ,&nbsp;Mengjie Yang ,&nbsp;Lei Fan ,&nbsp;Xiaoqing Guo ,&nbsp;Yujin Dai ,&nbsp;Yidan Wang ,&nbsp;Shuangqing Chen ,&nbsp;Zhengkai Zhang ,&nbsp;Yun Zhang","doi":"10.1016/j.jeurceramsoc.2024.116982","DOIUrl":"10.1016/j.jeurceramsoc.2024.116982","url":null,"abstract":"<div><div>This study investigates the effects of limiting current density and current step rate on the microstructure and hardness of current-step flash-sintered (CS-FS) disc-shaped MgAl<sub>2</sub>O<sub>4</sub> ceramics. The results indicated that, unlike conventional flash sintering, the temperature of the sample during the current-step flash started at a lower initial value and subsequently increased gradually. Furthermore, the differences in oxygen vacancies between the positive and negative sides of the CS-FS-ed MgAl<sub>2</sub>O<sub>4</sub> ceramics were significantly reduced. This led to the CS-FS samples exhibiting higher relative density, finer grain size, a more uniform microstructure, and increased hardness. The homogeneous microstructure resulted in consistent hardness across both sides of each CS-FS-ed sample. Additionally, as the limiting current density increased, the grain sizes near the positive and negative sides gradually enlarged, while the relative density initially increased before decreasing. A similar trend was observed when the current step rate decreased.</div></div>","PeriodicalId":17408,"journal":{"name":"Journal of The European Ceramic Society","volume":"45 3","pages":"Article 116982"},"PeriodicalIF":5.8,"publicationDate":"2024-10-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142434044","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
Preparation of magnetothermal Fe3O4/MgO/HA composite scaffolds for cancer hyperthermia by Vat Photopolymerization 通过槽式光聚合法制备用于癌症热疗的磁热 Fe3O4/MgO/HA 复合支架
IF 5.8 2区 材料科学 Q1 MATERIALS SCIENCE, CERAMICS Pub Date : 2024-10-11 DOI: 10.1016/j.jeurceramsoc.2024.116983
Chang Peng , Ming-Zhu Pan , Jia-Min Wu , Jin-Feng Yan , Qian-Xun Liu , Xiao-Yan Zhang , Xiu-Mei Wang , Yu-Sheng Shi
Bone defects resulting from bone tumor resections are often complicated with residual cancer cells. To address the challenge, the magnetothermal porous structured bone scaffolds of hydroxyapatite-Fe3O4-MgO (HA-FM) were fabricated by Vat Photopolymerization (VPP). This study improved curing behavior by doping Mg(OH)2 into Fe3O4 powder via the chemical deposition method. Mg(OH)2 functioned as a pore-forming agent during the sintering process, decomposing into MgO to enhance biocompatibility. A two-step debinding method combined with a carbon powder embedding sintering process was used employed to resolve the conflict between the removal of photosensitive resin and the oxidation of Fe3O4. After sintering at 1200°C, the porosity of the composite ceramics reached 69 % and a compressive strength of 2.28 MPa. In vitro mineralization tests showed that doping with Fe3O4 and Mg(OH)2 could promote the scaffolds’ degradation in simulated body fluid (SBF), beneficial to mineralization process. In vitro cell proliferation and adhesion experiments showed that ceramic samples were not cytotoxic and could promote osteogenic differentiation. The composite scaffolds exhibited magnetothermal properties, achieving a temperature increase of 8.2°C in the alternating magnetic field of 92 G and 100 kHz, indicating potential for cancer treatment.
骨肿瘤切除术造成的骨缺损往往与残留的癌细胞有关。为了应对这一挑战,研究人员采用蒸气光聚合(Vat Photopolymerization,VPP)技术制造了羟基磷灰石-Fe3O4-氧化镁(HA-FM)磁热多孔结构骨支架。本研究通过化学沉积法在 Fe3O4 粉末中掺入 Mg(OH)2 改善了固化行为。在烧结过程中,Mg(OH)2 可作为孔隙形成剂,分解成氧化镁,从而提高生物相容性。采用两步脱胶法结合碳粉包埋烧结工艺,解决了光敏树脂的去除与 Fe3O4 氧化之间的矛盾。在 1200°C 下烧结后,复合陶瓷的孔隙率达到 69%,抗压强度为 2.28 兆帕。体外矿化试验表明,掺入Fe3O4和Mg(OH)2可促进支架在模拟体液(SBF)中的降解,有利于矿化过程。体外细胞增殖和粘附实验表明,陶瓷样品没有细胞毒性,并能促进成骨分化。复合支架具有磁热特性,在 92 G 和 100 kHz 的交变磁场中温度可升高 8.2°C,这表明它具有治疗癌症的潜力。
{"title":"Preparation of magnetothermal Fe3O4/MgO/HA composite scaffolds for cancer hyperthermia by Vat Photopolymerization","authors":"Chang Peng ,&nbsp;Ming-Zhu Pan ,&nbsp;Jia-Min Wu ,&nbsp;Jin-Feng Yan ,&nbsp;Qian-Xun Liu ,&nbsp;Xiao-Yan Zhang ,&nbsp;Xiu-Mei Wang ,&nbsp;Yu-Sheng Shi","doi":"10.1016/j.jeurceramsoc.2024.116983","DOIUrl":"10.1016/j.jeurceramsoc.2024.116983","url":null,"abstract":"<div><div>Bone defects resulting from bone tumor resections are often complicated with residual cancer cells. To address the challenge, the magnetothermal porous structured bone scaffolds of hydroxyapatite-Fe<sub>3</sub>O<sub>4</sub>-MgO (HA-FM) were fabricated by Vat Photopolymerization (VPP). This study improved curing behavior by doping Mg(OH)<sub>2</sub> into Fe<sub>3</sub>O<sub>4</sub> powder via the chemical deposition method. Mg(OH)<sub>2</sub> functioned as a pore-forming agent during the sintering process, decomposing into MgO to enhance biocompatibility. A two-step debinding method combined with a carbon powder embedding sintering process was used employed to resolve the conflict between the removal of photosensitive resin and the oxidation of Fe<sub>3</sub>O<sub>4</sub>. After sintering at 1200°C, the porosity of the composite ceramics reached 69 % and a compressive strength of 2.28 MPa. In vitro mineralization tests showed that doping with Fe<sub>3</sub>O<sub>4</sub> and Mg(OH)<sub>2</sub> could promote the scaffolds’ degradation in simulated body fluid (SBF), beneficial to mineralization process. In vitro cell proliferation and adhesion experiments showed that ceramic samples were not cytotoxic and could promote osteogenic differentiation. The composite scaffolds exhibited magnetothermal properties, achieving a temperature increase of 8.2°C in the alternating magnetic field of 92 G and 100 kHz, indicating potential for cancer treatment.</div></div>","PeriodicalId":17408,"journal":{"name":"Journal of The European Ceramic Society","volume":"45 3","pages":"Article 116983"},"PeriodicalIF":5.8,"publicationDate":"2024-10-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142527705","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 energy-harvesting performance of (K, Na)NbO3-based ceramics through the synergistic effect of texture and defect engineering 通过纹理和缺陷工程的协同效应提高(K, Na)NbO3 基陶瓷的能量收集性能
IF 5.8 2区 材料科学 Q1 MATERIALS SCIENCE, CERAMICS Pub Date : 2024-10-11 DOI: 10.1016/j.jeurceramsoc.2024.116984
Yuzhi Zhai , Xudong Qi , Gang Tian , Jianxu Wang , Fapeng Yu , Zhigang Gai , Juan Du , Wenbin Su , Shiyi Guo , Limei Zheng
Textured CuO-doped KNN-based ceramics with [001]C orientation were developed to enhance energy harvesting performance. Textured ceramics doped with 0.3 mol% CuO exhibit remarkable piezoelectric coefficients d33 of 347 pC/N and g33 of 96 × 10−3 Vm/N, resulting in a higher figure of merit (d33 × g33 ∼ 33 × 10−12 m2/N) for evaluating energy conversion. The d33 and g33 increased by 105 % and 269 %, respectively, compared to those of randomly oriented ceramics. The piezoelectric energy harvester fabricated using the textured ceramic achieved an output power density of 3 μW/mm3, comparable to PZT-based energy harvesters. The enhancement in d33 is mainly due to favorable [00 l]C orientation. The orientation, along with the hardening effect caused by CuO doping, contributes to decreased dielectric coefficient εTr3, resulting in increased g33. The synergistic strategy is expected to facilitate the design high-performing, eco-friendly piezoelectric ceramics.
为了提高能量收集性能,我们开发了掺杂氧化铜的取向为 [001]C 的 KNN 基纹理陶瓷。掺杂了 0.3 mol% CuO 的纹理陶瓷显示出显著的压电系数 d33(347 pC/N)和 g33(96 × 10-3 Vm/N),因此在评估能量转换时具有更高的优越性(d33 × g33 ∼ 33 × 10-12 m2/N)。与随机取向陶瓷相比,d33 和 g33 分别增加了 105 % 和 269 %。使用纹理陶瓷制造的压电能量收集器的输出功率密度达到 3 μW/mm3,与基于 PZT 的能量收集器相当。d33 的增强主要归功于有利的 [00 l]C 取向。这种取向以及掺杂氧化铜所产生的硬化效应有助于降低介电系数εTr3,从而提高 g33。这种协同策略有望促进高性能、环保型压电陶瓷的设计。
{"title":"Improved energy-harvesting performance of (K, Na)NbO3-based ceramics through the synergistic effect of texture and defect engineering","authors":"Yuzhi Zhai ,&nbsp;Xudong Qi ,&nbsp;Gang Tian ,&nbsp;Jianxu Wang ,&nbsp;Fapeng Yu ,&nbsp;Zhigang Gai ,&nbsp;Juan Du ,&nbsp;Wenbin Su ,&nbsp;Shiyi Guo ,&nbsp;Limei Zheng","doi":"10.1016/j.jeurceramsoc.2024.116984","DOIUrl":"10.1016/j.jeurceramsoc.2024.116984","url":null,"abstract":"<div><div>Textured CuO-doped KNN-based ceramics with [001]<sub>C</sub> orientation were developed to enhance energy harvesting performance. Textured ceramics doped with 0.3 mol% CuO exhibit remarkable piezoelectric coefficients <em>d</em><sub>33</sub> of 347 pC/N and <em>g</em><sub>33</sub> of 96 × 10<sup>−3</sup> Vm/N, resulting in a higher figure of merit (<em>d</em><sub>33</sub> × <em>g</em><sub>33</sub> ∼ 33 × 10<sup>−12</sup> m<sup>2</sup>/N) for evaluating energy conversion. The <em>d</em><sub>33</sub> and <em>g</em><sub>33</sub> increased by 105 % and 269 %, respectively, compared to those of randomly oriented ceramics. The piezoelectric energy harvester fabricated using the textured ceramic achieved an output power density of 3 μW/mm<sup>3</sup>, comparable to PZT-based energy harvesters. The enhancement in <em>d</em><sub>33</sub> is mainly due to favorable [00 l]<sub>C</sub> orientation. The orientation, along with the hardening effect caused by CuO doping, contributes to decreased dielectric coefficient <em>ε</em><sup>T</sup><sub>r3</sub>, resulting in increased <em>g</em><sub>33</sub>. The synergistic strategy is expected to facilitate the design high-performing, eco-friendly piezoelectric ceramics.</div></div>","PeriodicalId":17408,"journal":{"name":"Journal of The European Ceramic Society","volume":"45 3","pages":"Article 116984"},"PeriodicalIF":5.8,"publicationDate":"2024-10-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142434045","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
Structural characteristics, P-V-L theory, Raman spectra, and microwave dielectric properties of (La1-xNdx)2(Zr0.96Ti0.04)3(MoO4)9 ceramics for LTCC applications 用于 LTCC 应用的 (La1-xNdx)2(Zr0.96Ti0.04)3(MoO4)9 陶瓷的结构特征、P-V-L 理论、拉曼光谱和微波介电性能
IF 5.8 2区 材料科学 Q1 MATERIALS SCIENCE, CERAMICS Pub Date : 2024-10-09 DOI: 10.1016/j.jeurceramsoc.2024.116974
Yuan-Bin Chen, Siyi Xiong
This article explores the microwave dielectric properties of (La1-xNdx)2(Zr0.96Ti0.04)3(MoO4)9 (x=0.1,0.3,0.5, and 0.7) ceramics prepared by solid-state reaction. Utilizing the Rietveld refinement technique in XRD, the sample is identified as a trigonal crystal system belonging to the R3¯c space group. SEM analysis indicates that relative density has a significant impact on the εr and Q×f of ceramics. The Q×f values of ceramics are closely related to the FWHM of the Raman spectra. At 750℃, (La0.5Nd0.5)2(Zr0.96Ti0.04)3(MoO4)9 ceramic exhibited excellent dielectric properties: εr = 10.4 (±0.08), Q×f = 149,300 (±3211) GHz, τf = −34.8 (±0.7) ppm/℃. To gain a deeper understanding of the intrinsic mechanisms governing the microwave dielectric properties of ceramics, analysis based on the P-V-L theory reveals that the La(Nd)-O bond and Mo-O bond contribute significantly to εr and Q×f, respectively.
本文探讨了固态反应制备的 (La1-xNdx)2(Zr0.96Ti0.04)3(MoO4)9(x=0.1、0.3、0.5 和 0.7)陶瓷的微波介电性能。利用 XRD 的里特维尔德细化技术,样品被确定为属于 R3¯c 空间群的三方晶系。SEM 分析表明,相对密度对陶瓷的 εr 和 Q×f 有显著影响。陶瓷的 Q×f 值与拉曼光谱的 FWHM 值密切相关。在 750℃时,(La0.5Nd0.5)2(Zr0.96Ti0.04)3(MoO4)9 陶瓷表现出优异的介电性能:εr = 10.4 (±0.08),Q×f = 149,300 (±3211) GHz,τf = -34.8 (±0.7) ppm/℃。为了更深入地了解陶瓷微波介电性能的内在机制,基于 P-V-L 理论的分析表明,La(Nd)-O 键和 Mo-O 键分别对 εr 和 Q×f 起着重要作用。
{"title":"Structural characteristics, P-V-L theory, Raman spectra, and microwave dielectric properties of (La1-xNdx)2(Zr0.96Ti0.04)3(MoO4)9 ceramics for LTCC applications","authors":"Yuan-Bin Chen,&nbsp;Siyi Xiong","doi":"10.1016/j.jeurceramsoc.2024.116974","DOIUrl":"10.1016/j.jeurceramsoc.2024.116974","url":null,"abstract":"<div><div>This article explores the microwave dielectric properties of (La<sub>1-x</sub>Nd<sub>x</sub>)<sub>2</sub>(Zr<sub>0.96</sub>Ti<sub>0.04</sub>)<sub>3</sub>(MoO<sub>4</sub>)<sub>9</sub> (x=0.1,0.3,0.5, and 0.7) ceramics prepared by solid-state reaction. Utilizing the Rietveld refinement technique in XRD, the sample is identified as a trigonal crystal system belonging to the <span><math><mrow><mi>R</mi><mover><mrow><mn>3</mn></mrow><mo>¯</mo></mover><mi>c</mi></mrow></math></span> space group. SEM analysis indicates that relative density has a significant impact on the ε<sub>r</sub> and Q×f of ceramics. The Q×f values of ceramics are closely related to the FWHM of the Raman spectra. At 750℃, (La<sub>0.5</sub>Nd<sub>0.5</sub>)<sub>2</sub>(Zr<sub>0.96</sub>Ti<sub>0.04</sub>)<sub>3</sub>(MoO<sub>4</sub>)<sub>9</sub> ceramic exhibited excellent dielectric properties: ε<sub>r</sub> = 10.4 (±0.08), Q×f = 149,300 (±3211) GHz, τ<sub>f</sub> = −34.8 (±0.7) ppm/℃. To gain a deeper understanding of the intrinsic mechanisms governing the microwave dielectric properties of ceramics, analysis based on the P-V-L theory reveals that the La(Nd)-O bond and Mo-O bond contribute significantly to ε<sub>r</sub> and Q×f, respectively.</div></div>","PeriodicalId":17408,"journal":{"name":"Journal of The European Ceramic Society","volume":"45 3","pages":"Article 116974"},"PeriodicalIF":5.8,"publicationDate":"2024-10-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142434043","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
High-entropy carbonitrides with superior oxidation resistance: Fabrication and investigation of oxidation behavior under non-isothermal and isothermal conditions 具有优异抗氧化性的高熵碳氮化物:非等温和等温条件下氧化行为的制造和研究
IF 5.8 2区 材料科学 Q1 MATERIALS SCIENCE, CERAMICS Pub Date : 2024-10-09 DOI: 10.1016/j.jeurceramsoc.2024.116980
Veronika Suvorova , Dmitrii Suvorov , Sergey Volodko , Maksim Poliakov , Lidiya Volkova , Andrey Nepapushev , Dmitry Moskovskikh
In this work, the influence of refractory Zr and Ti and their combination (Zr,Ti) on the oxidation behavior of the (Hf,Ta,Nb)(C,N) carbonitride under non-isothermal and isothermal conditions at 1200 °C was studied, the effect of nitrogen addition was demonstrated, and a possible oxidation mechanisms were identified. The best result was achieved for high-entropy carbonitride (Hf,Ta,Nb,Zr,Ti)(C,N). The introduction of nitrogen into the of high-entropy carbide lattice contributed to a decrease in the specific weight gain by 12 %, and the addition of Ti, Zr, and (Zr,Ti) to the (Hf,Ta,Nb)(C,N) – a decrease of 47, 65, and 83 %, respectively.
在这项工作中,研究了难熔 Zr 和 Ti 及其组合 (Zr,Ti) 在 1200 °C 的非等温和等温条件下对 (Hf,Ta,Nb)(C,N) 碳氮化物氧化行为的影响,证明了氮添加的效果,并确定了可能的氧化机制。高熵碳氮化物 (Hf,Ta,Nb,Zr,Ti)(C,N)取得了最佳结果。在高熵碳化物晶格中引入氮元素可使比增重减少 12%,而在(Hf,Ta,Nb)(C,N)中加入 Ti、Zr 和 (Zr,Ti) 则可使比增重分别减少 47%、65% 和 83%。
{"title":"High-entropy carbonitrides with superior oxidation resistance: Fabrication and investigation of oxidation behavior under non-isothermal and isothermal conditions","authors":"Veronika Suvorova ,&nbsp;Dmitrii Suvorov ,&nbsp;Sergey Volodko ,&nbsp;Maksim Poliakov ,&nbsp;Lidiya Volkova ,&nbsp;Andrey Nepapushev ,&nbsp;Dmitry Moskovskikh","doi":"10.1016/j.jeurceramsoc.2024.116980","DOIUrl":"10.1016/j.jeurceramsoc.2024.116980","url":null,"abstract":"<div><div>In this work, the influence of refractory Zr and Ti and their combination (Zr,Ti) on the oxidation behavior of the (Hf,Ta,Nb)(C,N) carbonitride under non-isothermal and isothermal conditions at 1200 °C was studied, the effect of nitrogen addition was demonstrated, and a possible oxidation mechanisms were identified. The best result was achieved for high-entropy carbonitride (Hf,Ta,Nb,Zr,Ti)(C,N). The introduction of nitrogen into the of high-entropy carbide lattice contributed to a decrease in the specific weight gain by 12 %, and the addition of Ti, Zr, and (Zr,Ti) to the (Hf,Ta,Nb)(C,N) – a decrease of 47, 65, and 83 %, respectively.</div></div>","PeriodicalId":17408,"journal":{"name":"Journal of The European Ceramic Society","volume":"45 3","pages":"Article 116980"},"PeriodicalIF":5.8,"publicationDate":"2024-10-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142420874","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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