首页 > 最新文献

Journal of The European Ceramic Society最新文献

英文 中文
Solution-based fabrication of high-performance K0.5Na0.5NbO3 thin films for surface haptics 表面触觉用高性能K0.5Na0.5NbO3薄膜的溶液制备
IF 6.2 2区 材料科学 Q1 MATERIALS SCIENCE, CERAMICS Pub Date : 2025-12-11 DOI: 10.1016/j.jeurceramsoc.2025.118077
Nagamalleswara Rao Alluri , Longfei Song , Stephanie Girod , Barnik Mandal , Juliette Cardoletti , Vid Bobnar , Torsten Granzow , Veronika Kovacova , Adrian-Marie Philippe , Emmanuel Defay , Sebastjan Glinsek
K0.5Na0.5NbO3 is among the most promising lead-free piezoelectrics. While its sputtered films match the performance of the champion piezoelectric Pb(Zr,Ti)O3, reproducible processing of high-quality and time-stable solution-deposited K0.5Na0.5NbO3 films remains challenging. Here, we report 1 µm-thick Mn-doped K0.5Na0.5NbO3 films prepared via a chemical solution deposition process, which have perfectly dense microstructure and uniform composition across their thickness. The films exhibit a high transverse piezoelectric coefficient (e31,f = −15.4 C/m2), high dielectric permittivity (εr ≈ 920), low dielectric losses (tanδ = 0.05) and can withstand electric fields up to at least 1 MV/cm. Their functional properties show excellent stability over time, and the synthesis process is reproducible. Furthermore, a surface acoustic haptic device based on K0.5Na0.5NbO3 thin-film actuators is demonstrated. The results validate the high potential of Mn-doped K0.5Na0.5NbO3 films to replace lead-based Pb(Zr,Ti)O3 films in piezoelectric applications.
K0.5Na0.5NbO3是最有前途的无铅压电材料之一。虽然其溅射薄膜的性能与冠军压电Pb(Zr,Ti)O3相匹配,但高质量和时间稳定的溶液沉积K0.5Na0.5NbO3薄膜的可重复性加工仍然具有挑战性。在这里,我们报道了通过化学溶液沉积工艺制备的1 μ m厚的mn掺杂K0.5Na0.5NbO3薄膜,该薄膜具有完美致密的微观结构和均匀的厚度组成。该薄膜具有较高的横向压电系数(e31,f =−15.4 C/m2),较高的介电常数(εr≈920),较低的介电损耗(tanδ = 0.05),并能承受至少1 MV/cm的电场。随着时间的推移,它们的功能特性表现出优异的稳定性,并且合成过程是可重复的。在此基础上,设计了一种基于K0.5Na0.5NbO3薄膜作动器的表面声触觉装置。结果验证了mn掺杂K0.5Na0.5NbO3薄膜在压电应用中取代铅基Pb(Zr,Ti)O3薄膜的高潜力。
{"title":"Solution-based fabrication of high-performance K0.5Na0.5NbO3 thin films for surface haptics","authors":"Nagamalleswara Rao Alluri ,&nbsp;Longfei Song ,&nbsp;Stephanie Girod ,&nbsp;Barnik Mandal ,&nbsp;Juliette Cardoletti ,&nbsp;Vid Bobnar ,&nbsp;Torsten Granzow ,&nbsp;Veronika Kovacova ,&nbsp;Adrian-Marie Philippe ,&nbsp;Emmanuel Defay ,&nbsp;Sebastjan Glinsek","doi":"10.1016/j.jeurceramsoc.2025.118077","DOIUrl":"10.1016/j.jeurceramsoc.2025.118077","url":null,"abstract":"<div><div>K<sub>0.5</sub>Na<sub>0.5</sub>NbO<sub>3</sub> is among the most promising lead-free piezoelectrics. While its sputtered films match the performance of the champion piezoelectric Pb(Zr,Ti)O<sub>3</sub>, reproducible processing of high-quality and time-stable solution-deposited K<sub>0.5</sub>Na<sub>0.5</sub>NbO<sub>3</sub> films remains challenging. Here, we report 1 µm-thick Mn-doped K<sub>0.5</sub>Na<sub>0.5</sub>NbO<sub>3</sub> films prepared via a chemical solution deposition process, which have perfectly dense microstructure and uniform composition across their thickness. The films exhibit a high transverse piezoelectric coefficient (<em>e</em><sub><em>31</em>,f</sub> = −15.4 C/m<sup>2</sup>), high dielectric permittivity (<em>ε</em><sub>r</sub> ≈ 920), low dielectric losses (tan<em>δ</em> = 0.05) and can withstand electric fields up to at least 1 MV/cm. Their functional properties show excellent stability over time, and the synthesis process is reproducible. Furthermore, a surface acoustic haptic device based on K<sub>0.5</sub>Na<sub>0.5</sub>NbO<sub>3</sub> thin-film actuators is demonstrated. The results validate the high potential of Mn-doped K<sub>0.5</sub>Na<sub>0.5</sub>NbO<sub>3</sub> films to replace lead-based Pb(Zr,Ti)O<sub>3</sub> films in piezoelectric applications.</div></div>","PeriodicalId":17408,"journal":{"name":"Journal of The European Ceramic Society","volume":"46 6","pages":"Article 118077"},"PeriodicalIF":6.2,"publicationDate":"2025-12-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145798202","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
Excellent comprehensive piezoelectric performance of textured 0.965(K0.48Na0.52)0.99Li0.01(Nb0.98Sb0.02)O3-0.035(Bi0.50Na0.50)ZrO3 ceramic 0.965(K0.48Na0.52)0.99Li0.01(Nb0.98Sb0.02)O3-0.035(Bi0.50Na0.50)ZrO3陶瓷具有优异的综合压电性能
IF 6.2 2区 材料科学 Q1 MATERIALS SCIENCE, CERAMICS Pub Date : 2025-12-11 DOI: 10.1016/j.jeurceramsoc.2025.118079
Jialiang Zhang, Lu Li, Fengyun Liu
The (K,Na)NbO3-based ceramics are an attractive type of lead-free piezoelectric materials. However, due to polymorphic phase transitions, obtaining an excellent comprehensive piezoelectric performance of high piezoelectric coefficient d33, large electromechanical coupling factors (representatively, kp, kt and k33) and good thermal stabilities of weak temperature dependence and little thermal-ageing degradation is significantly challenging. The 0.965(K0.48Na0.52)0.99Li0.01(Nb0.98Sb0.02)O3-0.035(Bi0.50Na0.50)ZrO3 composition was recently found to possess a great potential for resolving the issue. Its ordinary ceramic exhibits considerably good piezoelectric properties and thermal stabilities. The < 001> textured ceramic has a highly diffused orthorhombic-tetragonal phase transition, and shows a further enhanced temperature stability. It has d33 of 370 pC/N with little change up to 170 °C, and its kp varies between 0.605 and 0.525 in the temperature range from −60 °C to 150 °C. In general, this textured ceramic is well comparable to the famous commercial soft PZT-5A, and thus provides a large possibility for practical device applications.
(K,Na) nbo3基陶瓷是一种极具吸引力的无铅压电材料。然而,由于多晶相变的存在,获得高压电系数d33、大机电耦合系数kp、kt和k33以及温度依赖性弱、热老化退化小的良好热稳定性等优异的综合压电性能具有很大的挑战性。最近发现,0.965(K0.48Na0.52)0.99Li0.01(Nb0.98Sb0.02)O3-0.035(Bi0.50Na0.50)ZrO3组合物具有解决这一问题的巨大潜力。其普通陶瓷具有相当好的压电性能和热稳定性。<; 001>;织构陶瓷具有高度扩散的正交-四方相变,并进一步增强了温度稳定性。d33为370 pC/N,在170 ℃以下变化不大,kp在−60℃~ 150 ℃范围内变化在0.605 ~ 0.525之间。总的来说,这种纹理陶瓷与著名的商用软质PZT-5A相当,因此为实际器件应用提供了很大的可能性。
{"title":"Excellent comprehensive piezoelectric performance of textured 0.965(K0.48Na0.52)0.99Li0.01(Nb0.98Sb0.02)O3-0.035(Bi0.50Na0.50)ZrO3 ceramic","authors":"Jialiang Zhang,&nbsp;Lu Li,&nbsp;Fengyun Liu","doi":"10.1016/j.jeurceramsoc.2025.118079","DOIUrl":"10.1016/j.jeurceramsoc.2025.118079","url":null,"abstract":"<div><div>The (K,Na)NbO<sub>3</sub>-based ceramics are an attractive type of lead-free piezoelectric materials. However, due to polymorphic phase transitions, obtaining an excellent comprehensive piezoelectric performance of high piezoelectric coefficient <em>d</em><sub>33</sub>, large electromechanical coupling factors (representatively, <em>k</em><sub>p</sub>, <em>k</em><sub>t</sub> and <em>k</em><sub>33</sub>) and good thermal stabilities of weak temperature dependence and little thermal-ageing degradation is significantly challenging. The 0.965(K<sub>0.48</sub>Na<sub>0.52</sub>)<sub>0.99</sub>Li<sub>0.01</sub>(Nb<sub>0.98</sub>Sb<sub>0.02</sub>)O<sub>3</sub>-0.035(Bi<sub>0.50</sub>Na<sub>0.50</sub>)ZrO<sub>3</sub> composition was recently found to possess a great potential for resolving the issue. Its ordinary ceramic exhibits considerably good piezoelectric properties and thermal stabilities. The &lt; 001&gt; textured ceramic has a highly diffused orthorhombic-tetragonal phase transition, and shows a further enhanced temperature stability. It has <em>d</em><sub>33</sub> of 370 pC/N with little change up to 170 °C, and its <em>k</em><sub>p</sub> varies between 0.605 and 0.525 in the temperature range from −60 °C to 150 °C. In general, this textured ceramic is well comparable to the famous commercial soft PZT-5A, and thus provides a large possibility for practical device applications.</div></div>","PeriodicalId":17408,"journal":{"name":"Journal of The European Ceramic Society","volume":"46 6","pages":"Article 118079"},"PeriodicalIF":6.2,"publicationDate":"2025-12-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145798191","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
From powders to microfibers: Morphology-dependent phase transformation pathways in alumina-mullite ceramics 从粉末到微纤维:氧化铝-莫来石陶瓷中形态依赖的相变途径
IF 6.2 2区 材料科学 Q1 MATERIALS SCIENCE, CERAMICS Pub Date : 2025-12-10 DOI: 10.1016/j.jeurceramsoc.2025.118073
Qiang Liu , Xiaxue Zhang , Huiting Luo , Kai Cui , Lingjiao Zhan , Shuwei Yao
The phase transformation pathways in alumina-mullite ceramics are strongly influenced by precursor morphological dimensionality, where atomic-scale coordination environments are shown to critically affect crystallization kinetics. Through sol-gel synthesis of three distinct architectures—powders, nanofibers, and microfibers—we demonstrate that morphological scale controls the formation of aluminum coordination defects during pyrolysis. XRD and TEM analyses established morphology-dependent phase evolution: microfibers directly crystallize into orthorhombic mullite above 1000 °C, while nanofibers undergo sequential γ→θ alumina transitions prior to mullitization. Solid-state 27Al MAS NMR revealed that microfibers develop substantial pentacoordinated Al (AlO5), suggesting the generation of anionic vacancies that facilitate Si infiltration and enable mullite nucleation at temperatures as low as 800 °C. In contrast, nanofibers predominantly retain octahedral/tetrahedral Al configurations, which appear to impose kinetic barriers to Al/Si interdiffusion and preferentially stabilize γ-Al2O3. This work supports a vacancy-mediated diffusion mechanism, demonstrating that morphological engineering can effectively guide phase selection in multicomponent ceramic systems.
氧化铝-莫来石陶瓷的相变路径受前驱体形态维度的强烈影响,其中原子尺度的配位环境对结晶动力学有重要影响。通过溶胶-凝胶合成三种不同的结构——粉末、纳米纤维和微纤维——我们证明了形态尺度控制了热解过程中铝配位缺陷的形成。XRD和TEM分析表明,微纤维在1000℃以上直接结晶为正交莫来石,而纳米纤维在莫来石化之前经历了顺序的γ→θ氧化铝转变。固态27Al MAS NMR显示,微纤维产生了大量的五配位Al (AlO5),这表明阴离子空位的产生促进了Si的渗透,并使莫来石在低至800℃的温度下成核。相比之下,纳米纤维主要保留八面体/四面体Al构型,这似乎对Al/Si相互扩散施加了动力学障碍,并优先稳定γ-Al2O3。这项工作支持了空位介导的扩散机制,表明形态工程可以有效地指导多组分陶瓷系统的相选择。
{"title":"From powders to microfibers: Morphology-dependent phase transformation pathways in alumina-mullite ceramics","authors":"Qiang Liu ,&nbsp;Xiaxue Zhang ,&nbsp;Huiting Luo ,&nbsp;Kai Cui ,&nbsp;Lingjiao Zhan ,&nbsp;Shuwei Yao","doi":"10.1016/j.jeurceramsoc.2025.118073","DOIUrl":"10.1016/j.jeurceramsoc.2025.118073","url":null,"abstract":"<div><div>The phase transformation pathways in alumina-mullite ceramics are strongly influenced by precursor morphological dimensionality, where atomic-scale coordination environments are shown to critically affect crystallization kinetics. Through sol-gel synthesis of three distinct architectures—powders, nanofibers, and microfibers—we demonstrate that morphological scale controls the formation of aluminum coordination defects during pyrolysis. XRD and TEM analyses established morphology-dependent phase evolution: microfibers directly crystallize into orthorhombic mullite above 1000 °C, while nanofibers undergo sequential γ→θ alumina transitions prior to mullitization. Solid-state <sup>27</sup>Al MAS NMR revealed that microfibers develop substantial pentacoordinated Al (AlO<sub>5</sub>), suggesting the generation of anionic vacancies that facilitate Si infiltration and enable mullite nucleation at temperatures as low as 800 °C. In contrast, nanofibers predominantly retain octahedral/tetrahedral Al configurations, which appear to impose kinetic barriers to Al/Si interdiffusion and preferentially stabilize γ-Al<sub>2</sub>O<sub>3</sub>. This work supports a vacancy-mediated diffusion mechanism, demonstrating that morphological engineering can effectively guide phase selection in multicomponent ceramic systems.</div></div>","PeriodicalId":17408,"journal":{"name":"Journal of The European Ceramic Society","volume":"46 6","pages":"Article 118073"},"PeriodicalIF":6.2,"publicationDate":"2025-12-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145749574","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
Boosting the ultra-high temperature erosion stability of MoSi2 coating at 1800 ℃ by solid solution film-forming 采用固溶成膜的方法提高了MoSi2涂层在1800℃下的超高温侵蚀稳定性
IF 6.2 2区 材料科学 Q1 MATERIALS SCIENCE, CERAMICS Pub Date : 2025-12-10 DOI: 10.1016/j.jeurceramsoc.2025.118075
Ruixiong zhai , Taihong Huang , Dehao Kong , Qingshan Yang , Tao Wang , Chen Hua , Xiping Xiong , Yuwei Liang , Peng Song
To overcome the protection failure of MoSi2 coatings caused by the poor stability of the oxide scale at ultra-high temperatures, a solid solution film-forming strategy was proposed. The MoSi2–ZrB2 composite coating was successfully fabricated, and its erosion resistance at 1800 °C was systematically investigated. The results demonstrated that the MoSi2-ZrB2 composite coating exhibited superior high temperature erosion protection. After the ultra-high temperature erosion test, the mass erosion rate of MoSi2-ZrB2 composite coating was 0.013 mg/s, which is obviously lower than that the MoSi2 coating (0.133 mg/s). Compared to the MoSi2 coating, the MoSi2-ZrB2 composite coating maintained a dense and crack-free oxide scale. The enhanced performance originates from the formation of a highly stable composite glass phase (SiO2-ZrO2/ZrSiO4). Furthermore, the in-situ formation of the MoB phase effectively suppressed gases volatilization, synergistically improving the structural stability of the oxide layer and its oxygen-blocking capability.
为克服氧化膜在超高温下稳定性差导致MoSi2涂层保护失效的问题,提出了固溶体成膜策略。成功制备了MoSi2-ZrB2复合涂层,并对其在1800℃下的耐蚀性进行了系统的研究。结果表明,MoSi2-ZrB2复合涂层具有良好的耐高温侵蚀性能。经过超高温冲蚀试验,MoSi2- zrb2复合涂层的质量冲蚀速率为0.013 mg/s,明显低于MoSi2涂层的0.133 mg/s。与MoSi2涂层相比,MoSi2- zrb2复合涂层保持了致密且无裂纹的氧化层。性能的增强源于形成了高度稳定的复合玻璃相(SiO2-ZrO2/ZrSiO4)。此外,原位形成的MoB相有效地抑制了气体的挥发,协同提高了氧化层的结构稳定性和阻氧能力。
{"title":"Boosting the ultra-high temperature erosion stability of MoSi2 coating at 1800 ℃ by solid solution film-forming","authors":"Ruixiong zhai ,&nbsp;Taihong Huang ,&nbsp;Dehao Kong ,&nbsp;Qingshan Yang ,&nbsp;Tao Wang ,&nbsp;Chen Hua ,&nbsp;Xiping Xiong ,&nbsp;Yuwei Liang ,&nbsp;Peng Song","doi":"10.1016/j.jeurceramsoc.2025.118075","DOIUrl":"10.1016/j.jeurceramsoc.2025.118075","url":null,"abstract":"<div><div>To overcome the protection failure of MoSi<sub>2</sub> coatings caused by the poor stability of the oxide scale at ultra-high temperatures, a solid solution film-forming strategy was proposed. The MoSi<sub>2</sub>–ZrB<sub>2</sub> composite coating was successfully fabricated, and its erosion resistance at 1800 °C was systematically investigated. The results demonstrated that the MoSi<sub>2</sub>-ZrB<sub>2</sub> composite coating exhibited superior high temperature erosion protection. After the ultra-high temperature erosion test, the mass erosion rate of MoSi<sub>2</sub>-ZrB<sub>2</sub> composite coating was 0.013 mg/s, which is obviously lower than that the MoSi<sub>2</sub> coating (0.133 mg/s). Compared to the MoSi<sub>2</sub> coating, the MoSi<sub>2</sub>-ZrB<sub>2</sub> composite coating maintained a dense and crack-free oxide scale. The enhanced performance originates from the formation of a highly stable composite glass phase (SiO<sub>2</sub>-ZrO<sub>2</sub>/ZrSiO<sub>4</sub>). Furthermore, the in-situ formation of the MoB phase effectively suppressed gases volatilization, synergistically improving the structural stability of the oxide layer and its oxygen-blocking capability.</div></div>","PeriodicalId":17408,"journal":{"name":"Journal of The European Ceramic Society","volume":"46 6","pages":"Article 118075"},"PeriodicalIF":6.2,"publicationDate":"2025-12-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145749572","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
Fabrication of ZTA/ZTA joints with high strength based on interface interlocking strategy by using glass filler 采用玻璃填料制备基于界面联锁策略的高强度ZTA/ZTA接头
IF 6.2 2区 材料科学 Q1 MATERIALS SCIENCE, CERAMICS Pub Date : 2025-12-09 DOI: 10.1016/j.jeurceramsoc.2025.118072
Haolong Zheng , Weiwei Zhu , Mu Tang , Haohao Zou , Guoqing Zu , Ying Han , Xu Ran
In this study, the La2O3-Y2O3-B2O3-SiO2 glass filler was used to join zirconia toughened alumina (ZTA) ceramics. The three-dimensional interlocking interface structure formed between the brazing seam and the ceramic due to the in-situ dissolution of ZrO2 from the substrate, leading a strong interfacial bonding. Crystallization treatment promoted the formation of YNbO4 and Al2O3, which reduced the coefficient of thermal expansion (CTE) difference between the brazing seams and the ZTA ceramics. Owing to the improved interface structure and the matched CTE, the joints reached a flexural strength of 530 ± 20 MPa.
本研究采用La2O3-Y2O3-B2O3-SiO2玻璃填料加入氧化锆增韧氧化铝(ZTA)陶瓷。由于基体中ZrO2的原位溶解,钎焊焊缝与陶瓷之间形成三维互锁界面结构,界面结合牢固。晶化处理促进了YNbO4和Al2O3的形成,减小了钎焊焊缝与ZTA陶瓷之间的热膨胀系数(CTE)差异。通过改进界面结构和匹配CTE,接头的抗弯强度达到530 ± 20 MPa。
{"title":"Fabrication of ZTA/ZTA joints with high strength based on interface interlocking strategy by using glass filler","authors":"Haolong Zheng ,&nbsp;Weiwei Zhu ,&nbsp;Mu Tang ,&nbsp;Haohao Zou ,&nbsp;Guoqing Zu ,&nbsp;Ying Han ,&nbsp;Xu Ran","doi":"10.1016/j.jeurceramsoc.2025.118072","DOIUrl":"10.1016/j.jeurceramsoc.2025.118072","url":null,"abstract":"<div><div>In this study, the La<sub>2</sub>O<sub>3</sub>-Y<sub>2</sub>O<sub>3</sub>-B<sub>2</sub>O<sub>3</sub>-SiO<sub>2</sub> glass filler was used to join zirconia toughened alumina (ZTA) ceramics. The three-dimensional interlocking interface structure formed between the brazing seam and the ceramic due to the in-situ dissolution of ZrO<sub>2</sub> from the substrate, leading a strong interfacial bonding. Crystallization treatment promoted the formation of YNbO<sub>4</sub> and Al<sub>2</sub>O<sub>3</sub>, which reduced the coefficient of thermal expansion (CTE) difference between the brazing seams and the ZTA ceramics. Owing to the improved interface structure and the matched CTE, the joints reached a flexural strength of 530 ± 20 MPa.</div></div>","PeriodicalId":17408,"journal":{"name":"Journal of The European Ceramic Society","volume":"46 6","pages":"Article 118072"},"PeriodicalIF":6.2,"publicationDate":"2025-12-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145798199","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
Scratching of 2.5D C/SiC composites considering real abrasive morphology and material microstructure: Microscopic simulation and experimental study 考虑真实磨粒形貌和材料微观结构的2.5D C/SiC复合材料划伤:微观模拟和实验研究
IF 6.2 2区 材料科学 Q1 MATERIALS SCIENCE, CERAMICS Pub Date : 2025-12-08 DOI: 10.1016/j.jeurceramsoc.2025.118065
Ye Guo , Bing Chen , Rukai Liu , Junchang Liu , Fei Su , Zhaohui Deng
To address the oversimplification of abrasive morphology and composite structure in current 2.5D C/SiC composite scratching simulations, this study constructed a truncated octahedral abrasive model and established unidirectional (UD) and short-fiber reinforced polymer (SFRP) representative volume elements according to the composite's typical regional features. Four typical fiber region scratching simulations were conducted. Combined with experimental data, including scratching force, surface morphology, contour curves, and acoustic emission signals, material removal mechanisms were analyzed in depth. The results show that different fiber regions exhibit distinct mechanical responses and damage modes, influenced by carbon fiber anisotropy. At the same scratching depth, average force decreases in the order: 90° fiber region, needled fiber region, 0° fiber region, and SFRP region. With increasing depth, 90° region damage extends primarily longitudinally, while 0° region damage expands mainly transversely with less longitudinal extension. SFRP and needled regions show lighter damage in both directions.
针对目前2.5D C/SiC复合材料划伤模拟中磨料形貌和复合材料结构过于简单化的问题,本研究构建了截断八面体磨料模型,并根据复合材料的典型区域特征建立了单向(UD)和短纤维增强聚合物(SFRP)的代表性体积元。进行了四种典型的光纤区域划痕模拟。结合刮擦力、表面形貌、轮廓曲线和声发射信号等实验数据,深入分析了材料的去除机理。结果表明,受碳纤维各向异性的影响,不同纤维区域表现出不同的力学响应和损伤模式。在相同划痕深度下,平均力减小的顺序为:90°纤维区、针刺纤维区、0°纤维区、SFRP区。随着深度的增加,90°区域损伤主要纵向扩展,而0°区域损伤主要横向扩展,纵向扩展较少。SFRP和针刺区在两个方向上都表现出较轻的损伤。
{"title":"Scratching of 2.5D C/SiC composites considering real abrasive morphology and material microstructure: Microscopic simulation and experimental study","authors":"Ye Guo ,&nbsp;Bing Chen ,&nbsp;Rukai Liu ,&nbsp;Junchang Liu ,&nbsp;Fei Su ,&nbsp;Zhaohui Deng","doi":"10.1016/j.jeurceramsoc.2025.118065","DOIUrl":"10.1016/j.jeurceramsoc.2025.118065","url":null,"abstract":"<div><div>To address the oversimplification of abrasive morphology and composite structure in current 2.5D C/SiC composite scratching simulations, this study constructed a truncated octahedral abrasive model and established unidirectional (UD) and short-fiber reinforced polymer (SFRP) representative volume elements according to the composite's typical regional features. Four typical fiber region scratching simulations were conducted. Combined with experimental data, including scratching force, surface morphology, contour curves, and acoustic emission signals, material removal mechanisms were analyzed in depth. The results show that different fiber regions exhibit distinct mechanical responses and damage modes, influenced by carbon fiber anisotropy. At the same scratching depth, average force decreases in the order: 90° fiber region, needled fiber region, 0° fiber region, and SFRP region. With increasing depth, 90° region damage extends primarily longitudinally, while 0° region damage expands mainly transversely with less longitudinal extension. SFRP and needled regions show lighter damage in both directions.</div></div>","PeriodicalId":17408,"journal":{"name":"Journal of The European Ceramic Society","volume":"46 6","pages":"Article 118065"},"PeriodicalIF":6.2,"publicationDate":"2025-12-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145749569","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
Fracture criteria of self-healing ceramics determined by the competition between crack propagation and self-healing 裂纹扩展与自愈的竞争决定了自愈陶瓷的断裂准则
IF 6.2 2区 材料科学 Q1 MATERIALS SCIENCE, CERAMICS Pub Date : 2025-12-08 DOI: 10.1016/j.jeurceramsoc.2025.118071
JangWon Lee , Wataru Nakao
A method was investigated to utilize the competition behavior between crack propagation and crack degeneration due to self-healing in continuous fiber-reinforced self-healing composite ceramics (abbreviated as shFRC) as a new strength criterion. A stationary load test was performed at 1100 °C, and the overall elongation of the test specimen resulting was measured. At 65 MPa and 80 MPa, the crack hardly propagated, and the crack degeneration due to self-healing, so the crack arrest time became constant. At 90 MPa to 110 MPa, competition between crack propagation and crack degeneration due to self-healing occurred, but the crack was arrested. At 125 MPa to 140 MPa, crack propagation was inhibited, but eventually led to fracture. As a result, the maximum stress at which crack propagation due to self-healing can be arrested was determined to be 115 MPa. This stress corresponds to 80 % of the fracture strength and has been named the self-healing limit stress.
研究了一种利用连续纤维增强自愈复合陶瓷(shFRC)裂纹扩展与自愈退化之间的竞争行为作为新的强度准则的方法。在1100 °C下进行静载试验,并测量试样的总伸长率。在65 MPa和80 MPa时,裂纹几乎不扩展,裂纹自愈退化,裂纹止裂时间趋于恒定。在90 MPa ~ 110 MPa时,裂纹扩展与裂纹自愈退化相互竞争,但裂纹被抑制。在125 ~ 140 MPa时,裂纹扩展受到抑制,但最终导致断裂。结果表明,阻止裂纹自愈扩展的最大应力为115 MPa。该应力相当于断裂强度的80% %,被称为自愈极限应力。
{"title":"Fracture criteria of self-healing ceramics determined by the competition between crack propagation and self-healing","authors":"JangWon Lee ,&nbsp;Wataru Nakao","doi":"10.1016/j.jeurceramsoc.2025.118071","DOIUrl":"10.1016/j.jeurceramsoc.2025.118071","url":null,"abstract":"<div><div>A method was investigated to utilize the competition behavior between crack propagation and crack degeneration due to self-healing in continuous fiber-reinforced self-healing composite ceramics (abbreviated as shFRC) as a new strength criterion. A stationary load test was performed at 1100 °C, and the overall elongation of the test specimen resulting was measured. At 65 MPa and 80 MPa, the crack hardly propagated, and the crack degeneration due to self-healing, so the crack arrest time became constant. At 90 MPa to 110 MPa, competition between crack propagation and crack degeneration due to self-healing occurred, but the crack was arrested. At 125 MPa to 140 MPa, crack propagation was inhibited, but eventually led to fracture. As a result, the maximum stress at which crack propagation due to self-healing can be arrested was determined to be 115 MPa. This stress corresponds to 80 % of the fracture strength and has been named the self-healing limit stress.</div></div>","PeriodicalId":17408,"journal":{"name":"Journal of The European Ceramic Society","volume":"46 6","pages":"Article 118071"},"PeriodicalIF":6.2,"publicationDate":"2025-12-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145798196","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
Novel Mg7Ga2GeO12 microwave dielectric ceramics with ultralow-loss and low-permittivity for high-frequency packaging substrate 新型超低损耗低介电常数Mg7Ga2GeO12微波介质陶瓷用于高频封装衬底
IF 6.2 2区 材料科学 Q1 MATERIALS SCIENCE, CERAMICS Pub Date : 2025-12-08 DOI: 10.1016/j.jeurceramsoc.2025.118067
Hongji Zou , Jie Li , Ziyi Zhang , Ying Tang , Weiping Gong , Liang Fang
Novel low-permittivity Mg7Ga2GeO12 ceramics with unique crystal structure consisting of rock-salt and β-Ga2O3 blocks were prepared by the solid-state method. When sintered at 1380 °C, it showed ultra-high Q×f = 145,000 ± 300 GHz, low εr = 10.5 ± 0.1, and τf = −50.7 ± 1.0 ppm/°C. The positive deviation between the εr and εr(C–M) (8.7) of 21.2 % was due to the underestimating dielectric polarizability. The Phillips-Van Vechten-Levine (P-V-L) theory results indicated that the (Mg4/Ga1)-O bond had the greatest impact on the εr and thermal stability, while the (Ga5/Ge1)-O bond mainly contributes to lattice energy. The intrinsic dielectric properties were analyzed by infrared reflectivity spectra. To demonstrate its potential for practical applications, a dielectric resonator antenna (DRA) based on Mg7Ga2GeO12 ceramic was designed and fabricated, exhibiting a high gain (6.6 dBi) and radiation efficiency (> 98.3 %).
采用固态法制备了由岩盐和β-Ga2O3块体组成的具有独特晶体结构的新型低介电常数Mg7Ga2GeO12陶瓷。烧结在1380°C时,它显示超高Q×f = 145000 ± 300 GHz,低εr = 10.5  ±0.1 ,和τf = −50.7 ± 1.0 ppm /°C。εr与εr(C-M)(8.7)的正偏差为21.2% %,是由于低估了介电极化率。philips - van veechten - levine (P-V-L)理论结果表明,(Mg4/Ga1)-O键对εr和热稳定性的影响最大,而(Ga5/Ge1)-O键对晶格能的影响最大。利用红外反射光谱分析了材料的本征介电特性。为了证明其实际应用潜力,设计并制作了一种基于Mg7Ga2GeO12陶瓷的介质谐振器天线(DRA),具有较高的增益(6.6 dBi)和辐射效率(> 98.3% %)。
{"title":"Novel Mg7Ga2GeO12 microwave dielectric ceramics with ultralow-loss and low-permittivity for high-frequency packaging substrate","authors":"Hongji Zou ,&nbsp;Jie Li ,&nbsp;Ziyi Zhang ,&nbsp;Ying Tang ,&nbsp;Weiping Gong ,&nbsp;Liang Fang","doi":"10.1016/j.jeurceramsoc.2025.118067","DOIUrl":"10.1016/j.jeurceramsoc.2025.118067","url":null,"abstract":"<div><div>Novel low-permittivity Mg<sub>7</sub>Ga<sub>2</sub>GeO<sub>12</sub> ceramics with unique crystal structure consisting of rock-salt and <em>β</em>-Ga<sub>2</sub>O<sub>3</sub> blocks were prepared by the solid-state method. When sintered at 1380 °C, it showed ultra-high <em>Q</em>×<em>f</em> = 145,000 ± 300 GHz, low <em>ε</em><sub><em>r</em></sub> = 10.5 ± 0.1, and <em>τ</em><sub><em>f</em></sub> = −50.7 ± 1.0 ppm/°C. The positive deviation between the <em>ε</em><sub><em>r</em></sub> and <em>ε</em><sub><em>r</em>(C–M)</sub> (8.7) of 21.2 % was due to the underestimating dielectric polarizability. The Phillips-Van Vechten-Levine (P-V-L) theory results indicated that the (Mg4/Ga1)-O bond had the greatest impact on the <em>ε</em><sub><em>r</em></sub> and thermal stability, while the (Ga5/Ge1)-O bond mainly contributes to lattice energy. The intrinsic dielectric properties were analyzed by infrared reflectivity spectra. To demonstrate its potential for practical applications, a dielectric resonator antenna (DRA) based on Mg<sub>7</sub>Ga<sub>2</sub>GeO<sub>12</sub> ceramic was designed and fabricated, exhibiting a high gain (6.6 dBi) and radiation efficiency (&gt; 98.3 %).</div></div>","PeriodicalId":17408,"journal":{"name":"Journal of The European Ceramic Society","volume":"46 6","pages":"Article 118067"},"PeriodicalIF":6.2,"publicationDate":"2025-12-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145798188","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
Low-temperature pressure-less joining of SiCf/SiC via NITE sintering: Mechanical performance and steam oxidation resistance 低温无压烧结SiCf/SiC:力学性能和抗蒸汽氧化性
IF 6.2 2区 材料科学 Q1 MATERIALS SCIENCE, CERAMICS Pub Date : 2025-12-08 DOI: 10.1016/j.jeurceramsoc.2025.118070
Lingzhi Chen , Ce Zheng , Dongying Wang , Yichun Bi , Chaofan Yang , Shengkai Wang , Xiaoqiang Li
Developing a pressure-less joining process operable at tolerable temperatures is crucial for practical engineering deployment of SiCf/SiC thin-walled cladding tubes. Hereby, we invented a low-temperature pressure-less Nano-Infiltration and Transient Eutectic (NITE) joining method for SiCf/SiC composites using Al2O3 and Y2O3 sintering additives, achieving successful bonding at 1600 ℃ for 2.5 h without interfacial debonding. The joint microstructure consisted of SiC with finely distributed Y3Al5O12 intergranular phase, exhibiting excellent integrity and mechanical performance (shear strength of 46.7 ± 2.7 MPa). After 8 h steam oxidation at 1200 ℃, joints retained 77.9 % strength (36.4 ± 6.8 MPa) through protective SiO2/AlOOH layers and Y-silicate transformations. Successful SiCf/SiC cladding tube encapsulation demonstrated technical feasibility, with XCT revealing robust bonding despite minor inner-wall densification issues. This work establishes NITE as a viable solution for nuclear applications, combining favorable processing conditions with superior joint performance.
开发一种可在耐受温度下操作的无压力连接工艺对于SiCf/SiC薄壁包层管的实际工程部署至关重要。因此,我们发明了一种低温无压力的SiCf/SiC复合材料的纳米渗滤和瞬态共晶(NITE)连接方法,使用Al2O3和Y2O3烧结添加剂,在1600℃下,2.5 h下成功结合,没有界面脱落。节理组织由SiC和分布较细的Y3Al5O12晶间相组成,具有良好的整体性和力学性能(抗剪强度为46.7 ± 2.7 MPa)。经1200℃8 h蒸汽氧化处理后,通过SiO2/AlOOH保护层和y -硅酸盐相变,接头强度保持77.9% %(36.4 ± 6.8 MPa)。成功的SiCf/SiC包层管封装证明了技术上的可行性,XCT显示尽管存在较小的内壁致密化问题,但坚固的结合。这项工作建立了NITE作为核应用的可行解决方案,结合了有利的处理条件和优越的联合性能。
{"title":"Low-temperature pressure-less joining of SiCf/SiC via NITE sintering: Mechanical performance and steam oxidation resistance","authors":"Lingzhi Chen ,&nbsp;Ce Zheng ,&nbsp;Dongying Wang ,&nbsp;Yichun Bi ,&nbsp;Chaofan Yang ,&nbsp;Shengkai Wang ,&nbsp;Xiaoqiang Li","doi":"10.1016/j.jeurceramsoc.2025.118070","DOIUrl":"10.1016/j.jeurceramsoc.2025.118070","url":null,"abstract":"<div><div>Developing a pressure-less joining process operable at tolerable temperatures is crucial for practical engineering deployment of SiC<sub>f</sub>/SiC thin-walled cladding tubes. Hereby, we invented a low-temperature pressure-less Nano-Infiltration and Transient Eutectic (NITE) joining method for SiC<sub>f</sub>/SiC composites using Al<sub>2</sub>O<sub>3</sub> and Y<sub>2</sub>O<sub>3</sub> sintering additives, achieving successful bonding at 1600 ℃ for 2.5 h without interfacial debonding. The joint microstructure consisted of SiC with finely distributed Y<sub>3</sub>Al<sub>5</sub>O<sub>12</sub> intergranular phase, exhibiting excellent integrity and mechanical performance (shear strength of 46.7 ± 2.7 MPa). After 8 h steam oxidation at 1200 ℃, joints retained 77.9 % strength (36.4 ± 6.8 MPa) through protective SiO<sub>2</sub>/AlOOH layers and Y-silicate transformations. Successful SiC<sub>f</sub>/SiC cladding tube encapsulation demonstrated technical feasibility, with XCT revealing robust bonding despite minor inner-wall densification issues. This work establishes NITE as a viable solution for nuclear applications, combining favorable processing conditions with superior joint performance.</div></div>","PeriodicalId":17408,"journal":{"name":"Journal of The European Ceramic Society","volume":"46 6","pages":"Article 118070"},"PeriodicalIF":6.2,"publicationDate":"2025-12-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145749570","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
Synergistic tuning of electrical and thermal transport properties in Bi2SeS2 thermoelectric material via Ti/Cu co-doping Ti/Cu共掺杂对Bi2SeS2热电材料电输运和热输运性能的协同调节
IF 6.2 2区 材料科学 Q1 MATERIALS SCIENCE, CERAMICS Pub Date : 2025-12-08 DOI: 10.1016/j.jeurceramsoc.2025.118066
Rui-Hua Chen, Suniya Siddique, Hua-Jing Zhang, Ning Chen, Zhuo-Ming Xu, Zi-Long Zhang, Yue-Xing Chen, Zhuang-Hao Zheng, Fu Li
Herein, a Ti/Cu co-doping strategy is employed in Bi2SeS2 to optimize its electrical and thermal transport properties through carrier regulation and microstructure modulation. The Ti/Cu co-doped Bi2SeS2 samples were synthesized by mechanical alloying followed by spark plasma sintering. It is found that the co-doping boosts electrical conductivity while preserving a moderate Seebeck coefficient of 150–200 μV K−1. This yields a high power factor of 5.5 μW cm−1 K−2 at 773 K. Moreover, the lattice thermal conductivity is reduced to ∼0.25 W m−1 K−1, primarily due to effective phonon scattering induced by lattice strain and point defects. Finally, a peak zT of ∼0.80 is achieved at 773 K in Bi1.96Ti0.04SeS2-1 %Cu, surpassing the solely Cu-doped and Ti-doped counterparts by ∼22 % and 40 %, respectively. These findings reveal that multi-element doping is an effective approach for tailoring both charge and phonon transport, providing valuable insights for the design of advanced thermoelectric materials.
本文采用Ti/Cu共掺杂策略,通过载流子调控和微观结构调制优化Bi2SeS2的电学和热输运性能。采用机械合金化和火花等离子烧结法制备了Ti/Cu共掺杂Bi2SeS2样品。发现共掺杂提高了导电性能,同时保持了适中的塞贝克系数(150 ~ 200 μV K−1)。在773 K时产生5.5 μW cm−1 K−2的高功率因数。此外,晶格导热系数降低到~ 0.25 W m−1 K−1,主要是由于晶格应变和点缺陷引起的有效声子散射。最后,在Bi1.96Ti0.04SeS2-1 %Cu中,在773 K处达到了约0.80的峰值zT,分别比纯Cu掺杂和纯ti掺杂的对应物高出约22 %和40 %。这些发现表明,多元素掺杂是调整电荷和声子输运的有效方法,为设计先进的热电材料提供了有价值的见解。
{"title":"Synergistic tuning of electrical and thermal transport properties in Bi2SeS2 thermoelectric material via Ti/Cu co-doping","authors":"Rui-Hua Chen,&nbsp;Suniya Siddique,&nbsp;Hua-Jing Zhang,&nbsp;Ning Chen,&nbsp;Zhuo-Ming Xu,&nbsp;Zi-Long Zhang,&nbsp;Yue-Xing Chen,&nbsp;Zhuang-Hao Zheng,&nbsp;Fu Li","doi":"10.1016/j.jeurceramsoc.2025.118066","DOIUrl":"10.1016/j.jeurceramsoc.2025.118066","url":null,"abstract":"<div><div>Herein, a Ti/Cu co-doping strategy is employed in Bi<sub>2</sub>SeS<sub>2</sub> to optimize its electrical and thermal transport properties through carrier regulation and microstructure modulation. The Ti/Cu co-doped Bi<sub>2</sub>SeS<sub>2</sub> samples were synthesized by mechanical alloying followed by spark plasma sintering. It is found that the co-doping boosts electrical conductivity while preserving a moderate Seebeck coefficient of 150–200 μV K<sup>−1</sup>. This yields a high power factor of 5.5 μW cm<sup>−1</sup> K<sup>−2</sup> at 773 K. Moreover, the lattice thermal conductivity is reduced to ∼0.25 W m<sup>−1</sup> K<sup>−1</sup>, primarily due to effective phonon scattering induced by lattice strain and point defects. Finally, a peak <em>zT</em> of ∼0.80 is achieved at 773 K in Bi<sub>1.96</sub>Ti<sub>0.04</sub>SeS<sub>2</sub>-1 %Cu, surpassing the solely Cu-doped and Ti-doped counterparts by ∼22 % and 40 %, respectively. These findings reveal that multi-element doping is an effective approach for tailoring both charge and phonon transport, providing valuable insights for the design of advanced thermoelectric materials.</div></div>","PeriodicalId":17408,"journal":{"name":"Journal of The European Ceramic Society","volume":"46 6","pages":"Article 118066"},"PeriodicalIF":6.2,"publicationDate":"2025-12-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145749576","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
期刊
Journal of The European Ceramic Society
全部 Acc. Chem. Res. ACS Applied Bio Materials ACS Appl. Electron. Mater. ACS Appl. Energy Mater. ACS Appl. Mater. Interfaces ACS Appl. Nano Mater. ACS Appl. Polym. Mater. ACS BIOMATER-SCI ENG ACS Catal. ACS Cent. Sci. ACS Chem. Biol. ACS Chemical Health & Safety ACS Chem. Neurosci. ACS Comb. Sci. ACS Earth Space Chem. ACS Energy Lett. ACS Infect. Dis. ACS Macro Lett. ACS Mater. Lett. ACS Med. Chem. Lett. ACS Nano ACS Omega ACS Photonics ACS Sens. ACS Sustainable Chem. Eng. ACS Synth. Biol. Anal. Chem. BIOCHEMISTRY-US Bioconjugate Chem. BIOMACROMOLECULES Chem. Res. Toxicol. Chem. Rev. Chem. Mater. CRYST GROWTH DES ENERG FUEL Environ. Sci. Technol. Environ. Sci. Technol. Lett. Eur. J. Inorg. Chem. IND ENG CHEM RES Inorg. Chem. J. Agric. Food. Chem. J. Chem. Eng. Data J. Chem. Educ. J. Chem. Inf. Model. J. Chem. Theory Comput. J. Med. Chem. J. Nat. Prod. J PROTEOME RES J. Am. Chem. Soc. LANGMUIR MACROMOLECULES Mol. Pharmaceutics Nano Lett. Org. Lett. ORG PROCESS RES DEV ORGANOMETALLICS J. Org. Chem. J. Phys. Chem. J. Phys. Chem. A J. Phys. Chem. B J. Phys. Chem. C J. Phys. Chem. Lett. Analyst Anal. Methods Biomater. Sci. Catal. Sci. Technol. Chem. Commun. Chem. Soc. Rev. CHEM EDUC RES PRACT CRYSTENGCOMM Dalton Trans. Energy Environ. Sci. ENVIRON SCI-NANO ENVIRON SCI-PROC IMP ENVIRON SCI-WAT RES Faraday Discuss. Food Funct. Green Chem. Inorg. Chem. Front. Integr. Biol. J. Anal. At. Spectrom. J. Mater. Chem. A J. Mater. Chem. B J. Mater. Chem. C Lab Chip Mater. Chem. Front. Mater. Horiz. MEDCHEMCOMM Metallomics Mol. Biosyst. Mol. Syst. Des. Eng. Nanoscale Nanoscale Horiz. Nat. Prod. Rep. New J. Chem. Org. Biomol. Chem. Org. Chem. Front. PHOTOCH PHOTOBIO SCI PCCP Polym. Chem.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1