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Morphology-controlled self-assembly of hollow spherical heterostructured TiO2@BiOBr promotes visible-light degradation of antibiotic pollutants 形态控制的空心球形异质结构TiO2@BiOBr自组装促进抗生素污染物的可见光降解
IF 5.6 2区 材料科学 Q1 MATERIALS SCIENCE, CERAMICS Pub Date : 2026-01-01 DOI: 10.1016/j.ceramint.2025.12.069
Juanrong Chen , Yue shen , Junjie Ma , Chaozhong Sun , Sai Zhang , Sisi Xiao , Yingguan Xiao , Shunsheng Cao
Although BiOBr exhibits a good photodegradation activity for organic pollutants due to its special layered structure, low visible-light utilization and insufficiently exposed active sites limit its photocatalytic efficiency. To address these challenges, we construct TiO2@BiOBr (HTBB) photocatalyst by coupling hollow spherical structure and p-n heterojunction. The strong built-in electric field can boost efficient charge separation, while hollow spherical structure not only can provide abundant accessible active sites due to its unique two-sided available interfaces, but also can promote light absorption through multiple reflection mechanism. As a result, the degradation rate of levofloxacin (LVFX) over HTBB photocatalyst is as high as 96.25 % under visible light within 1 h and still maintains a high level (>90 %) after five successive cycles. Meanwhile, the photocatalytic performance of HTBB shows excellent harsh environment tolerance. Therefore, this work provides a new insight for constructing BiOBr-based hollow spherical photocatalysts for the treatment of antibiotic wastewater.
虽然由于其特殊的层状结构,BiOBr对有机污染物具有良好的光降解活性,但可见光利用率低,活性位点暴露不足,限制了其光催化效率。为了解决这些问题,我们通过将空心球形结构与p-n异质结耦合来构建TiO2@BiOBr (HTBB)光催化剂。强大的内置电场可以促进有效的电荷分离,而空心球形结构不仅由于其独特的双面可用界面可以提供丰富的可达活性位点,而且可以通过多种反射机制促进光的吸收。结果表明,HTBB光催化剂对左氧氟沙星(LVFX)在可见光下1 h内的降解率高达96.25%,连续5次循环后仍保持较高的降解率(> 90%)。同时,HTBB的光催化性能表现出优异的恶劣环境耐受性。因此,本研究为构建bibr基中空球形光催化剂处理抗生素废水提供了新的思路。
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引用次数: 0
Enhanced structural, dielectric, electrical, and optical properties of Ca2+/Sr2+ doped LaNbO4 ceramics Ca2+/Sr2+掺杂LaNbO4陶瓷的结构、介电、电学和光学性能增强
IF 5.6 2区 材料科学 Q1 MATERIALS SCIENCE, CERAMICS Pub Date : 2026-01-01 DOI: 10.1016/j.ceramint.2025.12.051
Samia Aydi , Mouhamed Mounir Bouzayeni , Iskandar Chaabane , Noweir Ahmad Alghamdi , Regis Barille , Abderrazek Oueslati
The development of multifunctional oxide ceramics for advanced energy-storage and optoelectronic applications motivates the investigation of doped LaNbO4 systems. In this work, La0.92Sr0.08NbO4-δ (LSNO) and La0.92Ca0.08NbO4-δ (LCNO) ceramics were synthesized via a conventional solid-state reaction route and thoroughly characterized. X-ray diffraction confirmed that both compositions crystallize in a monoclinic P21/C fergusonite-type structure, indicating effective incorporation of Sr2+ and Ca2+ at the La site. Dielectric measurements revealed a giant dielectric constant (ε′ ≈ 105) with very low dielectric loss (tan δ), demonstrating strong potential for high energy density capacitor applications. AC conductivity (σac) and impedance studies indicated thermally activated conduction, with a mechanism transitioning from non-overlapping small polaron tunneling (NSPT) at low temperatures to correlated barrier hopping (CBH) at elevated temperatures. Optical analyses showed a decrease in the band gap from 4.33eV (LSNO) to 4.12 eV (LCNO), enhancing light absorption and enabling tunable optoelectronic properties. The synergistic improvements in structural stability, dielectric performance, electrical conductivity, and optical functionality establish LSNO and LCNO ceramics as promising candidates for next-generation capacitors, semiconducting devices, and multifunctional optoelectronic applications.
用于先进储能和光电子应用的多功能氧化物陶瓷的发展激发了掺杂LaNbO4体系的研究。本文采用常规固相反应制备了La0.92Sr0.08NbO4-δ (LSNO)和La0.92Ca0.08NbO4-δ (LCNO)陶瓷,并对其进行了表征。x射线衍射证实,这两种成分结晶为单斜P21/C弗格森型结构,表明Sr2+和Ca2+在La位点有效结合。电介质测量结果表明,该电容器具有巨大的介电常数(ε′≈105)和极低的介电损耗(tan δ),具有很强的高能量密度电容器应用潜力。交流电导率(σac)和阻抗研究表明,该材料的热激活传导机制由低温下的非重叠小极化子隧穿(NSPT)向高温下的相关势垒跳变(CBH)转变。光学分析表明,带隙从4.33eV (LSNO)减小到4.12 eV (llcno),增强了光吸收并实现了可调谐的光电性能。在结构稳定性、介电性能、电导率和光学功能方面的协同改进使LSNO和LCNO陶瓷成为下一代电容器、半导体器件和多功能光电应用的有前途的候选者。
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引用次数: 0
Tailoring gradient porous ceramics via direct foaming: the role of seasonal temperature in slurry rheology and microstructure development 通过直接发泡剪裁梯度多孔陶瓷:季节温度在浆料流变学和微观结构发展中的作用
IF 5.6 2区 材料科学 Q1 MATERIALS SCIENCE, CERAMICS Pub Date : 2026-01-01 DOI: 10.1016/j.ceramint.2025.11.324
Gang Qi , Ruoyu Chen , Zhanmin Wang , Haichuan Wang , Chuanyang Cai , Minghui Li , Saisai Li , Canhua Li
Seasonal environmental conditions affect the temperature of raw materials, as well as preparation, and curing processes, thereby influencing the rheological behavior of porous ceramic slurries, the foaming process, and the final properties of the ceramics. In this study, gradient porous ceramics were prepared using silica fume by the direct foaming method under simulated seasonal temperatures, and the effect of working temperature on the rheology and foaming behavior of the slurry was investigated. The results showed that environmental temperature significantly influenced the rheological behavior, pore structure, and final properties of gradient porous ceramics. At 25 °C, the slurry exhibited the lowest viscosity (23,750 mPa s) and yield stress (30.2 Pa), while at 45 °C, viscosity and yield stress increased to 65,000 mPa s and 100.54 Pa, respectively. Solidification time was also prolonged from 6.5 h to 42.5 h with increasing temperature. These changes led to notable differences in pore size and distribution. Gradient structures were successfully formed at 15, 25, and 45 °C, whereas the sample at 35 °C showed irregular, disordered pores. Consequently, the samples fabricated at 15, 25, and 45 °C displayed gradient variations in apparent porosity, bulk density, and thermal conductivity. Specifically, the sample prepared at 25 °C exhibited the lowest total apparent porosity of 71.6 %, a bulk density of 0.50 g/cm3, and the lowest thermal conductivity ranging from 0.124 to 0.114 W/(m·K). The flexural strength in two directions measured 1.11 MPa and 1.03 MPa, while the corresponding compressive strength reached 2.95 MPa and 3.34 MPa, respectively. This study provides valuable insights into fabricating gradient porous ceramics via direct foaming under varying seasonal conditions.
季节性的环境条件会影响原材料的温度,以及制备和固化过程,从而影响多孔陶瓷浆料的流变行为、发泡过程和陶瓷的最终性能。在模拟季节温度条件下,采用硅灰直接发泡法制备梯度多孔陶瓷,研究了工作温度对料浆流变学和发泡性能的影响。结果表明,环境温度对梯度多孔陶瓷的流变行为、孔隙结构和最终性能有显著影响。在25°C时,浆料的粘度和屈服应力最低,分别为23,750 mPa s和30.2 Pa,而在45°C时,粘度和屈服应力分别增加到65,000 mPa s和100.54 Pa。随着温度的升高,凝固时间由6.5 h延长至42.5 h。这些变化导致了孔隙大小和分布的显著差异。梯度结构在15、25和45℃下成功形成,而在35℃下样品呈现不规则、无序的孔隙。因此,在15、25和45°C下制备的样品在表观孔隙度、体积密度和导热系数方面表现出梯度变化。其中,在25℃下制备的样品,总表观孔隙率最低,为71.6%,容重为0.50 g/cm3,导热系数最低,为0.124 ~ 0.114 W/(m·K)。两个方向的抗弯强度分别为1.11 MPa和1.03 MPa,对应的抗压强度分别为2.95 MPa和3.34 MPa。该研究为在不同季节条件下通过直接发泡制备梯度多孔陶瓷提供了有价值的见解。
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引用次数: 0
Effect of sintering temperature on the microstructure, magnetic, and dielectric properties of NiCuZn ferrites for microstrip antenna applications 烧结温度对微带天线用NiCuZn铁氧体微观结构、磁性和介电性能的影响
IF 5.6 2区 材料科学 Q1 MATERIALS SCIENCE, CERAMICS Pub Date : 2026-01-01 DOI: 10.1016/j.ceramint.2025.11.339
Xueying Wang , Yaoyao Luo , Kai Luo , Shao Kang , Shaobo Si , Ge Tang , Lei Wang , Zhenkang Zhang , Huaiwu Zhang
Magnetic and microstructural properties of NiCuZn ferrites are strongly dependent on sintering temperature, which strongly affects their performance in high-frequency applications. In this study, NiCuZn ferrite ceramics were prepared by the solid-phase reaction method, and the influence of sintering temperature on phase composition, grain growth, and magnetic behavior was investigated based on it as an independent variable. At the proper sintering temperature of 920 °C, a single-phase spinel structure with homogeneous grain morphology and high densification was obtained. Simultaneously, initial permeability (μ) increased obviously from 157.62 to 547.01, and the saturation magnetization (4πMs) reached 3339.94 Gauss. Meanwhile, the ferromagnetic resonance linewidth (ΔH) decreased greatly from 643.56 to 229.02 Oe, which reflected that the magnetic loss was reduced from the ferromagnetic resonance experiment. The optimized magnetic properties and improved dielectric characteristics suggest that NiCuZn ferrites sintered at 920 °C have the potential application in high-performance microstrip antenna substrates. Microstrip antennas based on ferrite-based substrates were simulated, and return loss and radiation characteristics were analyzed. The results show that when the magnetic bias condition is proper, with relatively high permittivity (ε′) and permeability (μ) of ferrite, the antenna can be miniaturized significantly. In addition, by reasonably designing the geometry of the antenna, the radiation characteristics of the antenna can be tuned to achieve the great performance of the whole antenna.
NiCuZn铁氧体的磁性和微观结构性能与烧结温度密切相关,烧结温度对NiCuZn铁氧体在高频应用中的性能有很大影响。本研究采用固相反应法制备了NiCuZn铁氧体陶瓷,并以烧结温度为自变量,研究了烧结温度对相组成、晶粒生长和磁性行为的影响。在920℃的烧结温度下,获得了晶粒形貌均匀、致密化程度高的单相尖晶石组织。同时,初始磁导率(μ)由157.62提高到547.01,饱和磁化强度(4πMs)达到3339.94高斯。同时,铁磁共振线宽(ΔH)从643.56 Oe大幅减小到229.02 Oe,说明铁磁共振实验降低了磁损失。优化后的磁性能和改善的介电特性表明,在920℃下烧结的NiCuZn铁氧体在高性能微带天线基板上具有潜在的应用前景。对基于铁氧体基板的微带天线进行了仿真,分析了其回波损耗和辐射特性。结果表明,在适当的偏磁条件下,铁氧体具有较高的介电常数(ε′)和磁导率(μ),可以实现天线的小型化。此外,通过合理设计天线的几何形状,可以对天线的辐射特性进行调谐,从而实现整体天线的优异性能。
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引用次数: 0
Synergistic experimental and first-principles insights into Sm3+ incorporation and dielectric performance of CdCu3Ti4O12 ceramics CdCu3Ti4O12陶瓷中Sm3+掺入和介电性能的协同实验和第一性原理研究
IF 5.6 2区 材料科学 Q1 MATERIALS SCIENCE, CERAMICS Pub Date : 2026-01-01 DOI: 10.1016/j.ceramint.2025.12.160
Sirawit Promsai , Atittaya Changchuea , Jakkree Boonlakhorn , Udomsilp Pinsook , Pornjuk Srepusharawoot
Cd1–3x/2SmxCu3Ti4O12 ceramics (x = 0, 0.025, and 0.05) were synthesized using a conventional solid-state reaction method, and all sintered samples exhibited the main CdCu3Ti4O12 phase. The addition of Sm3+ refined the grain size and produced a dense microstructure after sintering at 1000 °C for 3 h. The sample with x = 0.025 exhibited the best dielectric performance, with a high permittivity of 1.23 × 105, a low loss tangent of 0.090, and good thermal stability. The improved dielectric response is attributed to enhanced grain boundary resistance, which suppresses leakage conduction. Impedance spectroscopy and X-ray photoelectron spectroscopy confirm that oxygen vacancies generated during sintering are mainly localized within grain interiors, thereby promoting the formation of an internal barrier layer capacitor structure responsible for the giant dielectric permittivity. First-principles calculations revealed that Sm3+ preferentially substitutes at the Cd2+ site with minimal structural distortion, maintaining lattice stability. Oxygen vacancies preferentially form away from Sm3+ dopants and act as electron donors, thereby reducing Cu2+ to Cu+ and Ti4+ to Ti3+ via charge compensation. These processes promote hopping conduction and strengthen the dielectric response. The combined experimental and theoretical results demonstrate that both oxygen vacancy formation and microstructures critically govern the dielectric behavior of Sm3+-doped CdCu3Ti4O12, highlighting the effectiveness of Sm3+ doping in tailoring the microstructure and electrical properties for high-permittivity dielectric applications.
采用常规固相法合成了Cd1-3x /2SmxCu3Ti4O12陶瓷(x = 0、0.025和0.05),烧结样品均以CdCu3Ti4O12为主相。Sm3+的加入细化了晶粒尺寸,并在1000℃烧结3 h后形成致密的微观结构。当x = 0.025时,样品的介电常数高,为1.23 × 105,损耗切线低,为0.090,具有良好的热稳定性。介质响应的改善是由于晶界电阻的增强抑制了漏导。阻抗谱和x射线光电子能谱证实,烧结过程中产生的氧空位主要集中在晶粒内部,从而促进了内部势垒层电容器结构的形成,导致了巨大的介电常数。第一性原理计算表明,Sm3+优先取代Cd2+位点,结构畸变最小,保持晶格稳定性。氧空位优先在远离Sm3+掺杂物的地方形成,并充当电子供体,从而通过电荷补偿将Cu2+还原为Cu+,将Ti4+还原为Ti3+。这些过程促进了跳变传导,增强了介质响应。实验和理论结合的结果表明,氧空位的形成和微观结构对Sm3+掺杂CdCu3Ti4O12的介电性能起着关键的控制作用,突出了Sm3+掺杂在高介电常数介质应用中调整微观结构和电学性能的有效性。
{"title":"Synergistic experimental and first-principles insights into Sm3+ incorporation and dielectric performance of CdCu3Ti4O12 ceramics","authors":"Sirawit Promsai ,&nbsp;Atittaya Changchuea ,&nbsp;Jakkree Boonlakhorn ,&nbsp;Udomsilp Pinsook ,&nbsp;Pornjuk Srepusharawoot","doi":"10.1016/j.ceramint.2025.12.160","DOIUrl":"10.1016/j.ceramint.2025.12.160","url":null,"abstract":"<div><div>Cd<sub>1–3<em>x</em>/2</sub>Sm<sub><em>x</em></sub>Cu<sub>3</sub>Ti<sub>4</sub>O<sub>12</sub> ceramics (<em>x</em> = 0, 0.025, and 0.05) were synthesized using a conventional solid-state reaction method, and all sintered samples exhibited the main CdCu<sub>3</sub>Ti<sub>4</sub>O<sub>12</sub> phase. The addition of Sm<sup>3+</sup> refined the grain size and produced a dense microstructure after sintering at 1000 °C for 3 h. The sample with <em>x</em> = 0.025 exhibited the best dielectric performance, with a high permittivity of 1.23 × 10<sup>5</sup>, a low loss tangent of 0.090, and good thermal stability. The improved dielectric response is attributed to enhanced grain boundary resistance, which suppresses leakage conduction. Impedance spectroscopy and X-ray photoelectron spectroscopy confirm that oxygen vacancies generated during sintering are mainly localized within grain interiors, thereby promoting the formation of an internal barrier layer capacitor structure responsible for the giant dielectric permittivity. First-principles calculations revealed that Sm<sup>3+</sup> preferentially substitutes at the Cd<sup>2+</sup> site with minimal structural distortion, maintaining lattice stability. Oxygen vacancies preferentially form away from Sm<sup>3+</sup> dopants and act as electron donors, thereby reducing Cu<sup>2+</sup> to Cu<sup>+</sup> and Ti<sup>4+</sup> to Ti<sup>3+</sup> via charge compensation. These processes promote hopping conduction and strengthen the dielectric response. The combined experimental and theoretical results demonstrate that both oxygen vacancy formation and microstructures critically govern the dielectric behavior of Sm<sup>3+</sup>-doped CdCu<sub>3</sub>Ti<sub>4</sub>O<sub>12</sub>, highlighting the effectiveness of Sm<sup>3+</sup> doping in tailoring the microstructure and electrical properties for high-permittivity dielectric applications.</div></div>","PeriodicalId":267,"journal":{"name":"Ceramics International","volume":"52 3","pages":"Pages 3681-3693"},"PeriodicalIF":5.6,"publicationDate":"2026-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145996113","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
A unique coating film architecture makes Ce:YAG sapphire films suitable for high-power laser-driven lighting 独特的镀膜结构使Ce:YAG蓝宝石薄膜适合于高功率激光驱动照明
IF 5.6 2区 材料科学 Q1 MATERIALS SCIENCE, CERAMICS Pub Date : 2026-01-01 DOI: 10.1016/j.ceramint.2025.12.163
Ziyi Fang , Xu Liang , Meilin Fu , Xiangjia Sun , Jiao Liu , Zhiheng Zong , Zhaoping Chen , Jian Xu , Xiaojuan Liang , Weidong Xiang
The field of solid-state laser illumination is developing rapidly. Phosphor-in-glass film (PiF) has been proved to be a promising color-conversion material for high-quality laser illumination due to their excellent chromatic properties, tunability, and simple fabrication process. However, conventional fabrication methods that fix the phosphor layer directly onto small-sized therally conductive substrate struggle to simultaneously achieve both high luminous flux and high luminous efficiency. In this study, Ce:YAG PiF@Coating film (PiF@CF) was obtained by coating Ta2O5 composite film on the surface of sapphire substrate which was not coated with phosphor layer through a unique coating film design. The coated Ce:YAG PiF@CF achieves synergistic optimization of luminous efficiency (LE) and luminous flux (LF). While achieving a laser performance of 243.63 lm/W peak LE and holding 1641 lm @ 8.32 W, which is twice that of the uncoated Ce:YAG PiF (824.63 lm). In addition, the sample maintains an excellent thermal conductivity of 12.92 W/(m K) at 573 K. This study provides a new solution for high-power laser illumination fluorescence conversion materials that take into account the three aspects of luminous efficiency, luminous flux and heat dissipation performance through the coating process, laying an important foundation for its application in the fields of lighting and display.
固体激光照明领域发展迅速。玻璃内磷薄膜(PiF)由于其优异的色彩特性、可调性和简单的制备工艺,已被证明是一种有前途的高质量激光照明颜色转换材料。然而,将荧光粉层直接固定在小尺寸导热衬底上的传统制造方法难以同时实现高光通量和高发光效率。本研究通过独特的涂膜设计,将Ta2O5复合薄膜涂覆在未涂磷光体层的蓝宝石基底表面,得到Ce:YAG PiF@Coating薄膜(PiF@CF)。涂覆的Ce:YAG PiF@CF实现了发光效率(LE)和光通量(LF)的协同优化。同时实现了243.63 lm/W的峰值激光性能和1641 lm @ 8.32 W,这是未涂覆Ce:YAG PiF (824.63 lm)的两倍。此外,样品在573 K时保持了12.92 W/(m K)的优异导热系数。本研究通过涂层工艺为兼顾光效、光通量和散热性能三方面的高功率激光照明荧光转换材料提供了一种新的解决方案,为其在照明和显示领域的应用奠定了重要基础。
{"title":"A unique coating film architecture makes Ce:YAG sapphire films suitable for high-power laser-driven lighting","authors":"Ziyi Fang ,&nbsp;Xu Liang ,&nbsp;Meilin Fu ,&nbsp;Xiangjia Sun ,&nbsp;Jiao Liu ,&nbsp;Zhiheng Zong ,&nbsp;Zhaoping Chen ,&nbsp;Jian Xu ,&nbsp;Xiaojuan Liang ,&nbsp;Weidong Xiang","doi":"10.1016/j.ceramint.2025.12.163","DOIUrl":"10.1016/j.ceramint.2025.12.163","url":null,"abstract":"<div><div>The field of solid-state laser illumination is developing rapidly. Phosphor-in-glass film (PiF) has been proved to be a promising color-conversion material for high-quality laser illumination due to their excellent chromatic properties, tunability, and simple fabrication process. However, conventional fabrication methods that fix the phosphor layer directly onto small-sized therally conductive substrate struggle to simultaneously achieve both high luminous flux and high luminous efficiency. In this study, Ce:YAG PiF@Coating film (PiF@CF) was obtained by coating Ta<sub>2</sub>O<sub>5</sub> composite film on the surface of sapphire substrate which was not coated with phosphor layer through a unique coating film design. The coated Ce:YAG PiF@CF achieves synergistic optimization of luminous efficiency (LE) and luminous flux (LF). While achieving a laser performance of 243.63 lm/W peak LE and holding 1641 lm @ 8.32 W, which is twice that of the uncoated Ce:YAG PiF (824.63 lm). In addition, the sample maintains an excellent thermal conductivity of 12.92 W/(m K) at 573 K. This study provides a new solution for high-power laser illumination fluorescence conversion materials that take into account the three aspects of luminous efficiency, luminous flux and heat dissipation performance through the coating process, laying an important foundation for its application in the fields of lighting and display.</div></div>","PeriodicalId":267,"journal":{"name":"Ceramics International","volume":"52 3","pages":"Pages 3702-3710"},"PeriodicalIF":5.6,"publicationDate":"2026-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145996152","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
Interfacial adhesion of CVD-SiC coatings on graphite substrates: Role of temperature in microstructure and mechanical properties CVD-SiC涂层在石墨基体上的界面粘附:温度对微观结构和力学性能的影响
IF 5.6 2区 材料科学 Q1 MATERIALS SCIENCE, CERAMICS Pub Date : 2026-01-01 DOI: 10.1016/j.ceramint.2025.12.164
Qingzhi Ma , Renhao Hu , Xuechao Liu , Xuhua Lu , Jian Chen , Rulin Zhang , Yunzhou Xue , Shaolong He , Ying Wang , Lianyi Xu , Min Jin , Rongbin Li , Pan Gao
Silicon carbide (SiC) coatings are critical for protecting graphite substrates in high-performance applications, such as semiconductor manufacturing and aerospace, where extreme thermal and chemical environments demand robust adhesion and durability. This study investigates the temperature-driven microstructural evolution of SiC coatings deposited on graphite by chemical vapor deposition (CVD) at 1260 °C, 1280 °C, and 1320 °C, elucidating the mechanism of their impact on interfacial adhesion. Advanced analytical techniques, including field-emission scanning electron microscopy (FE-SEM), X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), white-light confocal microscopy, nanoindentation, and scratch testing, were employed to characterize the coatings. The results show that when the deposition temperature increases from 1260 °C to 1320 °C, the SiC coating grain aggregate transforms from an irregular structure to a truncated polyhedron structure, and the (111) surface texture coefficient increases significantly. Additionally, the SiC grain aggregates are relatively loose at low temperatures, whereas they form a continuous and dense fused structure at high temperatures. XPS analysis shows that with increasing temperature, the Si-C bond density increases and the stacking faults decrease, thereby enhancing the bonding strength between the coating and the substrate. It is worth noting that the critical bonding force increases from 20.8 N at 1260 °C to 28.5 N at 1320 °C, which is consistent with the increase in nanohardness. These findings highlight that within the studied 1260–1320 °C range, increasing the deposition temperature significantly improves the microstructure and adhesion of SiC coatings.
碳化硅(SiC)涂层对于高性能应用中保护石墨基板至关重要,例如半导体制造和航空航天,这些应用中极端的热和化学环境需要强大的附着力和耐久性。本文研究了1260℃、1280℃和1320℃下化学气相沉积(CVD)在石墨上沉积的SiC涂层的温度驱动显微组织演变,阐明了它们对界面粘附的影响机制。采用先进的分析技术,包括场发射扫描电镜(FE-SEM)、x射线衍射(XRD)、x射线光电子能谱(XPS)、白光共聚焦显微镜、纳米压痕和划痕测试,对涂层进行了表征。结果表明:当沉积温度从1260℃升高到1320℃时,SiC涂层晶粒集合体由不规则结构转变为截断多面体结构,(111)表面织构系数显著增大;此外,SiC晶粒聚集体在低温下相对松散,而在高温下形成连续致密的熔合结构。XPS分析表明,随着温度的升高,Si-C键密度增加,层错减少,从而增强了涂层与基体之间的结合强度。值得注意的是,临界结合力从1260℃时的20.8 N增加到1320℃时的28.5 N,这与纳米硬度的提高是一致的。研究结果表明,在1260 ~ 1320℃范围内,提高沉积温度可显著改善SiC涂层的显微组织和附着力。
{"title":"Interfacial adhesion of CVD-SiC coatings on graphite substrates: Role of temperature in microstructure and mechanical properties","authors":"Qingzhi Ma ,&nbsp;Renhao Hu ,&nbsp;Xuechao Liu ,&nbsp;Xuhua Lu ,&nbsp;Jian Chen ,&nbsp;Rulin Zhang ,&nbsp;Yunzhou Xue ,&nbsp;Shaolong He ,&nbsp;Ying Wang ,&nbsp;Lianyi Xu ,&nbsp;Min Jin ,&nbsp;Rongbin Li ,&nbsp;Pan Gao","doi":"10.1016/j.ceramint.2025.12.164","DOIUrl":"10.1016/j.ceramint.2025.12.164","url":null,"abstract":"<div><div>Silicon carbide (SiC) coatings are critical for protecting graphite substrates in high-performance applications, such as semiconductor manufacturing and aerospace, where extreme thermal and chemical environments demand robust adhesion and durability. This study investigates the temperature-driven microstructural evolution of SiC coatings deposited on graphite by chemical vapor deposition (CVD) at 1260 °C, 1280 °C, and 1320 °C, elucidating the mechanism of their impact on interfacial adhesion. Advanced analytical techniques, including field-emission scanning electron microscopy (FE-SEM), X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), white-light confocal microscopy, nanoindentation, and scratch testing, were employed to characterize the coatings. The results show that when the deposition temperature increases from 1260 °C to 1320 °C, the SiC coating grain aggregate transforms from an irregular structure to a truncated polyhedron structure, and the (111) surface texture coefficient increases significantly. Additionally, the SiC grain aggregates are relatively loose at low temperatures, whereas they form a continuous and dense fused structure at high temperatures. XPS analysis shows that with increasing temperature, the Si-C bond density increases and the stacking faults decrease, thereby enhancing the bonding strength between the coating and the substrate. It is worth noting that the critical bonding force increases from 20.8 N at 1260 °C to 28.5 N at 1320 °C, which is consistent with the increase in nanohardness. These findings highlight that within the studied 1260–1320 °C range, increasing the deposition temperature significantly improves the microstructure and adhesion of SiC coatings.</div></div>","PeriodicalId":267,"journal":{"name":"Ceramics International","volume":"52 3","pages":"Pages 3711-3718"},"PeriodicalIF":5.6,"publicationDate":"2026-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145996153","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
Customizing oxide debris of CoCrW alloy by adding Re to improve tribological properties while maintaining high mechanical strength and oxidation resistance 在CoCrW合金中加入稀土元素,在提高摩擦性能的同时保持较高的机械强度和抗氧化性
IF 5.6 2区 材料科学 Q1 MATERIALS SCIENCE, CERAMICS Pub Date : 2026-01-01 DOI: 10.1016/j.ceramint.2025.12.168
Kaili Song , Shasha Yang , Minghui Chen , Dongbiao Li , Xiaoyue Zhang , Gang Wang , Fuhui Wang
While traditional high-temperature self-lubricating composites with various solid lubricants demonstrate adequate tribological performance under mild conditions, they inherently suffer from two critical applied limitations: (i) competing trade-offs between tribological and mechanical properties, and (ii) accelerated oxidation arising from lubricant-derived oxidative voiding and cracks. Herein, we propose a new design philosophy for high-temperature self-lubricating alloys that strategically eliminates solid lubricant additions. Through oxidation regulation to customize oxide debris, a hard glaze layer is in situ formed on the wear surface at early stage of high-temperature friction, which provides enhanced tribological performances. This concept is realized by introducing merely 3 wt% Re into a CoCrWSi alloy (CCWS-3Re). It induces the transformation of oxide debris from CoO to the low-melting-point oxide of Co3O4. The low melting point and high atomic diffusion rate of Co3O4 promote sintering of wear debris and accelerate the formation of glaze layer. Comparing to the Re-free alloy, CCWS-3Re alloy exhibits a 97.5 % reduction in wear rate, accompanied by a 25 % decrease in friction coefficient under 800 °C sliding conditions. Since no solid lubricants are added, CCWS-3Re possesses a high yield strength of 470 MPa, meanwhile high oxidation resistance with a remarkable low parabolic rate constant of 1.24 × 10−4 mg2cm4h−1 at 800 °C.
虽然传统的高温自润滑复合材料与各种固体润滑剂在温和的条件下表现出足够的摩擦学性能,但它们固有地受到两个关键的应用限制:(i)摩擦学和机械性能之间的竞争权衡;(ii)由润滑剂衍生的氧化空洞和裂纹引起的加速氧化。在此,我们提出了一种新的高温自润滑合金设计理念,策略性地消除了固体润滑剂的添加。通过氧化调节,定制氧化碎片,在高温摩擦初期在磨损表面原位形成硬釉层,提高了摩擦学性能。这个概念是通过在CoCrWSi合金(CCWS-3Re)中仅引入3wt %的Re来实现的。它诱导氧化碎屑由CoO向Co3O4的低熔点氧化物转变。Co3O4的低熔点和高原子扩散速率促进了磨损碎片的烧结,加速了釉层的形成。与无re合金相比,CCWS-3Re合金在800℃滑动条件下的磨损率降低了97.5%,摩擦系数降低了25%。由于没有添加固体润滑剂,CCWS-3Re具有高达470 MPa的屈服强度,同时具有很高的抗氧化性,在800°C时抛物线速率常数为1.24 × 10−4 mg2cm4h−1。
{"title":"Customizing oxide debris of CoCrW alloy by adding Re to improve tribological properties while maintaining high mechanical strength and oxidation resistance","authors":"Kaili Song ,&nbsp;Shasha Yang ,&nbsp;Minghui Chen ,&nbsp;Dongbiao Li ,&nbsp;Xiaoyue Zhang ,&nbsp;Gang Wang ,&nbsp;Fuhui Wang","doi":"10.1016/j.ceramint.2025.12.168","DOIUrl":"10.1016/j.ceramint.2025.12.168","url":null,"abstract":"<div><div>While traditional high-temperature self-lubricating composites with various solid lubricants demonstrate adequate tribological performance under mild conditions, they inherently suffer from two critical applied limitations: (i) competing trade-offs between tribological and mechanical properties, and (ii) accelerated oxidation arising from lubricant-derived oxidative voiding and cracks. Herein, we propose a new design philosophy for high-temperature self-lubricating alloys that strategically eliminates solid lubricant additions. Through oxidation regulation to customize oxide debris, a hard glaze layer is <em>in situ</em> formed on the wear surface at early stage of high-temperature friction, which provides enhanced tribological performances. This concept is realized by introducing merely 3 wt% Re into a CoCrWSi alloy (CCWS-3Re). It induces the transformation of oxide debris from CoO to the low-melting-point oxide of Co<sub>3</sub>O<sub>4</sub>. The low melting point and high atomic diffusion rate of Co<sub>3</sub>O<sub>4</sub> promote sintering of wear debris and accelerate the formation of glaze layer. Comparing to the Re-free alloy, CCWS-3Re alloy exhibits a 97.5 % reduction in wear rate, accompanied by a 25 % decrease in friction coefficient under 800 °C sliding conditions. Since no solid lubricants are added, CCWS-3Re possesses a high yield strength of 470 MPa, meanwhile high oxidation resistance with a remarkable low parabolic rate constant of 1.24 × 10<sup>−4</sup> mg<sup>2</sup>cm<sup>4</sup>h<sup>−1</sup> at 800 °C.</div></div>","PeriodicalId":267,"journal":{"name":"Ceramics International","volume":"52 3","pages":"Pages 3758-3769"},"PeriodicalIF":5.6,"publicationDate":"2026-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145996157","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
Study on damage in ultrafast laser ablation of CaTiO3-MgTiO3 ceramic CaTiO3-MgTiO3陶瓷超快激光烧蚀损伤研究
IF 5.6 2区 材料科学 Q1 MATERIALS SCIENCE, CERAMICS Pub Date : 2026-01-01 DOI: 10.1016/j.ceramint.2025.12.170
Hong Shen , Hengfeng Yang , Yingbo Feng , Quan Xu
This study investigates the damage to ceramic substrates caused by ultrafast laser pulses during metal coating removal and explores the causes of color changes induced by varying laser energy intensities. EDS reveals no significant differences in elemental ratios between laser-processed and pristine surfaces after laser processing. However, high-energy laser irradiation alters the crystal structure. The laser-induced thermal effect results in the broadening of Raman spectral peaks and the disappearance of X-ray diffraction (XRD) peaks, indicating that the ceramic undergoes remelting and amorphization. This remelting process leads to the loss of the original microstructure, which consequently causes a decline in the ceramic's piezoelectric performance and frequency selectivity. The findings provide a theoretical foundation for the optimization of ultrafast laser processing to reduce thermal damage to ceramic substrates and to control discoloration.
本文研究了超快激光脉冲在金属涂层去除过程中对陶瓷基板的损伤,并探讨了不同激光能量强度引起颜色变化的原因。EDS显示,激光加工后的表面与原始表面的元素比没有显著差异。然而,高能激光照射改变了晶体结构。激光诱导的热效应导致陶瓷的拉曼光谱峰展宽,x射线衍射峰消失,表明陶瓷发生了重熔和非晶化。这种重熔过程导致原始微观结构的丧失,从而导致陶瓷的压电性能和频率选择性下降。研究结果为优化超快激光加工工艺以减少对陶瓷基板的热损伤和控制变色提供了理论基础。
{"title":"Study on damage in ultrafast laser ablation of CaTiO3-MgTiO3 ceramic","authors":"Hong Shen ,&nbsp;Hengfeng Yang ,&nbsp;Yingbo Feng ,&nbsp;Quan Xu","doi":"10.1016/j.ceramint.2025.12.170","DOIUrl":"10.1016/j.ceramint.2025.12.170","url":null,"abstract":"<div><div>This study investigates the damage to ceramic substrates caused by ultrafast laser pulses during metal coating removal and explores the causes of color changes induced by varying laser energy intensities. EDS reveals no significant differences in elemental ratios between laser-processed and pristine surfaces after laser processing. However, high-energy laser irradiation alters the crystal structure. The laser-induced thermal effect results in the broadening of Raman spectral peaks and the disappearance of X-ray diffraction (XRD) peaks, indicating that the ceramic undergoes remelting and amorphization. This remelting process leads to the loss of the original microstructure, which consequently causes a decline in the ceramic's piezoelectric performance and frequency selectivity. The findings provide a theoretical foundation for the optimization of ultrafast laser processing to reduce thermal damage to ceramic substrates and to control discoloration.</div></div>","PeriodicalId":267,"journal":{"name":"Ceramics International","volume":"52 3","pages":"Pages 3787-3795"},"PeriodicalIF":5.6,"publicationDate":"2026-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145996160","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
Dependence of the Mn valence state in complex oxide thin films derived from lanthanum manganite 锰酸镧复合氧化物薄膜中Mn价态的依赖性
IF 5.6 2区 材料科学 Q1 MATERIALS SCIENCE, CERAMICS Pub Date : 2026-01-01 DOI: 10.1016/j.ceramint.2025.12.152
Jelena Vukmirović , Ivan Stijepović , Bojan Miljević , Danica Piper , Paweł Pęczkowski , Piotr Zachariasz , Sara Joksović , Vladimir V. Srdić
Different lanthanum manganite-based thin films were prepared by polymer assisted deposition (PAD) and spin coating on the monocrystal SrTiO3 (001) and Si substrates, whereas double-layered film was obtained by combining PAD and sol-gel method to deposit second perovskite Ba0.7Sr0.3TiO3 layer. Valence states of ions were probed by X-ray absorption spectroscopy (XAS) at the SOLARIS National Synchrotron Radiation Centre in Kraków, Poland. It was found that manganese valence depends on substrate type, doping level, and BSTO buffer layer which is important to obtain single-phase complex oxide thin films.
采用聚合物辅助沉积(PAD)和自旋镀膜的方法在单晶SrTiO3(001)和Si衬底上制备了不同的锰酸镧基薄膜,采用PAD和溶胶-凝胶相结合的方法沉积了第二层钙钛矿Ba0.7Sr0.3TiO3,得到了双层薄膜。在波兰Kraków的SOLARIS国家同步辐射中心,用x射线吸收光谱(XAS)探测了离子的价态。发现锰的价态取决于衬底类型、掺杂水平和BSTO缓冲层,这对获得单相配合氧化物薄膜很重要。
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引用次数: 0
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Ceramics International
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