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HfO2-based thin films and devices 基于hfo2的薄膜和器件
IF 9.6 1区 材料科学 Q1 CHEMISTRY, PHYSICAL Pub Date : 2025-11-01 Epub Date: 2025-09-08 DOI: 10.1016/j.jmat.2025.101125
Xiaoguang Li, Min Hyuk Park, Ji-Yan Dai, Yuewei Yin
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引用次数: 0
Tailoring microwave dielectric properties of MgAl5/4(Li1/3Ti2/3)3/4O4 ceramics for multi-band dielectric resonant antenna 多波段介电谐振天线用MgAl5/4(Li1/3Ti2/3)3/4O4陶瓷的微波介电特性定制
IF 8.4 1区 材料科学 Q1 CHEMISTRY, PHYSICAL Pub Date : 2025-11-01 Epub Date: 2025-04-24 DOI: 10.1016/j.jmat.2025.101064
Zhicong Chen , Qianbiao Du , Guo Tian , Linzhao Ma , Longxiang Jiang , Chang Jiang , Zeyan Zhou , Hao Li
This study introduces a novel microwave dielectric ceramic, MgAl5/4(Li1/3Ti2/3)3/4O4, tailored for modern communication technologies. MgAl5/4(Li1/3Ti2/3)3/4O4 ceramics feature a composite spinel structure (Fd-3m space group) comprising MgAl2O4 and Li4Ti5O12 type phases. By substituting Al3+ of MgAl2O4 ceramic with the composite ion (Li1/3Ti2/3)3+, differences in elemental diffusion induced by sintering temperature (1200–1280 °C) significantly affect the microwave dielectric properties: a low εᵣ (11.83) and enhanced microwave properties (Q×f = 79,381 GHz and τf = −28.5 × 10−6/°C) at 1240 °C. With further optimization of the ceramics, a near-zero τf is realized in 0.93MgAl5/4(Li1/3Ti2/3)3/4O4-0.07CaTiO3 ceramics with excellent comprehensive performance (εr = 14.36, Q×f = 44,144 GHz). Building on this, a multi-band dielectric resonant antenna (DRA) was designed for applications in communication and aeronautical radio navigation, featuring a wide relative bandwidth of 39.37% (5.97–6.49 GHz and 7.19–9.83 GHz). This study presents an optimization strategy for obtaining microwave dielectric ceramics with low εr, high Q×f, excellent frequency-temperature stability, low sintering temperature, and low density.
本文介绍了一种为现代通信技术量身定制的新型微波介质陶瓷MgAl5/4(Li1/3Ti2/3)3/4O4。MgAl5/4(Li1/3Ti2/3)3/4O4陶瓷具有由MgAl2O4和Li4Ti5O12型相组成的复合尖晶石结构(Fd-3m空间群)。用复合离子(Li1/3Ti2/3)3+取代MgAl2O4陶瓷的Al3+,烧结温度(1200 ~ 1280℃)引起的元素扩散差异显著影响了MgAl2O4陶瓷的微波介电性能:1240℃时εᵣ(11.8)较低,微波性能(Q×f = 79,381 GHz, τf = -28.5×10−6/°C)增强。进一步优化陶瓷,得到综合性能优良的0.93MgAl5/4(Li1/3Ti2/3)3/4O4-0.07CaTiO3陶瓷的τf接近于零(εr = 14.36, Q×f = 44,144 GHz)。在此基础上,设计了一种适用于通信和航空无线电导航的多频段介质谐振天线(DRA),相对带宽为39.37% (5.97 ~ 6.49 GHz和7.19 ~ 9.83 GHz)。本研究提出了一种获得低εr、高Q×f、优异的频温稳定性、低烧结温度和低密度微波介质陶瓷的优化策略。
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引用次数: 0
Hard, strong, and tough cold-sintered α-quartz composites as high-performance structural ceramics 硬、强、韧的α-石英冷烧结复合材料是高性能结构陶瓷
IF 8.4 1区 材料科学 Q1 CHEMISTRY, PHYSICAL Pub Date : 2025-11-01 Epub Date: 2025-05-10 DOI: 10.1016/j.jmat.2025.101076
Peng Yan , Mingming Si , Yongping Liu, Yu Ren, Jie Min, Xu Wang, Qi Ding, Weizhong Jiang, Yuchi Fan, Wan Jiang
Cold-sintered ceramics typically exhibit inferior mechanical properties compared to high-temperature sintered counterparts. We demonstrate that introducing large internal stress through highly concentrated nanodiamonds (NDs) significantly enhances cold-sintered α-quartz composites to structural ceramic levels. At 500 MPa cold-sintering pressure, uniformly dispersed NDs generate 1.2 GPa local prestress via Young's modulus difference, while pressure-modulated internal stress is evidenced by dielectric property changes. The optimized composite achieves fracture toughness of (3.65 ± 0.21) MPa·m1/2 (180% increase) and Vickers hardness of 10.6 GPa (80% increase), matching some high-temperature-sintered ceramics. Toughening arises from prestress-driven crack deflection and crack tip bridging, while hardness enhancement stems from NDs' rigid constraint and high-pressure-induced dislocations in silica matrix. Compressive strength increases by 90% and fatigue life exceeds 1000 cycles, attributed to internal stress-strengthened grain boundaries and improved toughness. This work presents a transformative strategy for developing damage-resistant ceramics, meriting further exploration of scalability and engineering applications.
与高温烧结陶瓷相比,冷烧结陶瓷通常表现出较差的机械性能。研究表明,通过高浓度纳米金刚石(NDs)引入大内应力可显著提高冷烧结α-石英复合材料的结构陶瓷水平。在500 MPa冷烧结压力下,均匀分散的NDs通过杨氏模量差产生1.2 GPa的局部预应力,而介电性能的变化则证明了压力调节内应力。优化后的复合材料断裂韧性达到(3.65±0.21)MPa·m1/2(提高180%),维氏硬度达到10.6 GPa(提高80%),与部分高温烧结陶瓷相匹配。增韧来自于预应力驱动的裂纹挠曲和裂纹尖端桥接,而硬度增强来自于NDs的刚性约束和高压诱导的二氧化硅基体位错。抗压强度提高90%,疲劳寿命超过1000次,这是由于内应力增强了晶界,提高了韧性。这项工作为开发抗损伤陶瓷提供了一种变革性的策略,值得进一步探索可扩展性和工程应用。
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引用次数: 0
A hybrid processing technology for fabricating lead zirconate-based ceramics with high energy storage density, high efficiency, and low sintering temperature 一种制备高能量储存密度、高效率、低烧结温度的锆酸铅基陶瓷的混合加工技术
IF 8.4 1区 材料科学 Q1 CHEMISTRY, PHYSICAL Pub Date : 2025-11-01 Epub Date: 2025-05-24 DOI: 10.1016/j.jmat.2025.101077
Cangjin Li, Manwen Yao, Xi Yao, Chunyu Li
For multilayer ceramic capacitors, co-sintering of ceramics with inner electrodes is a crucial issue. This requires ceramic materials to have a low sintering temperature. In response to this criterion, a hybrid processing technology is proposed in this study. This technology involves mixing of calcined ceramic powders with sol solutions to obtain composite powders. Eventually, sintering temperature of the obtained composite material is reduced from 1300 °C to 1120 °C. This is originated from the introduction of more specific surface areas and more oxygen vacancies by sol solutions, leading to an enhancement of chemical reaction activity. The ceramic powders and the sol solutions used in this work are (Pb0.94La0.04)(Zr0.51Sn0.47Hf0.01Ti0.01)O3 and (Pb0.97La0.02)(Zr0.6Sn0.4)O3, respectively. Such composition design helps improve the dielectric constant and polarization intensity. While in the meantime, because of the strong interfacial resistance caused by sol solutions, interfacial insulation as well as electrical breakdown strength can be significantly improved. Consequently, a high energy storage density up to 12.4 J/cm3 and an efficiency of 92.4% is obtained in this work. Overall, this technology is applicable to a wide range of ceramic material systems, and provides an innovative design and manufacture of ceramics.
对于多层陶瓷电容器来说,陶瓷内电极共烧结是一个关键问题。这就要求陶瓷材料具有较低的烧结温度。针对这一准则,本研究提出了一种混合处理技术。该技术包括将煅烧的陶瓷粉末与溶胶溶液混合以获得复合粉末。最终,得到的复合材料的烧结温度从1300℃降低到1120℃。这是因为溶胶溶液引入了更大的比表面积和更多的氧空位,从而增强了化学反应活性。所制备的陶瓷粉体和溶胶溶液分别为(Pb0.94La0.04)(Zr0.51Sn0.47Hf0.01Ti0.01)O3和(Pb0.97La0.02)(Zr0.6Sn0.4)O3。这种成分设计有助于提高介电常数和极化强度。同时,由于溶胶溶液产生的强界面电阻,可以显著提高界面绝缘和电击穿强度。因此,在此工作中获得了高达12.4 J/cm3的高能量存储密度和92.4%的效率。总的来说,这项技术适用于广泛的陶瓷材料系统,并提供了一种创新的陶瓷设计和制造。
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引用次数: 0
Modulation in sintering characteristics and microwave dielectric properties of Ca3Co2SiV2O12 via Li+ inequivalent substitution Li+不等量取代对Ca3Co2SiV2O12烧结特性和微波介电性能的调制
IF 8.4 1区 材料科学 Q1 CHEMISTRY, PHYSICAL Pub Date : 2025-11-01 Epub Date: 2025-05-11 DOI: 10.1016/j.jmat.2025.101074
Zhenli Tao, Jiamao Li, Junxian Wang, Yuxuan Ren, Yunfeng Guo, Qinghe Yang, Zhihao Yuan, Rui Tian, Wenbo Wang
In this study, the inequivalent substitution of Ca2+ by Li+ in the Ca3Co2SiV2O12 compound was designed to modulate its sintering characteristics and microwave dielectric properties. The corresponding Ca3–xLi2xCo2SiV2O12 (CCSV-xLi, 0.01≤ x ≤ 0.07) ceramics were prepared via the conventional solid-state phase method, which could be densely sintered at a temperature below 1140 °C. Rietveld refinement results suggested that all the doped Li occupied the Ca-site as x ≤ 0.05 while superfluous Li positioned at the Co-site of CCSV when x = 0.07. This atomic occupancy had a remarkable effect on the degree of “rattling effect” and thus modulated the relative permittivity of ceramics, constantly increasing at x = 0.01–0.05 and slightly decreasing at x = 0.07. Raman spectra revealed that Q×f value was closely related to Raman shift and FWHM. Also, the Q×f value was partly influenced by oxygen vacancy concentration. The τf demonstrated an opposite tendency to the bond valence of the A-site and was affected by the “rattling effect”. The CCSV-0.05Li ceramic sintered at 1120 °C possessed excellent microwave dielectric properties: εr = 12.17, Q×f = 56,220 GHz, and τf = −8.5 × 10−6 °C−1.
在本研究中,设计了Ca3Co2SiV2O12化合物中Li+的不等量取代Ca2+来调节其烧结特性和微波介电性能。采用常规固相法制备相应的Ca3-xLi2xCo2SiV2O12 (CCSV-xLi, 0.01≤x≤0.07)陶瓷,在1140℃以下的温度下烧结致密。Rietveld细化结果表明,当x≤0.05时,所有掺杂的Li都占据了ca位点,而当x = 0.07时,多余的Li位于CLCSV的co位点。这种原子占据对“咔嗒效应”的程度有显著影响,从而调节了陶瓷的相对介电常数,在x = 0.01-0.05处不断增大,在x = 0.07处略有减小。拉曼光谱显示Q×f值与拉曼位移和FWHM密切相关。同时,Q×f值部分受氧空位浓度的影响。τf值表现出与a位键价相反的趋势,并受到“咔嗒效应”的影响。在1120℃下烧结的CCSV-0.05Li陶瓷具有优异的微波介电性能:εr = 12.17, Q×f = 56,220 GHz, τf = -8.5×10−6°C−1。
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引用次数: 0
Self-powered tunable photodetection via flexoelectric engineering of single-phase 2HMoS2 基于柔性电工程的单相2H-MoS2自供电可调谐光探测
IF 8.4 1区 材料科学 Q1 CHEMISTRY, PHYSICAL Pub Date : 2025-11-01 Epub Date: 2025-06-18 DOI: 10.1016/j.jmat.2025.101103
Junxi Yu , Yuan Zhang , Songjie Yang , Chunlin Song , Shiyao Xu , Boyuan Huang , Qingyuan Wang , Jiangyu Li
Two-dimensional (2D) molybdenum disulfide (MoS2) has shown considerable potential for photodetection, yet existing MoS2-based photodetectors require either external voltage bias or complex heterojunctions. In this work, we present a new device concept based on flexoelectric engineering of bulk photovoltaic effect (BPVE) of 2HMoS2, simplifying the device configuration considerably while enhancing its self-powered photodetection performance. By introducing a strain gradient in the suspended 2HMoS2, we break its inversion symmetry, resulting in BPVE in the otherwise centrosymmetric system. The significant flexoelectric polarization induced also facilitates efficient photocarrier separation, leading to a 41-fold enhancement in short-circuit photocurrent under a strain gradient of 0.95μm1. Furthermore, the flexoelectric-engineered photodetector can be dynamically tuned via air pressure, enabling multilevel photoconductance and achieving a responsivity of 191 mA/W. This performance surpasses existing self-powered MoS2-based photodetectors reported in literature, offering a strategy for enhanced photodetection.
二维(2D)二硫化钼(MoS2)已经显示出相当大的光探测潜力,但现有的基于MoS2的光电探测器需要外部电压偏置或复杂的异质结。在这项工作中,我们提出了一种基于2H-MoS2体光伏效应(BPVE)柔性电工程的新器件概念,大大简化了器件结构,同时提高了其自供电光探测性能。通过在悬浮的2H-MoS2中引入应变梯度,我们打破了它的反转对称性,从而在原本中心对称的体系中产生了BPVE。显著的挠曲电极化诱导也促进了有效的光载流子分离,导致在应变梯度下短路光电流增强41倍。此外,柔性电工程光电探测器可以通过空气压力动态调谐,实现多级光电导,并实现191 mA/W的响应率。这种性能超越了文献中报道的现有的基于mos2的自供电光电探测器,为增强光探测提供了一种策略。
{"title":"Self-powered tunable photodetection via flexoelectric engineering of single-phase 2HMoS2","authors":"Junxi Yu ,&nbsp;Yuan Zhang ,&nbsp;Songjie Yang ,&nbsp;Chunlin Song ,&nbsp;Shiyao Xu ,&nbsp;Boyuan Huang ,&nbsp;Qingyuan Wang ,&nbsp;Jiangyu Li","doi":"10.1016/j.jmat.2025.101103","DOIUrl":"10.1016/j.jmat.2025.101103","url":null,"abstract":"<div><div>Two-dimensional (2D) molybdenum disulfide (MoS<sub>2</sub>) has shown considerable potential for photodetection, yet existing MoS<sub>2</sub>-based photodetectors require either external voltage bias or complex heterojunctions. In this work, we present a new device concept based on flexoelectric engineering of bulk photovoltaic effect (BPVE) of 2H<img>MoS<sub>2</sub>, simplifying the device configuration considerably while enhancing its self-powered photodetection performance. By introducing a strain gradient in the suspended 2H<img>MoS<sub>2</sub>, we break its inversion symmetry, resulting in BPVE in the otherwise centrosymmetric system. The significant flexoelectric polarization induced also facilitates efficient photocarrier separation, leading to a 41-fold enhancement in short-circuit photocurrent under a strain gradient of <span><math><mn>0.95</mn><mspace></mspace><msup><mi>μm</mi><mrow><mo>−</mo><mn>1</mn></mrow></msup></math></span>. Furthermore, the flexoelectric-engineered photodetector can be dynamically tuned <em>via</em> air pressure, enabling multilevel photoconductance and achieving a responsivity of 191 mA/W. This performance surpasses existing self-powered MoS<sub>2</sub>-based photodetectors reported in literature, offering a strategy for enhanced photodetection.</div></div>","PeriodicalId":16173,"journal":{"name":"Journal of Materiomics","volume":"11 6","pages":"Article 101103"},"PeriodicalIF":8.4,"publicationDate":"2025-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144311736","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"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
Room-temperature densified Al2O3-H3BO3 ceramics with excellent microwave dielectric properties and thermal conductivity for chip packaging 具有优异微波介电性能和导热性的室温致密Al2O3-H3BO3陶瓷
IF 8.4 1区 材料科学 Q1 CHEMISTRY, PHYSICAL Pub Date : 2025-11-01 Epub Date: 2025-05-09 DOI: 10.1016/j.jmat.2025.101069
Zhan Zeng , Jin Cheng , Xinwei Xu , Hongye Wang , Yani Lu , Liang Sun , Naichao Chen , Xiaoyu Li , Boshen Zhang , Hong Wang
As electronic devices become increasingly miniaturized and demand greater integration, traditional packaging technologies face substantial challenges in meeting the needs for high-frequency performance and system reliability. Ceramic materials, known for their excellent dielectric properties and thermal stability, are promising candidates for advanced packaging applications. However, conventional high-temperature densification processes, which often exceed 1000 °C, restrict their compatibility with temperature-sensitive components in modern electronic systems. To overcome this limitation, we propose a novel approach to densify Al2O3H3BO3 ceramic at room temperature under low uniaxial stress. It is found that a H3BO3 facilitates plastic deformation in the medium of deionized water, enhancing the densification of Al2O3H3BO3 ceramics even at minimal uniaxial stress. The resulting material exhibits a high relative density of over 96% and possesses excellent microwave dielectric properties (relative permittivity εr: 2.84–5.37; Q×f values: 12,924–69,000 GHz; resonant frequency τf values: −156.94 10−6 °C−1 to −73.42 10−6 °C−1) and thermal conductivity (λ values: 1.96–5.96 W·m−1·K−1). After co-firing with a silicon wafer, the ceramic maintains its structural integrity, with no observable atomic diffusion at the ceramic-silicon interface, rendering it a potential candidate for advanced packaging and integration technologies.
随着电子器件的小型化和集成度的提高,传统的封装技术在满足高频性能和系统可靠性方面面临着巨大的挑战。陶瓷材料以其优异的介电性能和热稳定性而闻名,是先进封装应用的有希望的候选者。然而,传统的高温致密化工艺通常超过1000°C,限制了它们与现代电子系统中温度敏感元件的兼容性。为了克服这一限制,我们提出了一种在室温下低单轴应力下致密化Al2O3-H3BO3陶瓷的新方法。发现H3BO3在去离子水介质中有利于塑性变形,即使在最小的单轴应力下也能增强Al2O3-H3BO3陶瓷的致密性。所得材料的相对密度高达96%以上,具有优异的微波介电性能(相对介电常数:2.84 ~ 5.37;取值范围:12924 - 69,000 GHz;谐振频率值:−156.94 10-6·°C-1 ~−73.42 10-6·°C-1)和导热系数(值:1.96 ~ 5.96 W·m-1·K-1)。在与硅片共烧后,陶瓷保持其结构完整性,在陶瓷-硅界面没有观察到原子扩散,使其成为先进封装和集成技术的潜在候选者。
{"title":"Room-temperature densified Al2O3-H3BO3 ceramics with excellent microwave dielectric properties and thermal conductivity for chip packaging","authors":"Zhan Zeng ,&nbsp;Jin Cheng ,&nbsp;Xinwei Xu ,&nbsp;Hongye Wang ,&nbsp;Yani Lu ,&nbsp;Liang Sun ,&nbsp;Naichao Chen ,&nbsp;Xiaoyu Li ,&nbsp;Boshen Zhang ,&nbsp;Hong Wang","doi":"10.1016/j.jmat.2025.101069","DOIUrl":"10.1016/j.jmat.2025.101069","url":null,"abstract":"<div><div>As electronic devices become increasingly miniaturized and demand greater integration, traditional packaging technologies face substantial challenges in meeting the needs for high-frequency performance and system reliability. Ceramic materials, known for their excellent dielectric properties and thermal stability, are promising candidates for advanced packaging applications. However, conventional high-temperature densification processes, which often exceed 1000 °C, restrict their compatibility with temperature-sensitive components in modern electronic systems. To overcome this limitation, we propose a novel approach to densify Al<sub>2</sub>O<sub>3</sub><img>H<sub>3</sub>BO<sub>3</sub> ceramic at room temperature under low uniaxial stress. It is found that a H<sub>3</sub>BO<sub>3</sub> facilitates plastic deformation in the medium of deionized water, enhancing the densification of Al<sub>2</sub>O<sub>3</sub><img>H<sub>3</sub>BO<sub>3</sub> ceramics even at minimal uniaxial stress. The resulting material exhibits a high relative density of over 96% and possesses excellent microwave dielectric properties (relative permittivity <span><math><msub><mi>ε</mi><mi>r</mi></msub></math></span>: 2.84–5.37; <span><math><mrow><mi>Q</mi><mo>×</mo><mi>f</mi></mrow></math></span> values: 12,924–69,000 GHz; resonant frequency <span><math><msub><mi>τ</mi><mi>f</mi></msub></math></span> values: −156.94 10<sup>−6</sup> °C<sup>−1</sup> to −73.42 10<sup>−6</sup> °C<sup>−1</sup>) and thermal conductivity (<span><math><mrow><mi>λ</mi></mrow></math></span> values: 1.96–5.96 W·m<sup>−1</sup>·K<sup>−1</sup>). After co-firing with a silicon wafer, the ceramic maintains its structural integrity, with no observable atomic diffusion at the ceramic-silicon interface, rendering it a potential candidate for advanced packaging and integration technologies.</div></div>","PeriodicalId":16173,"journal":{"name":"Journal of Materiomics","volume":"11 6","pages":"Article 101069"},"PeriodicalIF":8.4,"publicationDate":"2025-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143926348","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"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 quality CuInP2S6 single crystal for intrinsic electric property 高品质的CuInP2S6单晶具有本征电性能
IF 8.4 1区 材料科学 Q1 CHEMISTRY, PHYSICAL Pub Date : 2025-11-01 Epub Date: 2025-04-18 DOI: 10.1016/j.jmat.2025.101067
Changjin Guo , Yu Tan , Jiajun Zhu , Jiyang Xie , Chengding Gu , Wanbiao Hu
What is the nature of the electric (dielectric/ferroelectric) properties of CuInP2S6 (CIPS)? CIPS, considered an emerging two-dimensional (2D) ferroelectric, has been well explored in various properties and applications. However, the most important and fundamental nature, i.e. dielectric/ferroelectric property, has been controversial, because high-quality CIPS samples are grossly deficient. In this work, single crystal CIPS is successfully synthesized by the chemical vapour transport method, which presents “high quality” in terms of high purity, excellent crystallinity, uniform composition, and defect-free structure etc. that are confirmed through comprehensive characterization techniques. With performing high-quality single crystal, we fully uncover the intrinsic electric properties of CIPS through accurately identifying the atomic arrangement, electron configuration, magnetic, dielectric, and ferroelectric properties that should reach a consensus on such a disputed CIPS material. These findings serve as a pivotal benchmark for a comprehensive understanding of the inherent electric characteristics of CIPS, offering valuable insights for its future modifications and applications in various applications.
CuInP2S6 (CIPS)的电(介电/铁电)性质是什么?CIPS被认为是一种新兴的二维(2D)铁电材料,在各种性质和应用方面得到了很好的探索。然而,最重要和最基本的性质,即介电/铁电性质,一直存在争议,因为高质量的CIPS样品严重缺乏。本研究成功地通过化学气相输运法合成了单晶CIPS,通过综合表征技术,证实了单晶CIPS在纯度高、结晶度好、成分均匀、结构无缺陷等方面具有“高品质”。通过制备高质量的单晶,通过对原子排列、电子排布、磁性、介电性和铁电性的准确识别,充分揭示了CIPS的内在电学性质,对这一有争议的CIPS材料应达成共识。这些发现是全面了解CIPS固有电特性的关键基准,为其未来的修改和在各种应用中的应用提供了有价值的见解。
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引用次数: 0
Ultrahigh energy storage performance via defect engineering in Sr0.7Bi0.2TiO3 lead-free relaxor ferroelectrics 通过 Sr0.7Bi0.2TiO3 无铅弛豫铁电体中的缺陷工程实现超高储能性能
IF 8.4 1区 材料科学 Q1 CHEMISTRY, PHYSICAL Pub Date : 2025-11-01 Epub Date: 2025-04-21 DOI: 10.1016/j.jmat.2025.101065
Yutao Luo , Tianyang Zheng , Song Liu , Yunfei Liu , Yinong Lyu , Jin Luo
With the development of advanced electronic memory and the advocacy of environmental friendliness, lead-free relaxor ferroelectric capacitors with slim hysteresis loops have received great attention in high power energy storage applications. However, various emerging defects in Sr0.7Bi0.2TiO3 based relaxor ferroelectric films can result in inferior energy storage performance. In this work, Mn doping is utilized to modify the defects caused by the excessive Bi compensation in the Sr0.7Bi0.2TiO3 relaxor ferroelectric thin films. Those Mn doped Sr0.7Bi0.2TiO3 thin films exhibits significantly improved recoverable energy storage density by more than one order of magnitude with an ultrahigh energy storage density (126 J/cm3). By analyzing the change of the chemical environment and using the scanning transmission electron microscopy, we reveal these improved energy storage performances arises from the formation of defect dipoles of Mn2+ at B site with oxygen vacancies, suppressing the volume of oxygen vacancies and titanium vacancies simultaneously, and the slush-like “single domain” structure with fluctuated B-site cation displacements stabilized and confined in a single nano-sized crystal grain. This chemical modification strategy in this work can serve as a regular approach to suppress the defects and improve the energy storage performance in ferroelectric thin films with volatile elements.
随着先进电子存储技术的发展和对环境友好的倡导,具有细磁滞回线的无铅弛豫铁电电容器在大功率储能领域的应用受到了广泛的关注。然而,Sr0.7Bi0.2TiO3基弛豫铁电薄膜中出现的各种缺陷导致其储能性能较差。本文采用Mn掺杂的方法对Sr0.7Bi0.2TiO3弛豫铁电薄膜中由于Bi补偿过多而产生的缺陷进行了修正。Mn掺杂的Sr0.7Bi0.2TiO3薄膜的可回收储能密度显著提高了一个数量级以上,达到了126 J/cm3的超高储能密度。通过对化学环境变化的分析和扫描透射电镜的分析,我们发现这些储能性能的提高是由于Mn2+在具有氧空位的B位形成缺陷偶极子,同时抑制了氧空位和钛空位的体积,并且具有波动的B位阳离子位移的泥状“单畴”结构稳定并被限制在单个纳米晶粒中。本研究的化学改性策略可作为抑制含挥发性元素铁电薄膜缺陷和提高其储能性能的常规方法。
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引用次数: 0
Observation of tunable terahertz optical response in nanoscale lithium ferrite driven by magnetic field and laser 磁场和激光驱动下纳米铁氧体锂可调谐太赫兹光响应的观察
IF 8.4 1区 材料科学 Q1 CHEMISTRY, PHYSICAL Pub Date : 2025-11-01 Epub Date: 2025-05-02 DOI: 10.1016/j.jmat.2025.101068
Zhen Zhou , Lvkang Shen , Xiaohua Xing , Keyu Tan , Die Zou , Qiankun Zhang , Rui Zhu , Zhiyong Wang , Jianquan Yao , Ming Liu , Liang Wu
With the advancement of spintronics, tunability has emerged as a highly sought-after attribute of magnetic materials. Nevertheless, the comprehension of the terahertz (THz) optical characteristics of tunable magnetic materials driven by external excitation fields remains limited, necessitating further qualitative and quantitative investigation. Here we demonstrate the tunable optical properties of the LiFe5O8 (LFO)/F-Mica structure under magnetic field by a THz time-domain spectroscopy (THz-TDS) system. The prepared LFO/F-Mica structure shows significant changes in dielectric properties and absorption coefficients under different magnetic fields, which is attributed to the interaction of the magnetic field with the spins of ordered magnetic ions (Fe3+) located in a non-centrosymmetric coordination environment. In addition, we investigate the specific contribution of the external laser field to the THz optical parameters of the LFO/F-Mica. The dielectric properties and THz optical response of LFO/F-Mica significantly depend on the laser power under 532 nm laser pumping. The modulation effects of these diverse external fields reveal the potential of lithium ferrites for applications in the THz band. These findings offer valuable insights for the development of tunable multifunctional THz magnetic devices, with potential applications in the fields of communications, medicine, and nondestructive testing.
随着自旋电子学的进步,磁性材料的可调性已成为一种备受追捧的特性。然而,外界激发场驱动的可调谐磁性材料的太赫兹(THz)光学特性的理解仍然有限,需要进一步的定性和定量研究。本文利用太赫兹时域光谱(THz- tds)系统证明了LiFe5O8 (LFO)/F-Mica结构在磁场作用下的可调谐光学特性。制备的LFO/F-Mica结构在不同磁场下的介电性能和吸收系数发生了显著变化,这是由于磁场与位于非中心对称配位环境中的有序磁性离子(Fe3+)的自旋相互作用所致。此外,我们还研究了外部激光场对LFO/F-Mica的太赫兹光学参数的具体贡献。LFO/F-Mica的介电特性和太赫兹光学响应与532 nm激光泵浦下的激光功率密切相关。这些不同外场的调制效应揭示了锂铁氧体在太赫兹波段应用的潜力。这些发现为开发可调谐多功能太赫兹磁器件提供了有价值的见解,在通信、医学和无损检测领域具有潜在的应用前景。
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引用次数: 0
期刊
Journal of Materiomics
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