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Weak Li-O bonds and small grains enable fast ion diffusion and electron transport for LiFePO4 cathode 弱锂键(Li-O)和小晶粒可实现磷酸铁锂阴极的快速离子扩散和电子传输
IF 1 2区 材料科学 Q1 Engineering Pub Date : 2024-05-20 DOI: 10.1016/j.mtadv.2024.100502
Han-xin Wei, Dao-fa Ying, Jing-ju Liu, Yang Lv, Yu-tao Liu, Jiang-feng Wang, Xuan-lin Gong, Mu-yang Zhou, Zuo-sheng Li, Kuo Chen, Luo-jia Chen, Chuan-ping Wu, Bao-hui Chen
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引用次数: 0
Structural, optical and electrical properties in multilayer SnS2(1-x)Se2(x) compounds for energy, thermoelectric and photocatalytic application 用于能源、热电和光催化应用的多层 SnS2(1-x)Se2(x)化合物的结构、光学和电学特性
IF 1 2区 材料科学 Q1 Engineering Pub Date : 2024-05-20 DOI: 10.1016/j.mtadv.2024.100498
Thalita Maysha Herninda, Zi-Ying Chen, Ching-Hwa Ho
Band gap engineering is crucial in the development of two-dimensional layered materials in nanoelectronics, optoelectronics, and photonics fields. In this study, we present characteristics of layered SnSSe (0 ≤ x ≤ 1) ternary alloys grown via chemical vapor transport (CVT) with tunable compositions. Polarized micro-Raman spectroscopy shows the existence of intralayer E and A modes in all the compositions. The A mode demonstrates a pronounced resonant intensity, whilst the E mode is significantly weaker. In the ternary compositions, two groups of E and A modes undergo shift, reflecting lattice and bond transitions from S-rich to Se-rich compositions. Micro-thermoreflectance and optical transmission spectroscopy reveal tunable optical properties consistent with the alloy-composition change. All samples exhibit a single band-edge transition peak, shifting from 1.3 eV (for pure SnSe) to 2.3 eV (for pure SnS), indicating high-quality alloy nanosheets of SnSSe. The optical and electrical applications, such as photodegradation, photoconductivity, and thermoelectric performance are also explored. The alteration in selenium composition within SnSSe is observed to significantly influence potential applications of the materials. The materials with a predominant selenium composition exhibit superior electrical and thermoelectric properties, whereas those with a sulfur-dominant composition manifest enhanced optical characteristics. The engineered 2D structures presents promising opportunities for investigating their fundamental physical properties and also exploring their wide-range applications in electronic and optoelectronic devices, as well as in the field of energy and photocatalytic application.
带隙工程对于二维层状材料在纳米电子学、光电子学和光子学领域的发展至关重要。在本研究中,我们介绍了通过化学气相传输(CVT)生长的具有可调成分的层状 SnSSe(0 ≤ x ≤ 1)三元合金的特性。偏振微拉曼光谱显示,在所有成分中都存在层内 E 和 A 模式。A 模式具有明显的共振频率,而 E 模式则明显较弱。在三元成分中,两组 E 和 A 模式发生了转变,反映了从富 S 成分到富 Se 成分的晶格和键的转变。显微热反射光谱和透射光谱显示了与合金成分变化相一致的可调光学特性。所有样品都显示出单个带边转变峰,从 1.3 eV(纯 SnSe)转变到 2.3 eV(纯 SnS),表明了高质量的 SnSSe 合金纳米片。此外,还探讨了光降解、光导和热电性能等光学和电学应用。据观察,SnSSe 中硒成分的变化会对材料的潜在应用产生重大影响。硒成分占主导地位的材料具有优异的电学和热电性能,而硫成分占主导地位的材料则具有更强的光学特性。这种工程二维结构为研究其基本物理性质以及探索其在电子和光电设备、能源和光催化应用领域的广泛应用提供了大好机会。
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引用次数: 0
“ Review and perspective on additive manufacturing of refractory high entropy alloys” "难熔高熵合金增材制造的回顾与展望"
IF 1 2区 材料科学 Q1 Engineering Pub Date : 2024-05-15 DOI: 10.1016/j.mtadv.2024.100497
Muhammad Raies Abdullah, Zhen Peng
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引用次数: 0
Enabling high-fidelity personalised pharmaceutical tablets through multimaterial inkjet 3D printing with a water-soluble excipient 通过使用水溶性辅料的多材料喷墨 3D 打印技术实现高保真个性化药片
IF 1 2区 材料科学 Q1 Engineering Pub Date : 2024-05-14 DOI: 10.1016/j.mtadv.2024.100493
Geoffrey Rivers, Anna Lion, Nur Rofiqoh Eviana Putri, Graham A. Rance, Cara Moloney, Vincenzo Taresco, Valentina Cuzzucoli Crucitti, Hannah Constantin, Maria Inês Evangelista Barreiros, Laura Ruiz Cantu, Christopher J. Tuck, Felicity R.A.J. Rose, Richard J.M. Hague, Clive J. Roberts, Lyudmila Turyanska, Ricky D. Wildman, Yinfeng He
Additive manufacturing offers manufacture of personalised pharmaceutical tablets through design freedoms and material deposition control at an individual voxel level. This control goes beyond geometry and materials choices: inkjet based 3D printing enables the precise deposition (10–80 μm) of multiple materials, which permits integration of precise doses with tailored release rates; in the meanwhile, this technique has demonstrated its capability of high-volume personalised production. In this paper we demonstrate how two dissimilar materials, one water soluble and one insoluble, can be co-printed within a design envelope to dial up a range of release rates including slow (0.98 ± 0.04 mg/min), fast (4.07 ± 0.25 mg/min) and multi-stepped (2.17 ± 0.04 mg/min then 0.70 ± 0.13 mg/min) dissolution curves. To achieve this, we adopted poly-4-acryloylmorpholine (poly-ACMO) as a new photocurable water-soluble carrier and demonstrated its contemporaneous deposition with an insoluble monomer. The water soluble ACMO formulation with aspirin incorporated was successfully printed and cured under UV light and a wide variety of shapes with material distributions that control drug elution was successfully fabricated by inkjet based 3D printing technique, suggesting its viability as a future personalised solid dosage form fabrication routine.
通过在单个体素水平上的设计自由度和材料沉积控制,快速成型制造技术为个性化药片的制造提供了可能。这种控制不仅限于几何形状和材料选择:基于喷墨技术的三维打印可实现多种材料的精确沉积(10-80 μm),从而可以整合具有定制释放率的精确剂量;同时,这种技术已经证明了其大批量个性化生产的能力。在本文中,我们展示了如何在设计包络线内共同印制两种不同的材料(一种是水溶性材料,另一种是不溶性材料),以调节一系列释放速率,包括慢速(0.98 ± 0.04 mg/min)、快速(4.07 ± 0.25 mg/min)和多级(2.17 ± 0.04 mg/min,然后是 0.70 ± 0.13 mg/min)溶出曲线。为此,我们采用了聚 4-丙烯酰吗啉(poly-ACMO)作为新型光固化水溶性载体,并演示了其与不溶性单体同时沉积的过程。含有阿司匹林的水溶性 ACMO 制剂在紫外光下成功打印固化,并通过基于喷墨的三维打印技术成功制造出各种形状的材料分布,从而控制了药物的洗脱,这表明其作为未来个性化固体制剂制造工艺的可行性。
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引用次数: 0
Pressure-induced hypercoordination of iodine and dimerization of I2O6H in strontium di-iodate hydrogen-iodate (Sr(IO3)2HIO3) 压力诱导的二碘酸氢锶-碘酸锶(Sr(IO3)2HIO3)中碘的超配位和 I2O6H 的二聚反应
IF 1 2区 材料科学 Q1 Engineering Pub Date : 2024-05-13 DOI: 10.1016/j.mtadv.2024.100495
D. Errandonea, H.H.H. Osman, R. Turnbull, D. Diaz-Anichtchenko, A. Liang, J. Sanchez-Martin, C. Popescu, D. Jiang, H. Song, Y. Wang, F.J. Manjon
In this work, we report evidence of pressure-induced changes in the crystal structure of Sr(IO)HIO connected to changes the coordination of the iodine atom and the of the configuration of HIO and IO units. The changes favor iodine hypercoordination and happen in two steps on sample compression. Firstly, at 2.5 GPa, [HIO]·[IO] complexes are formed, and secondly, at 4.5 GPa, these complexes form dimers of [HIO]·[IO]·[IO]·[HIO]. The evidence is obtained from a combined experimental and theoretical study performed up to 20 GPa. Synchrotron powder X-ray diffraction, Raman spectroscopy, and optical-absorption experiments have been complemented with density-functional theory calculations, including the study of the topology of the electron density. The changes observed in the crystal structure are related to the transformation of secondary (halogen) bonds into electron-deficient multicenter bonds. The paper also discusses the effect of pressure on the compressibility of the Sr(IO)HIO crystal structure, its phonons, the electronic band gap, and the refractive index. Sr(IO)HIO was found to be highly compressible with an anisotropic compressibility. The softening of the internal I–O vibrations of IO units was also observed, together with a decrease of the band-gap energy (from 4.1 eV at 0 GPa to 3.7 eV at 20 GPa), a band-gap crossing, and a change in the topology of the band structure, with Sr(IO)HIO transforming from a direct gap semiconductor at 0 GPa to an indirect gap semiconductor beyond 6 GPa.
在这项工作中,我们报告了 Sr(IO)HIO 晶体结构因压力而发生变化的证据,这些变化与碘原子的配位以及 HIO 和 IO 单元的构型变化有关。这些变化有利于碘的超配位,并在样品压缩时分两步发生。首先,在 2.5 GPa 时,形成 [HIO]-[IO] 复合物;其次,在 4.5 GPa 时,这些复合物形成 [HIO]-[IO]-[IO]-[HIO] 的二聚体。这些证据来自于一项高达 20 GPa 的实验和理论研究。同步辐射粉末 X 射线衍射、拉曼光谱和光吸收实验得到了密度泛函理论计算的补充,包括对电子密度拓扑结构的研究。在晶体结构中观察到的变化与次级(卤素)键转变为缺电子多中心键有关。论文还讨论了压力对 Sr(IO)HIO 晶体结构的可压缩性、声子、电子带隙和折射率的影响。研究发现,Sr(IO)HIO 具有各向异性的高度可压缩性。此外,还观察到 IO 单元内部 I-O 振动的软化,以及带隙能的降低(从 0 GPa 时的 4.1 eV 降至 20 GPa 时的 3.7 eV)、带隙交叉和带状结构拓扑的变化,Sr(IO)HIO 从 0 GPa 时的直接隙半导体转变为 6 GPa 以上的间接隙半导体。
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引用次数: 0
In situ TEM investigation of nickel catalytic graphitization 镍催化石墨化的原位 TEM 研究
IF 1 2区 材料科学 Q1 Engineering Pub Date : 2024-05-13 DOI: 10.1016/j.mtadv.2024.100494
Jaemin Kim, Seungwoo Son, Myeonggi Choe, Zonghoon Lee
With the increasing demand for production of graphitic materials for various applications, it becomes crucial to get a fundamental understanding of how graphene layers grow on metal catalysts. Here, we performed an heating transmission electron microscopy (TEM) study to understand the mechanism of graphitization of amorphous carbon (a-C) on Ni catalyst by following graphene growth at atomic resolution in real time. By discerning the NiC phase from the pure Ni phase during the graphitic carbon growth process, we demonstrate that growth occurs through the carbide graphitization of NiC. Additionally, during the graphitization, Ni diffusion has a crucial effect on the structure of the resulting graphene. Under our experimental conditions, we observed graphene contains islands of multilayers. Based on our experimental results, we suggest a mechanism for graphitization of the a-C/Ni system and explain the dynamics resulting from Ni diffusion. Our study can contribute to the control of graphitization by using Ni catalyst in the production of graphene and other graphitic materials.
随着各种应用领域对石墨材料生产的需求日益增长,从根本上了解石墨烯层如何在金属催化剂上生长变得至关重要。在此,我们进行了一项加热透射电子显微镜(TEM)研究,通过以原子分辨率实时跟踪石墨烯的生长,了解无定形碳(a-C)在镍催化剂上的石墨化机制。通过分辨石墨碳生长过程中的 NiC 相和纯 Ni 相,我们证明了生长是通过 NiC 的碳化物石墨化实现的。此外,在石墨化过程中,镍的扩散对生成的石墨烯的结构有着至关重要的影响。在我们的实验条件下,我们观察到石墨烯含有多层的岛屿。基于我们的实验结果,我们提出了 a-C/Ni 体系的石墨化机制,并解释了镍扩散所产生的动态变化。我们的研究有助于在石墨烯和其他石墨材料的生产中使用镍催化剂来控制石墨化。
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引用次数: 0
Performance improvement of blue light micro-light emitting diodes (< 20 μm) by neutral beam etching process 通过中性束蚀刻工艺提高蓝光微型发光二极管(< 20 μm)的性能
IF 1 2区 材料科学 Q1 Engineering Pub Date : 2024-05-11 DOI: 10.1016/j.mtadv.2024.100496
Yu-Hsuan Hsu, Yun-Cheng Hsu, Chien-Chung Lin, Yi-Hsin Lin, Dong-Sing Wuu, Hao-Chung Kuo, Seiji Samukawa, Ray-Hua Horng
In this study, micro-light emitting diodes array (μLEDs) with dimensions of 5 μm and 15 μm chip size were fabricated using Neutral Beam Etching (NBE) processes. Size-dependent issues of μLEDs processed by traditional inductively coupled plasma-reactive ion etching (ICPRIE) were alleviated by NBE technology, which exhibited lower equivalent resistance, turn-on voltage, and Ideality factor as compared with those of μLEDs by ICPRIE. Additionally, higher light output power of μLEDs processed by NBE with both 5 μm and 15 μm resulted in higher EQE 7.6 % and 7.7 % than those of μLEDs processed by ICPRIE. Furthermore, the size effect led to a decrease in EQE values of the ICPRIE sample by 0.4 %, but only a 0.1 % decay in NBE. Overall, samples fabricated by the NBE process exhibited superior optoelectronic characteristics. Finally, non-radiative recombination behaviors on the mesa sidewall were verified by cathodoluminescence analysis, showing significant decay in ICPRIE samples but not in NBE samples. These results demonstrated the potential of the NBE process for fabricating small chip sizes blue-light μLEDs required for high-brightness, high-efficiency, and high-resolution μLED displays.
本研究采用中性束蚀刻(NBE)工艺制造了芯片尺寸分别为 5 μm 和 15 μm 的微型发光二极管阵列(μLED)。通过 NBE 技术,传统电感耦合等离子体反应离子蚀刻(ICPRIE)工艺处理的 μLED 的尺寸相关问题得到了缓解,与 ICPRIE 工艺处理的 μLED 相比,NBE 工艺处理的 μLED 具有更低的等效电阻、导通电压和理想系数。此外,采用 NBE 技术处理的 5 μm 和 15 μm μLED 的光输出功率更高,与采用 ICPRIE 技术处理的 μLED 相比,EQE 分别提高了 7.6% 和 7.7%。此外,尺寸效应导致 ICPRIE 样品的 EQE 值下降了 0.4%,但 NBE 仅下降了 0.1%。总体而言,采用 NBE 工艺制作的样品具有更优越的光电特性。最后,通过阴极发光分析验证了介子侧壁上的非辐射重组行为,结果显示 ICPRIE 样品有显著衰减,而 NBE 样品则没有。这些结果证明了 NBE 工艺在制造高亮度、高效率和高分辨率 μLED 显示器所需的小芯片尺寸蓝光 μLED 方面的潜力。
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引用次数: 0
Strategies for robust electrocatalytic activity of 2D materials: ORR, OER, HER, and CO2RR 增强二维材料电催化活性的策略:ORR、OER、HER 和 CO2RR
IF 1 2区 材料科学 Q1 Engineering Pub Date : 2024-05-08 DOI: 10.1016/j.mtadv.2024.100488
Ali Raza, Jahan Zeb Hassan, Usman Qumar, Ayesha Zaheer, Zaheer Ud Din Babar, Vincenzo Iannotti, Antonio Cassinese
Electrocatalysis utilizing 2D materials is an encouraging approach for advancing sustainable energy conversion technologies. This review explores the strategies employed to achieve robust electrocatalytic activity of 2D materials in key reactions, namely, the OER, HER, and CORR. The distinct structural and electrical characteristics of 2D materials offer opportunities for rapid catalytic performance, indicating significant energy efficiency and selectivity. We systematically discuss the factors governing the electrocatalytic efficiency of two-dimensional materials, including their intrinsic properties, surface modification techniques, heterostructure engineering, and the role of defects. Furthermore, we summarize the recent advances in experimental and theoretical studies to understand the fundamental mechanisms of 2D materials with respect to their catalytic behavior. For the HER, OER, and ORR, defect engineering, phase engineering, interface engineering, and heteroatom doping techniques have been explored. In addition, in the case of the CORR, surface modification, surface-structure tuning, and electrolyte and electrolyzer optimization strategies were examined. This review emphasizes prospective two-dimensional materials as efficient and sustainable electrocatalysts for energy conversion processes. Moreover, it provides future insights into this rapidly evolving field and highlights the possible challenges. In conclusion, it aims to serve as a remarkable resource for researchers seeking to harness the potential response of two-dimensional materials for sustainable energy conversion applications.
利用二维材料进行电催化是推进可持续能源转换技术的一种令人鼓舞的方法。本综述探讨了二维材料在关键反应(即 OER、HER 和 CORR)中实现强大电催化活性的策略。二维材料独特的结构和电学特性为实现快速催化性能提供了机会,并显示出显著的能源效率和选择性。我们系统地讨论了影响二维材料电催化效率的因素,包括其固有特性、表面改性技术、异质结构工程以及缺陷的作用。此外,我们还总结了为了解二维材料催化行为的基本机制而进行的实验和理论研究的最新进展。对于 HER、OER 和 ORR,我们探索了缺陷工程、相工程、界面工程和杂原子掺杂技术。此外,还研究了 CORR 的表面改性、表面结构调整以及电解质和电解槽优化策略。本综述强调了二维材料作为能源转换过程中高效、可持续的电催化剂的前景。此外,它还提供了对这一快速发展领域的未来见解,并强调了可能面临的挑战。总之,本综述旨在为寻求利用二维材料的潜在反应进行可持续能源转换应用的研究人员提供重要资源。
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引用次数: 0
First integration of Ni barrier layer for enhanced threshold switching characteristics in Ag/HfO2-based TS device 在基于 Ag/HfO2 的 TS 器件中首次集成镍阻挡层以增强阈值开关特性
IF 1 2区 材料科学 Q1 Engineering Pub Date : 2024-05-03 DOI: 10.1016/j.mtadv.2024.100492
Daeyoung Chu, Sanghyun Kang, Gwon Kim, Juho Sung, Jaehyuk Lim, Yejoo Choi, Donghwan Han, Changhwan Shin
Utilizing Ag/HfO with nickel (Ni) as a barrier layer, a novel threshold switching (TS) device is devised to overcome challenges such as low reliability, high threshold voltage, and high leakage current. Compared against an Ag/Ti/HfO-based TS device, the Ag/Ni/HfO-based TS device exhibits improved electrical characteristics: yield enhancement from 31.7 % to 40.0 %, enhanced endurance from ∼10 cycles to ∼300 cycles, and suppression in off-state current (I) from 1.2 × 10 A to 5.2 × 10 A under a high compliance current (e.g., 10 A). The results obtained through transmission electron microscopy (TEM), energy-dispersive X-ray spectroscopy (EDS), and atomic force microscopy (AFM) support the evidence of those accomplishments. Reducing the effective area of the TS device improves control over erratically generated filaments and the electric field within the switching layer, resulting in enhanced performance such as a reduced threshold voltage (V ∼0.35 V), minimized V variability (∼0.01 V), decreased a threshold current (I, i.e., the leakage current in the off-state before activation, ∼5.2 × 10 A), and maximum conductance (∼5.0 × 10 S) of low-resistance state. These findings suggest that the optimized Ag/Ni/HfO-based TS device can serve as a practical solution for low-power applications.
利用镍(Ni)作为阻挡层的 Ag/HfO 设计了一种新型阈值开关(TS)器件,以克服低可靠性、高阈值电压和高漏电流等挑战。与基于 Ag/Ti/HfO 的 TS 器件相比,基于 Ag/Ni/HfO 的 TS 器件具有更好的电气特性:良率从 31.7% 提高到 40.0%;耐久性从 10 次循环提高到 300 次循环;在高顺从电流(如 10 A)条件下,离态电流 (I) 从 1.2 × 10 A 抑制到 5.2 × 10 A。通过透射电子显微镜(TEM)、能量色散 X 射线光谱(EDS)和原子力显微镜(AFM)获得的结果也证明了这些成就。减小 TS 器件的有效面积可改善对开关层内不规则产生的灯丝和电场的控制,从而提高性能,如降低阈值电压(V ∼ 0.35 V)、最大限度地减少 V 变化(∼ 0.01 V)、减小阈值电流(I,即关断状态下的漏电流)、5.2 × 10 A)和低电阻状态的最大电导(∼5.0 × 10 S)。这些研究结果表明,经过优化的 Ag/Ni/HfO 基 TS 器件可以作为低功耗应用的实用解决方案。
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引用次数: 0
Wet-spinning of reduced graphene oxide composite fiber by mechanical synergistic effect with graphene scrolling method 利用机械协同效应和石墨烯卷绕法湿法纺制还原氧化石墨烯复合纤维
IF 1 2区 材料科学 Q1 Engineering Pub Date : 2024-05-03 DOI: 10.1016/j.mtadv.2024.100491
Chae-Lin Park, Du Won Kim, Sujin Ryu, Joonmyung Choi, Young-Chul Song, Keon Jung Kim, Sang Won Lee, Seongjae Oh, Doyoung Kim, Young Hwan Bae, Hyun Kim, Seon-Jin Choi, Jaehoon Ko, Shi Hyeong Kim, Hyunsoo Kim
Carbon-based fibers have attracted attention in various field owing to their exceptional properties, including high tensile strength, thermal stability, and electrical conductivity. In particular, graphene-based high-strength fibers are promising materials in aerospace, automotive, and marine sectors. Recently, the hybrid fiber, consisting of carbon nanotubes (CNTs) and graphene with enhanced toughness was reported by deflecting cracks and enabling high deformation. However, complex synthesis and structural optimization of composite fiber with two different materials make challenge for mass production. Here, we introduce a novel graphene composite fiber, consisting of reduced graphene oxide (rGO) and scrolled rGO (SrGO), showing remarkable toughness. A multidimensional-state solution with 2D rGO and 1D SrGO was obtained by using a simple sonication technique. Mass production of high-toughness composite fibers was achieved via wet-spinning, with enhanced toughness attributed to microstructure optimization by controlling the SrGO ratio. Additionally, the use of poly(vinyl alcohol) (PVA) as the matrix facilitated high deformation, resulting in a remarkable 90.7 % increase in mechanical toughness without complex composite material synthesis.
碳基纤维因其卓越的性能,包括高拉伸强度、热稳定性和导电性,在各个领域都备受关注。尤其是石墨烯基高强度纤维,是航空航天、汽车和船舶领域前景广阔的材料。最近,有报道称由碳纳米管(CNT)和石墨烯组成的混合纤维通过偏转裂缝和实现高变形来增强韧性。然而,两种不同材料复合纤维的复杂合成和结构优化给大规模生产带来了挑战。在此,我们介绍一种新型石墨烯复合纤维,它由还原型氧化石墨烯(rGO)和卷曲型氧化石墨烯(SrGO)组成,具有显著的韧性。通过使用简单的超声技术,我们获得了具有二维 rGO 和一维 SrGO 的多维态溶液。通过湿法纺丝实现了高韧性复合纤维的批量生产,通过控制 SrGO 的比例实现了微结构的优化,从而提高了韧性。此外,使用聚乙烯醇(PVA)作为基体可促进高变形,从而在不合成复杂复合材料的情况下显著提高了 90.7% 的机械韧性。
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引用次数: 0
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