通过纳米级多界面相结构工程实现高导热性和强抗弯强度的金刚石/铝复合材料

IF 10 2区 材料科学 Q1 MATERIALS SCIENCE, MULTIDISCIPLINARY Materials Today Physics Pub Date : 2024-09-27 DOI:10.1016/j.mtphys.2024.101563
Ping Zhu , Qiang Zhang , Yixiao Xia , Yifu Ma , Huasong Gou , Xue Liang , Gaohui Wu
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引用次数: 0

摘要

金刚石/铝复合材料作为新一代热管理材料,在抑制 Al4C3 的形成和提高性能之间进退两难。在此,我们提出了一种纳米级多界面相结构工程策略,利用磁控溅射和真空热处理相结合的方法,获得具有纳米级 TiC-Ti 层的金刚石颗粒。延长真空加热时间会增加 TiC 的含量,但会导致在金刚石(100)和(111)面上形成的 TiC 的形态和覆盖率出现显著差异。第一性原理计算显示,金刚石(100)/钛的附着功和 C-Ti 反应倾向强于金刚石(111)/钛,从而阐明了金刚石/钛和金刚石/TiC 之间界面性质的差异。提前获得的金刚石-TiC-Ti 构型有助于制备金刚石-TiC-Al(Al3Ti)结构的复合材料,多界面相结构有利于改善界面结合、调整声学失配和抑制 Al4C3 的形成。(800 °C 0.5 h)@Ti 涂层金刚石(100 μm)/铝多界面相复合材料表现出优异的热导率(646 W m-1 K-1)和出色的抗弯强度(358 MPa),超过微分有效介质模型理论预测值的 90%。(800 °C 0.5 h)@Ti 涂层金刚石/铝复合材料的性能比传统的 Ti 涂层金刚石/铝复合材料高出约 30%。增加热处理时间形成的 TiC 层更厚且不连续,导致复合材料的热导率降低,Al4C3 的抑制作用减弱。我们通过多尺度表征阐明了与金刚石取向相关的界面结构形成机制。在热导率预测模型的基础上,考虑了不同金刚石取向对应的界面结构,预测值与实验结果具有良好的一致性。通过界面改性工程,我们克服了引入改性层抑制 Al-C 反应的同时导致界面热阻增加的两难问题,为界面热传输机制的研究提供了启示。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Achieving high thermal conductivity and strong bending strength diamond/aluminum composite via nanoscale multi-interface phase structure engineering
Diamond/aluminum composites, as a new generation of thermal management materials, are caught in the dilemma between inhibiting the formation of Al4C3 and improving the performance. Herein, we proposed a strategy for nanoscale multi-interface phase structure engineering, utilizing a combination of magnetron sputtering and vacuum heat treatment to obtain diamond particles with nanoscale TiC-Ti layers. Prolonging the vacuum heating time increases the content of TiC, but results in significant differences in the morphology and coverage of TiC formed on the diamond(100) and (111) facets. First-principles calculations reveal that the work of adhesion and C-Ti reaction tendency of diamond(100)/Ti are stronger than those of diamond(111)/Ti, clarifying the difference in interfacial properties between diamond/Ti and diamond/TiC. Diamond-TiC-Ti configuration obtained in advance contributes to fabricating the composite with diamond-TiC-Al(Al3Ti) structure, and the multi-interface phase structure is beneficial to improve the interface bonding, adjust the acoustic mismatch, and inhibit the formation of Al4C3. (800 °C 0.5 h)@Ti-coated diamond(100 μm)/aluminum composite with the multi-interface phase exhibits excellent thermal conductivity(646 W m−1 K−1) and outstanding bending strength(358 MPa), exceeding 90 % of the theoretical prediction of the differential effective medium model. The performance of (800 °C 0.5 h)@Ti-coated diamond/aluminum composite is about 30 % higher than that of traditional Ti-coated diamond/aluminum composite. The TiC layer formed by increasing the heat treatment time is thicker and discontinuous, leading to a decrease in the thermal conductivity of the composite and a weakening effect of Al4C3 inhibition. We clarified the formation mechanism of interface structure related to diamond orientation by multi-scale characterization. Based on the thermal conductivity prediction models, the interface structures corresponding to different diamond orientations were considered, and the predicted values showed good consistency with the experimental results. By interface modification engineering, we overcome the dilemma of introducing modified layer to inhibit Al-C reaction while leading to additional interface thermal resistance, providing insights into the interfacial thermal transport mechanism.
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来源期刊
Materials Today Physics
Materials Today Physics Materials Science-General Materials Science
CiteScore
14.00
自引率
7.80%
发文量
284
审稿时长
15 days
期刊介绍: Materials Today Physics is a multi-disciplinary journal focused on the physics of materials, encompassing both the physical properties and materials synthesis. Operating at the interface of physics and materials science, this journal covers one of the largest and most dynamic fields within physical science. The forefront research in materials physics is driving advancements in new materials, uncovering new physics, and fostering novel applications at an unprecedented pace.
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