Facile Preparation of an Intrinsically Low Dielectric and High Thermal Conductivity Biobased (Magnolol) Polysiloxane Film

IF 5.1 1区 化学 Q1 POLYMER SCIENCE Macromolecules Pub Date : 2024-12-26 DOI:10.1021/acs.macromol.4c01794
Guoming Yuan, Hui Yang, Xiaole Zheng, Kunxin Wang, Zhijun Liu, Yuemiao Zhang, Yanhan Tao, Kun Wu, Peiwei Hong, Jun Shi, Li Yang
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Abstract

In response to the limitations imposed on the microelectronics industry by electronic crosstalk losses and signal delays, as well as the rapid accumulation of heat, intrinsically low dielectric and high thermal conductivity materials are in urgent demand. Here, a self-curable biobased silane precursor (M@KH590) with a biphenyl unit was synthesized. A series of films (magnolol polysiloxane films (MPSOs)) were prepared using simple sol–gel film conversion and annealing and modulated intermolecular forces and molecular structure. The red-shift of the UV–vis absorption indicated that a larger π–π conjugated system was established. As a result, the through-plane thermal conductivity of MPSO-140 was 0.601 W·m–1·K–1, which was more than three times that of the pure polysiloxane material. Meanwhile, MPSO-140 exhibited excellent intrinsic low dielectric properties (Dk = 2.52, Df = 0.000572, and f = 100 MHz). This was mainly attributed to the reduction of highly polar substances and groups as well as the difficulty in polarizing a π–π conjugated system. Based on rigid biphenyl units and high cross-link density, the tensile strength and modulus of MPSO-140 were 17.42 MPa and 2.61 GPa, respectively, showing prominent mechanical properties. In addition, MPSO-140 exhibited excellent water resistance (water contact angle and 72 h water absorption of 104.8° and 0.19%, respectively) and electrical insulation, showing great potential for practical applications. The study broadened the way toward overcoming the contradiction between low dielectric and high thermal conductivity by simultaneously introducing large free volume and modulating the intermolecular forces and molecular structure in a simple and effective way.

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由于电子串扰损耗和信号延迟以及热量的快速积累对微电子工业造成了限制,因此急需本征低介电系数和高导热系数的材料。在此,我们合成了一种具有联苯单元的自固化生物基硅烷前体(M@KH590)。通过简单的溶胶-凝胶薄膜转化和退火,并调节分子间作用力和分子结构,制备了一系列薄膜(木兰醇聚硅氧烷薄膜(MPSOs))。紫外-可见吸收的红移表明建立了较大的π-π共轭体系。因此,MPSO-140 的通面热导率为 0.601 W-m-1-K-1,是纯聚硅氧烷材料的三倍多。同时,MPSO-140 表现出优异的固有低介电常数特性(Dk = 2.52,Df = 0.000572,f = 100 MHz)。这主要归因于高极性物质和基团的减少,以及 π-π 共轭体系难以极化。基于刚性联苯单元和高交联密度,MPSO-140 的拉伸强度和模量分别为 17.42 MPa 和 2.61 GPa,显示出突出的机械性能。此外,MPSO-140 还具有优异的耐水性(水接触角和 72 小时吸水率分别为 104.8°和 0.19%)和电绝缘性,在实际应用中具有巨大潜力。该研究通过同时引入大自由体积,并以简单有效的方式调节分子间作用力和分子结构,为克服低介电系数和高导热系数之间的矛盾拓宽了道路。
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来源期刊
Macromolecules
Macromolecules 工程技术-高分子科学
CiteScore
9.30
自引率
16.40%
发文量
942
审稿时长
2 months
期刊介绍: Macromolecules publishes original, fundamental, and impactful research on all aspects of polymer science. Topics of interest include synthesis (e.g., controlled polymerizations, polymerization catalysis, post polymerization modification, new monomer structures and polymer architectures, and polymerization mechanisms/kinetics analysis); phase behavior, thermodynamics, dynamic, and ordering/disordering phenomena (e.g., self-assembly, gelation, crystallization, solution/melt/solid-state characteristics); structure and properties (e.g., mechanical and rheological properties, surface/interfacial characteristics, electronic and transport properties); new state of the art characterization (e.g., spectroscopy, scattering, microscopy, rheology), simulation (e.g., Monte Carlo, molecular dynamics, multi-scale/coarse-grained modeling), and theoretical methods. Renewable/sustainable polymers, polymer networks, responsive polymers, electro-, magneto- and opto-active macromolecules, inorganic polymers, charge-transporting polymers (ion-containing, semiconducting, and conducting), nanostructured polymers, and polymer composites are also of interest. Typical papers published in Macromolecules showcase important and innovative concepts, experimental methods/observations, and theoretical/computational approaches that demonstrate a fundamental advance in the understanding of polymers.
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