Core@Double-Shell结构纳米复合材料:通往高介电常数和低损耗材料的途径

IF 5.4 2区 医学 Q2 MATERIALS SCIENCE, BIOMATERIALS ACS Biomaterials Science & Engineering Pub Date : 2016-09-07 DOI:10.1021/acsami.6b06650
Yanhui Huang, Xingyi Huang*, Linda S. Schadler, Jinliang He, Pingkai Jiang
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引用次数: 63

摘要

本文报道了利用core@double-shell纳米结构增强聚合物纳米复合材料的电能存储能力和抑制介电损耗的进展。采用表面引发原子转移自由基聚合(ATRP)方法,在BaTiO3纳米颗粒上接枝聚(2-羟乙基甲基丙烯酸酯)-嵌段聚(甲基丙烯酸甲酯)和聚丙烯酸钠-嵌段聚(2-羟乙基甲基丙烯酸酯)嵌段共聚物,制备了两种类型的core@double-shell钛酸钡(BaTiO3)无基体纳米复合材料。选用具有高介电常数或高导电性的内壳聚合物,以提供较大的极化;选用封装的外壳聚合物,以保持较大的电阻率和较低的损耗。通过有限元模拟研究了所制备的纳米复合材料的介电性能和接枝聚合物的弛豫行为。研究表明,在这种多壳纳米结构中,限制更导电(损耗)的相是实现高介电常数和保持低损耗的关键。这种有前途的多壳策略可以推广到各种聚合物中,以开发新型纳米复合材料。
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Core@Double-Shell Structured Nanocomposites: A Route to High Dielectric Constant and Low Loss Material

This work reports the advances of utilizing a core@double-shell nanostructure to enhance the electrical energy storage capability and suppress the dielectric loss of polymer nanocomposites. Two types of core@double-shell barium titanate (BaTiO3) matrix-free nanocomposites were prepared using a surface initiated atom transfer radical polymerization (ATRP) method to graft a poly(2-hydroxylethyle methacrylate)-block-poly(methyl methacrylate) and sodium polyacrylate-block-poly(2-hydroxylethyle methacrylate) block copolymer from BaTiO3 nanoparticles. The inner shell polymer is chosen to have either high dielectric constant or high electrical conductivity to provide large polarization, while the encapsulating outer shell polymer is chosen to be more insulating as to maintain a large resistivity and low loss. Finite element modeling was conducted to investigate the dielectric properties of the fabricated nanocomposites and the relaxation behavior of the grafted polymer. It demonstrates that confinement of the more conductive (lossy) phase in this multishell nanostructure is the key to achieving a high dielectric constant and maintaining a low loss. This promising multishell strategy could be generalized to a variety of polymers to develop novel nanocomposites.

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来源期刊
ACS Biomaterials Science & Engineering
ACS Biomaterials Science & Engineering Materials Science-Biomaterials
CiteScore
10.30
自引率
3.40%
发文量
413
期刊介绍: ACS Biomaterials Science & Engineering is the leading journal in the field of biomaterials, serving as an international forum for publishing cutting-edge research and innovative ideas on a broad range of topics: Applications and Health – implantable tissues and devices, prosthesis, health risks, toxicology Bio-interactions and Bio-compatibility – material-biology interactions, chemical/morphological/structural communication, mechanobiology, signaling and biological responses, immuno-engineering, calcification, coatings, corrosion and degradation of biomaterials and devices, biophysical regulation of cell functions Characterization, Synthesis, and Modification – new biomaterials, bioinspired and biomimetic approaches to biomaterials, exploiting structural hierarchy and architectural control, combinatorial strategies for biomaterials discovery, genetic biomaterials design, synthetic biology, new composite systems, bionics, polymer synthesis Controlled Release and Delivery Systems – biomaterial-based drug and gene delivery, bio-responsive delivery of regulatory molecules, pharmaceutical engineering Healthcare Advances – clinical translation, regulatory issues, patient safety, emerging trends Imaging and Diagnostics – imaging agents and probes, theranostics, biosensors, monitoring Manufacturing and Technology – 3D printing, inks, organ-on-a-chip, bioreactor/perfusion systems, microdevices, BioMEMS, optics and electronics interfaces with biomaterials, systems integration Modeling and Informatics Tools – scaling methods to guide biomaterial design, predictive algorithms for structure-function, biomechanics, integrating bioinformatics with biomaterials discovery, metabolomics in the context of biomaterials Tissue Engineering and Regenerative Medicine – basic and applied studies, cell therapies, scaffolds, vascularization, bioartificial organs, transplantation and functionality, cellular agriculture
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