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Fabrication Densification and Replica Molding of 3D Carbon Nanotube Microstructures

机译:3D碳纳米管微结构的制造致密化和仿制成型

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摘要

The introduction of new materials and processes to microfabrication has, in large part, enabled many important advances in microsystems, lab-on-a-chip devices, and their applications. In particular, capabilities for cost-effective fabrication of polymer microstructures were transformed by the advent of soft lithography and other micromolding techniques 1, 2, and this led a revolution in applications of microfabrication to biomedical engineering and biology. Nevertheless, it remains challenging to fabricate microstructures with well-defined nanoscale surface textures, and to fabricate arbitrary 3D shapes at the micro-scale. Robustness of master molds and maintenance of shape integrity is especially important to achieve high fidelity replication of complex structures and preserving their nanoscale surface texture. The combination of hierarchical textures, and heterogeneous shapes, is a profound challenge to existing microfabrication methods that largely rely upon top-down etching using fixed mask templates. On the other hand, the bottom-up synthesis of nanostructures such as nanotubes and nanowires can offer new capabilities to microfabrication, in particular by taking advantage of the collective self-organization of nanostructures, and local control of their growth behavior with respect to microfabricated patterns. Our goal is to introduce vertically aligned carbon nanotubes (CNTs), which we refer to as CNT "forests", as a new microfabrication material. We present details of a suite of related methods recently developed by our group: fabrication of CNT forest microstructures by thermal CVD from lithographically patterned catalyst thin films; self-directed elastocapillary densification of CNT microstructures; and replica molding of polymer microstructures using CNT composite master molds. In particular, our work shows that self-directed capillary densification ("capillary forming"), which is performed by condensation of a solvent onto the substrate with CNT microstructures, significantly increases the packing density of CNTs. This process enables directed transformation of vertical CNT microstructures into straight, inclined, and twisted shapes, which have robust mechanical properties exceeding those of typical microfabrication polymers. This in turn enables formation of nanocomposite CNT master molds by capillary-driven infiltration of polymers. The replica structures exhibit the anisotropic nanoscale texture of the aligned CNTs, and can have walls with sub-micron thickness and aspect ratios exceeding 50:1. Integration of CNT microstructures in fabrication offers further opportunity to exploit the electrical and thermal properties of CNTs, and diverse capabilities for chemical and biochemical functionalization 3.
机译:将新材料和新工艺引入微细加工,在很大程度上使微系统,片上实验室设备及其应用取得了许多重要进展。尤其是,随着软光刻技术和其他微成型技术 1、2 的出现,高性价比制造聚合物微结构的能力得到了改变,这引发了微制造在生物医学工程和生物学中的应用革命。然而,制造具有良好定义的纳米级表面纹理的微结构以及以微米级制造任意3D形状仍然具有挑战性。母模的鲁棒性和形状完整性的保持对于实现复杂结构的高保真复制并保留其纳米级表面纹理尤为重要。分层纹理和异构形状的结合对现有的微加工方法提出了严峻的挑战,这些方法在很大程度上依赖于使用固定掩模模板进行自上而下的蚀刻。另一方面,纳米结构(例如纳米管和纳米线)的自下而上的合成可以为微细加工提供新的功能,特别是通过利用纳米结构的集体自组织以及相对于微细加工图案的局部控制其生长行为。我们的目标是引入一种垂直对齐的碳纳米管(CNT),我们将其称为CNT“森林”,作为一种新型的微细加工材料。我们介绍了我们小组最近开发的一系列相关方法的详细信息:通过热CVD从光刻图案化的催化剂薄膜制造CNT森林微结构;碳纳米管的自导向弹性毛细管致密化;并使用CNT复合母模对聚合物微结构进行仿制成型。特别地,我们的工作表明,通过将溶剂缩合到具有CNT微结构的基材上进行的自定向毛细管致密化(“毛细管形成”)显着提高了CNT的堆积密度。该工艺能够将垂直的CNT微结构定向转化为直的,倾斜的和扭曲的形状,其机械性能比典型的微加工聚合物强。反过来,这使得能够通过毛细管驱动的聚合物渗透形成纳米复合CNT主模。复制结构显示出排列的CNT的各向异性纳米级纹理,并且可以具有亚微米厚度和长宽比超过50:1的壁。 CNT微观结构在制造中的集成为进一步利用CNT的电学和热学性质以及化学和生物化学功能化 3 的各种功能提供了进一步的机会。

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