Deng D S, Orf N D, Abouraddy A F, Stolyarov A M, Joannopoulos J D, Stone H A, Fink Y
Research Laboratory of Electronics, Department of Materials Science and Engineering, Massachusetts Institute of Technology, 77 Massachusetts Avenue, Cambridge, Massachusetts 02139, USA.
Nano Lett. 2008 Dec;8(12):4265-9. doi: 10.1021/nl801979w.
We report a novel physical phenomenon in which a cylindrical shell undergoing a scaling process evolves into an ordered array of filaments upon reaching a characteristic thickness. We observe that the tendency to breakup is related to the material viscosity in a manner reminiscent of capillary instability. However, unlike the classical breakup of a fluid cylinder into droplets, the structural evolution in our system occurs exclusively in the cross sectional plane while uniformity is maintained in the axial direction. We propose a fluid front instability mechanism to account for the observed phenomena. The fleeting evolution of fluid breakup from a thin film to a filament array is captured in the frozen state by a thermal drawing process which results in extended lengths of solid sub-100 nm filaments encapsulated within a polymer fiber. Hundreds of glassy semiconductor filament arrays are precisely oriented within a polymer fiber matrix making electrical connections trivial. This approach offers unique opportunities for fabrication of nanometer scale devices of unprecedented lengths allowing simplified access and connectivity.
我们报告了一种新的物理现象,即经历缩放过程的圆柱壳在达到特征厚度时会演变成有序的细丝阵列。我们观察到,破裂的趋势与材料粘度有关,这让人联想到毛细管不稳定性。然而,与流体圆柱体分裂成液滴的经典破裂不同,我们系统中的结构演化仅发生在横截面平面内,而轴向保持均匀性。我们提出了一种流体前沿不稳定性机制来解释所观察到的现象。通过热拉伸过程,流体从薄膜到细丝阵列的短暂演化在冻结状态下被捕获,这导致聚合物纤维中封装了长度延伸的亚100纳米固体细丝。数百个玻璃态半导体细丝阵列在聚合物纤维基质中精确取向,使得电连接变得简单。这种方法为制造前所未有的长度的纳米级器件提供了独特的机会,简化了接入和连接。