Starko-Bowes Ryan, Pramanik Sandipan
Electrical and Computer Engineering, University of Alberta.
J Vis Exp. 2013 Jun 18(76):50706. doi: 10.3791/50706.
In recent years π-conjugated organic semiconductors have emerged as the active material in a number of diverse applications including large-area, low-cost displays, photovoltaics, printable and flexible electronics and organic spin valves. Organics allow (a) low-cost, low-temperature processing and (b) molecular-level design of electronic, optical and spin transport characteristics. Such features are not readily available for mainstream inorganic semiconductors, which have enabled organics to carve a niche in the silicon-dominated electronics market. The first generation of organic-based devices has focused on thin film geometries, grown by physical vapor deposition or solution processing. However, it has been realized that organic nanostructures can be used to enhance performance of above-mentioned applications and significant effort has been invested in exploring methods for organic nanostructure fabrication. A particularly interesting class of organic nanostructures is the one in which vertically oriented organic nanowires, nanorods or nanotubes are organized in a well-regimented, high-density array. Such structures are highly versatile and are ideal morphological architectures for various applications such as chemical sensors, split-dipole nanoantennas, photovoltaic devices with radially heterostructured "core-shell" nanowires, and memory devices with a cross-point geometry. Such architecture is generally realized by a template-directed approach. In the past this method has been used to grow metal and inorganic semiconductor nanowire arrays. More recently π-conjugated polymer nanowires have been grown within nanoporous templates. However, these approaches have had limited success in growing nanowires of technologically important π-conjugated small molecular weight organics, such as tris-8-hydroxyquinoline aluminum (Alq3), rubrene and methanofullerenes, which are commonly used in diverse areas including organic displays, photovoltaics, thin film transistors and spintronics. Recently we have been able to address the above-mentioned issue by employing a novel "centrifugation-assisted" approach. This method therefore broadens the spectrum of organic materials that can be patterned in a vertically ordered nanowire array. Due to the technological importance of Alq3, rubrene and methanofullerenes, our method can be used to explore how the nanostructuring of these materials affects the performance of aforementioned organic devices. The purpose of this article is to describe the technical details of the above-mentioned protocol, demonstrate how this process can be extended to grow small-molecular organic nanowires on arbitrary substrates and finally, to discuss the critical steps, limitations, possible modifications, trouble-shooting and future applications.
近年来,π共轭有机半导体已成为多种不同应用中的活性材料,包括大面积、低成本显示器、光伏、可印刷和柔性电子产品以及有机自旋阀。有机材料具有以下优点:(a)低成本、低温加工;(b)电子、光学和自旋传输特性的分子水平设计。主流无机半导体不易具备这些特性,这使得有机材料在以硅为主导的电子市场中占据了一席之地。第一代有机基器件主要关注通过物理气相沉积或溶液处理生长的薄膜几何结构。然而,人们已经认识到有机纳米结构可用于提高上述应用的性能,并且已经投入了大量精力探索有机纳米结构的制造方法。一类特别有趣的有机纳米结构是其中垂直取向的有机纳米线、纳米棒或纳米管以规则排列的高密度阵列形式组织起来的结构。这种结构具有高度的通用性,是各种应用的理想形态结构,如化学传感器、分裂偶极子纳米天线、具有径向异质结构“核壳”纳米线的光伏器件以及具有交叉点几何结构的存储器件。这种结构通常通过模板导向方法实现。过去,这种方法已用于生长金属和无机半导体纳米线阵列。最近,π共轭聚合物纳米线已在纳米多孔模板内生长。然而,这些方法在生长技术上重要的π共轭小分子有机材料(如三(8 - 羟基喹啉)铝(Alq3)、红荧烯和甲烷富勒烯)的纳米线方面取得的成功有限,这些材料广泛应用于有机显示器、光伏、薄膜晶体管和自旋电子学等不同领域。最近,我们通过采用一种新颖的“离心辅助”方法解决了上述问题。因此,该方法拓宽了可在垂直有序纳米线阵列中图案化的有机材料范围。由于Alq3、红荧烯和甲烷富勒烯在技术上的重要性,我们的方法可用于探索这些材料的纳米结构化如何影响上述有机器件的性能。本文的目的是描述上述方案的技术细节,展示该过程如何扩展到在任意衬底上生长小分子有机纳米线,最后讨论关键步骤、局限性、可能的改进、故障排除和未来应用。