Department of Chemistry and International Institute of Nanotechnology, Northwestern University, Evanston, Illinois 60208, USA.
ACS Nano. 2010 Jan 26;4(1):259-66. doi: 10.1021/nn901383d.
The assembly mechanism by which hundreds of thousands of two-segment gold-polypyrrole nanorods are assembled into kinetically controlled shape-directed superstructures is examined to predict the range of nanoparticle sizes and materials that can be utilized in their formation. Four processes are responsible for assembly: templating, capillary force assembly, adhesion, and polymer hydration. It is shown that templating, where rods are prepositioned for assembly, is scale invariant and that the energy-minimized state after this step is highly disordered. In addition, we predict that superstructures can be made independently from patterns of rods separated by a distance as small as six times the inter-rod spacing. Both modeling and experiment show that adhesion and polymer dehydration, which induces curvature in the superstructures, are applicable to other materials. However, the high surface energy and low elastic modulus of polypyrrole are advantageous toward generating three-dimensional structures, inducing curvature at gold/polypyrrole length ratios as large as 7:1.
数以十万计的两段式金-聚吡咯纳米棒通过何种组装机制形成具有动力学控制的形状导向超结构,这一组装机制受到了研究人员的关注,以期预测可用于形成超结构的纳米颗粒尺寸和材料的范围。有四个过程负责组装:模板、毛细力组装、粘附和聚合物水合作用。研究表明,模板预定位是一种标度不变的过程,经过这一步骤后,能量最小化的状态是高度无序的。此外,我们预测超结构可以独立于棒之间的距离图案形成,只要棒之间的距离小于棒间距的六倍即可。模型和实验都表明,粘附和聚合物脱水(导致超结构产生曲率)适用于其他材料。然而,聚吡咯的高表面能和低弹性模量有利于生成三维结构,在金/聚吡咯长度比高达 7:1 的情况下,诱导曲率的产生。