Cross Emily R, Sproules Stephen, Schweins Ralf, Draper Emily R, Adams Dave J
School of Chemistry , University of Glasgow , Glasgow G12 8QQ , U.K.
Large Scale Structures Group , Institut Laue-Langevin , 71 Avenue des Martyrs, CS 20156 , F-38042 Grenoble Cedex 9 , France.
J Am Chem Soc. 2018 Jul 18;140(28):8667-8670. doi: 10.1021/jacs.8b05359. Epub 2018 Jul 3.
Multicomponent supramolecular gels have great potential for optoelectronics. Ideally, we could control the self-assembly of multiple components across many length scales, from the primary assembled structures to how these are arranged in space. This would allow energy transfer between p-type and n-type fibers to be controlled. Usually, a single network is formed and analyzed. It is not clear how most networks could be modified, and certainly not how these might be differentiated. Here, we address both of these issues. We show how the different components in a multicomponent gel can be differentiated by small-angle neutron scattering using contrast-matching experiments. The rate of self-assembly can be used to vary the networks that are formed, leading directly to changes in the efficiency of electron transfer. The assembly kinetics can therefore be used to prepare different networks from the same primary building blocks and primary self-assembled structures. We expect that these advances will allow multicomponent systems to become effective electronic materials.
多组分超分子凝胶在光电子学领域具有巨大潜力。理想情况下,我们能够在从初级组装结构到其在空间中的排列方式等多个长度尺度上控制多种组分的自组装。这将使得p型和n型纤维之间的能量转移得以控制。通常,会形成并分析单个网络。目前尚不清楚大多数网络如何能够被修饰,更不确定如何区分它们。在此,我们解决这两个问题。我们展示了如何通过使用对比匹配实验的小角中子散射来区分多组分凝胶中的不同组分。自组装速率可用于改变所形成的网络,直接导致电子转移效率的变化。因此,组装动力学可用于从相同的基本构建单元和初级自组装结构制备不同的网络。我们预计这些进展将使多组分系统成为有效的电子材料。