Laboratory of Biosensors and Bioelectronics , Institute for Biomedical Engineering, ETH Zurich , Gloriastrasse 35 , 8092 Zurich , Switzerland.
Langmuir. 2018 Jul 3;34(26):7827-7843. doi: 10.1021/acs.langmuir.8b01411. Epub 2018 Jun 21.
In this study, we present a detailed investigation of the morphology of binary colloidal structures formed by self-assembly at air/water interface of particles of two different sizes, with a size ratio such that the larger particles do not retain a hexagonal arrangement in the binary assembly. While the structure and symmetry of binary mixtures in which such hexagonal order is preserved has been thoroughly scrutinized, binary colloids in the regime of nonpreservation of the hexagonal order have not been examined with the same level of detail due also to the difficulty in finding analysis tools suitable to recognize hidden symmetries in seemingly amorphous and disordered arrangements. For this purpose, we resorted to a combination of different analysis tools based on computational geometry and computational topology to get a comprehensive picture of the morphology of the assemblies. By carrying out an extensive investigation of binary assemblies in this regime with variable concentration of smaller particles with respect to larger particles, we identify the main patterns that coexist in the apparently disordered assemblies and detect transitions in the symmetries upon increase in the number of small particles. As the concentration of small particles increases, large particle arrangements become more dilute and a transition from hexagonal to rhombic and square symmetries occurs, accompanied also by an increase in clusters of small particles; the relative weight of each specific symmetry can be controlled by varying the composition of the assemblies. The demonstration of the possibility to control the morphology of apparently disordered binary colloidal assemblies by varying experimental conditions and the definition of a route for the investigation of disordered assemblies are important for future studies of complex colloidal patterns to understand self-assembly mechanisms and to tailor the physical properties of colloidal assemblies.
在这项研究中,我们详细研究了由两种不同大小的粒子在空气/水界面自组装形成的二元胶体结构的形态,其大小比使得较大的粒子在二元组装中不会保持六边形排列。虽然已经彻底研究了保持这种六边形有序的二元混合物的结构和对称性,但由于难以找到适合识别看似无定形和无序排列中隐藏对称性的分析工具,因此没有以相同的细节水平检查保持六边形有序的二元胶体。为此,我们求助于基于计算几何和计算拓扑学的不同分析工具的组合,以全面了解组装体的形态。通过对该体系中具有不同浓度的较小粒子相对于较大粒子的二元组装体进行广泛研究,我们确定了在看似无序组装体中共存的主要模式,并在小粒子数量增加时检测到对称性的转变。随着小粒子浓度的增加,大粒子排列变得更加稀疏,从六边形到菱形和正方形对称性发生转变,同时小粒子簇也增加;通过改变组装体的组成,可以控制每种特定对称性的相对权重。通过改变实验条件来控制显然无序的二元胶体组装体的形态的可能性的证明以及对无序组装体的研究途径的定义,对于未来研究复杂胶体图案以理解自组装机制和调整胶体组装体的物理性质非常重要。