Department of Physics and Center for Nanophysics and Advanced Materials, University of Maryland, College Park, Maryland 20742, USA.
Department of Electrical and Computer Engineering, University of Maryland, College Park, Maryland 20742, USA.
Nat Commun. 2017 Feb 2;8:14312. doi: 10.1038/ncomms14312.
Cooperative chirality phenomena extensively exist in biomolecular and organic systems via intra- and inter-molecular interactions, but study of inorganic materials has been lacking. Here we report, experimentally and theoretically, cooperative chirality in colloidal cinnabar mercury sulfide nanocrystals that originates from chirality interplay between the crystallographic lattice and geometric morphology at different length scales. A two-step synthetic scheme is developed to allow control of critical parameters of these two types of handedness, resulting in different chiral interplays expressed as observables through materials engineering. Furthermore, we adopt an electromagnetic model with the finite element method to elucidate cooperative chirality in inorganic systems, showing excellent agreement with experimental results. Our study enables an emerging class of nanostructures with tailored cooperative chirality that is vital for fundamental understanding of nanoscale chirality as well as technology applications based on new chiroptical building blocks.
协同手性现象通过分子内和分子间相互作用广泛存在于生物分子和有机体系中,但对无机材料的研究却一直缺乏。在这里,我们通过实验和理论报告了胶体辰砂硫化汞纳米晶体中的协同手性,这种协同手性源于晶体格子和不同长度尺度上的几何形态之间的手性相互作用。我们开发了一种两步合成方案,可以控制这两种手性的关键参数,从而通过材料工程实现不同的手性相互作用的表达。此外,我们采用具有有限元法的电磁场模型来阐明无机体系中的协同手性,实验结果与理论结果吻合较好。我们的研究为具有定制协同手性的一类新兴纳米结构提供了可能,这对于深入理解纳米尺度手性以及基于新手性构建基元的技术应用至关重要。