Self-organized supramolecular assemblies are widespread in nature and technology in the form of liquid crystals, colloids, and gels. The reversible nature of non-covalent bonding leads to dynamic functions such as stimuli-responsive switching and self-healing, which are unachievable from an isolated molecule. However, multiple intermolecular interactions generate diverse conformational and configurational molecular motions over various time scales in their self-assembled states, and their specific dynamics remains unclear. In the present study, we have experimentally unveiled the static structures and dynamical behaviors in columnar colloidal liquid crystals by a coherent X-ray scattering technique using refined model samples. We have found that controlling the size distribution of the colloidal nanoplates dramatically changed their static and dynamic properties. Furthermore, the resulting dynamical behaviors obtained by X-ray photon correlation spectroscopy have been successfully decomposed into multiple distinct modes, allowing us to explore the dynamical origin in the colloidal liquid-crystalline state. The present approaches using a columnar liquid crystal may contribute to a better understanding of the dynamic nature of molecular assemblies and dense colloidal systems and bring valuable insights into rational design of functional properties of self-assembled materials such as stimuli-responsive liquid crystals, self-healing gels, and colloidal crystals. For these materials, the motion of constituent particles and molecules in the self-assembled state is a key factor for structural formation and dynamically responsive performance.
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