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Updated: Jul 6, 2026

Self-assembling Morphologies Obtained from Helical Polycarbodiimide Copolymers and Their Triazole Derivatives
Published on: February 7, 2017
Thermal-Responsive Self-Assembly of Organic Crystals With Asymmetric Architectures
Ying-Xin Ma1, Ya-Nan Zhu1, Xue-Dong Wang1
1State Key Laboratory of Bioinspired Interfacial Materials Science, Institute of Functional Nano & Soft Materials (FUNSOM), Soochow University, Suzhou, P. R. China.
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The miniaturization and integration of electronic/photonic devices demand precise control over light at the micro-scale. However, achieving tailored optical anisotropy through intrinsic material design, rather than external components, remains a significant challenge. Herein, we report a general and programmable strategy for the growth of one-dimensional organic crystals with precisely tunable asymmetric architectures via a spatially defined temperature gradient. By leveraging the competitive, facet-dependent growth kinetics under a thermal bias, continuous and precise control over the structural asymmetry is achieved in single crystals, with a tunable morphological anisotropy ranging from 9% to 81%. The resulting asymmetric crystals exhibit a pronounced direction-dependent optical response, yielding a photoluminescence intensity contrast ratio as high as 113.3, which scales directly with the degree of structural asymmetry. This work establishes a material-based platform for applying direction-dependent photonic properties directly into crystal morphology, paving the way for advanced organic photonic materials with built-in anisotropy.

