Affiliation:
1. College of Chemistry Chemical Engineering and Materials Science Soochow University Suzhou 215123 P. R. China
2. Institute of Functional Nano & Soft Materials (FUNSOM) Jiangsu Key Laboratory for Carbon‐Based Functional Materials & Devices Soochow University Suzhou 215123 P. R. China
3. National Engineering Laboratory for Modern Silk College of Textile and Clothing Engineering Soochow University Suzhou 215123 P. R. China
4. School of Physics and Electronics Shandong Normal University Jinan 250014 P. R. China
Abstract
AbstractPrecise fabrication of organic micro/nanostructures with regular morphology has gained a considerable concern in developing high‐performance optoelectronic devices, which is still a huge challenge to realize tunable morphology without the dependence on molecule packing arrangement. Herein, a thermodynamic/kinetic controlled self‐assembly for triphenylene‐7,7,8,8‐tetracyanoquinodimethane (TP‐TCNQ) cocrystal, with well‐defined microwires and microplates based on the same crystal structure, is proposed. With the low solution concentration of C = 5 mm, the comparable growth rates along [011] driven by π–π interaction and along [100] driven by charge‐transfer (CT) interaction facilitate the formation of thermodynamically favored shape of microplates. In contrast, the prominent CT interaction along [100] leads to the construction of microwires at kinetic state under high‐concentration solution of C = 10 mm. Furthermore, the prepared TP‐TCNQ microwires and microplates demonstrate isotropic photonic transmissions with the low optical loss coefficient of 0.033 and 0.042 dB µm−1, respectively. This strategy provides a novel avenue to finely construct the organic microcrystals with desired morphology for potential optoelectronics.
Funder
National Natural Science Foundation of China
Natural Science Foundation of Jiangsu Province
Science and Technology Support Program of Jiangsu Province
Subject
Atomic and Molecular Physics, and Optics,Electronic, Optical and Magnetic Materials
Cited by
6 articles.
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