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通过微间距空气升华法生长 1D 与 2D 共晶。

1D versus 2D cocrystals growth via microspacing in-air sublimation.

机构信息

State Key Laboratory of Crystal Materials, Shandong University, 250100, Jinan, Shandong, People's Republic of China.

出版信息

Nat Commun. 2019 Feb 15;10(1):761. doi: 10.1038/s41467-019-08712-1.

Abstract

Organic cocrystals possess valuable properties owing to the synergistic effect of the individual components. However, the growth of molecular cocrystals is still in its primary stage. Here we develop a microspacing in-air sublimation method to grow organic cocrystals, and furthermore to realize morphology control on them, which is essential for structure-property relations. A series of polycyclic aromatic hydrocarbon (PAH)‒1,2,4,5-tetracyanobenzene (TCNB) complexes cocrystals are grown directly on the substrate, with the morphology tunable from 1D needle-like to 2D plate-like on demand. Spatially resolved photoluminescence spectra analyses on different cocrystals display morphology dependent and anisotropic optical waveguiding properties. In situ observation and energy calculations of the crystallization processes reveal the formation mechanism being from a competition between growth kinetics-defined crystal habit and the thermodynamics driving force. This growth technique may serve the future demand for tunable morphology organic cocrystals in different functional applications.

摘要

有机共晶由于各组分的协同作用而具有有价值的性质。然而,分子共晶的生长仍处于初级阶段。在这里,我们开发了一种微间距空气升华法来生长有机共晶,并进一步实现对它们的形态控制,这对于结构-性质关系至关重要。一系列多环芳烃 (PAH) - 1,2,4,5-四氰基苯 (TCNB) 复合物共晶直接在衬底上生长,其形态可按需从 1D 针状调变为 2D 板状。对不同共晶的空间分辨光致发光光谱分析显示出形态依赖性和各向异性的光学波导性质。结晶过程的原位观察和能量计算揭示了形成机制是由生长动力学定义的晶体习性和热力学驱动力之间的竞争决定的。这种生长技术可能满足未来在不同功能应用中对可调形态有机共晶的需求。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3554/6377649/51dbae0473d8/41467_2019_8712_Fig1_HTML.jpg

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