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廖良生教授课题组在Nature Communications上发表论文
发布时间:2019-10-24 点击:14

题目:

Hierarchical Self-assembly of Organic Heterostructure Nanowires


作者:

Ming-Peng Zhuo1, Jun-Jie Wu1, Xue-Dong Wang1,*, Yi-Chen Tao1, Yi Yuan1, Liang-Sheng Liao1,2,*


单位:

1Institute of Functional Nano & Soft Materials (FUNSOM), Collaborative Innovation Center of Suzhou Nanoscience and Technology, Soochow University, 199 Ren-AiRoad, Suzhou 215123, China.

2Institute of Organic Optoelectronics, JITRI, Wujiang, Suzhou, Jiangsu 215211, P. R. China.


摘要:

Organic heterostructures (OHSs) integrating the intrinsic heterostructure characters as well as the organic semiconductor properties have attracted intensive attention in material chemistry. However, the precise bottom-up synthesis of OHSs is still challenging owing to the general occurrence of homogeneous-nucleation and the difficult manipulation of noncovalent interactions. Herein, we present the rational synthesis of the longitudinally/horizontally epitaxial growth of one-dimensional OHSs including triblock and core/shell nanowires with quantitatively-manipulated microstructure via a hierarchical self-assembly method by regulating the noncovalent interactions: hydrogen bond (−15.66 kcal mol−1) > halogen bond (−4.90 kcal mol−1) > π-π interaction (−0.09 kcal mol−1). In the facet-selective epitaxial growth strategy, the lattice-matching and the surface-interface energy balance respectively facilitate the realization of triblock and core/shell heterostructures. This hierarchical self-assembly approach opens up avenues to the fine synthesis of OHSs. We foresee application possibilities in integrated optoelectronics, such as the nanoscale multiple input/out optical logic gate with high-fidelity signal.


影响因子:

12.353


分区情况:

一区


链接:

https://www.nature.com/articles/s41467-019-11731-7


责任编辑:朱文昌




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