Epitaxial growth of dual-color-emitting organic heterostructures via binary solvent synergism driven sequential crystallization

被引:24
作者
Yin, Baipeng [1 ]
Gu, Jianmin [1 ,2 ]
Feng, Man [1 ]
Zhang, Guang Cong [1 ]
Zhang, Ziming [1 ]
Zhong, Jinling [1 ]
Zhang, Chuang [3 ]
Wen, Bin [2 ]
Zhao, Yong Sheng [3 ]
机构
[1] Yanshan Univ, Hebei Key Lab Appl Chem, Sch Environm & Chem Engn, Qinhuangdao 066004, Hebei, Peoples R China
[2] Yanshan Univ, State Key Lab Metastable Mat Sci & Technol MMST, Qinhuangdao 066004, Hebei, Peoples R China
[3] Chinese Acad Sci, Key Lab Photochem, Inst Chem, Beijing 100190, Peoples R China
基金
中国博士后科学基金; 中国国家自然科学基金;
关键词
ELECTROGENERATED CHEMILUMINESCENCE; SELECTIVE GROWTH; NANOWIRE HETEROSTRUCTURES; NANOSTRUCTURES; ARCHITECTURES;
D O I
10.1039/c8nr08066f
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The controlled construction of organic heterostructured architectures derived from molecules with similar nucleation thresholds and concentrations has been rare and remains a great challenge. Herein, we report a sequential epitaxial growth to synthesize dual-color-emitting organic heterostructures with 9,10-bis(phenylethynyl) anthracene (BPEA) microwire trunks and tris-(8-hydroxyquinoline) aluminium (Alq3) microstructure branches by an anti-solvent induced sequential crystallization strategy. During the epitaxial growth process, the hydrogen-bonding interactions of the antisolvent and solvent cause a large change in the solubility and crystallization rate of BPEA and Alq3 molecules in the mixed system, which facilitates sequential crystallization of organic molecule pairs with similar nucleation thresholds and concentrations into desired heterostructures by manipulating the synergism of antisolvents and solvents. The Forster resonant energy transfer process in heterostructures could be modulated by varying the structure of heterostructures, such as the shape, amount and angles of the branches. The present synthesis strategy provides a unique insight into the detailed formation mechanism of complex organic heterostructures, further guiding the construction of more functional heterostructure materials.
引用
收藏
页码:7111 / 7116
页数:6
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