光致发光
成核
单斜晶系
材料科学
分子间力
正交晶系
激光阈值
发光
分子
星团(航天器)
相(物质)
光电子学
纳米技术
结晶学
化学
晶体结构
有机化学
波长
计算机科学
程序设计语言
作者
Qing Liao,Xin Guo Wang,Shaokai Lv,Zhenzhen Xu,Yi Zhang,Hongbing Fu
出处
期刊:ACS Nano
[American Chemical Society]
日期:2018-04-26
卷期号:12 (6): 5359-5367
被引量:55
标识
DOI:10.1021/acsnano.8b00150
摘要
Controlled fabrication of organic polymorphisms with well-defined dimensions and tunable luminescent properties plays an important role in developing optoelectronic devices, sensors, and biolabeling agents but remains a challenge due to the weak intermolecular interactions among organic molecules. Herein, we developed a two-step solution self-assembly method for the controlled preparation of blue-emissive or green-emissive microribbons (MRs) of difluoroboron avobenzone (BF2AVB) by adjusting the cluster-mediated nucleation and subsequent one-dimensional growth processes. We found that blue-emissive MRs belong to the monoclinic phase, in which BF2AVB molecules form slipped π-stacks, resulting in J-aggregates with the solid-state photoluminescence efficiency φ = 68%. Meanwhile, green-emissive MRs are ascribed to the orthorhombic phase and exhibit cofacial π-stacks, which lead to H-aggregates with φ = 24%. Furthermore, these as-prepared MRs can both act as polymorph-dependent Fabry-Pérot resonators for lasing oscillators. The strategy described here might offer significant promise for the coherent light source of optoelectronic devices.
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