材料科学
光致发光
聚合物
低语长廊波浪
成核
发光
共轭体系
光子学
纳米技术
激光器
光电子学
接受者
化学工程
光学
复合材料
化学
物理
有机化学
工程类
谐振器
凝聚态物理
作者
Soh Kushida,Daniel Braam,Thang Duy Dao,Hitoshi Saitô,Kosuke Shibasaki,Satoshi Ishii,Tadaaki Nagao,Akinori Saeki,Junpei Kuwabara,Takaki Kanbara,Masashi Kijima,A. Lorke,Yohei Yamamoto
出处
期刊:ACS Nano
[American Chemical Society]
日期:2016-05-02
卷期号:10 (5): 5543-5549
被引量:60
标识
DOI:10.1021/acsnano.6b02100
摘要
Highly luminescent π-conjugated polymeric microspheres were fabricated through self-assembly of energy-donating and energy-accepting polymers and their blends. To avoid macroscopic phase separation, the nucleation time and growth rate of each polymer in the solution were properly adjusted. Photoluminescence (PL) studies showed that efficient donor-to-acceptor energy transfer takes place inside the microspheres, revealing that two polymers are well-blended in the microspheres. Focused laser irradiation of a single microsphere excites whispering gallery modes (WGMs), where PL generated inside the sphere is confined and resonates. The wavelengths of the PL lines are finely tuned by changing the blending ratio, accompanying the systematic yellow-to-red color change. Furthermore, when several microspheres are coupled linearly, the confined PL propagates the microspheres through the contact point, and a cascade-like process converts the PL color while maintaining the WGM characteristics. The self-assembly strategy for the formation of polymeric nano- to microstructures with highly miscible polymer blends will be advantageous for optoelectronic and photonic device applications.
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