三聚体
芴
聚氨酯
荧光
光化学
聚合物
材料科学
有机发光二极管
发光二极管
蓝光
高分子化学
化学
光电子学
光学
二聚体
复合材料
有机化学
物理
图层(电子)
作者
Wenxin Huang,Xinyu Liang,Qingqing Lu,Rui Gao,Lubing Bai,Yingru Lin,Jing Yang,Lizhi Wang,Zhiqiang Zhuo,Wenchao Zhao,Ning Sun,Lili Sun,Yamin Han,Xiang An,Jinyi Lin,Wei Huang
出处
期刊:Macromolecules
[American Chemical Society]
日期:2025-04-09
卷期号:58 (8): 3787-3794
被引量:1
标识
DOI:10.1021/acs.macromol.5c00447
摘要
Intrinsically stretchable materials play a pivotal role in the advancement of flexible electronics. However, simultaneously achieving excellent mechanical stretchability and superior optoelectronic properties in light-emitting polymers remains a formidable challenge. Here, we present a novel fluorescent polyurethane (PU) synthesized by integrating a fluorene-based trimer (TrF) as the hard segment and polydimethylsiloxane (PDMS) as the soft segment. This molecular design imparts the polymer with a maximum elongation at a break of 125%, coupled with efficient deep-blue photoluminescence with a quantum yield of 50.2%. Besides, the interchain hydrogen bonds between urethane groups facilitate polymer solution gelation by forming noncovalent cross-linked networks. Polymer light-emitting diodes (PLEDs) based on this novel polymer were successfully fabricated, demonstrating a turn-on voltage of 3.8 V and a maximum luminance of 120 cd m–2. These results underscore the feasibility of integrating stretchability with optoelectronic functionality, emphasizing the critical balance between the mechanical flexibility and optoelectronic properties.
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