基于有机发光二极管全共轭骨架的固有可拉伸电致发光弹性体

IF 5.2 1区 化学 Q1 POLYMER SCIENCE
Yi Wan, Hao-Tian Yuan, Qianwei Xu, Fang Liu, Nianlong Cai, Qian Xue, Xiang-Chun Li* and Wen-Yong Lai*, 
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引用次数: 0

摘要

可拉伸有机发光二极管(oled)能够承受长时间的变形,代表了柔性和可拉伸电子领域的重要发展方向。内在可拉伸的电致发光弹性体(isee)对于实现oled的可拉伸性至关重要。然而,目前可用的基于软链调制的非共轭主干网的电致发光聚合物往往难以保持器件的光电性能。在此,我们提出了一种通过全共轭聚合物骨架的软链调制来平衡光电性能和拉伸性的分子设计策略。所得弹性体的拉伸伸长率为166%,屈服强度为0.34 MPa。当作为oled的发射层使用时,该器件显示出5 V的低导通电压。研究结果为柔性和可拉伸电子器件提供了一种有效的分子设计策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Intrinsically Stretchable Electroluminescent Elastomers Based on Fully Conjugated Backbones for Organic Light-Emitting Diodes

Intrinsically Stretchable Electroluminescent Elastomers Based on Fully Conjugated Backbones for Organic Light-Emitting Diodes

Intrinsically Stretchable Electroluminescent Elastomers Based on Fully Conjugated Backbones for Organic Light-Emitting Diodes

Stretchable organic light-emitting diodes (OLEDs) are capable of withstanding prolonged deformation, representing a significant direction for advancement within the field of flexible and stretchable electronics. Intrinsically stretchable electroluminescent elastomers (ISEEs) are essential for achieving stretchability in OLEDs. Nonetheless, currently available electroluminescent polymers based on nonconjugated backbones modulated by soft chains often struggle to maintain the optoelectronic performance of the devices. Herein, we proposed a molecular design strategy to balance the optoelectronic performance and stretchability by the soft-chain modulation of fully conjugated polymer backbones. The resulting elastomers exhibit a tensile elongation of 166% and a yield strength of 0.34 MPa. When employed as the emitting layer in OLEDs, the device demonstrated a low turn-on voltage of 5 V. The results suggest an effective molecular design strategy for flexible and stretchable electronics.

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来源期刊
Macromolecules
Macromolecules 工程技术-高分子科学
CiteScore
9.30
自引率
16.40%
发文量
942
审稿时长
2 months
期刊介绍: Macromolecules publishes original, fundamental, and impactful research on all aspects of polymer science. Topics of interest include synthesis (e.g., controlled polymerizations, polymerization catalysis, post polymerization modification, new monomer structures and polymer architectures, and polymerization mechanisms/kinetics analysis); phase behavior, thermodynamics, dynamic, and ordering/disordering phenomena (e.g., self-assembly, gelation, crystallization, solution/melt/solid-state characteristics); structure and properties (e.g., mechanical and rheological properties, surface/interfacial characteristics, electronic and transport properties); new state of the art characterization (e.g., spectroscopy, scattering, microscopy, rheology), simulation (e.g., Monte Carlo, molecular dynamics, multi-scale/coarse-grained modeling), and theoretical methods. Renewable/sustainable polymers, polymer networks, responsive polymers, electro-, magneto- and opto-active macromolecules, inorganic polymers, charge-transporting polymers (ion-containing, semiconducting, and conducting), nanostructured polymers, and polymer composites are also of interest. Typical papers published in Macromolecules showcase important and innovative concepts, experimental methods/observations, and theoretical/computational approaches that demonstrate a fundamental advance in the understanding of polymers.
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