热塑性聚氨酯
材料科学
玻璃化转变
拉曼光谱
光致发光
复合材料
聚氨酯
扫描电子显微镜
聚合物
热塑性塑料
聚合物混合物
极限抗拉强度
化学工程
共聚物
弹性体
光学
物理
光电子学
工程类
作者
Patrícia Santiago de Oliveira Patrício,Hállen Daniel Rezende Calado,Flávio A. Oliveira,A. Righi,Bernardo R. A. Neves,Glaura G. Silva,L. A. Cury
标识
DOI:10.1088/0953-8984/18/32/002
摘要
A correlation between thermal, optical and morphological properties of self-sustained films formed from blends of poly(3-hexylthiophene) (P3HT) and thermoplastic polyurethane (TPU), with 1, 10 and 20 wt% of P3HT in TPU, is established. Images of scanning electron microscopy (SEM) show the formation of domains of P3HT into the TPU matrix, characterizing the blend material as heterogeneous. The heat capacity (Cp) dependence on P3HT contents was investigated in a large temperature interval. In the region of the TPU glass transition, the difference between the experimental and predicted ΔCp values is more pronounced for the 1 wt% case, which strongly suggests that in this case there is a higher influence of the P3HT chains on the TPU matrix. The SEM images for the 1 wt% blended film present the formation of the smallest P3HT domains in the TPU matrix. The relatively high reduction of the PL intensity of the pure electronic transition peak in the 1 wt% blended film, in comparison to the other blended films and also to a pure P3HT film, favours the assumption that the smallest P3HT domains are at the origin of a more structural disordered character. This fact is in agreement with the results obtained by Raman spectroscopy and also by photoluminescence resolved by polarization in stretched self-sustained films, showing an ample correlation between morphological, thermal and optical properties of these blended materials. In addition, the thermoplastic properties of the polyurethane configure very good conditions for tensile drawing of P3HT and other conjugated polymer molecules.
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