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Competition between substrate-mediated π-π stacking and surface-mediated T(g) depression in ultrathin conjugated polymer films.

机译:超薄共轭聚合物薄膜中底物介导的π-π堆积与表面介导的T(g)抑制之间的竞争。

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摘要

We report surface and interface effects in dynamics and chain conformation in the thin film of conjugated polymer PCDTBT. To probe dynamic anomalies, we measure the glass transition temperature (T(g)) of PCDTBT films as a function of thickness, and find that there is a significant depression in T(g) for films less than 100 nm thick; a result qualitatively similar to that observed in many other polymer film systems. However, for films less than 40 nm, the T(g) converges to a constant value of 20 K below its bulk value. Grazing incidence X-ray diffraction shows depth-dependent molecular organization that is associated with the unusual thickness-dependent dynamics.
机译:我们报告了共轭聚合物PCDTBT薄膜的动力学和链构象中的表面和界面效应。为了探测动态异常,我们测量了PCDTBT薄膜的玻璃化转变温度(T(g))与厚度的关系,发现厚度小于100 nm的薄膜的T(g)明显降低。该结果在质量上与许多其他聚合物薄膜系统中观察到的结果相似。但是,对于小于40 nm的薄膜,T(g)会收敛到一个低于其体积值20 K的恒定值。掠入射X射线衍射显示出与深度有关的分子组织,这与异常的与厚度有关的动力学有关。

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