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局部刚度对聚噻吩熵驱动微观动力学的影响。

Impact of Local Stiffness on Entropy Driven Microscopic Dynamics of Polythiophene.

作者信息

Gupta Sudipta, Chatterjee Sourav, Zolnierczuk Piotr, Nesterov Evgueni E, Schneider Gerald J

机构信息

Department of Chemistry, Louisiana State University, Baton Rouge, LA, 70803, USA.

Jülich Centre for Neutron science (JCNS) and outstation at SNS, POB 2008, 1 Bethel Valley Road, TN, 37831, Oak Ridge, USA.

出版信息

Sci Rep. 2020 Jun 19;10(1):9966. doi: 10.1038/s41598-020-66354-6.

Abstract

We exploited the high temporal and spatial resolution of neutron spin echo spectroscopy to investigate the large-scale dynamics of semiflexible conjugated polymer chains in solutions. We used a generalized approach of the well-established Zimm model of flexible polymers to describe the relaxation mode spectra of locally stiff polythiophene chains. The Zimm mode analysis confirms the existence of beads with a finite length that corresponds to a reduced number of segmental modes in semiflexible chains. Irrespective of the temperature and the molecular weight of the conjugated polymer, we witness a universal behavior of the local chain stiffness and invariability of the bead length. Our experimental findings indicate possibly minor role of the change in π-electron conjugation length (and therefore conjugated backbone planar to non-planar conformational transition) in the observed thermochromic behavior of polythiophene but instead point on the major role of chain dynamics in this phenomenon. We also obtained the first experimental evidence of an existence of a single-chain glass state in conjugated polymers.

摘要

我们利用中子自旋回波光谱的高时间和空间分辨率,研究了溶液中半柔性共轭聚合物链的大规模动力学。我们采用了成熟的柔性聚合物齐姆模型的广义方法,来描述局部刚性聚噻吩链的弛豫模式光谱。齐姆模式分析证实了存在具有有限长度的珠子,这对应于半柔性链中节段模式数量的减少。无论共轭聚合物的温度和分子量如何,我们都观察到局部链刚性的普遍行为以及珠子长度的不变性。我们的实验结果表明,在聚噻吩观察到的热致变色行为中,π电子共轭长度的变化(以及因此共轭主链从平面构象到非平面构象的转变)可能起次要作用,而链动力学在这一现象中起主要作用。我们还获得了共轭聚合物中存在单链玻璃态的首个实验证据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/43a0/7305133/0d1483870a48/41598_2020_66354_Fig1_HTML.jpg

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