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Two-dimensional subnanometer confinement of ethylene glycol and Poly(ethylene oxide) by neutron spectroscopy: Molecular size effects

机译:中子光谱法对乙二醇和聚环氧乙烷的二维亚纳米级限制:分子大小效应

摘要

We explore the effects of chain size on the structure and dynamics of ethylene glycol (EG) and poly(ethylene oxide) (PEO) intercalated in graphite oxide (GO). To this end, EG as well as a PEO series of increasing chain length have been studied by means of high-resolution inelastic neutron spectroscopy. The neutron experiments are complemented by X-ray diffraction, differential scanning calorimetry, Fourier-transform infrared spectroscopy, and Raman scattering. We find that EG is accommodated in a layer of thickness ∼3 Å within the GO substrate and adopts a preferential, yet largely disordered, gauche conformation. Longer PEO chains give rise to a layer thickness in the range ∼3.0-3.4 Å characterized by planar zigzag (trans-trans-trans) conformations. Moreover, we observe a strong reduction of vibrational motions for the confined EG and polymer phases, as clearly evidenced by the disappearance, shift, and/or broadening of mode-specific inelastic neutron scattering spectral features, as well as by the complete suppression of crystallization. All of these effects are surprisingly insensitive to the length of the PEO chains. © 2012 American Chemical Society.
机译:我们探索链大小对插在氧化石墨(GO)中的乙二醇(EG)和聚环氧乙烷(PEO)的结构和动力学的影响。为此,已经通过高分辨率非弹性中子光谱学研究了EG以及增加链长的PEO系列。 X射线衍射,差示扫描量热法,傅立叶变换红外光谱和拉曼散射对中子实验进行了补充。我们发现,EG被容纳在GO衬底内约3Å的厚度的层中,并采用了一种优先的但无序的gauche构象。较长的PEO链会形成约3.0-3.4Å的层厚,其特征为平面之字形(反式-反式-反式)构型。此外,我们观察到有限的EG和聚合物相的振动运动大大降低,这由模式特定的非弹性中子散射光谱特征的消失,移动和/或加宽以及完全抑制结晶清楚地证明了。所有这些作用令人惊讶地对PEO链的长度不敏感。 ©2012美国化学学会。

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