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超冷和玻璃态阿司匹林慢动力学的准弹性中子散射研究。

Quasi-elastic neutron scattering studies of the slow dynamics of supercooled and glassy aspirin.

机构信息

Neutron Scattering Science Division and Joint Institute for Neutron Sciences, Oak Ridge National Laboratory, Oak Ridge, TN 37831, USA.

出版信息

J Phys Condens Matter. 2012 Feb 15;24(6):064112. doi: 10.1088/0953-8984/24/6/064112. Epub 2012 Jan 25.

Abstract

Aspirin, also known as acetylsalicylic acid (ASA), is not only a wonderful drug, but also a good glass former. Therefore, it serves as an important molecular system to study the near-arrest and arrested phenomena. In this paper, a high-resolution quasi-elastic neutron scattering (QENS) technique is used to investigate the slow dynamics of supercooled liquid and glassy aspirin from 410 down to 350 K. The measured QENS spectra can be analyzed with a stretched exponential model. We find that (i) the stretched exponent β(Q) is independent of the wavevector transfer Q in the measured Q range and (ii) the structural relaxation time τ(Q) follows a power-law dependence on Q. Consequently, the Q-independent structural relaxation time τ(0) can be extracted for each temperature to characterize the slow dynamics of aspirin. The temperature dependence of τ(0) can be fitted with the mode-coupling power law, the Vogel-Fulcher-Tammann equation and a universal equation for fragile glass forming liquids recently proposed by Tokuyama in the measured temperature range. The calculated dynamic response function χ(T)(Q, t) using the experimentally determined self-intermediate scattering function of the hydrogen atoms of aspirin shows direct evidence of the enhanced dynamic fluctuations as the aspirin is increasingly supercooled, in agreement with the fixed-time mean squared displacement ⟨x(2)⟩ and the non-Gaussian parameter α(2) extracted from the elastic scattering.

摘要

阿司匹林,也被称为乙酰水杨酸(ASA),不仅是一种极好的药物,还是一种良好的玻璃形成剂。因此,它成为研究近程和被捕获现象的重要分子体系。在本文中,我们采用高分辨率准弹性中子散射(QENS)技术研究了过冷液体和玻璃态阿司匹林从 410K 到 350K 的慢动力学。测量得到的 QENS 谱可以用拉伸指数模型进行分析。我们发现:(i)在测量的 Q 范围内,拉伸指数β(Q)与波矢转移 Q 无关;(ii)结构弛豫时间τ(Q)与 Q 呈幂律关系。因此,可以从每个温度下提取出与 Q 无关的结构弛豫时间τ(0)来描述阿司匹林的慢动力学。τ(0)随温度的变化可以用模式耦合幂律、Vogel-Fulcher-Tammann 方程和 Tokuyama 最近提出的通用脆弱玻璃形成液体方程来拟合。使用阿司匹林氢原子的实验确定的自相互散射函数计算的动态响应函数 χ(T)(Q,t)直接证明了阿司匹林在过冷过程中动态波动的增强,这与固定时间均方位移 ⟨x(2)⟩和弹性散射中提取的非高斯参数 α(2)一致。

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