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对称哑铃状分子在液体中的动态阻滞:小分子伸长时的重取向跳跃

Dynamic arrest in a liquid of symmetric dumbbells: reorientational hopping for small molecular elongations.

作者信息

Moreno Angel J, Chong Song-Ho, Kob Walter, Sciortino Francesco

机构信息

Dipartimento di Fisica and Istituto Nazionale per la Fisica della Materia (INFM)-Centri di Ricerca e Sviluppo (CRS)-Statistical Mechanics and Complexity (SMC), Universitá di Roma La Sapienza, Piazzale Aldo Moro 2, 00185 Rome, Italy.

出版信息

J Chem Phys. 2005 Nov 22;123(20):204505. doi: 10.1063/1.2085030.

Abstract

We present extensive equilibrium and out-of-equilibrium molecular-dynamics simulations of a liquid of symmetric dumbbell molecules, for constant packing fraction, as a function of temperature and molecular elongation. We compute diffusion constants as well as odd and even orientational correlators. The notations odd and even refer to the parity of the order l of the corresponding Legendre l polynomial, evaluated for the orientation of the molecular axis relative to its initial position. Rotational degrees of freedom of order l are arrested if, in the long-time limit, the corresponding orientational l correlator does not decay to zero. It is found that for large elongations translational and rotational degrees of freedom freeze at the same temperature. For small elongations only the even rotational degrees of freedom remain coupled to translational motions and arrest at a finite common temperature. On the contrary, the odd rotational degrees of freedom remain ergodic at all investigated temperatures. Hence, in the translationally arrested state, each molecule remains trapped in the cage formed by its neighboring molecules, but is able to perform 180 degrees rotations, which lead to relaxation only for the odd orientational correlators. The temperature dependence of the characteristic time of these residual rotations is well described by an Arrhenius law. Finally, we discuss the evidence in favor of the presence of the type-A transition for the odd rotational degrees of freedom, as predicted by mode-coupling theory for small molecular elongations. This transition is distinct from the type-B transition, associated with the arrest of the translational and even rotational degrees of freedom for small elongations, and with all degrees of freedom for large elongations. Odd orientational correlators are computed for small elongations at very low temperatures in the translationally arrested state. The obtained results suggest that hopping events restore the ergodicity of the odd rotational degrees of freedom at temperatures far below the A transition.

摘要

我们针对对称哑铃形分子液体,在恒定堆积分数下,给出了作为温度和分子伸长函数的广泛平衡态和非平衡态分子动力学模拟。我们计算了扩散常数以及奇数和偶数取向关联函数。奇数和偶数的表示法是指相应勒让德(l)多项式的阶数(l)的奇偶性,是针对分子轴相对于其初始位置的取向进行评估的。如果在长时间极限下,相应的取向(l)关联函数不衰减至零,则阶数为(l)的转动自由度被冻结。结果发现,对于大伸长情况,平动和转动自由度在相同温度下冻结。对于小伸长情况,只有偶数转动自由度仍与平动运动耦合,并在有限的共同温度下冻结。相反,奇数转动自由度在所有研究温度下都保持遍历性。因此,在平动被冻结的状态下,每个分子都被困在由其相邻分子形成的笼中,但能够进行(180)度旋转,这仅导致奇数取向关联函数的弛豫。这些残余旋转的特征时间的温度依赖性可以很好地用阿仑尼乌斯定律来描述。最后,我们讨论了支持奇数转动自由度存在(A)型转变的证据,这是由模式耦合理论针对小分子伸长情况所预测的。这种转变与(B)型转变不同,(B)型转变与小伸长情况下平动和偶数转动自由度的冻结以及大伸长情况下所有自由度的冻结相关。在平动被冻结的状态下,在非常低的温度下针对小伸长情况计算了奇数取向关联函数。所得结果表明,跳跃事件在远低于(A)转变的温度下恢复了奇数转动自由度的遍历性。

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