Zhang Hao, Douglas Jack F
Department of Chemical and Materials Engineering, University of Alberta, AB T6G 2V4 Canada.
Soft Matter. 2013 Jan 1;9(4):1266-1280. doi: 10.1039/C2SM27533C.
Recent studies of the dynamics of diverse condensed amorphous materials have indicated significant heterogeneity in the local mobility and a progressive increase in collective particle motion upon cooling that takes the form of string-like particle rearrangements. In a previous paper (Part I), we examined the possibility that fluctuations in potential energy and particle mobility associated with this 'dynamic heterogeneity' might offer information about the scale of collective motion in glassy materials based on molecular dynamics simulations of the glassy interfacial region of Ni nanoparticles (NPs) at elevated temperatures. We found that the noise exponent associated with fluctuations in the Debye-Waller factor, a mobility related quantity, was directly proportional to the scale of collective motion under a broad range of conditions, but the noise exponent associated with () fluctuations was seemingly to . In the present work, we focus on this unanticipated difference between potential energy and mobility fluctuations by examining these quantities at an atomic scale. We find that the string atoms exhibit a jump-like motion between two well-separated bands of energy states and the rate at which these jumps occur seems to be consistent with the phenomenology of the 'slow-beta' relaxation process of glass-forming liquids. Concurrently with these local () jumps, we also find 'quake-like' particle displacements having a power-law distribution in magnitude so that particle displacement fluctuations within the strings are strikingly different from local () fluctuations. An analysis of these () fluctuations suggests that we are dealing with 'discrete breather' excitations in which large energy fluctuations develop in arrays of non-linear oscillators by virtue of large anharmonicity in the interparticle interactions and discreteness effects associated with particle packing. We quantify string collective motions on a fast caging times scale (picoseconds) and explore the significance of these collective motions for understanding the Boson peak of glass-forming materials.
最近对多种凝聚态非晶材料动力学的研究表明,局部流动性存在显著的不均匀性,并且在冷却时集体粒子运动呈渐进增加,其形式为串状粒子重排。在之前的一篇论文(第一部分)中,我们基于高温下镍纳米颗粒(NPs)玻璃态界面区域的分子动力学模拟,研究了与这种“动态不均匀性”相关的势能和粒子流动性波动是否可能提供有关玻璃态材料中集体运动尺度的信息。我们发现,与德拜 - 瓦勒因子(一个与流动性相关的量)波动相关的噪声指数,在广泛的条件下与集体运动尺度成正比,但与()波动相关的噪声指数似乎与()无关。在本工作中,我们通过在原子尺度上研究这些量,关注势能和流动性波动之间这种意外的差异。我们发现,串状原子在两个能量状态分隔良好的能带之间呈现跳跃式运动,这些跳跃发生的速率似乎与玻璃形成液体的“慢β”弛豫过程的现象学一致。与这些局部()跳跃同时发生的是,我们还发现“类似地震”的粒子位移,其大小具有幂律分布,使得串内的粒子位移波动与局部()波动显著不同。对这些()波动的分析表明,我们正在处理“离散呼吸子”激发,其中由于粒子间相互作用中的大非谐性以及与粒子堆积相关的离散效应,在非线性振荡器阵列中会产生大的能量波动。我们在快速笼蔽时间尺度(皮秒)上对串状集体运动进行量化,并探索这些集体运动对于理解玻璃形成材料的玻色子峰的意义。