Finney John L, Woodcock Leslie V
Department of Physics and Astronomy and London Centre for Nanotechnology, University College London, UK.
J Phys Condens Matter. 2014 Nov 19;26(46):463102. doi: 10.1088/0953-8984/26/46/463102. Epub 2014 Oct 22.
We review the scientific history of random close packing (RCP) of equal spheres, advocated by J D Bernal as a more plausible alternative to the non-ideal gas or imperfect crystal as a structural model of simple liquids. After decades of neglect, computer experiments are revealing a central role for RCP in the theory of liquids. These demonstrate that the RCP amorphous state of hard spheres can be well defined, is reproducible, and has the thermodynamic status of a metastable ground state. Further evidence from simulations of square-well model liquids indicates an extended role of RCP as an amorphous ground state that terminates a supercooled liquid coexistence line, suggesting likewise for real liquids. A phase diagram involving percolation boundaries has been proposed in which there is no merging of liquid and gas phases, and no critical singularity as assumed by van der Waals. Rather, the liquid phase continuously spans all temperatures, but above a critical dividing line on the Gibbs density surface, it is bounded by a percolation transition and separated from the gas phase by a colloidal supercritical mesophase. The colloidal-like inversion in the mesophase as it changes from gas-in-liquid to liquid-in-gas can be identified with the hypercritical line of Bernal. We therefore argue that the statistical theory of simple liquids should start from the RCP reference state rather than the ideal gas. Future experimental priorities are to (i) find evidence for an amorphous ground state in real supercooled liquids, (ii) explore the microscopic structures of the supercritical mesophase, and (iii) determine how these change from gas to liquid, especially across Bernal's hypercritical line. The theoretical priority is a statistical geometrical theory of RCP. Only then might we explain the coincident values of the RCP packing fraction with Buffon's constant, and the RCP residual entropy with Boltzmann's ideal gas constant.
我们回顾了等径球体随机密堆积(RCP)的科学史,这是由J D 伯纳尔提出的,作为非理想气体或不完美晶体的一种更合理替代方案,作为简单液体的结构模型。在被忽视数十年后,计算机实验揭示了RCP在液体理论中的核心作用。这些实验表明,硬球的RCP非晶态可以被很好地定义、可重复,并且具有亚稳态基态的热力学状态。来自方阱模型液体模拟的进一步证据表明,RCP作为非晶态基态的作用得到了扩展,它终止了过冷液体共存线,这同样适用于真实液体。有人提出了一个涉及渗流边界的相图,其中液相和气相不会合并,也没有范德瓦尔斯假设的临界奇点。相反,液相连续跨越所有温度,但在吉布斯密度表面上的一条临界分界线之上,它由渗流转变界定,并通过胶体超临界中间相与气相分离。中间相从气液变为液气时类似胶体的反转可以与伯纳尔的超临界线相识别。因此,我们认为简单液体的统计理论应该从RCP参考态而不是理想气体开始。未来的实验重点是:(i)在真实过冷液体中找到非晶态基态的证据;(ii)探索超临界中间相的微观结构;(iii)确定这些结构如何从气相转变为液相,特别是跨越伯纳尔的超临界线时。理论重点是RCP的统计几何理论。只有这样,我们才可能解释RCP堆积分数与布丰常数的巧合值,以及RCP剩余熵与玻尔兹曼理想气体常数的巧合值。