如何在纳米尺度上计算密度波动。

IF 5.5 1区 化学 Q2 CHEMISTRY, PHYSICAL
Journal of Chemical Theory and Computation Pub Date : 2025-01-14 Epub Date: 2024-12-27 DOI:10.1021/acs.jctc.4c01047
Peter Krüger
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引用次数: 0

摘要

基于点状粒子的粒子数波动的标准定义忽略了排除的体积效应。这导致了一个大的和系统的有限尺寸尺度和非物理表面项在等温可压缩性。我们通过引入一个考虑到粒子有限大小的修正的对分布函数来纠正这些错误。对于一维的硬球流体,我们证明了压缩率是严格与尺寸无关的,并从用新理论计算的数值波动中再现了这一结果。一般来说,目前的方法消除了主要的有限尺寸效应,这使得在非常小的采样体积中精确计算密度波动成为可能,与单一粒径相当。这些发现为从涨落理论获得纳米尺度的局部压缩率开辟了道路。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

How to Compute Density Fluctuations at the Nanoscale.

How to Compute Density Fluctuations at the Nanoscale.

How to Compute Density Fluctuations at the Nanoscale.

How to Compute Density Fluctuations at the Nanoscale.

The standard definition of particle number fluctuations based on point-like particles neglects the excluded volume effect. This leads to a large and systematic finite-size scaling and an unphysical surface term in the isothermal compressibility. We correct these errors by introducing a modified pair distribution function that takes account of the finite size of the particles. For the hard sphere fluid in one-dimension, we show that the compressibility is strictly size-independent, and we reproduce this result from the number fluctuations calculated with the new theory. In general, the present method eliminates the leading finite-size effect, which makes it possible to compute density fluctuations accurately in very small sampling volumes, comparable to a single particle size. These findings open the way for obtaining the local compressibility from fluctuation theory at the nanometer scale.

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来源期刊
Journal of Chemical Theory and Computation
Journal of Chemical Theory and Computation 化学-物理:原子、分子和化学物理
CiteScore
9.90
自引率
16.40%
发文量
568
审稿时长
1 months
期刊介绍: The Journal of Chemical Theory and Computation invites new and original contributions with the understanding that, if accepted, they will not be published elsewhere. Papers reporting new theories, methodology, and/or important applications in quantum electronic structure, molecular dynamics, and statistical mechanics are appropriate for submission to this Journal. Specific topics include advances in or applications of ab initio quantum mechanics, density functional theory, design and properties of new materials, surface science, Monte Carlo simulations, solvation models, QM/MM calculations, biomolecular structure prediction, and molecular dynamics in the broadest sense including gas-phase dynamics, ab initio dynamics, biomolecular dynamics, and protein folding. The Journal does not consider papers that are straightforward applications of known methods including DFT and molecular dynamics. The Journal favors submissions that include advances in theory or methodology with applications to compelling problems.
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