使用各种随机化技术获得的磷酸铁玻璃模型中的中阶:分子动力学研究

IF 5.5 1区 化学 Q2 CHEMISTRY, PHYSICAL
Shakti Singh*, Manan Dholakia* and Sharat Chandra*, 
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引用次数: 0

摘要

众所周知,眼镜具有中程序(MRO),但它们与任何实验可测量的量之间的联系仍然是模糊的。从玻璃衍射实验中获得的结构因子S(q)中的第一个尖锐衍射峰(FSDP)与这个MRO有关(~ 7-15 Å),但了解这个普遍峰的基本起源仍然是一个开放的问题。我们通过混合方法(我们内部开发的MC代码+分子动力学模拟)生成的原子模型,解决了复杂玻璃(即磷酸铁玻璃(IPG))的这个问题。IPG是一种具有重要技术意义的玻璃,在废物玻璃化、生物活性玻璃、激光玻璃材料、电池负极材料等方面都有应用,被视为硼硅酸盐玻璃的强化替代品。我们通过生成不同初始配置和随机化技术的玻璃模型进行了比较研究。通过对SRO和环分布的对相关函数、键角分布和配位数、结构因子的FSDP和MRO的空隙尺寸分布的研究,首先利用现有的SRO和MRO数据对所建立的IPG模型进行了验证。研究氧的配位环境有助于通过拓扑约束理论来理解玻璃的形成。然后,为了了解S(q)中FSDP的基本来源,根据模型中存在的单个环尺寸计算结构因子。这些个体S(q)在总实验S(q)中的相对贡献是使用逆拟合方法估计的。因此得到的贡献与考虑q范围的模型中的环大小百分比直接相关。特别是,从MC模型中获得的熔融淬火模型作为初始结构,可以重现IPG中看到的大多数实验特征。通过这一练习,我们可以将原子玻璃模型的环分布与复杂类玻璃IPG的FSDP在S(q)中的实验可测量量联系起来。这给环分布提供了物理意义,同时也证明了这种结构描述符是在玻璃模拟模型中验证MRO的有用工具。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Medium-Range Order in Iron Phosphate Glass Models Obtained Using Various Randomization Techniques: A Molecular Dynamics Study

Medium-Range Order in Iron Phosphate Glass Models Obtained Using Various Randomization Techniques: A Molecular Dynamics Study

Glasses are known to have medium-range order (MRO), but their link to any experimentally measurable quantity is still ambiguous. The first sharp diffraction peak (FSDP) in structure factor S(q) obtained from diffraction experiments on glasses has been associated with this MRO (∼7–15 Å), but understanding the fundamental origin of this universal peak is still an open problem. We have addressed this issue for a complex glass, i.e., iron phosphate glass (IPG), through atomistic models generated from a hybrid approach (our in-house-developed MC code + molecular dynamics simulation). IPG is a technologically important glass with applications in waste vitrification, bioactive glass, laser glass material, anode material for batteries, etc., and is seen as a strengthened substitute for borosilicate glasses. We performed a comparative study by generating glass models from different initial configurations and randomization techniques. The developed IPG models were first validated with existing data on short-range order (SRO) and MRO through the study of pair correlation functions, bond angle distributions, and coordination number for SRO and rings distribution, FSDP in structure factor, and void size distribution for MRO. The study of coordination environment of oxygen is specifically shown to aid in understanding glass formation through topological constraint theory. Thereafter, to understand the fundamental origin of FSDP in S(q), structure factors were calculated corresponding to the individual ring sizes present in the model. The relative contribution of these individual S(q)’s in the total experimental S(q) is estimated using an inverse fitting approach. The contributions thus obtained directly correlated with ring size percentages in the models for the considered q-range. In particular, the melt-quenched model obtained from the MC model as an initial structure is found to reproduce most experimental features seen in IPG. Through this exercise, we can connect the rings distribution of an atomistic glass model with an experimentally measurable quantity like FSDP in S(q) for a complex glass-like IPG. This gives physical meaning to the rings distribution while also proving that this structural descriptor is a useful tool for validation of MRO in simulation-produced models of glass.

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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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