液态硫中短链的证据。

IF 3.1 2区 化学 Q3 CHEMISTRY, PHYSICAL
Chris J Benmore, Ganesh Sivaraman
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引用次数: 0

摘要

高能 X 射线对分布函数测量结果表明,在整个 λ 转变过程中,液态硫中第一层外壳的平均配位数为 1.86 ± 0.04,而不是普遍认为的 2.0。这表明在熔化时,液态硫并不完全由 S8 环组成,还拥有大量的短链。X 射线结构因子的前峰和第一个衍射峰的强度以及对分布函数的第三个峰高在 λ 转变温度 Tλ 时都出现了偏差,这与 S8 环的断裂和低聚物聚合的开始有关。在熔化时第一和第二层外壳之间的所谓 "禁区 "中,还观察到大量非键合或松散键合的 "间隙原子",其平均配位数为 0.20 ± 0.005。研究发现,间隙原子的数量会在λ转变时减少到最低,但大部分会持续存在于高温聚合液体中。正如最近的分子动力学模拟所提出的,短链和附近间隙原子的存在是启动 S8 环向链转变所需的两个主要因素。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Evidence of short chains in liquid sulfur.

High energy x-ray pair distribution function measurements show the average coordination number of the first shell in liquid sulfur is 1.86 ± 0.04 across the λ-transition, not precisely 2.0 as widely accepted. This indicates that upon melting, liquid sulfur does not comprise solely of S8 rings but also possesses a significant number of short chains. Intensities of the pre-peak and first diffraction peak of the x-ray structure factor and third peak height of the pair distribution function all show deviations at the λ-transition temperature Tλ, associated with the break-up of S8 rings and the start of oligomer polymerization. A significant number of non-bonded or loosely bonded "interstitial atoms," with an average coordination number of 0.20 ± 0.005, are also observed in the so-called "forbidden zone" between the first and second shells upon melting. The number of interstitial atoms is found to decrease to a minimum at the λ-transition, but the majority persist into the high temperature polymerized liquid. The existence of short chains and nearby interstitial atoms represent the two main factors required to initiate the S8-ring to chain transition, as proposed by recent molecular dynamics simulations.

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来源期刊
Journal of Chemical Physics
Journal of Chemical Physics 物理-物理:原子、分子和化学物理
CiteScore
7.40
自引率
15.90%
发文量
1615
审稿时长
2 months
期刊介绍: The Journal of Chemical Physics publishes quantitative and rigorous science of long-lasting value in methods and applications of chemical physics. The Journal also publishes brief Communications of significant new findings, Perspectives on the latest advances in the field, and Special Topic issues. The Journal focuses on innovative research in experimental and theoretical areas of chemical physics, including spectroscopy, dynamics, kinetics, statistical mechanics, and quantum mechanics. In addition, topical areas such as polymers, soft matter, materials, surfaces/interfaces, and systems of biological relevance are of increasing importance. Topical coverage includes: Theoretical Methods and Algorithms Advanced Experimental Techniques Atoms, Molecules, and Clusters Liquids, Glasses, and Crystals Surfaces, Interfaces, and Materials Polymers and Soft Matter Biological Molecules and Networks.
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