基于分子动力学、分子中原子量子理论和非共价相互作用的Fe3+和Ni2+离子在深共晶溶剂和水溶液中相互作用的理论研究

IF 4.3 3区 化学 Q2 CHEMISTRY, MULTIDISCIPLINARY
Laudenor Amorim, Renato Veríssimo de Oliveira, Lucas Lima Bezerra, Pierre Basílio Almeida Fechine, Adriana Nunes Correia, Pedro de Lima-Neto and Norberto de Kássio Vieira Monteiro*, 
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引用次数: 0

摘要

与水和传统溶剂相比,深度共晶溶剂(DES)有几个优点,使其成为一种替代方案,特别是在需要更好的溶剂化、更高的热稳定性和更低的环境影响的应用中。本研究旨在分析Fe3+和Ni2+离子在两种水(300和5580分子)和基于氯化胆碱和乙二醇(1ChCl:2EG)的共晶溶剂中的行为。使用的计算方法包括分子动力学、分子中原子的量子理论(QTAIM)和非共价相互作用模拟。对径向分布函数乘以数密度[g(r)ρ]和累积数(CN)的分析表明,在水最多的体系中,金属离子与水分子之间的相互作用最强。QTAIM确定了键临界点、电子密度[ρ(r)]、电子密度[∇2ρ(r)]的拉普拉斯函数和电子局域函数(η, ELF),从而可以对相互作用进行分析。比较了金属离子在水中和在乙烷中的极化率;极化率的递增顺序为Fe3+ <;Ni2 + & lt;Fe2+,其中Fe3+由于其高电荷和较小的离子半径而具有最小的极化性。在Fe2+或Fe3+加入Ni2+的混合体系中,具有相同电荷的金属种类在水和DES中竞争相似。由于溶剂的极性和介电常数比水低,DES中的分子间力较弱。在含水量最高(5580分子)的体系中,Fe3+离子被最大的水分子包围,其次是Fe2+和Ni2+。这些结果可能有助于更好地理解这些离子在不同介质中的溶剂化和行为,这对电沉积、电池和腐蚀抑制的应用具有重要意义。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Theoretical Study of Fe3+ and Ni2+ Ion Interactions in Ethaline as the Deep Eutectic Solvent and Water Solutions Using Molecular Dynamics, Quantum Theory of Atoms in Molecules, and Non-Covalent Interactions

Deep eutectic solvents (DES) have several advantages compared to water and traditional solvents, making them an alternative, especially in applications that require better solvation, greater thermal stability, and a lower environmental impact. This study aimed to analyze the behavior of Fe3+ and Ni2+ ions in two quantities of water (300 and 5580 molecules) and in a eutectic solvent based on choline chloride and ethylene glycol (1ChCl:2EG). The computational methods used involved molecular dynamics, quantum theory of atoms in molecules (QTAIM), and noncovalent interactions simulations. Analysis of the radial distribution function multiplied by the number density [g(r)ρ] and the cumulative number (CN) indicated that the interactions between the metal ions and the water molecules were strongest for the systems with the most water. QTAIM determined the bond critical point, the electron density [ρ(r)], the Laplacian of the electronic density [∇2ρ(r)], and the electron localization function (η, ELF), allowing the interactions to be analyzed. Polarizability of the metal ions in both water and ethaline was compared; the increasing order of polarizability was Fe3+ < Ni2+ < Fe2+, with Fe3+ being the least polarizable due to its high charge and smaller ionic radius. In the mixed systems with Fe2+ or Fe3+ added to Ni2+, the metal species with the same charge competed similarly in water and DES. The intermolecular forces in DES are weaker due to the solvent’s lower polarity and dielectric constant than water. In the systems with the highest water content (5580 molecules), Fe3+ ions were surrounded by the largest water molecules, followed by Fe2+ and Ni2+. These results may help to better understand the solvation and behavior of these ions in different media, which has implications for use in electrodeposition, batteries, and corrosion inhibition.

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来源期刊
ACS Omega
ACS Omega Chemical Engineering-General Chemical Engineering
CiteScore
6.60
自引率
4.90%
发文量
3945
审稿时长
2.4 months
期刊介绍: ACS Omega is an open-access global publication for scientific articles that describe new findings in chemistry and interfacing areas of science, without any perceived evaluation of immediate impact.
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