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揭示熔盐体系中离子迁移数的微观起源:一种通向精确“黄金法则”的动力学理论方法

Unveiling the Microscopic Origin of Ion Transference Numbers in Molten Salt Systems: A Kinetic Theory Approach to an Accurate "Golden Rule".

作者信息

Gheribi Aïmen E

机构信息

Department of Mechanical, Industrial and Aerospace Engineering, Concordia University, 1455 De Maisonneuve Blvd. W, Montreal, Quebec H3G 1M8, Canada.

出版信息

ACS Omega. 2025 Mar 3;10(10):10272-10282. doi: 10.1021/acsomega.4c09587. eCollection 2025 Mar 18.

Abstract

In recent years, there has been a renewed interest in accurately quantifying the ion's transference number within molten salts. Surprisingly, despite efforts to address the severe lack of experimental data, there is still no reliable theoretical framework that establishes a clear link between the transference number and simulated phase trajectories through atomistic simulations or a dependable theoretical relationship for precise estimation. In general, overcoming limitations in both experimental and fundamental aspects, transference numbers are typically estimated by either considering the Nernst-Einstein (NE) approximation or employing the so-called "golden rules". However, it is worth noting that neither the Nernst-Einstein approximation nor the "golden rules" provide a truly accurate prediction. This work concentrates on establishing a robust theoretical framework to accurately define transference number boundaries and averages within molten salt systems. This is achieved by integrating principles from kinetic theory with an in-depth exploration of the electronic structure and local ordering of molten salts. Unlike prevailing theoretical approaches that are heavily reliant on Einstein's concept of ion mobility, which correlate with self-diffusion, the proposed theoretical framework is fundamentally grounded in the inherent mobility of ions. In summary, the introduction of this original "golden rule" showcases robust predictive capabilities, effectively addressing the scarcity of diverse observations gleaned from various experimental sources in the literature. Finally, the proposed formalism is extended to complex molten salts through a microscopic consideration of the impact of the cation associated with the anion upon its diffusional cross-section. Based on this, the cationic transference number of all divalent metal halide molten salts is predicted to be very close to that reported in the literature.

摘要

近年来,人们对准确量化熔盐中离子的迁移数重新产生了兴趣。令人惊讶的是,尽管努力解决实验数据严重匮乏的问题,但仍然没有可靠的理论框架能够通过原子模拟在迁移数和模拟相轨迹之间建立明确的联系,也没有用于精确估计的可靠理论关系。一般来说,为了克服实验和基础方面的局限性,迁移数通常通过考虑能斯特 - 爱因斯坦(NE)近似或采用所谓的“黄金规则”来估计。然而,值得注意的是,能斯特 - 爱因斯坦近似和“黄金规则”都不能提供真正准确的预测。这项工作专注于建立一个强大的理论框架,以准确界定熔盐体系中的迁移数边界和平均值。这是通过将动力学理论的原理与对熔盐电子结构和局部有序性的深入探索相结合来实现的。与主要依赖爱因斯坦离子迁移率概念(与自扩散相关)的现有理论方法不同,所提出的理论框架从根本上基于离子的固有迁移率。总之,这种原创“黄金规则”的引入展示了强大的预测能力,有效地解决了文献中来自各种实验来源的多样观测数据稀缺的问题。最后,通过微观考虑与阴离子相关的阳离子对其扩散截面的影响,将所提出的形式主义扩展到复杂熔盐。基于此,预测所有二价金属卤化物熔盐的阳离子迁移数与文献报道的非常接近。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/28ae/11923847/90e7e62abcd5/ao4c09587_0001.jpg

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