Electronic fluctuations, cation clustering, and ionic dynamics in molten silver iodide

Molten salts are high-temperature ionic liquids whose unique combination of strong Coulombic interactions, large polarizabilities, and high ionic conductivities makes them central to energy storage, metallurgy, and nuclear technology. Understanding the delicate balance of Coulomb forces, short-range repulsion, and electronic polarization, particularly regarding the role that electronic fluctuations play in their structure and dynamics, is critical for predictively designing molten salts for applications of interest. We investigate the importance of electronic fluctuations in molten AgI using density functional theory, a universal machine learning model (Orb), and a classical, empirical pairwise model of interionic interactions. We find that the polarizability of iodide ions screens cation-cation interactions, leading to pronounced cation clustering. Iodide's directional polarization fluctuations enhance Ag+ diffusion, manifesting as enhanced force fluctuations and structure in the time-dependent friction experienced by the cations. The coupling between iodide polarization fluctuations and silver diffusion creates a dynamic asymmetry; Ag+ motion is tightly linked to the instantaneous polarization of neighboring I-, whereas I- dynamics are relatively unperturbed by electronic fluctuations. For all structural and dynamic quantities investigated, the Orb model is in excellent agreement with density functional theory-based simulations, highlighting the ability of this universal neural network potential to capture many-body polarization effects. In contrast, the empirical force field fails to reproduce key structural and dynamic quantities involving cations, ultimately because it neglects dynamic electronic fluctuations. Our findings connect liquid-state ionic dynamics to the "electronic paddle-wheel" mechanism of ionic diffusion in superionic solids and motivate further exploration of polarization fluctuation effects in complex electrolytes and ionic liquids.

Authors

Institutions

Publication Details

Journal
The Journal of Chemical Physics
Published
2025-12-17
DOI
https://doi.org/10.1063/5.0301431
Primary Topic
Molten salt chemistry and electrochemical processes
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Electronic fluctuations, cation clustering, and ionic dynamics in molten silver iodide

Harender S. Dhattarwal, Richard C. Remsing
The Journal of Chemical Physics
Molten salt chemistry and electrochemical processes
article

Electronic fluctuations, cation clustering, and ionic dynamics in molten silver iodide

Harender S. Dhattarwal, Richard C. Remsing
article en

Abstract

Molten salts are high-temperature ionic liquids whose unique combination of strong Coulombic interactions, large polarizabilities, and high ionic conductivities makes them central to energy storage, metallurgy, and nuclear technology. Understanding the delicate balance of Coulomb forces, short-range repulsion, and electronic polarization, particularly regarding the role that electronic fluctuations play in their structure and dynamics, is critical for predictively designing molten salts for applications of interest. We investigate the importance of electronic fluctuations in molten AgI using density functional theory, a universal machine learning model (Orb), and a classical, empirical pairwise model of interionic interactions. We find that the polarizability of iodide ions screens cation-cation interactions, leading to pronounced cation clustering. Iodide's directional polarization fluctuations enhance Ag+ diffusion, manifesting as enhanced force fluctuations and structure in the time-dependent friction experienced by the cations. The coupling between iodide polarization fluctuations and silver diffusion creates a dynamic asymmetry; Ag+ motion is tightly linked to the instantaneous polarization of neighboring I-, whereas I- dynamics are relatively unperturbed by electronic fluctuations. For all structural and dynamic quantities investigated, the Orb model is in excellent agreement with density functional theory-based simulations, highlighting the ability of this universal neural network potential to capture many-body polarization effects. In contrast, the empirical force field fails to reproduce key structural and dynamic quantities involving cations, ultimately because it neglects dynamic electronic fluctuations. Our findings connect liquid-state ionic dynamics to the "electronic paddle-wheel" mechanism of ionic diffusion in superionic solids and motivate further exploration of polarization fluctuation effects in complex electrolytes and ionic liquids.

The Journal of Chemical PhysicsVol. 163(23)
Rutgers, The State University of New Jersey (US), Environmental and Occupational Health Sciences Institute (US)
Openalex Percentile: Top 62%
Molten salt chemistry and electrochemical processes
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.