2026-09-22T11:06:37Z https://www.ideals.illinois.edu/oai-pmh

oai:www.ideals.illinois.edu:2142/132462 2026-02-20 col_2142_5131 col_2142_14787 com_2142_5130 com_2142_9630 com_2142_234

application/pdf en text Submission original under an indefinite embargo labeled 'Open Access'. The submission was exported from vireo on 2026-02-19 without embargo terms The student, Hananeh Oliaei, accepted the attached license on 2025-09-08 at 12:39. The student, Hananeh Oliaei, submitted this Dissertation for approval on 2025-09-08 at 12:46. This Dissertation was approved for publication on 2025-09-11 at 09:23. DSpace SAF Submission Ingestion Package generated from Vireo submission #22790 on 2026-02-19 at 18:24:14 Spectra at speed: neural force fields for IR spectroscopy in ionic liquids Oliaei, Hananeh 2025-09-11 Aluru, Narayana R van der Zande, Arend Smith, Kyle C Zhang, Yingjie IR spectroscopy Machine learning force field Ionic liquid eng Ionic liquids (ILs) are salts composed entirely of ions and often remain liquid near room temperature. Their structural tunability grants unique properties, making them valuable in catalysis, separations, and electrochemical energy storage. Understanding their microscopic structure and dynamics is key to optimizing such applications. Infrared (IR) spectroscopy provides molecular-level insight into IL conformations, hydrogen bonding, and ionic interactions, but interpreting spectra requires connecting measured bands to specific vibrational motions. Computational modeling bridges this gap: ab initio molecular dynamics (AIMD) simulations offer high accuracy, but their high computational cost restricts system size and timescale. Classical molecular dynamics (MD) can address larger systems and longer simulations but often misrepresents vibrational mode ordering and intensities. Machine learning (ML)–based force fields offer a promising alternative, delivering both accuracy and efficiency. Yet most are trained on isolated molecules, neglecting condensed-phase effects, long-range correlations, or electronic polarization. Furthermore, accurate IR predictions require precise dipole moments, which are commonly estimated from arbitrary, method-dependent partial charges. In this work, we address these challenges for a prototypical IL. First, for an isolated ion pair, we develop a hybrid framework combining Deep Potential (DP) and Deep Wannier (DW) models to predict potential energy, forces, and Maximally Localized Wannier Function (MLWF)–based dipole moments. Nanosecond-scale DPMD simulations reproduce AIMD results with improved convergence from extended sampling. Second, we extend the Neural Equivariant Interatomic Potential (NequIP) to a liquid system, enabling simultaneous prediction of energies, forces, virial tensors, and dipole moments. NequIP’s symmetry-preserving message-passing architecture effectively captures both short- and long-range interactions, achieving AIMD-level accuracy for radial distribution functions, diffusion coefficients, conformer populations, and IR spectra. The model also generalizes to larger systems than those used in the development stage, granting access to structural organization beyond the reach of small-cell AIMD. 2025-12 Thesis https://hdl.handle.net/2142/132462 Copyright 2025 Hananeh Oliaei Mechanical Sci & Engineering Mechanical Engineering University of Illinois Urbana-Champaign Ph.D. Dissertation