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Seung Kyu Min

Publications and source records attributed to Seung Kyu Min.

10 recordsLinked to original sources

Bayesian E(3)-Equivariant Interatomic Potential with Iterative Restratification of Many-body Message Passing

Machine learning potentials (MLPs) have become essential for large-scale atomistic simulations, enabling ab initio-level accuracy with computational efficiency. However, current MLPs struggle with uncertainty quantification, limiting their reliability for active learning, calibration, and out-of-distribution (OOD) detection. We address these challenges by developing Bayesian E(3) equivariant MLPs with iterative restratification of many-body message passing. Our approach introduces the joint energy-force negative log-likelihood (NLL$_\text{JEF}$) loss function, which explicitly models uncertainty in both energies and interatomic forces, yielding substantially improved accuracy compared to conventional NLL losses. We systematically benchmark multiple Bayesian approaches, including deep ensembles with mean-variance estimation, stochastic weight averaging Gaussian, improved variational online Newton, and Laplace approximation by evaluating their performance on uncertainty prediction, OOD detection, calibration, and active learning tasks. We further demonstrate that NLL$_\text{JEF}$ facilitates efficient active learning by quantifying energy and force uncertainties. Using Bayesian active learning by disagreement (BALD), our framework outperforms random sampling and energy-uncertainty-based sampling. Our results demonstrate that Bayesian MLPs achieve competitive accuracy with state-of-the-art models while enabling uncertainty-guided active learning, OOD detection, and energy/forces calibration. This work establishes Bayesian equivariant neural networks as a powerful framework for developing uncertainty-aware MLPs for atomistic simulations at scale.

cs.LG↗

Unifying Decoherence and Phase Evolution in Mixed Quantum-Classical Dynamics through Exact Factorization

We propose mixed quantum-classical equations of motion that unify electronic coherence and phase evolution simultaneously within the exact factorization framework. Our derivation shows that incorporating the second-order electron-nuclear correlation terms from the exact coupled time-dependent Schrödinger equations is essential to recover both correct phase dynamics and complete electronic (de)coherence, including their effect on nuclear forces. Benchmark calculations on one- and two-dimensional model systems confirm that the approach accurately captures key nonadiabatic features. The equations therefore provide a rigorous first-principles foundation for mixed quantum-classical description of coupled electron-nuclear dynamics, bringing electronic coherence and phase evolution-long treated through separate heuristic corrections-into a single unified and systematically derived framework.

physics.chem-ph↗

Oscillator-qubit generalized quantum signal processing for vibronic models: a case study of uracil cation

Hybrid oscillator-qubit processors have recently demonstrated high-fidelity control of both continuous- and discrete-variable information processing. However, most of the quantum algorithms remain limited to homogeneous quantum architectures. Here, we present a compiler for hybrid oscillator-qubit processors, implementing state preparation and time evolution. In hybrid oscillator-qubit processors, this compiler invokes generalized quantum signal processing (GQSP) to constructively synthesize arbitrary bosonic phase gates with moderate circuit depth O(log(1/{\varepsilon})). The approximation cost is scaled by the Fourier bandwidth of the target bosonic phase, rather than by the degree of nonlinearity. Armed with GQSP, nonadiabatic molecular dynamics can be decomposed with arbitrary-phase potential propagators. Compared to fully discrete encodings, our approach avoids the overhead of truncating continuous variables, showing linear dependence on the number of vibration modes while trading success probability for circuit depth. We validate our method on the uracil cation, a canonical system whose accurate modeling requires anharmonic vibronic models, estimating the cost for state preparation and time evolution.

quant-ph↗

Roadmap for Molecular Benchmarks in Nonadiabatic Dynamics

Simulating the coupled electronic and nuclear response of a molecule to light excitation requires the application of nonadiabatic molecular dynamics. However, when faced with a specific photophysical or photochemical problem, selecting the most suitable theoretical approach from the wide array of available techniques is not a trivial task. The challenge is further complicated by the lack of systematic method comparisons and rigorous testing on realistic molecular systems. This absence of comprehensive molecular benchmarks remains a major obstacle to advances within the field of nonadiabatic molecular dynamics. A CECAM workshop, Standardizing Nonadiabatic Dynamics: Towards Common Benchmarks, was held in May 2024 to address this issue. This Perspective highlights the key challenges identified during the workshop in defining molecular benchmarks for nonadiabatic dynamics. Specifically, this work outlines some preliminary observations on essential components needed for simulations and proposes a roadmap aiming to establish, as an ultimate goal, a community-driven, standardized molecular benchmark set.

physics.chem-ph↗

Machine Learning Nonadiabatic Dynamics: Eliminating Phase Freedom of Nonadiabatic Couplings with the State-Intraction State-Averaged Spin-Restricted Ensemble-Referenced Kohn-Sham Approach

Excited-state molecular dynamics (ESMD) simulations near conical intersections (CIs) pose significant challenges when using machine learning potentials (MLPs). Although MLPs have gained recognition for their integration into mixed quantum-classical (MQC) methods, such as trajectory surface hopping (TSH), and their capacity to model correlated electron-nuclear dynamics efficiently, difficulties persist in managing nonadiabatic dynamics. Specifically, singularities at CIs and double-valued coupling elements result in discontinuities that disrupt the smoothness of predictive functions. Partial solutions have been provided by learning diabatic Hamiltonians with phaseless loss functions to these challenges. However, a definitive method for addressing the discontinuities caused by CIs and double-valued coupling elements has yet to be developed. Here, we introduce the phaseless coupling term, $Δ^2$, derived from the square of the off-diagonal elements of the diabatic Hamiltonian in the state-interaction state-averaged spin-restricted ensemble-referenced Kohn-Sham (SI-SA-REKS, briefly SSR)(2,2) formalism. This approach improves the stability and accuracy of the MLP model by addressing the issues arising from CI singularities and double-valued coupling functions. We apply this method to the penta-2,4-dieniminium cation (PSB3), demonstrating its effectiveness in improving MLP training for ML-based nonadiabatic dynamics. Our results show that the $Δ^2$ based ML-ESMD method can reproduce ab initio ESMD simulations, underscoring its potential and efficiency for broader applications, particularly in large-scale and long-timescale ESMD simulations.

physics.chem-ph↗

A study of the decoherence correction derived from the exact factorization approach for non-adiabatic dynamics

We present a detailed study of the decoherence correction to surface-hopping that was recently derived from the exact factorization approach. Ab initio multiple spawning calculations that use the same initial conditions and same electronic structure method are used as a reference for three molecules: ethylene, methaniminium cation, and fulvene, for which non-adiabatic dynamics follows a photo-excitation. A comparison with the Granucci-Persico energy-based decoherence correction, and the augmented fewest-switches surface-hopping scheme shows that the three decoherence-corrected methods operate on individual trajectories in a qualitatively different way, but results averaged over trajectories are similar for these systems.

physics.chem-ph↗

Quantum-Classical Non-Adiabatic Dynamics: Coupled- vs. Independent-Trajectory Methods

Trajectory-based mixed quantum-classical approaches to coupled electron-nuclear dynamics suffer from well-studied problems such as the lack of (or incorrect account for) decoherence in the trajectory surface hopping method and the inability of reproducing the spatial splitting of a nuclear wave packet in Ehrenfest-like dynamics. In the context of electronic non-adiabatic processes, these problems can result in wrong predictions for quantum populations and in unphysical outcomes for the nuclear dynamics. In this paper we propose a solution to these issues by approximating the coupled electronic and nuclear equations within the framework of the exact factorization of the electron-nuclear wave function. We present a simple quantum-classical scheme based on coupled classical trajectories, and test it against the full quantum mechanical solution from wave packet dynamics for some model situations which represent particularly challenging problems for the above-mentioned traditional methods.

quant-ph↗

A coupled-trajectory quantum-classical approach to decoherence in non-adiabatic processes

We present a novel quantum-classical approach to non-adiabatic dynamics, deduced from the coupled electronic and nuclear equations in the framework of the exact factorization of the electron-nuclear wave function. The method is based on the quasi-classical interpretation of the nuclear wave function, whose phase is related to the classical momentum and whose density is represented in terms of classical trajectories. In this approximation, electronic decoherence is naturally induced as effect of the coupling to the nuclei and correctly reproduces the expected quantum behaviour. Moreover, the splitting of the nuclear wave packet is captured as consequence of the correct approximation of the time-dependent potential of the theory. This new approach offers a clear improvement over Ehrenfest-like dynamics. The theoretical derivation presented in the Letter is supported by numerical results that are compared to quantum mechanical calculations.

physics.chem-ph↗

Semiclassical analysis of the electron-nuclear coupling in electronic non-adiabatic processes

In the context of the exact factorization of the electron-nuclear wave function, the coupling between electrons and nuclei beyond the adiabatic regime is encoded (i) in the time-dependent vector and scalar potentials and (ii) in the electron-nuclear coupling operator. The former appear in the Schroedinger-like equation that drives the evolution of the nuclear degrees of freedom, whereas the latter is responsible for inducing non-adiabatic effects in the electronic evolution equation. As we have devoted previous studies to the analysis of the vector and scalar potentials, in this paper we focus on the properties of the electron-nuclear coupling operator, with the aim of describing a numerical procedure to approximate it within a semiclassical treatment of the nuclear dynamics.

physics.chem-ph↗

The exact forces on classical nuclei in non-adiabatic charge transfer

The decomposition of electronic and nuclear motion presented in~[A. Abedi, N. T. Maitra, and E. K. U. Gross, Phys. Rev. Lett. 105, 123002 (2010)] yields a time-dependent potential that drives the nuclear motion and fully accounts for the coupling to the electronic subsystem. Here we show that propagation of an ensemble of independent classical nuclear trajectories on this exact potential yields dynamics that are essentially indistinguishable from the exact quantum dynamics for a model non-adiabatic charge transfer problem. We point out the importance of step and bump features in the exact potential that are critical in obtaining the correct splitting of the quasiclassical nuclear wave packet in space after it passes through an avoided crossing between two Born-Oppenheimer surfaces, and analyze their structure. Lastly, an analysis of the exact potentials in the context of trajectory surface hopping procedure is presented, including preliminary investigations of velocity-adjustment, and the force-induced decoherence effect.

physics.chem-ph↗