arXiv subjects

Qingyong Meng

Publications and source records attributed to Qingyong Meng.

9 recordsLinked to original sources

arXiv2026

Implementation Possibility of Quantum Simulation for Quantum Molecular Dynamics

In this work, we explore the implementation possibility of quantum simulation for quantum molecular dynamics, in particular for reaction dynamics, though several implementations have already reported through quantum-classical mixed simulations ({\it Acc. Chem. Res.} {\bf 54} (2021), 4229 and {\it J. Phys. Chem. Lett.} {\bf xx} (2026), XXXX). To analyze this aspect, we examine (1) the conjugacy relation between quantum simulator and the target molecular system, (2) the wave function correspondence in quantum algorithm and classical algorithm for multi-dimensional dynamics, (3) problems arisen from real-valued classical algorithms, and finally (4) geometric phase arisen from the separation among the degrees of freedom (DOFs). As is well known, the aforementioned first and second points play fundamental roles in quantum simulation of quantum many-body systems, and the third and fourth points are theoretical issues that might introduce problems in classical and quantum computing. In this work, we mainly focus on the third and fourth points by analysis of the first two points by reviewing previously reported quantum-classical mixed implementations of quantum simulation. We also consider gauge freedom in high-dimensional quantum molecular dynamics that has been introduced recently, and then discuss possibility of advantages and disadvantages of quantum simulation for molecular reaction dynamics.

physics.chem-ph↗

arXiv2026

The $[3+1]$ Formulation of Chemical Dynamics in Curved Spacetime under the Eulerian Observer

Traditionally, gravity is generally considered to exert an extremely weak effect in chemistry because the Newtonian gravitation is typically negligible compared to the dominant Coulomb potentials in a molecular system. In this work, we porpose a primitive framework of chemical dynamics in curved spacetime through fiducial-observer $[3+1]$ formulation by revising the nuclear Hamiltonian operator through the metric tensor of configuration space rather than by adding Newtonian gravitation in the potential energy term, where the absolute-sapce and universal-time viewpoint of Galileo is adopted. Using frames fixed on normal observers in the $[3+1]$ formalism ensures possibility of this treatment. Taking spherically symmetric curved spacetime ({\it i.e.} Schwarzschild spacetime) as numerical demonstration, we explore (1) the H + H$_2$ reaction dynamics, (2) the H$_2$ + H$_2$ scattering dynamics, (3) dynamics of dissociative chemsorption of H$_2$O on Cu(111), (4) the spectrum band of anthracene cation, and (5) the Berry phase in the nuclear wave function of a 98D surface scattering model. These calculations predict that (i) reaction or scattering probability and (ii) spectrum band decrease abruptly to zero as the spacetime curvature increases; meanwhile, the geometric phase is unaffected by the spacetime curvature. Finally, discussions on these numerical results, together with perspectives on the applications of quantum field theory to chemical dynamics in curved spacetime are given.

physics.chem-ph↗

arXiv2026

A Primary Unified Geometric Framework of Molecular Reaction Dynamics Based on the Variational Principle

This work describes a geometric framework on molecular reaction dynamics based on the variational principle, where the Schr{ö}dinger equation must be solved to ``see'' how a reaction occurs. First, the mathematical preliminaries are given by discussing the principle of least action and the mountain pass theorem. Second, we discuss the physical preliminaries, including the principle of equivalence for deriving the kinetic energy operator (KEO) and artificial intelligence (AI) techniques to build the potential energy surface (PES) in general spacetime. Moreover, we simplified electromagnetic interactions in curved spacetime within the molecular system and consequently, we are able to construct the nuclear Hamiltonian in nonzero curvature spacetime. This indicates possibility to introduce gauge fields through the curvature, such as additional term in the nuclear KEO near a conical intersection. Third, the single-particle approximation provides a powful ansatz to solve the Schr{ö}dinger equation by variational principle. Thus, one can formulate the variational approaches for either electronic structure or quantum dynamics. In this work, based on previous discussions ({\it Phys. Chem. Chem. Phys.} {\bf 27} (2025), 20397) we unified them by a geometric description, where the geometric phase is naturally introduced. Finally, due to optimization characteristic of the present theory, further discussions on the present theory from optimization insight are also given, including two postulates, generative AI techniques, role of perturbation, and Markov process in optimization.

physics.chem-ph↗

arXiv2025

A Multi-Electronic-State Model to Interpret the Apparent Anomalous Arrhenius Curve of OH + HO$_2$ $\to$ O$_2$ + H$_2$O

A comprehensive multi-electronic-state model for OH + HO2 -> O2 + H2O has been developed through extensive multi-reference configuration interaction (MRCI) calculations, aiming to elucidate two key experimental observations: (1) an unusually deep and narrow ``well'' in the Arrhenius curve near 1100K and (2) a slightly negative temperature dependence in the range of 200K~500K. Moreover, the present model can serve as the basis for constructing multi-state Hamiltonian in multi-dimensional quantum dynamics calculations. The present model incorporates eight state-to-state processes involving OH (X) + HO2 (X/A), where three of four processes associated with HO2 (X) are exothermic, while those associated with HO2 (A) have three endothermic channels with the smallest barrier of 0.107 eV. At temperatures below 500K, the processes of HO2 (A) remain inaccessible, and the dominance of exothermic pathways results in a temperature-independent rate constant. To enable HO2 excitation at temperatures above 900K, a black-body radiation model that facilitates endothermic processes is introduced and reproduces the reduction factor of 0.3711 at 1100K. This value falls within the experimentally observed range of 0.30~0.76. Furthermore, a recombination process involving HO2 (A) is proposed to provide additional reduction of the rate constant. In conjunction with our previous works (J. Chem. Phys. 152 (2020), 134309 and J. Chem. Theory Comput. 20 (2024), 597), predicted values of the rate constants are well agree with experiments. At elevated temperatures exceeding 1242K (namely >0.107eV), the overall rate constant becomes temperature-dependent due to the activation of endothermic processes, leading to a distinct well in the Arrhenius curve between 900K and 1242K.

physics.chem-ph↗

arXiv2025

Hierarchical Wavepacket Propagation Framework via ML-MCTDH for Molecular Reaction Dynamics

This work presents a computational framework for studying reaction dynamics via wavepacket propagation, employing the multiconfiguration time-dependent Hartree (MCTDH) method and its multilayer extension (ML-MCTDH) as the core methodologies. The core idea centers on the concept of modes that combine several coordinates along with their hierarchical separations because the degrees of freedom are too numerous to be efficiently treated as a single mode. First, the system is partitioned into several fragments within the same layer, and these fragments are further decomposed. Repeating this process, a hierarchical separation of modes emerges, until modes of a manageable size are achieved. Accordingly, the coordinates frame can be designed hierarchically. Second, the kinetic energy operator (KEO) is derived as a sum-of-products (SOP) of single-particle differential operators through polyspherical approach, while the potential energy surface (PES) is expressed in a similar SOP form of single-particle potentials (SPPs) through (1) reconstruction approaches using an existing PES or (2) direct approaches based on a computed database. Third, the nuclear wave function is expressed in a multi-layer expansion form, where each term is a product of single-particle functions (SPFs) that are further expanded by the SPFs in deeper layer. This expansion form is also adopted by variational eigensolver for electronic wave function. Finally, the Dirac-Frenkel variational principle leads to a set of working equations whose solutions reproduce reaction dynamics. In addition, the hierarchical framework can be rearranged by the mathematical language of tensor network (TN) or tree tensor network (TTN). In this work, we compare the methods represented by function with those in the form of TN or TTN. We also discuss the limitations of the present framework and propose solutions, providing further perspectives.

physics.chem-ph↗

arXiv2025

Berry Phase Effects of Nuclei in Chemical Reaction Dynamics

In calculations on quantum state-resolved dynamics of a chemical reaction, reactants are usually prepared in separated eigenstates of individual fragments, and their direct-product is then evolved in time. In this work, we focus on the essence in separating them and the Berry phase effects of the nuclear wave function. By the present theory, mechanism of inter/intramolecular energy redistribution is also proposed to deeply understand reactive dynamics with multirovibrational states. To demonstrate the phase transition of the nuclear wave function, two three-dimensional (3D) models reductively describing the molecular reaction are developed to simulate transport of the system along a closed path in a parameter space represented of inter/intramolecular energy transfers. Employing these 3D models, extensive multiconfigurational time-dependent Hartree (MCTDH) calculations are performed to solve the time-dependent nuclear Schr{ö}dinger equation at various initial conditions. Moreover, 98D multilayer MCTDH (ML-MCTDH) calculations are launched to demonstrate the transition of Berry phase. These calculations clearly indicate that the wave function can change sign allowing quantum interference in the parameter space. Discussions on the separation of the reactants are made, while perspectives on the Berry phase effects predicted by the present work are given from the viewpoint of differential geometry. As a conclusion remark, the Berry phase effects on molecular dynamics are also thoroughly compared with those on electronic properties (see, for example, {\it Rev. Mod. Phys.} {\bf 82} (2010), 1959) and mode/bond-specific reactivity (see, for example, {\it Nat. Chem.} {\bf 14} (2022), 545).

physics.chem-ph↗

arXiv2024

Canonical-Polyadic-Decomposition of the Potential Energy Surface Fitted by Warm-Started Support Vector Regression

In this work, we propose a decoupled support vector regression (SVR) approach for direct canonical polyadic decomposition (CPD) of a potential energy surface (PES) through a set of discrete training energy data. This approach, denoted by CPD-SVR, is able to directly construct the PES in CPD with a more compressed form than previously developed Gaussian process regression (GPR) for CPD, denoted by CPD-GRP ({\it J. Phys. Chem. Lett.} {\bf 13} (2022), 11128). Similar to CPD-GPR, the present CPD-SVR method requires the multi-dimension kernel function in a product of a series of one-dimensional functions. We shall show that, only a small set of support vectors play a role in SVR prediction making CPD-SVR predict lower-rank CPD than CPD-GPR. To save computational cost in determining support vectors, we propose a warm-started (ws) algorithm where a pre-existed crude PES is employed to classify the training data. With the warm-started algorithm, the present CPD-SVR approach is extended to the CPD-ws-SVR approach. Then, we test CPD-ws-SVR and compare it with CPD-GPR through constructions and applications of the PESs of H + H$_2$, H$_2$ + H$_2$, and H$_2$/Cu(111). To this end, the training data are computed by existed PESs. Calculations on H + H$_2$ predict a good agreement of dynamics results among various CPD forms, which are constructed through different approaches.

physics.chem-ph↗

arXiv2021

Theoretical Chemistry Course for Students in Chemistry

In this work, the teaching content of a theoretical-chemistry (TC) course is reformed, establishing a theoretical contents from micro- to macro-system, and comprehensively introducing the theory of chemical reaction to undergraduate students in chemistry. In order to develop such TC course based on the general physical-chemistry course, we focus on the last-mile problem between the physics and chemistry courses to train the critical thinking of undergraduate students in chemistry. To clearly show this, a reduction scheme of polymer molecular dynamics was discussed as an example, which shows a different theoretical content in polymer chemistry. Moreover, we propose a series of experiences and dependent measures that can provide information regarding students' levels of knowledge and understanding. This assessment quiz was designed to test students on the fundamental concepts and applications of TC, such as dynamics, statistical ensemble, kinetics, and so on. From the actual teaching for 36 students, it was found that these students performed significantly improvement from the present TC content. Further analysis of each individual question revealed that approximately two-third of the students learn new knowledge. Although the present TC course might be considered to be a certain degree of difficulty for chemists, these analyses show that students can effectively accept these complicated concepts.

physics.ed-ph↗

arXiv2021

High-dimensional Quantum Dynamics Study on Excitation-Specific Surface Scattering including Lattice Effects of a Five-Atoms Surface Cell

In this work high-dimensional (21D) quantum dynamics calculations on mode-specific surface scattering of a carbon monoxide molecule on a copper (100) surface with lattice effects of a five-atom surface cell are performed through the multilayer multiconfiguration time-dependent Hartree (ML-MCTDH) method. We employ a surface model in which five surface atoms near the impact site are treated as fully flexible quantum particles while all other more distant atoms are kept at fixed locations. To efficiently perform the 21D ML-MCTDH wavepacket propagation, the potential energy surface is transferred to canonical polyadic decomposition form with the aid of a Monte Carlo based method. Excitation-specific sticking probabilities of CO on Cu(100) are computed and lattice effects caused by the flexible surface atoms are demonstrated by comparison with sticking probabilities computed for a rigid surface. The dependence of the sticking probability of the initial state of the system is studied, and it is found that the sticking probability is reduced, when the surface atom on the impact site is initially vibrationally excited.

physics.chem-ph↗