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Takeshi Sato

Publications and source records attributed to Takeshi Sato.

At least 19 recordsLinked to original sources

Efficient Quantum Circuits for Electronic Hamiltonian Simulation without Pauli Expansion

Electronic Hamiltonian simulation is commonly formulated by mapping fermionic operators to qubit operators and subsequently expanding the resulting ladder-operator products into Pauli strings. While general, this procedure obscures the higher-level fermionic structure and can hide opportunities for circuit optimization. Building on ladder-string-pair (Lasp) diagonalization originally developed for Hamiltonian simulation of partial differential equations, we construct time-evolution circuits for the second-quantized electronic Hamiltonian without performing a Pauli expansion. For the most general case of complex-valued coefficients, we present a time-evolution circuit for a two-body fermionic Lasp operator that corresponds to 16 Pauli strings in the Pauli-expansion approach but does not suffer from Trotter error at this stage. Expanding the optimization scope from a single operator to a triad of three fermionic Lasp operators sharing the same four spin-orbital indices enables systematic cancellation of CX gates, reducing the CX-gate count from 36 to 12 in the example considered, still without introducing Trotter error at this stage. For $n$ spin orbitals, further expanding the optimization scope to a sequence of $O(n)$ suitably ordered triads enables a cascade of CX-gate reductions across triad boundaries, reducing the CX-gate count from $O(n^2)$ to $O(n)$. The Lasp-based approach also naturally accommodates controlled time evolution and yields further optimizations for real-valued Hamiltonians. These results demonstrate that the Lasp-based approach enables more efficient time-evolution circuits by preserving high-level circuit structures and thereby expanding the scope of optimization, providing a systematic route toward more efficient electronic Hamiltonian simulation.

quant-ph

A deviatoric-stress closure for constitutive modeling of viscoelastic dynamics

Standard rheological measurements yield only selected stress components; thus, inferring tensorial constitutive equations from experimentally accessible observables is complicated. We propose a constitutive formulation written in terms of a deviatoric stress tensor, whose trace is zero, rather than the extra stress tensor. From rheometric data including shear stress, first and second normal stress differences under shear, and elongational stress under uniaxial elongation, we can construct a deviatoric stress state without the indeterminate isotropic stress. The deviatoric-stress dynamics is represented by a closure inferred through symbolic regression, constrained to satisfy material objectivity and a given linear Maxwell response. To demonstrate the proposed formulation, two closures inferred from stress responses of the Giesekus and Larson models successfully captured untrained transient-flow responses under planar elongation and mixed shear/uniaxial elongations at deformation rates around an inverse relaxation time. Steady rheological functions of the closures agreed with the original models in the linear-response regime and over a deformation-rate range connected to the training data, whereas deviations and divergent responses appeared at larger deformation rates outside the training regime. These results demonstrate that the proposed deviatoric-stress formulation provides a practical route for constitutive modeling of observable linear and nonlinear viscoelastic dynamics, while clarifying its range of validity under strong deformation.

cond-mat.soft

Auger Spectroscopy via Generative Quantum Eigensolver: A Quantum Approach to Molecular Excitations

Auger electron spectroscopy, a way of characterizing electronic structure through core-level decay processes, is widely used in materials characterization; however direct calculation from molecular geometry requires accurate treatment of many excited states, posing a challenge for classical methods. We present a hybrid quantum-classical workflow for calculating Auger spectra that combines the generative quantum eigensolver (GQE) for ground-state preparation, the quantum self-consistent equation-of-motion method for excited-state calculations, and the one-centre approximation for Auger transition rates. GQE uses a GPT-2 model to generate quantum circuits for ground-state optimization, allowing our workflow to benefit from HPC parallelization and GPU-acceleration for favourable scaling with system size. We demonstrate the validity of our workflow by calculating the Auger spectrum of water with the STO-3G basis set and demonstrating qualitative and quantitative agreement with spectra obtained using completely classical full configuration interaction calculations, from the computational literature, and from the experimental literature. We also find that for water, substituting the variational quantum eigensolver (VQE) for GQE results in near-identical spectra, but that the ground state estimator generated by GQE contains about half the total gate count as that generated by VQE.

quant-ph

Bridging Quantum Computing and Nuclear Structure: Atomic Nuclei on a Trapped-Ion Quantum Computer

We demonstrate quantum simulations of strongly correlated nuclear many-body systems on the RIKEN-Quantinuum Reimei trapped-ion quantum computer, targeting ground states of oxygen, calcium, and nickel isotopes. By combining a hard-core-boson representation of the nuclear shell model with a pair-unitary coupled-cluster doubles ansatz, we achieve sub-percent relative error in the ground-state energies compared to noise-free statevector simulations. Our approach leverages symmetry-aware state preparation and particle-number post-selection to efficiently capture pairing correlations characteristic of systems with same-species nucleons. These findings highlight the viability of high-fidelity trapped-ion platforms for nuclear physics applications and provide a foundation for scaling to more complex nuclear systems.

nucl-th

Time-dependent Hole States in Multiconfigurational Time-Dependent Hartree-Fock Approaches: A Time-Domain Generalization of Extended Koopmans' Theorem

We introduce a framework for resolving electron-hole dynamics within wavefunction-based multiconfigurational time-dependent Hartree-Fock (MCTDHF) theory. Central to this framework is a time-domain generalization of the extended Koopmans' theorem, which rigorously defines time-dependent hole states through single-electron removal. From this foundation, we prove the existence of exact equations of motion for time-dependent Dyson orbitals, enabling instantaneous construction of photofragments' reduced density matrices. The formalism further yields a systematic procedure to extract hole-resolved observables, such as channel-resolved photoelectron momentum distributions, directly from time-dependent \textit{ab initio} wavefunctions. As a demonstration, we employ an attosecond $ω-2ω$ laser strategy to control hole dynamics, thereby resolving a long-standing challenge in MCTDHF simulations. This advance opens a pathway for exploring correlated multielectron dynamics in atoms and molecules under ultrafast laser fields.

physics.atom-ph

Development of Rheological Constitutive Modeling Method Using a Sparse Identification Algorithm: A Case Study for Extensional Flows

Deriving constitutive models (CMs) from numerical data has been an attractive approach as a systematic CM building method. One recent study is Rheo-SINDy, which extended the sparse identification of nonlinear dynamics (SINDy) method to rheology. Although the Rheo-SINDy framework discovered an approximate CM from numerical data under shear flow, its versatility has not been investigated. To clarify its applicability to other types of flows, this study applied Rheo-SINDy to numerically generated data under extensional flow conditions. As baseline tests for extensional flow, we considered two problems: (i) whether the Rheo-SINDy framework can reproduce the famous Giesekus model from data generated by that model, and (ii) whether it can derive an approximate CM from data generated by a dumbbell model with a finite extensible nonlinear elastic (FENE) spring. For problem (i), we confirmed that Rheo-SINDy can identify the exact expression of the Giesekus model under extensional flow. For problem (ii), the Rheo-SINDy framework discovered a relatively simple expression of the approximate CM by manually designing the library matrix based on rheological knowledge. The identified approximate CM can reasonably predict extensional rheological properties of the FENE dumbbell model, including an extrapolation region. These findings demonstrate the fundamental validity of using Rheo-SINDy under extensional flow.

physics.flu-dyn

Reduced density matrix description of high-harmonic generation in multi-electron atoms: exploring sub-cycle correlation effects

High-harmonic generation (HHG) is one of the fundamental processes at the heart of attosecond physics. Traditionally viewed as an effective single-particle effect, recent advances have focused on contributions beyond this single-particle picture to the harmonic spectrum, as well as on probing electron correlations through HHG in atoms, molecules, and solids. In this paper, we introduce a reduced density matrix description to explore and to quantify correlation effects on a sub-cycle time scale and apply this approach to prototypical multi-electron atoms. By comparing noble gas atoms (He, Ne) with alkaline earth atoms (Be, Mg) exposed to driving fields with similar Keldysh parameters, we show that the sub-cycle variation of correlation parameters differs markedly for noble gases and alkaline earth atoms. We provide an intuitive explanation of these surprising effects based on the dynamics of natural orbitals and discuss the effect of this ultrafast correlation dynamics on the HHG spectrum.

physics.atom-ph

Coherent Control of Ion-Photoelectron Dynamics through Rabi Oscillations: An ab initio study

We present first-principles numerical simulations of photoionization in neon induced by bichromatic extreme ultraviolet pulses with frequencies $ω$ and $2ω$, specially chosen to make $ω$ equal to the energy difference between the $2s$ and $2p$ subshells. This allows for the production of photoelectrons from the $2s$ shell by $2ω$ pulse and from the $2p$ shell by $ω$ pulse with the same energy. Using the multi-configurational time-dependent Hartree-Fock method, we explore how Rabi coupling between subshells generates coherence between the corresponding photoelectron wave packets. Our \textit{ab initio} calculations confirm the analytical results derived from the essential-states approach in [K. L. Ishikawa, K. C. Prince, and K. Ueda, J. Phys. Chem. A 127, 10638 (2023)], validating the theoretical predictions. Although we focus on the Ne $2p$ and $2s$ subshells, our approach is applicable to a broad range of systems exhibiting photoionization from multiple subshells. The laser parameters employed in our simulations are available in modern Free Electron Lasers (FELs), and we anticipate that this work could stimulate experimental investigations using FELs to study ion-photoelectron coherence and entanglement.

physics.atom-ph

Time-dependent Hole States in Multiconfigurational Time-Dependent Hartree-Fock Approaches: Applications in Photoionization of Water Molecule

By simulating the real-time multielectron wavefunction with the multi-configurational time-dependent Hartree-Fock (MCTDHF) approach, we conduct an \textit{ab initio} study of the single-photon ionization process of a body-fixed water molecule ($\mathrm{H_2O}$) driven by attosecond pulses. To this end, we present a full-dimensional implementation of the MCTDHF method based on one-center expansions, allowing for the simulation of arbitrarily polarized lasers and multi-center polyatomic potentials. With a rigorous definition of the time-dependent hole state (TDHS) using the time-domain generalization of extended Koopmans' theorem (TD-EKT), we derive the reduced ion density matrix within the MCTDHF framework, which inherently encodes the total and channel-resolved photoionization cross sections of $\mathrm{H_2O}$. The cross sections obtained are benchmarked against existing experimental and theoretical results, validating the TDHS formalism. Furthermore, by adjusting the phase delay and intensity ratio of a pair of orthogonally polarized attosecond pulses, we explore the ultrafast control of attosecond coherence between electronic states of $\mathrm{H_2O^+}$.

physics.atom-ph

Rheo-SINDy: Finding a Constitutive Model from Rheological Data for Complex Fluids Using Sparse Identification for Nonlinear Dynamics

Rheology plays a pivotal role in understanding the flow behavior of fluids by discovering governing equations that relate deformation and stress, known as constitutive equations. Despite the importance of these equations, current methods for deriving them lack a systematic methodology, often relying on sense of physics and incurring substantial costs. To overcome this problem, we propose a novel method named Rheo-SINDy, which employs the sparse identification of nonlinear dynamics (SINDy) algorithm for discovering constitutive models from rheological data. Rheo-SINDy was applied to five distinct scenarios, four with well-established constitutive equations and one without predefined equations. Our results demonstrate that Rheo-SINDy successfully identified accurate models for the known constitutive equations and derived physically plausible approximate models for the scenario without established equations. Notably, the identified approximate models can accurately reproduce nonlinear shear rheological properties, especially at steady state, including shear thinning. These findings validate the robustness of Rheo-SINDy in handling data complexities and underscore its efficacy as a tool for advancing the development of data-driven approaches in rheology.

cond-mat.soft

Time-dependent orbital-optimized coupled-cluster methods families for fermion-mixtures dynamics

Five time-dependent orbital optimized coupled-cluster (TD-ooCC) methods, of which four can converge to the complete active space self-consistent-field method, are presented for fermion-mixtures with arbitrary fermion kinds and numbers. Truncation schemes maintaining the intragroup orbital rotation invariance, as well as equations of motion of CC amplitudes and orbitals, are derived. Present methods are compact CC-parameterization alternatives to the time-dependent multiconfiguration self-consistent-field method for systems consisting of arbitrarily different kinds and numbers of interacting fermions. Theoretical analysis of applications of present methods to various chemical systems are reported.

physics.chem-ph

Accurate and precise quantum computation of valence two-neutron systems

Developing methods to solve nuclear many-body problems with quantum computers is an imperative pursuit within the nuclear physics community. Here, we introduce a quantum algorithm to accurately and precisely compute the ground state of valence two-neutron systems leveraging presently available Noisy Intermediate-Scale Quantum devices. Our focus lies on the nuclei having a doubly-magic core plus two valence neutrons in the $ p $, $ sd $, and $ pf $ shells, i.e. ${}^6$He, ${}^{18}$O, and ${}^{42}$Ca, respectively. Our ansatz, quantum circuit, is constructed in the pair-wise form, taking into account the symmetries of the system in an explicit manner, and enables us to reduce the number of qubits and the number of CNOT gates required. The results on a real quantum hardware by IBM Quantum Platform show that the proposed method gives very accurate results of the ground-state energies, which are typically within $ 0.1 \, \% $ error in the energy for ${}^6$He and ${}^{18}$O and at most $ 1 \, \% $ error for ${}^{42}$Ca. Furthermore, our experiments using real quantum devices also show the pivotal role of the circuit layout design, attuned to the connectivity of the qubits, in mitigating errors.

nucl-th

Efficient simulation of multielectron dynamics in molecules under intense laser pulses: Implementation of the multiconfiguration time-dependent Hartree-Fock method based on the adaptive finite element method

We present an implementation of the multiconfiguration time-dependent Hartree-Fock method based on the adaptive finite element method for molecules under intense laser pulses. For efficient simulations, orbital functions are propagated by a stable propagator using the short iterative Arnoldi scheme and our implementation is parallelized for distributed memory computing. This is demonstrated by simulating high-harmonic generation from a water molecule and achieves a simulation of multielectron dynamics with overwhelmingly less computational time, compared to our previous work.

quant-ph

Time-dependent multiconfiguration self-consistent-field and time-dependent optimized coupled-cluster methods for intense laser-driven multielectron dynamics

We review time-dependent multiconfiguration self-consistent-field (TD-MCSCF) method and time-dependent optimized coupled-cluster (TD-OCC) method for first-principles simulations of high-field phenomena such as tunneling ionization and high-order harmonic generation in atoms and molecules irradiated by a strong laser field. These methods provide a flexible and systematically improvable description of the multielectron dynamics by expressing the all-electron wavefunction by configuration interaction expansion or coupled-cluster expansion, using time-dependent one-electron orbital functions. The time-dependent variational principle plays a key role to derive these methods satisfying gauge invariance and Ehrenfest theorem. The real-time/real-space implementation with an absorbing boundary condition enables the simulation of high-field processes involving multiple excitation and ionization. We present a detailed, comprehensive discussion of such features of TD-MCSCF and TD-OCC methods.

physics.chem-ph

Time-dependent optimized coupled-cluster method with doubles and perturbative triples [TD-OCCD(T)] for first principles simulation of multielectron dynamics

We report the formulation of a new, cost-effective approximation method in the time-dependent optimized coupled-cluster (TD-OCC) framework [T. Sato et al., J. Chem. Phys. 148, 051101 (2018)] for first-principles simulations of multielectron dynamics in an intense laser field. The method, designated as TD-OCCD(T), is a time-dependent, orbital-optimized extension of the "gold-standard" CCSD(T) method in the ground-state electronic structure theory. The equations of motion for the orbital functions and the coupled-cluster amplitudes are derived based on the real-valued time-dependent variational principle using the fourth-order Lagrangian. The TD-OCCD(T) is size extensive and gauge invariant, and scales as O(N^7) with respect to the number of active orbitals N. The pilot application of the TD-OCCD(T) method to the strong-field ionization and high-order harmonic generation from a Kr atom is reported in comparison with the results of the previously developed methods, such as the time-dependent complete-active-space self-consistent field (TD-CASSCF), TD-OCC with double and triple excitations (TD-OCCDT), TD-OCC with double excitations (TD-OCCD), and the time-dependent Hartree-Fock (TDHF) methods.

physics.chem-ph

Variational Quantum Simulation for Periodic Materials

We present a quantum-classical hybrid algorithm that simulates electronic structures of periodic systems such as ground states and quasiparticle band structures. By extending the unitary coupled cluster (UCC) theory to describe crystals in arbitrary dimensions, for a hydrogen chain, we numerically demonstrate that the UCC ansatz implemented on a quantum circuit can be successfully optimized with a small deviation from the exact diagonalization over the entire range of the potential energy curves. Furthermore, by using the quantum subspace expansion method, in which we truncate the Hilbert space within the linear response regime from the ground state, the quasiparticle band structure is computed as charged excited states. Our work establishes a powerful interface between the rapidly developing quantum technology and modern material science.

quant-ph

Implementation of a time-dependent multiconfiguration self-consistent-field method for coupled electron-nuclear dynamics in diatomic molecules driven by intense laser pulses

We present an implementation of a time-dependent multiconfiguration self-consistent-field (TD-MCSCF) method [R. Anzaki et al., Phys. Chem. Chem. Phys. 19, 22008 (2017)] with the full configuration interaction expansion for coupled electron-nuclear dynamics in diatomic molecules subject to a strong laser field. In this method, the total wave function is expressed as a superposition of different configurations constructed from time-dependent electronic Slater determinants and time-dependent orthonormal nuclear basis functions. The primitive basis functions of nuclei and electrons are strictly independent of each other without invoking the Born-Oppenheimer approximation. Our implementation treats the electronic motion in its full dimensionality on curvilinear coordinates, while the nuclear wave function is propagated on a one-dimensional stretching coordinate with rotational nuclear motion neglected. We apply the present implementation to high-harmonic generation and dissociative ionization of a hydrogen molecule and discuss the role of electron-nuclear correlation.

physics.atom-ph

Time-dependent optimized coupled-cluster method for multielectron dynamics IV: Approximate consideration of the triple excitation amplitudes

We present a cost-effective treatment of the triple excitation amplitudes in the time-dependent optimized coupled-cluster (TD-OCC) framework called TD-OCCDT(4) for studying intense laser-driven multielectron dynamics. It considers triple excitation amplitudes correct up to fourth-order in many-body perturbation theory and achieves a computational scaling of O(N7), with N being the number of active orbital functions. This method is applied to the electron dynamics in Ne and Ar atoms exposed to an intense near-infrared laser pulse with various intensities. We benchmark our results against the time-dependent complete-active-space self-consistent field (TD-CASSCF), time-dependent optimized coupled-cluster with double and triple excitations (TD-OCCDT), time-dependent optimized coupled-cluster with double excitations (TD-OCCD), and the time-dependent Hartree-Fock (TDHF) methods to understand how this approximate scheme performs in describing nonperturbatively nonlinear phenomena, such as field-induced ionization and high-harmonic generation. We find that the TD-OCCDT(4) method performs equally well as the TD-OCCDT method, almost perfectly reproducing the results of fully-correlated TD-CASSCF with a more favorable computational scaling.

physics.chem-ph