Oct 2026· Journal of the American Chemical Society· 0 citations· 77 references
TL;DR
Sample-based Quantum Diagonalization is extended to AIMD and SQD-vibrational analysis, establishing SQD-AIMD and SQD-vibrational analysis as practical and scalable frameworks for simulating chemical reaction dynamics and elucidating reaction mechanisms on near-term quantum hardware, extending quantum computing applications beyond static electronic structure calculations.
Abstract
Quantum computers offer the potential to simulate chemical systems beyond the capabilities of classical computers. However, current quantum computing approaches to ab initio molecular dynamics (AIMD) and vibrational analysis largely rely on the Variational Quantum Eigensolver (VQE), whose circuit depth, iterative optimization, and measurement overhead hinder the practical simulation of molecular systems. Here, we extend Sample-based Quantum Diagonalization (SQD), a quantum sampling-based electronic-structure method, to AIMD and vibrational analysis on noisy quantum hardware. The resulting framework enables nuclear forces and Hessians to be derived from quantum-computed electronic energies, facilitating molecular dynamics and characterization of potential energy surfaces. We demonstrate the approach using diverse molecular processes, including H2 bond vibration, the proton-exchange reaction (H+ + H2), the bimolecular nucleophilic substitution (SN2) reaction (Cl– + CH3Cl), and proton-transfer dynamics between two water molecules involving transient formation of the Zundel cation (H2O···H+···OH2). Across these systems, SQD-AIMD trajectories and vibrational frequencies obtained with noisy quantum hardware/noise-models show excellent agreement with classical reference calculations and substantially improved accuracy relative to previously reported VQE-based simulations. Importantly, the SQD-based approach eliminates costly variational optimization and significantly reduces measurement requirements relative to VQE, enabling AIMD simulations spanning approximately 500 timesteps (∼200 fs), substantially longer than previously reported AIMD simulations on quantum hardware. These results establish SQD-AIMD and SQD-vibrational analysis as practical and scalable frameworks for simulating chemical reaction dynamics and elucidating reaction mechanisms on near-term quantum hardware, extending quantum computing applications beyond static electronic structure calculations.
Nonorthogonal variational quantum simulation (NOVQS) is introduced, which applies linear combinations of parameterized quantum states to real- and imaginary-time evolutions and provides a flexible route to enhancing wavefunction expressivity under circuit-depth constraints.
Predicting anharmonic vibrational spectra is a complex computational task, which becomes quickly infeasible as molecular size and the number of vibrational basis functions increase, leading to an exponential growth of the underlying Hilbert space. Here, we employ a sample-based quantum diagonalization (SQD) framework t...
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Nuclear quantum effects are critical for describing proton transfer and hydrogen bonding, but their incorporation into quantum chemistry calculations is often computationally prohibitive on classical hardware. A promising alternative are quantum computers due to their linear scaling in the space requirements with syste...
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Introduction:
Quantum computing has the potential to transform scientific computing by providing efficient algorithms for solving large-scale numerical problems that arise in engineering and materials science. However, integrating quantum algorithms into multiscale mechanics remains largely unexplored due to the com...
Ying-Bin Chen, Shao-Ping Xiao· Academia Quantum· 0 citations
Quantum computing offers a promising route for electronic-structure calculations, but practical condensed-matter applications often require solving large families of related Hamiltonians arising from $\mathbf{k}$-point sampling, compositional variation, defects, and changes in system size. Here, we develop strategies f...
Saurabh Shivpuje, Vinit Singh, Manas Sajjan et al.· 0 citations
Charge transfer (CT) is the delocalization of electron density from a donor to an acceptor. It is a crucial component of noncovalent interactions that significantly influences hydrogen bonding, ion solvation, and the structure of aqueous and biomolecular systems. Because direct experimental measurement of CT is chall...
Piotr Cieplak, Ray Luo, Yong Duan· Journal of Physical Chemistr...· 0 citations
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