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This study demonstrates a practical method for extending quantum coherence on superconducting processors using Variational Trotter Compression, enabling high-fidelity simulations of complex systems like the H2 molecule and Fermi-Hubbard model. By successfully extracting eigenenergies with precision comparable to exact diagonalization, the work establishes a robust framework for simulating strongly correlated regimes on near-term hardware.
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High-Resolution Dynamical Eigenspectroscopy via Variational Trotter Compression on a Superconducting Qubit Processor

arXiv2 min read

arXiv:2609.05838v1 Announce Type: new Abstract: The pursuit of high-resolution eigenspectroscopy on noisy intermediate-scale quantum devices is often hindered by the trade-off between circuit depth and coherence time. In this work, we introduce and experimentally demonstrate a dynamical eigenspectroscopy protocol that extracts fine-grained energy structures from time-dependent survival amplitudes. To overcome the finite coherence window of current superconducting processors, we employ Variational Trotter Compression (VTC) as a practical means to extend the duration of high-fidelity unitary evolution. Using a multi-connected 9-qubit superconducting processor, we reconstruct the time-domain autocorrelation signal via quantum state tomography for the H2 molecule at different bond lengths and for the Fermi-Hubbard model across different correlation regimes. Through multi-frequency fitting and Fourier analysis, the extracted eigenenergies agree with the exact-diagonalization values to within 2x10^-3, including the near-degenerate levels in the strongly interacting regime. Our results establish experimental dynamical spectroscopy as a robust and generalizable framework for simulating both quantum chemistry and strongly correlated lattice systems, bridging weak- and strong-coupling regimes on near-term quantum hardware.

Abstract:The pursuit of high-resolution eigenspectroscopy on noisy intermediate-scale quantum devices is often hindered by the trade-off between circuit depth and coherence time. In this work, we introduce and experimentally demonstrate a dynamical eigenspectroscopy protocol that extracts fine-grained energy structures from time-dependent survival amplitudes. To overcome the finite coherence window of current superconducting processors, we employ Variational Trotter Compression (VTC) as a practical means to extend the duration of high-fidelity unitary evolution. Using a multi-connected 9-qubit superconducting processor, we reconstruct the time-domain autocorrelation signal via quantum state tomography for the H2 molecule at different bond lengths and for the Fermi-Hubbard model across different correlation regimes. Through multi-frequency fitting and Fourier analysis, the extracted eigenenergies agree with the exact-diagonalization values to within 2x10^-3, including the near-degenerate levels in the strongly interacting regime. Our results establish experimental dynamical spectroscopy as a robust and generalizable framework for simulating both quantum chemistry and strongly correlated lattice systems, bridging weak- and strong-coupling regimes on near-term quantum hardware.

arXiv:2609.05838 [quant-ph]

(or arXiv:2609.05838v1 [quant-ph] for this version)

https://doi.org/10.48550/arXiv.2609.05838 Focus to learn more arXiv-issued DOI via DataCite (pending registration)

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