VanQver: The Variational and Adiabatically Navigated Quantum Eigensolver

TL;DR

VanQver introduces a variational adiabatic quantum algorithm with a navigator Hamiltonian, significantly reducing annealing time for molecular ground-state energy estimation on NISQ hardware.

Contribution

It proposes a novel variational approach with a navigator Hamiltonian to enhance adiabatic quantum computation efficiency.

Findings

Achieves chemical accuracy two to three orders faster than standard AQC.

Demonstrates improved ground-state energy estimation for molecules H₂, P4, and LiH.

Shows potential for more efficient quantum algorithms on NISQ devices.

Abstract

The accelerated progress in manufacturing noisy intermediate-scale quantum (NISQ) computing hardware has opened the possibility of exploring its application in transforming approaches to solving computationally challenging problems. The important limitations common among all NISQ computing technologies are the absence of error correction and the short coherence time, which limit the computational power of these systems. Shortening the required time of a single run of a quantum algorithm is essential for reducing environment-induced errors and for the efficiency of the computation. We have investigated the ability of a variational version of adiabatic quantum computation (AQC) to generate an accurate state more efficiently compared to existing adiabatic methods. The standard AQC method uses a time-dependent Hamiltonian, connecting the initial Hamiltonian with the final Hamiltonian. In the current approach, a navigator Hamiltonian is introduced which has a non-zero amplitude only in the middle of the annealing process. Both the initial and navigator Hamiltonians are determined using variational methods. A hermitian cluster operator, inspired by coupled-cluster theory and truncated to single and double excitations/de-excitations, is used as a navigator Hamiltonian. A comparative study of our variational algorithm (VanQver) with that of standard AQC, starting with a Hartree--Fock Hamiltonian, is presented. The results indicate that the introduction of the navigator Hamiltonian significantly improves the annealing time required to achieve chemical accuracy by two to three orders of magnitude. The efficiency of the method is demonstrated in the ground-state energy estimation of molecular systems, namely, H$_2$, P4, and LiH.