Resolving Correlated States of Benzyne on a Quantum Computer with an Error-Mitigated Quantum Contracted Eigenvalue Solver

The simulation of strongly correlated many-electron systems is one of the most promising applications for near-term quantum devices. Here we use a class of eigenvalue solvers (presented in Phys. Rev. Lett. 126, 070504 (2021)) in which a contraction of the Schrödinger equation is solved for the two-electron reduced density matrix (2-RDM) to resolve the energy splittings of ortho-, meta-, and para-isomers of benzyne ${\textrm C_6} {\textrm H_4}$. In contrast to the traditional variational quantum eigensolver, the contracted quantum eigensolver solves an integration (or contraction) of the many-electron Schrödinger equation onto the two-electron space. The quantum solution of the anti-Hermitian part of the contracted Schrödinger equation (qACSE) provides a scalable approach with variational parameters that has its foundations in 2-RDM theory. Experimentally, a variety of error mitigation strategies enable the calculation, including a linear shift in the 2-RDM targeting the iterative nature of the algorithm as well as a projection of the 2-RDM onto the convex set of approximately $N$-representable 2-RDMs defined by the 2-positive (DQG) $N$-representability conditions. The relative energies exhibit single-digit millihartree errors, capturing a large part of the electron correlation energy, and the computed natural orbital occupations reflect the significant differences in the electron correlation of the isomers.

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