Quantum simulation of electronic structure with a transcorrelated Hamiltonian

Quantum simulation of electronic structure with a transcorrelated Hamiltonian: improved accuracy with a smaller footprint on the quantum computer

Researchers at IBM Research and Mercedez–Benz Research have demonstrated quantum simulations of electronic structure with a transformed Hamiltonian that includes some electron correlation effects.

The transcorrelated Hamiltonian used in this work is efficiently constructed classically, at polynomial cost, by an approximate similarity transformation with an explicitly correlated two-body unitary operator. This Hamiltonian is Hermitian, includes no more than two-particle interactions, and is free of electron–electron singularities.

The team investigated the effect of such a transformed Hamiltonian on the accuracy and computational cost of quantum simulations by focusing on a widely used solver for the Schrödinger equation, namely the Variational Quantum Eigensolver (VQE) method, based on the unitary coupled cluster with singles and doubles (q-UCCSD) Ansatz.

Nevertheless, the formalism presented in the paper translates straightforwardly to other quantum algorithms for chemistry. Their results demonstrated that a transcorrelated Hamiltonian, paired with extremely compact bases, produces explicitly correlated energies comparable to those from much larger bases.

For the chemical species studied here, explicitly correlated energies based on an underlying 6-31G basis had cc-pVTZ quality.

The use of the very compact transcorrelated Hamiltonian reduces the number of CNOT gates required to achieve cc-pVTZ quality by up to two orders of magnitude, and the number of qubits by a factor of three.

The paper has been published in the Physical Chemistry Chemical Physics.