Infrared-dressed entanglement of cold open-shell polar molecules for universal matchgate quantum computing

Abstract

Implementing a scalable quantum information processor using polar molecules in optical lattices requires precise control over the long-range dipole-dipole interaction between molecules in selected lattice sites. We present here a scheme using trapped open-shell $^2\Sigma$ polar molecules that allows dipolar exchange processes between nearest and next-nearest neighbors to be controlled to construct a generalized transverse Ising spin Hamiltonian with tunable $XX$, $YY$ and $XY$ couplings in the rotating frame of the driving lasers. The scheme requires a moderately strong bias magnetic field with near-infrared light to provide local tuning of the qubit energy gap, and mid-infrared pulses to perform rotational state transfer via stimulated Raman adiabatic passage. No interaction between qubits is present in the absence of the infrared driving. We analyze the fidelity of the resulting two-qubit matchgate, and demonstrate its robustness as a function of the driving parameters. We discuss a realistic application of the system for universal matchgate quantum computing in optical lattices.