Preparation and coherent manipulation of toroidal moments in molecules (2504.08701v1)

Abstract: Molecules with an odd number of electrons are expected to display paramagnetic behaviour in a uniform magnetic field. Instead, a vanishing magnetization is often measured in a family of lanthanide complexes known as Single Molecule Toroics. The anomaly can be explained in terms of degenerate quantum states in which electron spins and orbital currents give rise to time-odd and space-odd magnetic vortices known as toroidal moments, carrying a vanishing magnetic dipole. Resilient to stray magnetic fields and susceptible to electric manipulation, toroidal moments are sparking growing interest for applications in spintronics, magnonics, and photonics. While macroscopic toroidal moments have been observed in extended systems such as bulk low-dimensional non-collinear ferromagnets, theoretically predicted quantum toroidal states in molecules are yet to be observed, as it is currently unclear how to split degenerate states carrying counter-rotating vortices via existing experimental setups. Here we propose a realistic experimental protocol to polarize and observe molecular toroidal moments using pulsed microwave radiation. Modelling the spin-dynamics in a pulsed MW-field, we find that three resonant MW-pulses, delivered either sequentially or simultaneously, to a class of MDy$_6$ (M = Al$^{3+}$, Cr$^{3+}$) molecules consisting of coupled Dy$_3$ toroidal moieties, can selectively and coherently transfer population to a long-lived polarized toroidal state. The ensuing magneto-electric properties can then be used as a read-out mechanism. Our results provide a strategy to measure and coherently manipulate toroidal states in molecular systems, which is expected to trigger applications of molecular toroidal states to quantum technologies.