Unveiling phonons in a molecular qubit with four-dimensional inelastic neutron scattering and density functional theory.

Phonons are the main source of relaxation in molecular nanomagnets, and different mechanisms have been proposed in order to explain the wealth of experimental findings. However, very limited experimental investigations on phonons in these systems have been performed so far, yielding no information about their dispersions. Here we exploit state-of-the-art single-crystal inelastic neutron scattering to directly measure for the first time phonon dispersions in a prototypical molecular qubit. Both acoustic and optical branches are detected in crystals of [VO(acac)$${}_{2}$$] along different directions in the reciprocal space. Using energies and polarisation vectors calculated with state-of-the-art Density Functional Theory, we reproduce important qualitative features of [VO(acac)$${}_{2}$$] phonon modes, such as the presence of low-lying optical branches. Moreover, we evidence phonon anti-crossings involving acoustic and optical branches, yielding significant transfers of the spin-phonon coupling strength between the different modes. Molecular nanomagnets have potential applications for storing both classical and quantum information, with benefit of the high scalability of chemical synthesis. Here the authors use state-of-the-art experimental and theoretical methods to investigate phonons in a molecular qubit candidate.