Thermalization of magnons in yttrium-iron garnet: nonequilibrium functional renormalization group approach

Using a nonequilibrium functional renormalization group (FRG) approach we calculate the time evolution of the momentum distribution of a magnon gas in contact with a thermal phonon bath. As a cutoff for the FRG procedure we use a hybridization parameter {\Lambda} giving rise to an artificial damping of the phonons. Within our truncation of the FRG flow equations the time evolution of the magnon distribution is obtained from a rate equation involving cutoff-dependent nonequilibrium self-energies, which in turn satisfy FRG flow equations depending on cutoff-dependent transition rates. Our approach goes beyond the Born collision approximation and takes the feedback of the magnons on the phonons into account. We use our method to calculate the thermalization of a quasi two-dimensional magnon gas in the magnetic insulator yttrium-iron garnet after a highly excited initial state has been generated by an external microwave field. We obtain good agreement with recent experiments.Comment: 16 pages, 6 figures, final versio

Phonon-induced disorder in dynamics of optically pumped metals from non-linear electron-phonon coupling

The non-equilibrium dynamics of matter excited by light may produce electronic phases that do not exist in equilibrium, such as laser-induced high-$T_c$ superconductivity. Here we simulate the dynamics of a metal driven at $t=0$ by a pump that excites dipole-active vibrational modes that couple quadratically to electrons, and study the evolution of its electronic and vibrational observables. We provide evidence for enhancement of local electronic correlations, including double occupancy, accompanied by rapid loss of long-range spatial phase coherence. Concurrently, the onsite vibrational reduced density matrix evolves from its initial coherent state to one with a predominantly diagonal structure whose distribution qualitatively resembles the coherent state Poisson character. This rapid loss of coherence controls the electronic dynamics as the system evolves towards a correlated electron-phonon long-time state. We show that a simple model based on an effective disorder potential generated by the oscillator dephasing dynamics for the electrons provides an explanation for the flattening in momentum of electronic correlations. Our results provide a basis within which to understand correlation dynamics of vibrationally coupled electrons in pump-probe experiments.Comment: 7 pages main text + 3 pages appendices, 5 figures main text + 2 figures appendice