The expected return time to the original state is a key concept characterizing systems obeying both classical or quantum dynamics. We consider iterated open quantum dynamical systems in finite dimensional Hilbert spaces, a broad class of systems that includes classical Markov chains and unitary discrete time quantum walks on networks. Starting from a pure state, the time evolution is induced by repeated applications of a general quantum channel, in each timestep followed by a measurement to detect whether the system has returned to the original state. We prove that if the superoperator is unital in the relevant Hilbert space (the part of the Hilbert space explored by the system), then the expectation value of the return time is an integer, equal to the dimension of this relevant Hilbert space. We illustrate our results on partially coherent quantum walks on finite graphs. Our work connects the previously known quantization of the expected return time for bistochastic Markov chains and for unitary quantum walks, and shows that these are special cases of a more general statement. The expected return time is thus a quantitative measure of the size of the part of the Hilbert space available to the system when the dynamics is started from a certain state.
We study spin liquid phases of spin-5/2 alkaline earth atoms on a honeycomb lattice at finite temperatures. Our analysis is based on a Gutzwiller projection variational approach recast to a path-integral formalism. In the framework of a saddle-point approximation we determine spin liquid phases with lowest free energy and study their temperature dependence. We identify a critical temperature, where all the spin liquid phases melt and the system goes to the paramagnetic phase. We also study the stability of the saddle-point solutions and show that a time-reversal symmetry breaking state, a so called chiral spin liquid phase is realized even at finite temperatures. We also determine the spin structure factor, which, in principle, is an experimentally measurable quantity and is the basic tool to map the spectrum of elementary excitations of the system.
We work out a simple, pulsed pump-probe measurement scheme to measure the homogeneous linewidth of an atomic transition in an inhomogeneously broadened spectral line in a solid state environment. We apply the theory to the I_11/2 -- I_15/2 optical transition of erbium in LiNbO_3:Er^3+ crystal. Beside obtaining the homogeneous linewidth, we have estimated the population relaxation time as well.
