A quantum thermodynamic cycle with a chiral multiferroic working substance such as LiCu2O2 is presented. Shortcuts to adiabaticity are employed to achieve an efficient, finite time quantum thermodynamic cycle which is found to depend on the spin ordering. The emergent electric polarization associated with the chiral spin order, i.e. the magnetoelectric coupling, renders possible steering of the spin order by an external electric field and hence renders possible an electric-field control of the cycle. Due to the intrinsic coupling between of the spin and the electric polarization, the cycle performs an electro-magnetic work. We determine this work's mean square fluctuations, the irreversible work, and the output power of the cycle. We observe that the work mean square fluctuations are increased with the duration of the adiabatic strokes while the irreversible work and the output power of the cycle show a non-monotonic behavior. In particular the irreversible work vanishes at the end of the quantum adiabatic strokes. This fact confirms that the cycle is reversible. Our theoretical findings evidence the existence of a system inherent maximal output power. By implementing a Lindblad master equation we quantify the role of thermal relaxations on the cycle efficiency. We also discuss the role of entanglement encoded in the non-collinear spin order as a resource to affect the quantum thermodynamic cycle.

Following the theoretical approach by Xiao et al [Phys. Rev. B 81, 214418 (2010)] to the spin Seebeck effect, we calculate the mean value of the total spin current flowing through a normalmetal/ferromagnet interface. The spin current emitted from the ferromagnet to the normal metal is evaluated in the framework of the Fokker-Planck approach for the stochastic Landau-Lifshitz-Gilbert equation. We show that the total spin current depends not only on the temperature difference between the electron and the magnon baths, but also on the external magnetic field and magnetic anisotropy. Apart from this, the spin current is shown to saturate with increasing magnon temperature, and the saturation temperature increases with increasing magnetic field and/or magnetic anisotropy.

Quantum dynamics of magnetic order in a chiral multiferroic chain is studied. We consider two different scenarios: Ultrashort terahertz (THz) excitations or a sudden electric field quench. Performing analytical and numerical exact diagonalization calculations we trace the pulse induced spin dynamics and extract quantities that are relevant to quantum information processing. In particular, we analyze the dynamics of the system chirality, the von Neumann entropy, the pairwise and the many body entanglement. If the characteristic frequencies of the generated states are non-commensurate then a partial loss of pair concurrence occurs. Increasing the system size this effect becomes even more pronounced. Many particle entanglement and chirality are robust and persist in the incommensurate phase. To analyze the dynamical quantum transitions for the quenched and pulsed dynamics we combined the Weierstrass factorization technique for entire functions and Lanczos exact diagonalization method. For a small system we obtained analytical results including the rate function of Loschmidt echo. Exact numerical calculations for a system up to 40 spins confirm phase transition. Quenchinduced dynamical transitions have been extensively studied recently. Here we show that related dynamical transitions can be achieved and controlled by appropriate electric field pulses.

The influence of the dynamical Stark shift on the thermal entanglement and the efficiency of the quantum Otto cycle is studied for the su(1,1) Tavis-Cummings system. It is shown that the degree of the thermal entanglement becomes larger as the dynamical Stark shift increases. In contrast, the efficiency of the Otto cycle is degraded with an increase of the values of dynamical Stark shift. Expressions for the efficiency coefficient are derived. Using those expressions we identify the maximal efficiency of the quantum Otto cycle from the experimentally measured values of the dynamical Stark shift PACS numbers:

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