In the realm of open quantum systems, steady states and high-harmonic generation (HHG) existing far from equilibrium have become core pillars of ultrafast science. Most solid-state research explores charge HHG with limited investigations into spin degrees of freedom. In this study, we theoretically address spin HHG in the steady state resulting from the terahertz laser-driven spin-phonon coupling in a dissipative dimerized spin-1/2 chain. Instead of directly driving spins using time-dependent magnetic fields, we employ the magnetophononic mechanism, where the laser first drives the lattice, and then the excited lattice subsequently drives the spins. We investigate the role of various model parameters for optimizing HHG. Increasing the laser amplitude amplifies spin HHG beyond the perturbative regime, enhancing both harmonic amplitudes and orders. We find that configuring the drive frequency far below the spin band yields the highest harmonic order. Additionally, we provide a theory matching the numerical results under weak spin-phonon coupling and propose an experimental procedure to probe the emission spectrum of spin HHG.
In the realm of open quantum systems, steady states and high-harmonic generation (HHG) existing far from equilibrium have become core pillars of ultrafast science. Most solid-state research explores charge HHG with limited investigations into spin degrees of freedom. In this study, we theoretically address spin HHG in the steady state resulting from the terahertz laser-driven spin-phonon coupling in a dissipative dimerized spin-1/2 chain. Instead of directly driving spins using time-dependent magnetic fields, we employ the magnetophononic mechanism, where the laser first drives the lattice, and then the excited lattice subsequently drives the spins. We investigate the role of various model parameters for optimizing HHG. Increasing the laser amplitude amplifies spin HHG beyond the perturbative regime, enhancing both harmonic amplitudes and orders. We find that configuring the drive frequency far below the spin band yields the highest harmonic order. Additionally, we provide a theory matching the numerical results under weak spin-phonon coupling and propose an experimental procedure to probe the emission spectrum of spin HHG.
The advent of high-intensity ultrafast laser pulses has opened new opportunities for controlling and designing quantum materials. In particular, terahertz (THz) pulses can resonantly drive optical phonon modes, enabling dynamic manipulation of lattice degrees of freedom. In this work, we investigate the ultrafast quantum thermodynamics of optical phonon mode driven by a THz pulse by treating the phonon as an open quantum system coupled to a thermal environment within a Caldeira-Leggett-type framework. We derive the quantum heat current between the phonon and the bath and analyze its behavior under realistic pulse protocols. Our results demonstrate that ultrafast laser driving can reveal and even induce significant deviations from the commonly adopted Markovian approximation, thereby providing a pathway to probe and control non-Markovian dissipation in driven solid-state systems.
We study a dimerized spin-1/2 chain, such as CuGeO3, hosting triplon excitations coupled to optical phonons under weak terahertz laser driving. Both phonons and triplons weakly lose energy into the surrounding baths, forming a nonequilibrium steady state. In the strong phonon-triplon coupling regime, phonons near the two-triplon continuum hybridize strongly with triplons. Using mean-field Lindblad dynamics, we show that strong hybridization induces sharp first-order phase transitions---either single or simultaneous double---in the emission spectrum, mainly due to nonlinearities in the chain and the instantaneous breaking of spatial inversion symmetry, as captured by the phonon displacement. Using mean-field Floquet analysis of harmonic modes in both sectors, we analytically confirm the existence of these phase transitions. Furthermore, we map the complete steady-state phase diagram by varying key control parameters and provide experimentally relevant parameters for observing these transitions in laser-driven CuGeO3.
Quantum high-harmonic generation (HHG) is a prominent and growing field of research with potential capabilities of providing high photon-number entangled states of light. However, there is an open debate regarding the theory level required for correctly describing the quantum aspects of HHG, such as squeezing or entanglement. Previous approaches either semi-classically sampled the quantum electromagnetic field distribution, or employed perturbation theory utilizing the semi-classical simulations as a starting point. Both of these schemes miss out key quantum-optical features as self-consistent numerical simulations of the electron-photon wavefunction are not performed at any stage. In this Letter, we develop a full quantum theory for multipartite entanglement in HHG, solving exactly the light-matter interaction Hamiltonian in a given Hilbert space, and employ it for evaluating the quantum correlations of emitted photons. We show that HHG entanglement oscillates with the driving laser power and exhibits multiple local maxima, which allows fine-tuning HHG entanglement. Such features arise for both above-threshold harmonics and between above- and below-threshold harmonics. By analyzing different types of atomic targets, we find that the long-range behavior of driven electrons can qualitatively change the resulting entanglement, potentially leading to non-universal behavior across systems. Lastly, we show that focal averaging over classical degrees of freedom in fact plays a key role in entanglement measures and can change the qualitative behavior of observables. Our work establishes the state-of-the art in exploring entanglement features in HHG, and paves way for analysis and engineering of entangled multi-photon states in the XUV and ultrafast regime for more complex matter systems.
High-order harmonic generation (HHG) is one of the most commonly studied nonlinear optical phenomena, originating in the ultrafast dynamics of electrons in atomic gases and semiconductors. It has attracted much attention because of its nonperturbative nature and potential for future attosecond laser pulse sources. On the theory side, a semiclassical picture based on tunneling ionization of electrons is successfully used in explaining key characteristics of the HHG. This model assumes that electric fields nonperturbatively excite electrons beyond the ionization potential or the band gap. Thus, intuitively, a larger gap should lead to an exponentially smaller HHG emission. Despite this intuition, the HHG in the Mott insulator Ca2RuO4 has shown an unconventional exponential increase with respect to the gap width. This experiment implies effects beyond the semiclassical theory. However, most theoretical works have focused on the dependence of the HHG on external control parameters, and the gap dependence of the HHG is poorly understood even in noninteracting systems. Thus, it is essential to clarify the gap dependence of the HHG in a fully quantum mechanical approach. Here, we analyze numerically exactly the gap dependence of the HHG in two-level systems. We find an increase in the strength of the HHG when the Rabi frequency is large compared to the gap width. Furthermore, the relaxation and scattering of electrons increase the visibility of this gap dependence. Finally, we find that the enhancement rate follows a universal scaling law regardless of the driving frequency. The existence of this gap dependence in two-level systems suggests that this unconventional gap dependence is a universal behavior that can be found not only in Mott insulators but also in atomic gases and semiconductors.
The generation of higher-order harmonic radiation originating from the interaction of intense laser pulses with matter is typically described semiclassically: While the electronic structure and dynamics of matter is described quantum mechanically, the intense light field is described classically---and accordingly the generated harmonic radiation. However, pioneering experiments on quantum optical properties of high-order harmonic generation (HHG) in atomic gases from the group of P. Tzallas [I. Gonoskov et al., Sci. Rep. 6, 32821 (2016) and N. Tsatrafyllis et al., Nat. Commun. 8, 15170 (2017)], and theoretical investigations from the group of M. Lewenstein [M. Lewenstein et al., Nat. Phys. 17, 1104 (2021) and P. Stammer et al., Phys. Rev. Lett. 128, 123603 (2022)] have impressively demonstrated that light's quantum properties are observable in the strong-field realm. In this paper, we develop a quantum optical description of HHG in a bulk semiconductor originating from the nonlinear Bloch current. This mechanism of HHG, known as the intraband current, constitutes the major contribution to the emission spectrum for harmonic with energies of quanta roughly below the bandgap. Under certain approximations, employing a quantum description of both light and matter, we obtain analytical solutions, which allow us to analyze the classical and quantum optical characteristics of the fundamental mode of light and the harmonic modes. We find intricate but sufficiently mild modifications of the photon statistics of the fundamental mode and coherent displacements depending on the parameters of the driving laser field. Similar to high-harmonic generation in atoms, the fundamental and emitted harmonic field modes are entangled. Moreover, our analytical model predicts parameter ranges where these quantum optical properties will be most pronounced, allowing protocols for quantum information processing with high photon numbers over a large range of frequencies.
Harnessing the most advanced capabilities of quantum technologies will require the ability to control macroscopic quantum states of matter. Quantum magnetic materials provide a valuable platform for realizing highly entangled many-body quantum systems, and have been used to investigate phenomena ranging from quantum phase transitions (QPTs) to fractionalization, topological order and the entanglement structure of the quantum wavefunction. Although multiple studies have controlled their properties by static applied pressures or magnetic fields, dynamical control at the fundamental timescales of their magnetic interactions remains completely unexplored. However, major progress in the technology of ultrafast laser pulses has enabled the dynamical modification of electronic properties, and now we demonstrate the ultrafast control of quantum magnetism. This we achieve by a magnetophononic mechanism, the driving of coherent lattice displacements to produce a resonant excitation of the quantum spin dynamics. Specifically, we apply intense terahertz laser pulses to excite a collective spin state of the quantum antiferromagnet SrCu2(BO3)2 by resonance with the nonlinear mixing frequency of the driven phonons that modulate the magnetic interactions. Our observations indicate a universal mechanism for controlling nonequilibrium quantum many-body physics on timescales many orders of magnitude faster than those achieved to date.