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arXiv:1402.0881 · Physical Review B

Laser-induced magnetization curve

Shintaro Takayoshi, Masahiro Sato, Takashi Oka

Published Dec 3, 2014• 62 citations
arXivHTMLPDF

Abstract

We propose an all optical ultrafast method to highly magnetize general quantum magnets using a circularly polarized terahertz laser. The key idea is to utilize a circularly polarized laser and its chirping. Through this method, one can obtain magnetization curves of a broad class of quantum magnets as a function of time even without any static magnetic field. We numerically demonstrate the laser-induced magnetization process in realistic quantum spin models and find a condition for the realization. The onset of magnetization can be described by a many-body version of Landau-Zener mechanism. In a particular model, we show that a plateau state with topological properties can be realized dynamically.

DOI
10.1103/physrevb.90.214413

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We propose an all optical ultrafast method to highly magnetize general quantum magnets using a circularly polarized terahertz laser. The key idea is to utilize a circularly polarized laser and its chirping. Through this method, one can obtain magnetization curves of a broad class of quantum magnets as a function of time even without any static magnetic field. We numerically demonstrate the laser-induced magnetization process in realistic quantum spin models and find a condition for the realization. The onset of magnetization can be described by a many-body version of Landau-Zener mechanism. In a particular model, we show that a plateau state with topological properties can be realized dynamically.
We theoretically predict a nonequilibrium phase transition in quantum spin systems induced by a laser, which provides a purely quantum-mechanical way of coherently controlling magnetization. Namely, when a circularly polarized laser is applied to a spin system, the magnetic component of a laser is shown to induce a magnetization normal to the plane of polarization, leading to an ultrafast phase transition. We first demonstrate this phenomenon numerically for an S=1S=1S=1 antiferromagnetic Heisenberg spin chain, where a new state emerges with magnetization perpendicular to the polarization plane of the laser in place of the topologically ordered Haldane state. We then elucidate its physical mechanism by mapping the system to an effective static model. The theory also indicates that the phenomenon should occur in general quantum spin systems with a magnetic anisotropy. The required laser frequency is in the terahertz range, with the required intensity being within a prospective experimental feasibility.
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.
The effect of the circularly polarized laser field on quantum spin systems in the steady-state regime, in which relaxation plays the central role, has been studied. The dynamical mean-field-like theory predicts several general results for the behavior of the time-average magnetization caused by the laser field. The induced magnetization oscillates with the frequency of the laser field (while Rabi-like oscillations, which modulate the latter in the dynamical regime, are damped by the relaxation in the steady-state regime). At high frequencies, that magnetization is determined by the value to which the relaxation process is directed. At low frequencies the slope of that magnetization as a function of the frequency is determined by the strength of the laser field. The anisotropy determines the resonance behavior of the time-averaged magnetization in both the ferromagnetic and antiferromagnetic cases with nonzero magnetic anisotropy. Nonlinear effects (in the magnitude of the laser field) have been considered. The effect of the laser field on quantum spin systems is maximal in resonance, where the time-averaged magnetization, caused by the laser field, is changed essentially. Out of resonance the changes in the magnetization are relatively small. The resonance effect is caused by the nonzero magnetic anisotropy. The resonance frequency is small (proportional to the anisotropy value) for spin systems with ferromagnetic interactions and enhanced by exchange interactions in the spin systems with antiferromagnetic couplings. We show that it is worthwhile to study the laser-field-induced magnetization of quantum spin systems caused by the high-frequency laser field in the steady-state regime in ``easy-axis'' antiferromagnetic spin systems (e.g., in Ising-like antiferromagnetic spin-chain materials). The effects of the Dzyaloshinskii-Moriya interaction and the spin-frustration couplings (in the case of the zigzag spin chain) have been analyzed.
Strong laser-induced magnetization of oxygen gas at room temperature and atmospheric pressure is achieved experimentally on the subnanosecond time scale. The method is based on controlling the electronic spin of paramagnetic molecules by means of manipulating their rotation with an optical centrifuge. Spin-rotational coupling results in a high degree of spin polarization on the order of one Bohr magneton per centrifuged molecule. Owing to the nonresonant interaction with the laser pulses, the demonstrated technique is applicable to a broad class of paramagnetic rotors. Executed in a high-density gas, it may offer an efficient way of generating macroscopic magnetic fields remotely (as shown in this work) and producing a large amount of spin-polarized electrons.
The time evolution of magnetization induced by circularly polarized light in an S=1S=1S=1 Heisenberg chain with large easy-plane anisotropy is studied numerically and analytically. Results at constant light frequency $\mathrm{\ensuremath{\Omega}}={\mathrm{\ensuremath{\Omega}}}_{0}$ are interpreted in terms of absorption lines of the electronic spin resonance spectrum. The application of time-dependent frequency $\mathrm{\ensuremath{\Omega}}=\mathrm{\ensuremath{\Omega}}(t)$ light, so called chirping, is shown to be an efficient procedure in order to obtain within a short time a large, controlled value of the magnetization Mz{M}^{z}Mz. Furthermore, comparison with a two-level model provides a qualitative understanding of the induced magnetization process.
We investigate second-order magnetic responses of quantum magnets against ac magnetic fields. We focus on the case where the zzz component of the spin is conserved in the unperturbed Hamiltonian and the driving field is applied in the xyxyxy plane. We find that linearly polarized driving fields induce a second-harmonic response, while circularly polarized fields generate only a zero-frequency response, leading to a magnetization with a direction determined by the helicity. Employing an unbiased numerical method, we demonstrate the nonlinear magnetic effect driven by the circularly polarized field in the XXZ model and show that the magnitude of the magnetization can be predicted by the dynamical spin structure factor in the linear response regime.