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Optics Express

Non-instantaneous third-order optical response of gases in low-frequency fields

Felipe Morales, Maria Richter, Misha Ivanov, Anton Husakou

Published May 20, 2022• 4 citations
Publisher

Abstract

It is commonly assumed that for low-intensity short optical pulses far from resonance, the third-order optical nonlinear response is instantaneous. We solve the three-dimensional time-dependent Schrödinger equation for the hydrogen atom and show that this is not the case: the polarization is not simply proportional to the cube of the electric field even at low intensities. We analyze the fundamental-frequency and third-harmonic nonlinear susceptibilities of hydrogen, investigate their dependence on intensity, and find that the delays in the Kerr response rapidly approach the femtosecond time-scale at higher intensities, while the delays in the third harmonic generation remain much lower. We also propose an experimental scheme to detect and characterize the above effects.

DOI
10.1364/oe.458765

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It is commonly assumed that for low-intensity short optical pulses far from resonance, the third-order optical nonlinear response is instantaneous. We solve the three-dimensional time-dependent Schrödinger equation for the hydrogen atom and show that this is not the case: the polarization is not simply proportional to the cube of the electric field even at low intensities. We analyze the fundamental-frequency and third-harmonic nonlinear susceptibilities of hydrogen, investigate their dependence on intensity, and find that the delays in the Kerr response rapidly approach the femtosecond time-scale at higher intensities, while the delays in the third harmonic generation remain much lower. We also propose an experimental scheme to detect and characterize the above effects.
We investigate the third order harmonic generation for model atoms interacting with intense short laser pulses. We focus on the cases where the ponderomotive energy is not big enough to generate high-order harmonics, and where resonant transitions between bound states are also as important as multi-photon ionization and low-order harmonic generation. We find that the third order harmonic intensity from a model hydrogen atom can decrease as the laser frequency draws near a resonance between bound states. We explain this result by looking into the ionization and Rabi oscillation from the numerical calculation of the time-dependent 1-D Schrödinger equation. In order to support our explanation we also investigate the populations of bound states that play an important role in this atomic process.
Polarization response that appears in silver vapors in the field of a high-intensity femtosecond Ti:sapphire laser has been studied by the direct numerical integration of the time-dependent Schrödinger equation. The regions of applicability have been determined for perturbation theory and the power series expansion of the polarization in the field. The contribution of free electrons to the response at the frequency of the interacting field has been calculated, which is due to the photoionization process and limits the Kerr effect. An important contribution of laser-excited atomic states to nonlinear atomic responses of neutral atoms has been demonstrated.
Accurate modeling of optical nonlinearities is crucial to describe macroscopic laser propagation in a medium, including sum frequency generation, spectral broadening due to self-phase modulation, various ionization processes and soliton formation. For incident laser light the response of the medium is given by the induced polarization of the microscopic system. The polarization is usually expanded in a Taylor series for the electric field amplitude, which is truncated after the first non-linear term being of third order for isotropic media. A third-order nonlinearity leads to the well-known optical Kerr effect, where the refractive index of the medium becomes intensity dependent via n = n0+ n2I. This leads to an inherent problem when modeling laser propagation in two or more spatial dimensions, linked to the formal divergence (n2> 0) of the refractive index for increasing intensity.
We study harmonic generation by a single atom exposed to two short perpendicularly polarized laser pulses. The two perpendicular electric fields oscillate at two different frequencies ${\ensuremath{\omega}}_{1}$ and ${\ensuremath{\omega}}_{2}$. Hence, the resultant field has a polarization which depends on time. Since harmonics are emitted when the resultant oscillating field is linearly polarized, it is expected that a short pulse of harmonics may be emitted if the external field is linearly polarized during a short period of time. We show that, indeed, the atom may emit an ultrashort pulse of a given harmonic. This result has been obtained by time-frequency analyzing the acceleration of the induced dipole moment with a filter whose frequency bandwidth is smaller than twice the frequency of the external field. Our calculation of the dipole acceleration is based on the numerical solution of the time-dependent Schr\"odinger equation. We then address the question of how far it is possible to reduce the duration of the emitted pulse of one given harmonic by adjusting both ${\ensuremath{\omega}}_{1}$ and ${\ensuremath{\omega}}_{2}$ and keeping the amplitude of this pulse significant. In order to answer to this question, we used the quantum version of the two-step model [M. Lewenstein et al., Phys. Rev. A 49, 2117 (1994)].
Introduction In 1961, just a few months after Maiman invented the ruby laser, Franken focused the pulses emitted from such a laser, of wavelength 694 nm, on a quartz plate, and examined the spectrum of the light transmitted using a simple prism (see Figure 7.1). He thus discovered that ultra-violet light of wavelength 347 nm was emerging from the quartz plate. Clearly, as it propagated through the quartz, the light of frequency ω had generated the second harmonic, of frequency 2ω. It thus transpires that in optics, as in any other part of physics, a system subjected to a strong enough sinusoidal excitation will leave the linear response regime. Nonlinearities cause harmonics of the excitation frequency to appear. But what intensity is needed before nonlinear effects will appear? One might think that a natural scale would be the electric field of the nucleus at the location of an atomic electron. In the case of the hydrogen atom in its ground state, this field is about, or 3 × 10 11 V.m −1 . (Here e is the charge of the electron, and a 0 the Bohr radius, of the order of 5 × 10 −11 m). In fact, experiment shows that, in the transparency zone of a dielectric material like quartz, a field of just 10 7 V.m −1 (corresponding to a light intensity of 2.5 kW.cm −2 ) is sufficient for nonlinear effects to appear perturbatively.
We present a simple model for the nonlinear optical response of atomic gases for pulses with center wavelengths in the transparency region and peak fields for which ionization is not prevalent. By comparing with simulations based on the Schrödinger equation for a hydrogen atom we demonstrate that the model accurately captures the dispersion of the nonlinear polarization as well as noninstantaneous effects for a variety of photon energies and also a two-color pulse. Our approach should be of utility in simulating near- and mid-infrared pulse propagation in dielectric media for which extreme nonlinear effects can arise.