Challenges
Datasets
Workspaces
Papers
Discussions
Leaderboard
Log inSign up
Challenges
Datasets
Workspaces
Papers
Discussions
Leaderboard
Blog
Job Board
Q3AS

© 2026 Aqora Quantum S.A.S.

TermsPrivacyLegal Notice

Journal of the Optical Society of America B

Fluctuating laser field that induces a blueshift in harmonic generation

Emilio Fiordilino, Francesca Morales, Rosalba Daniele

Published Jan 1, 1998• 0 citations
Publisher

Abstract

The spectrum of a two-level atom in the presence of a multimode laser pulse is calculated. The field is allowed to fluctuate in amplitude or in phase; the emitted spectrum has richer emission lines than in the case of the nonfluctuating field and shows peaks shifted toward the blue with respect to the traditional harmonic peaks. The position of the lines is predicted by the formula ω2n+1=(2n+1)(1+Δ)ωL with Δ being a parameter that can be found numerically. In this way the fluctuations seem to result in an effective increase of the laser frequency.

DOI
10.1364/josab.15.000118

Related papers

Laser Pulse Shape Effects in Harmonic Generation from a Two-level Atom

Emilio Fiordilino, Vincenzo Miceli

The harmonic spectrum emitted by a two-level atom driven by a resonant laser field is calculated. The spectrum is seen to depend on the shape of the pulse. In the case of an asymmetric pulse profile, harmonic emission is present also at a relatively low intensity field.

Journal of Modern Optics•Jul 1, 1994•23 citations

Optical mixing of frequencies of a strong bichromatic field interacting with a three-level atom

Constantine Mavroyannis

We have studied the excitation spectrum arising from the optical mixing of the frequencies of a strong bichromatic field interacting with a three-level atom, where the two initially populated modes ωa and ωb are equal to the two atomic transition frequencies, respectively. In the limit of high photon densities, the excitation spectrum near the frequency ω = ωa – 2ωb has been calculated as a function of the parameter η = Ωa2/Ωb2, where Ωa and Ωb are the Rabi frequencies of the two laser fields, respectively. For [Formula: see text] and for weak fields for which [Formula: see text], the spectral function describes a Lorentzian line peaked at the frequency ω = ωa – 2ωb and has a width of the order of γ0, where γ0/2 is the natural width for a two-level atom. When Ωb2 > γ02 and [Formula: see text], the band at ω = ωa – 2ωb splits into two bands described by two Lorentzian lines peaked at ω = ωa – 2ωb ± Ωb/√2 and have spectral widths of the order of 3γ0/4. The ratio of the height of the band ω = ωa – 2ωb to the height ω = ωa – 2ωb ± Ωb/2 is 3:2. The probability amplitudes for both bands take large negative values indicating that optical amplification of the signal field may be expected to occur at these frequencies. When Ωa = Ωb = Ω, η = 1, and for Ω2 < γ02, the spectral function describes a single band at ω = ωa – 2ωb while for Ω2 > γ02, the single band splits into five pairs of bands which are separated from the frequency ω = ωa – 2ωb by frequency shifts which are equal to: ± Ω/√2, [Formula: see text], ± Ω, ± Ω√2, and ± Ω√3, respectively, and have spectral widths of the order of 3γ0/4. For [Formula: see text] and for laser fields for which Ωa2 > γ02 and Ωb2 > γ02, the spectral function consists of three pairs of bands. The probability amplitudes for these bands vary linearly with η and may take large values for [Formula: see text]. A complete discussion of the excitation spectrum as well as a graphical representation of the derived results has been given.

Canadian Journal of Physics•Dec 1, 1981•16 citations

High-order harmonic emission from a three-level atom in a laser field

Pasquale Caldara, Emilio Fiordilino

The spectrum emitted by a three-level atom in the presence of a weak laser field is given together with the population dynamics and the phase of the Fourier transform of the acceleration. Calculations show that the spectrum can be very different from that emitted by a two-level atom. When the trapping conditions are obtained, the coupling to the third level can result in a large change in the spectrum.

Journal of Modern Optics•Apr 1, 1999•6 citations

Wavelet analysis of short harmonics generated in presence of a two colour laser field

Salvatore De Luca, Emilio Fiordilino

The Morlet wavelet spectrum of the radiation emitted by a two level atom in presence of two laser pulses with very close frequency is obtained. The wavelet spectrum gives information on the time evolution of the full spectrum and of a particular line. The beating condition stimulates the atom to emit pulses of harmonics with duration of the order of a few optical cycles of the pumping radiation. Pulse trains of 3 optical cycles (FWHM) are observed.

Journal of Modern Optics•Sep 1, 1998•13 citations

Optical mixing of frequencies of a strong bichromatic field interacting with a three-level atom. II. Numerical results

Constantine Mavroyannis, K.J. Woloschuk, D. A. Hutchinson +1 more

We have numerically calculated the excitation spectra arising from the 3rd order mixing of the frequencies ωa and ωb of two laser fields interacting with a three-level atom, where each laser field resonantly couples the ground state with each excited state of the atom, respectively. In the limit of high photon densities, the excitation spectra near the reduced frequency X = (ω−ωa + 2ωb)/γ0 ≈ 0 are considered as a function of the reduced Rabi frequencies ηa and ηb of the two laser fields, respectively and γ0 is the spontaneous emission probability. For ηa < ηb the spectra consist of a doublet peaked at [Formula: see text] and its intensity is constant. When ηa = ηb, the spectra are composed of five pairs of bands peaked at [Formula: see text], and [Formula: see text]. When ηa < ηb the computed spectra consist of five pairs of bands, where the intensities of the peaks at [Formula: see text] and [Formula: see text] are positive indicating absorption, those at [Formula: see text] are negative implying amplification, and the two pairs of peaks at [Formula: see text] have positive and negative components describing the mixed process of absorption–amplification. The intensities of these bands are found to vary as (ηa/ηb)2 for (ηa/ηb) > 1 and, therefore, the intensities of the bands are immensely enhanced as the value of the ratio (ηa/ηb) increases. The computed spectra for a wide selection of Rabi frequencies are graphically presented and compared with those derived by analytical methods.

Canadian Journal of Physics•Feb 1, 1982•14 citations

Theory of resonance fluorescence in a fluctuating laser field

W. Vogel, D.‐G. Welsch, K. Wódkiewicz

A method of calculation of multiple-time correlation functions of the resonance fluorescence light from a two-level atom driven by a realistic laser field with phase and amplitude fluctuations is developed. Both kinds of fluctuations are assumed to be Gaussian. The phase fluctuations are treated in the phase-diffusion model. The averaging over the amplitude fluctuations can be performed in a closed way when the relative mean-square amplitude fluctuation is small compared with the ratio of the amplitude correlation decay rate to the characteristic atomic relaxation rate. There is no restriction to Markovian amplitude fluctuations. Arbitrary values for the mean Rabi frequency are allowed. Results are presented for the intensity, the intensity correlation function, and the spectrum of the fluorescent light. It is shown that even in the case when the relative strength of the amplitude fluctuations is small, significant effects can occur due to the finite correlation length of the fluctuations. The results for fast amplitude correlation decay correspond to the situation without amplitude fluctuations. When the correlation time of the amplitude fluctuations becomes comparable with the atomic relaxation times, the Rabi oscillations of the intensity and the intensity correlation function are nearly washed out, and non-Lorentzian line shapes for the side peaks in the spectrum are observed. It is found that the ratio of the heights of the central peak to the side peak increases with increasing correlation time.

Physical Review A•Sep 1, 1983•20 citations
The spectrum of a two-level atom in the presence of a multimode laser pulse is calculated. The field is allowed to fluctuate in amplitude or in phase; the emitted spectrum has richer emission lines than in the case of the nonfluctuating field and shows peaks shifted toward the blue with respect to the traditional harmonic peaks. The position of the lines is predicted by the formula ω2n+1=(2n+1)(1+Δ)ωL with Δ being a parameter that can be found numerically. In this way the fluctuations seem to result in an effective increase of the laser frequency.
We have studied the excitation spectrum arising from the optical mixing of the frequencies of a strong bichromatic field interacting with a three-level atom, where the two initially populated modes ωa and ωb are equal to the two atomic transition frequencies, respectively. In the limit of high photon densities, the excitation spectrum near the frequency ω = ωa – 2ωb has been calculated as a function of the parameter η = Ωa2/Ωb2, where Ωa and Ωb are the Rabi frequencies of the two laser fields, respectively. For [Formula: see text] and for weak fields for which [Formula: see text], the spectral function describes a Lorentzian line peaked at the frequency ω = ωa – 2ωb and has a width of the order of γ0, where γ0/2 is the natural width for a two-level atom. When Ωb2 > γ02 and [Formula: see text], the band at ω = ωa – 2ωb splits into two bands described by two Lorentzian lines peaked at ω = ωa – 2ωb ± Ωb/√2 and have spectral widths of the order of 3γ0/4. The ratio of the height of the band ω = ωa – 2ωb to the height ω = ωa – 2ωb ± Ωb/2 is 3:2. The probability amplitudes for both bands take large negative values indicating that optical amplification of the signal field may be expected to occur at these frequencies. When Ωa = Ωb = Ω, η = 1, and for Ω2 < γ02, the spectral function describes a single band at ω = ωa – 2ωb while for Ω2 > γ02, the single band splits into five pairs of bands which are separated from the frequency ω = ωa – 2ωb by frequency shifts which are equal to: ± Ω/√2, [Formula: see text], ± Ω, ± Ω√2, and ± Ω√3, respectively, and have spectral widths of the order of 3γ0/4. For [Formula: see text] and for laser fields for which Ωa2 > γ02 and Ωb2 > γ02, the spectral function consists of three pairs of bands. The probability amplitudes for these bands vary linearly with η and may take large values for [Formula: see text]. A complete discussion of the excitation spectrum as well as a graphical representation of the derived results has been given.
We have numerically calculated the excitation spectra arising from the 3rd order mixing of the frequencies ωa and ωb of two laser fields interacting with a three-level atom, where each laser field resonantly couples the ground state with each excited state of the atom, respectively. In the limit of high photon densities, the excitation spectra near the reduced frequency X = (ω−ωa + 2ωb)/γ0 ≈ 0 are considered as a function of the reduced Rabi frequencies ηa and ηb of the two laser fields, respectively and γ0 is the spontaneous emission probability. For ηa < ηb the spectra consist of a doublet peaked at [Formula: see text] and its intensity is constant. When ηa = ηb, the spectra are composed of five pairs of bands peaked at [Formula: see text], and [Formula: see text]. When ηa < ηb the computed spectra consist of five pairs of bands, where the intensities of the peaks at [Formula: see text] and [Formula: see text] are positive indicating absorption, those at [Formula: see text] are negative implying amplification, and the two pairs of peaks at [Formula: see text] have positive and negative components describing the mixed process of absorption–amplification. The intensities of these bands are found to vary as (ηa/ηb)2 for (ηa/ηb) > 1 and, therefore, the intensities of the bands are immensely enhanced as the value of the ratio (ηa/ηb) increases. The computed spectra for a wide selection of Rabi frequencies are graphically presented and compared with those derived by analytical methods.
A method of calculation of multiple-time correlation functions of the resonance fluorescence light from a two-level atom driven by a realistic laser field with phase and amplitude fluctuations is developed. Both kinds of fluctuations are assumed to be Gaussian. The phase fluctuations are treated in the phase-diffusion model. The averaging over the amplitude fluctuations can be performed in a closed way when the relative mean-square amplitude fluctuation is small compared with the ratio of the amplitude correlation decay rate to the characteristic atomic relaxation rate. There is no restriction to Markovian amplitude fluctuations. Arbitrary values for the mean Rabi frequency are allowed. Results are presented for the intensity, the intensity correlation function, and the spectrum of the fluorescent light. It is shown that even in the case when the relative strength of the amplitude fluctuations is small, significant effects can occur due to the finite correlation length of the fluctuations. The results for fast amplitude correlation decay correspond to the situation without amplitude fluctuations. When the correlation time of the amplitude fluctuations becomes comparable with the atomic relaxation times, the Rabi oscillations of the intensity and the intensity correlation function are nearly washed out, and non-Lorentzian line shapes for the side peaks in the spectrum are observed. It is found that the ratio of the heights of the central peak to the side peak increases with increasing correlation time.