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Physical Review A

Efficient frequency conversion of incoherent fluorescent light

M. Katsuragawa, Jian Liang, Fam Le Kien, K. Hakuta

Published Jan 3, 2002• 35 citations
Publisher

Abstract

We demonstrate efficient replication of an incoherent fluorescent light with the ${1770\ensuremath{-}\mathrm{c}\mathrm{m}}^{\mathrm{\ensuremath{-}}1}$ broad bandwidth into its Raman sidebands with frequency spacing of 4150 ${\mathrm{cm}}^{\mathrm{\ensuremath{-}}1}$ in a thin hydrogen crystal. We achieve a high conversion efficiency of 22% per sideband using a sufficiently large Raman coherence prepared by two collinearly propagating ns laser fields.

DOI
10.1103/physreva.65.025801

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Journal of Nonlinear Optical Physics & Materials•Dec 1, 2004•2 citations
We demonstrate efficient replication of an incoherent fluorescent light with the 1770\ensuremath−cm\ensuremath−1{1770\ensuremath{-}\mathrm{c}\mathrm{m}}^{\mathrm{\ensuremath{-}}1}1770\ensuremath−cm\ensuremath−1 broad bandwidth into its Raman sidebands with frequency spacing of 4150 cm\ensuremath−1{\mathrm{cm}}^{\mathrm{\ensuremath{-}}1}cm\ensuremath−1 in a thin hydrogen crystal. We achieve a high conversion efficiency of 22% per sideband using a sufficiently large Raman coherence prepared by two collinearly propagating ns laser fields.
Summary form only given. Recently we have shown using solid hydrogen that stimulated Raman scattering (SRS) can evolve spontaneously from the weak-coupling regime to the strong-coupling regime in which parametric anti-Stokes generation occurs without the restriction of phase-matching. In the present work, we extend this strong-coupling SRS to a more general parametric Raman sideband generation. We show using solid hydrogen as a nonlinear medium that the adiabatically-prepared Raman-coherence can beat with broadband incoherent fluorescence light and efficiently replicate the incoherence nature to the Raman sideband.
Parametric Raman sideband generation is investigated using strongly driven Raman coherence in solid hydrogen. We show that the Raman coherence prepared with two coaxial single-mode lasers beats with multimode laser radiation with very broad bandwidth and efficiently replicates the broadband nature to the Raman sidebands without the restriction of phase matching. We demonstrate that this efficient replication occurs mainly on the negative side of Raman detuning, where the medium adiabatically follows the antiphased state.
Recent experiments have shown that coherent molecular oscillations may generate a comb of coherent collinear sidebands with 50,000 cm/sup -1/ of spectral bandwidth. The essence of this technique is the use of a Raman transition with a sufficiently large coherence that the generation and phase slip length are of the same order. The coherence is established by driving the molecular transition with two single-mode laser fields slightly detuned from the Raman resonance, so as to excite a single molecular superposition state. This talk will summarize the characteristics of this light source and describe two recent experiments which show the mutual coherence of the generated sidebands.
We demonstrate the efficient generation of Raman sidebands in a medium coherently prepared in a dark state by continuous-wave low-intensity laser radiation. Our experiment is performed in sodium vapor excited in $\ensuremath{\Lambda}$ configuration on the D1{D}_{1}D1​ line by two laser fields of resonant frequencies ${\ensuremath{\omega}}_{1}$ and ${\ensuremath{\omega}}_{2},$ and probed by a third field ${\ensuremath{\omega}}_{3}.$ First-order sidebands for frequencies ${\ensuremath{\omega}}_{1},$ ${\ensuremath{\omega}}_{2}$ and up to the third-order sidebands for frequency ${\ensuremath{\omega}}_{3}$ are observed. The generation starts at a power as low as 10 \ensuremath{\mu}W for each input field. Dependences of the intensities of both input and generated waves on the frequency difference $({\ensuremath{\omega}}_{1}\ensuremath{-}{\ensuremath{\omega}}_{2}),$ on the frequency ${\ensuremath{\omega}}_{3},$ and on the optical density are investigated.
We use molecular deuterium and two driving lasers to demonstrate collinear generation of mutually coherent equidistant sidebands, covering $50000{\mathrm{cm}}^{\ensuremath{-}1}$ of spectral bandwidth and ranging from $2.94\ensuremath{\mu}\mathrm{m}$ to 195 nm in wavelength. The essential idea is the adiabatic preparation of a single, highly coherent ( $|{\ensuremath{\rho}}_{\mathrm{ab}}|\phantom{\rule{0ex}{0ex}}=\phantom{\rule{0ex}{0ex}}0.33$) molecular eigenstate.
We investigated the Raman coherence characteristics in the solid hydrogen film deposited on a sapphire substrate. By using Raman coherence prepared with two single-frequency pulsed lasers, we generated the multiorder coherent Raman sidebands in solid hydrogen film. High-order Raman sidebands were obtained under strong pumping conditions (≥230 MW/cm2). The generated anti-Stokes(AS)–Raman sidebands extended from ultraviolet (292 nm for AS5 band) to visible (565 nm for AS1 band) region. The multiorder Raman sideband generation is thought to be due to the parametric coupling of pump and coupling lasers. The frequency conversion efficiency shows the maximum (14%) at the pumping intensity of 360 MW/cm2. From the experiment that makes the multimode probe beam beat with the prepared Raman coherence, we found that the prepared Raman coherence replicates the probe beam to its Raman sidebands.