We demonstrate an all-optical delay line in hot cesium vapor that tunably delays 275 ps input pulses up to 6.8 ns and 740 input ps pulses up to 59 ns (group index of approximately 200) with little pulse distortion. The delay is made tunable with a fast reconfiguration time (hundreds of ns) by optically pumping out of the atomic ground states.
We demonstrate temporal group delays in coherently-coupled high-Q multi-cavity photonic crystals, in an all-optical analogue to electromagnetically induced transparency. We report deterministic control of the group delay up to 4x the single cavity lifetime in our CMOS-fabricated room-temperature chip. Supported by three-dimensional numerical simulations and theoretical analyses, our multi-pump beam approach enables control of the multi-cavity resonances and inter-cavity phase, in both single and double transparency peaks. The standing-wave wavelength-scale photon localization allows direct scalability for chip-scale optical pulse trapping and coupled-cavity QED.
The Fresnel-Fizeau effect of transverse drag, in which the trajectory of a light beam changes due to transverse motion of the optical medium, is usually extremely small and hard to detect. We observe transverse drag in a moving hot-vapor cell, utilizing slow light due to electromagnetically induced transparency (EIT). The drag effect is enhanced by a factor 360,000, corresponding to the ratio between the light speed in vacuum and the group velocity under EIT conditions. We study the contribution of the thermal atomic motion, which is much faster than the mean medium velocity, and identify the regime where its effect on the transverse drag is negligible.
We uncover a highly nontrivial dependence of the spin-noise (SN) resonance broadening induced by the intense probe beam. The measurements were performed by probing the cell with cesium vapor at the wavelengths of the transition ${6}^2S_{1/2} leftrightarrow {6}^2P_{3/2}$ ($mathrm{D}_2$ line) with the unresolved hyperfine structure of the excited state. The light-induced broadening of the SN resonance was found to differ strongly at different slopes of the $mathrm{D}_2$ line and, generally, varied nonmonotonically with light power. We discuss the effect in terms of the phenomenological Bloch equations for the spin fluctuations and demonstrate that the SN broadening behavior strongly depends on the relation between the pumping and excited-level decay rates, the spin precession, and decoherence rates. To reconcile the puzzling experimental results, we propose that the degree of optical perturbation of the spin-system is controlled by the route of the excited-state relaxation of the atom or, in other words, that the act of optical excitation of the atom does not necessarily break down completely its ground-state coherence and continuity of the spin precession. Spectral asymmetry of the effect, in this case, is provided by the position of the closed transition $F = 4 leftrightarrow F = 5$ at the short-wavelength side of the line. This hypothesis, however, remains to be proven by microscopic calculations.
Transparent materials do not absorb light but have profound influence on the phase evolution of transmitted radiation. One consequence is chromatic dispersion, i.e., light of different frequencies travels at different velocities, causing ultrashort laser pulses to elongate in time while propagating. Here we experimentally demonstrate ultrathin nanostructured coatings that resolve this challenge: we tailor the dispersion of silicon nanopillar arrays such that they temporally reshape pulses upon transmission using slow light effects and act as ultrashort laser pulse compressors. The coatings induce anomalous group delay dispersion in the visible to near-infrared spectral region around 800 nm wavelength over an 80 nm bandwidth. We characterize the arrays performance in the spectral domain via white light interferometry and directly demonstrate the temporal compression of femtosecond laser pulses. Applying these coatings to conventional optics renders them ultrashort pulse compatible and suitable for a wide range of applications.
We present experimental and numerical studies of nonlinear magneto-optical rotation (NMOR) in rubidium vapor excited with resonant light tuned to the $5^2!S_{1/2}rightarrow 6^2!P_{1/2}$ absorption line (421~nm). Contrary to the experiments performed to date on the strong $D_1$ or $D_2$ lines, in this case, the spontaneous decay of the excited state $6^2!P_{1/2}$ may occur via multiple intermediate states, affecting the dynamics, magnitude and other characteristics of NMOR. Comparing the experimental results with the results of modelling based on Auzinsh et al., Phys. Rev. A 80, 1 (2009), we demonstrate that despite the complexity of the structure, NMOR can be adequately described with a model, where only a single excited-state relaxation rate is used.
Ryan M. Camacho
,Michael V. Pack
,John C. Howell
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(2007)
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"Wide-bandwidth, tunable, multiple-pulse-width optical delays using slow light in cesium vapor"
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Ryan Camacho
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