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Frontiers in Optics

A Double Resonance Atomic Prism

David J. Starling, Steven M. Bloch, Praveen K. Vudyasetu, Joseph S. Choi, Bethany Little, John C. Howell

Published Jan 1, 2012• 0 citations
Publisher

Abstract

We demonstrate an atomic prism exhibiting high spectral resolution by discriminating frequency modes 50 MHz apart. We achieve high transmission by working between two rubidium resonances and spatially separate beams resulting from four-wave mixing [1].
DOI
10.1364/fio.2012.fth3d.4

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We present an atomic prism spectrometer that utilizes the steep linear dispersion between two strongly absorbing hyperfine resonances of rubidium. We resolve spectral lines 50 MHz apart and, utilizing a larger part of the available spectrum than only between the two resonances, we spatially separate collinear pump, signal, and idler beams resulting from a four-wave mixing process. Due to the high transparency possible between the resonances, these results have applications in the filtering of narrow-band entangled photons and interaction-free measurements.
This thesis presents the applications of some of the coherent processes in a three-level atomic system, to control spatial and temporal properties of a signal pulse. We use two Raman absorption resonances in rubidium vapor separated by a few MHz to achieve a rapidly tunable slow-light system. We control the slow-light characteristics all-optically by tuning the frequency and power of a coupling beam. A dual absorption slow-light system is known to cause less pulse broadening than a single transmission resonance system, and thus, a tunable double absorption system is advantageous. We use a four-wave mixing process to demonstrate pulse storage in rubidium vapor for times much greater than the pulse width. We demonstrate storage of both the temporal and spatial profile of the pulse. We overcome the diffusion of spatial information during the storage in warm atomic vapor by storing the Fourier transform of the image instead of an image with a flat phase. The Raman absorption resonance is also used to control the transverse refractive index profile of the signal beam. The refractive index of the signal interacting with a coupling beam in a Raman process is dependent on the coupling beam intensity. We use a first order Laguerre-Gaussian (LG01) coupling beam to create a waveguide like transverse refractive index profile. We demonstrate propagation of a focused signal beam for lengths much greater than the Rayleigh length. Finally, we demonstrate a dual absorption atomic prism, which is capable
Abstract A cell with a submicron thickness was used to measure the broadening and shift of the D1 and D2 lines of Rb atoms by neon. The resolution of hypefine components is achieved by a combination of two techniques. First, the Rb vapor column thickness in the direction of propagation of the laser radiation was chosen equal to half of its wavelength λ under conditions of resonance with the atomic transition frequency. For rubidium atoms λ/2 ~ 400 nm. At a nanocell thickness L ~ λ/2, in the transmission spectrum A(ν), the spectral lines of atomic transitions are narrowed due to the exclusion of Doppler broadening. Second, further narrowing of the detected signals was achieved by the double differentiation of the transmission spectrum, A''(ν). The transmission spectra of pure rubidium vapor and rubidium vapor with the addition of neon have been measured at different pressures. The measured values of the shift coefficients of the D1 and D2 lines of rubidium in the presence of Ne were –1.1 ± 0.2 MHz/Torr and –2.1 ± 0.2 MHz/Torr, respectively. The broadening coefficients of the D1 and D2 lines coincide and are equal to 10 ± 1 MHz/Torr. Due to its high spectral resolution, this technique allows separate measurements for each individual transition.