Fluorescence spectrum of optical molasses

Early experiments on ultracold optical molasses relied on time-of-flight and other ballistic techniques to measure the temperature of atoms released from the molasses.1,2 At the extremely low temperatures observed, the size of the molasses, the effects of gravity, the probe that detected the falling atoms, and the way in which the laser beams forming the molasses were turned off produced a large systematic uncertainty in the temperature determination. Here, we report a direct measurement of the Doppler width of the fluorescence spectrum of Na atoms still viscously confined in the molasses. We determined this spectrum using an optical heterodyne technique and we believe this to be the first time an atomic fluorescence spectrum has been heterodyned. The temperature deduced from the Doppler width is in good agreement with that determined using improved time-of-flight techniques. The heterodyne technique has the added advantage of providing spatially resolved temperature measurements. In addition to the nominally 600-kHz wide Doppler peak, we see a much narrower (60-kHz wide) peak which we tentatively ascribe to Dicke narrowing due to confinement by optical forces.Early experiments on ultracold optical molasses relied on time-of-flight and other ballistic techniques to measure the temperature of atoms released from the molasses.1,2 At the extremely low temperatures observed, the size of the molasses, the effects of gravity, the probe that detected the falling atoms, and the way in which the laser beams forming the molasses were turned off produced a large systematic uncertainty in the temperature determination. Here, we report a direct measurement of the Doppler width of the fluorescence spectrum of Na atoms still viscously confined in the molasses. We determined this spectrum using an optical heterodyne technique and we believe this to be the first time an atomic fluorescence spectrum has been heterodyned. The temperature deduced from the Doppler width is in good agreement with that determined using improved time-of-flight techniques. The heterodyne technique has the added advantage of providing spatially resolved temperature measurements. In addition to the nominally 600-kHz wide Doppler peak, we see a much narrower (60-kHz wide) peak which we tentatively ascribe to Dicke narrowing due to confinement by optical forces.

Annual Meeting Optical Society of AmericaJan 1, 19890 citations

Spectrum of resonance fluorescence and cooling dynamics in quantized one-dimensional molasses: Effects of laser configuration

Richard Taïeb, P. Marte, Ralph Dum +1 more

We study theoretically the spectrum of resonance fluorescence and laser-cooling dynamics corresponding to quantized atomic motion in one-dimensional optical molasses. We consider an atom with a ${\mathit{J}}_{\mathit{g}}$ =1\ensuremath{\rightarrow} ${\mathit{J}}_{\mathit{e}}$ =2 transition interacting with two counterpropagating laser beams. The laser light is assumed to be linearly polarized with an angle \ensuremath{\theta} between the polarization vectors. We discuss the spectrum of resonance fluorescence, the spectroscopy of band structure in the optical potentials, and the population of the vibrational quantum levels as a function of the angle between the polarization vectors.We study theoretically the spectrum of resonance fluorescence and laser-cooling dynamics corresponding to quantized atomic motion in one-dimensional optical molasses. We consider an atom with a ${\mathit{J}}_{\mathit{g}}$=1\ensuremath{\rightarrow}${\mathit{J}}_{\mathit{e}}$=2 transition interacting with two counterpropagating laser beams. The laser light is assumed to be linearly polarized with an angle \ensuremath{\theta} between the polarization vectors. We discuss the spectrum of resonance fluorescence, the spectroscopy of band structure in the optical potentials, and the population of the vibrational quantum levels as a function of the angle between the polarization vectors.

Physical Review AJun 1, 199321 citations

We study theoretically the spectrum of resonance fluorescence and laser-cooling dynamics corresponding to quantized atomic motion in one-dimensional optical molasses. We consider an atom with a

{\mathit{J}}_{\mathit{g}}

=1\ensuremath{\rightarrow}

{\mathit{J}}_{\mathit{e}}

=2 transition interacting with two counterpropagating laser beams. The laser light is assumed to be linearly polarized with an angle \ensuremath{\theta} between the polarization vectors. We discuss the spectrum of resonance fluorescence, the spectroscopy of band structure in the optical potentials, and the population of the vibrational quantum levels as a function of the angle between the polarization vectors.