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Quantum Electronics and Laser Science Conference

Software atom in laser spectroscopy

Juha Javanainen

Published May 2, 1993• 0 citations
OpenAlex

Abstract

We have developed computer programs for numerical experiments on laser-atom interactions. First, subroutines have been written that build a software atom with an arbitrary level scheme from elementary specifications, such as angular momenta and energies of the atomic levels. Second, the key operations of the semiclassical theory of laser spectroscopy have been implemented as transformations acting on the software atom. The software atom was initially used in investigations of the motion of an atom in three-dimensional optical molasses,1 Here we discuss two new applications, saturation and resonance fluorescence of a multistate atom.

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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.

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Laser spectroscopy of hot atomic vapours: from ’scope to theoretical fit

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Abstract The spectroscopy of hot atomic vapours is a hot topic. Many of the work-horse techniques of contemporary atomic physics were first demonstrated in hot vapours. Alkali-metal atomic vapours are ideal media for quantum-optics experiments as they combine: a large resonant optical depth; long coherence times; and well-understood atom–atom interactions. These features aid with the simplicity of both the experimental set up and the theoretical framework. The topic attracts much attention as these systems are ideal for studying both fundamental physics and has numerous applications, especially in sensing electromagnetic fields and quantum technology. This tutorial reviews the necessary theory to understand the Doppler broadened absorption spectroscopy of alkali-metal atoms, and explains the data taking and processing necessary to compare theory and experiment. The aim is to provide a gentle introduction to novice scientists starting their studies of the spectroscopy of thermal vapours while also calling attention to the application of these ideas in the contemporary literature. In addition, the work of expert practitioners in the field is highlighted, explaining the relevance of three extensively-used software packages that complement the presentation herein.

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In two recent experiments Verkerk et al. and our group have observed quantization of the center-of-mass motion of laser cooled atoms in sub-wavelength sized potential wells formed by the light field of a 1-dimensional optical molasses. Our 1-dimensional optical molasses consists of a pair of counterpropagating laser beams of orthogonal, linear polarization, creating a series of potential wells separated by {lambda}/4. Polarization gradient laser cooling reduces the thermal energy of the atoms until they are trapped in well resolved vibrational levels near the bottom of the wells. Transitions between these vibrational levels are seen in a high resolution spectrum of fluorescence, where they give rise to a Rayleigh peak centered at the laser frequency, and well resolved Raman sidebands shifted by a frequency {plus_minus}{omega}, typically on the order of 100 kHz. We find quantitative agreement between the measured level separation h{omega} and the results of a calculation of the bandstructure in the periodic optical potential. Based on the observed ratio of the strength of the blue to the red sideband we determine the temperature of the atoms, and find agreement with theoretical predictions. Based on the level spacing and temperature we find the atoms to be localized to {approx}/15, withmore » up to 50-60% of the population of the trapped atoms in the vibrational ground state. We observe intriguing differences between fluorescence radiated by localized atoms, and the fluorescence radiated by non-localized atoms in a 1-dimensional optical molasses composed of a pair of counterpropagating laser beams of opposite circular polarization. The prospect of observing quantum motion and spatial order in 2 and 3 dimensions, and the consequences for the spectrum of fluorescence, will be discussed.« less

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Wiley eBooks•Feb 17, 2010•48 citations
We have developed computer programs for numerical experiments on laser-atom interactions. First, subroutines have been written that build a software atom with an arbitrary level scheme from elementary specifications, such as angular momenta and energies of the atomic levels. Second, the key operations of the semiclassical theory of laser spectroscopy have been implemented as transformations acting on the software atom. The software atom was initially used in investigations of the motion of an atom in three-dimensional optical molasses,1 Here we discuss two new applications, saturation and resonance fluorescence of a multistate atom.
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 Jg{\mathit{J}}_{\mathit{g}}Jg​=1\ensuremath{\rightarrow}Je{\mathit{J}}_{\mathit{e}}Je​=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.
Abstract The spectroscopy of hot atomic vapours is a hot topic. Many of the work-horse techniques of contemporary atomic physics were first demonstrated in hot vapours. Alkali-metal atomic vapours are ideal media for quantum-optics experiments as they combine: a large resonant optical depth; long coherence times; and well-understood atom–atom interactions. These features aid with the simplicity of both the experimental set up and the theoretical framework. The topic attracts much attention as these systems are ideal for studying both fundamental physics and has numerous applications, especially in sensing electromagnetic fields and quantum technology. This tutorial reviews the necessary theory to understand the Doppler broadened absorption spectroscopy of alkali-metal atoms, and explains the data taking and processing necessary to compare theory and experiment. The aim is to provide a gentle introduction to novice scientists starting their studies of the spectroscopy of thermal vapours while also calling attention to the application of these ideas in the contemporary literature. In addition, the work of expert practitioners in the field is highlighted, explaining the relevance of three extensively-used software packages that complement the presentation herein.
We study theoretically the spectrum of resonance fluoresence from one-dimensional molasses consisting of two-level atoms with Zeeman substructure. The center-of-mass motion of the atom is treated fully quantum mechanically. The spectrum shows sidebands due to transitions between vibrational levels in optical potentials generated by the laser light. Detailed results are presented for the Jg{\mathit{J}}_{\mathit{g}}Jg​=1/2\ensuremath{\rightarrow}Je{\mathit{J}}_{\mathit{e}}Je​=3/2 atomic transition in a laser configuration with two counterpropagating waves with orthogonal polarizations. We have solved the corresponding quantum master equation and calculated the relevant autocorrelation function of the atomic dipole using (i) a direct numerical solution of the master equation, (ii) a wave-function simulation of the master equation and correlation function employing periodic time-dependent Bloch wave functions, and (iii) a semiclassical bipotential calculation for the spectrum including a simple quantum correction.
In two recent experiments Verkerk et al. and our group have observed quantization of the center-of-mass motion of laser cooled atoms in sub-wavelength sized potential wells formed by the light field of a 1-dimensional optical molasses. Our 1-dimensional optical molasses consists of a pair of counterpropagating laser beams of orthogonal, linear polarization, creating a series of potential wells separated by {lambda}/4. Polarization gradient laser cooling reduces the thermal energy of the atoms until they are trapped in well resolved vibrational levels near the bottom of the wells. Transitions between these vibrational levels are seen in a high resolution spectrum of fluorescence, where they give rise to a Rayleigh peak centered at the laser frequency, and well resolved Raman sidebands shifted by a frequency {plus_minus}{omega}, typically on the order of 100 kHz. We find quantitative agreement between the measured level separation h{omega} and the results of a calculation of the bandstructure in the periodic optical potential. Based on the observed ratio of the strength of the blue to the red sideband we determine the temperature of the atoms, and find agreement with theoretical predictions. Based on the level spacing and temperature we find the atoms to be localized to {approx}/15, withmore » up to 50-60% of the population of the trapped atoms in the vibrational ground state. We observe intriguing differences between fluorescence radiated by localized atoms, and the fluorescence radiated by non-localized atoms in a 1-dimensional optical molasses composed of a pair of counterpropagating laser beams of opposite circular polarization. The prospect of observing quantum motion and spatial order in 2 and 3 dimensions, and the consequences for the spectrum of fluorescence, will be discussed.« less
Covering the most important knowledge on optical pumping of atoms, this ready reference is backed by numerous examples of modelling computation for optical pumped systems. The authors show for the first time that modern scientific computing software makes it practical to analyze the full, multilevel system of optically pumped atoms. To make the discussion less abstract, the authors have illustrated key points with sections of MATLAB codes. To make most effective use of contemporary mathematical software, it is especially useful to analyze optical pumping situations in the Liouville spa