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Register a new userForbidden atomic transitions driven by an intensity-modulated laser trap
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Spectroscopy is an essential tool in understanding and manipulating quantum systems, such as atoms and molecules. The model describing spectroscopy includes a multipole-field interaction, which leads to established spectroscopic selection rules, and an interaction that is quadratic in the field, which is often neglected. However, spectroscopy using the quadratic (ponderomotive) interaction promises two significant advantages over spectroscopy using the multipole-field interaction: flexible transition rules and vastly improved spatial addressability of the quantum system. For the first time, we demonstrate ponderomotive spectroscopy by using optical-lattice-trapped Rydberg atoms, pulsating the lattice light at a microwave frequency, and driving a microwave atomic transition that would otherwise be forbidden by established spectroscopic selection rules. This new ability to measure frequencies of previously inaccessible transitions makes possible improved determinations of atomic characteristics and constants underlying physics. In the spatial domain, the resolution of ponderomotive spectroscopy is orders of magnitude better than the transition frequency (and the corresponding diffraction limit) would suggest, promising single-site addressability in a dense particle array for quantum control and computing applications. Future advances in technology may allow ponderomotive spectroscopy to be extended to ground-state atoms and trapped molecules.
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We report the first observation of a non-dipole transition in an ultra-cold atomic vapor. We excite the 3P-4P electric quadrupole (E2) transition in $^{23}$Na confined in a Magneto-Optical Trap(MOT), and demonstrate its application to high-resolution spectroscopy by making the first measurement of the hyperfine structure of the 4P$_{1/2}$ level and extracting the magnetic dipole constant A $=$ 30.6 $pm$ 0.1 MHz. We use cw OODR (Optical-Optical Double Resonance) accompanied by photoinization to probe the transition.
Magnetic field-induced giant modification of probabilities for seven components of 6S1/2 (Fg=3) - 6P3/2 (Fe=5) transition of Cs D2 line forbidden by selection rules is observed experimentally for the first time. For the case of excitation with circularly-polarized laser radiation, the probability of Fg=3,mF=-3 - Fe=5,mF=-2 transition becomes the largest among 25 transitions of Fg=3 - Fe=2,3,4,5 group in a wide range of magnetic field 200 - 3200 G. Moreover, the modification is the largest among D2 lines of alkali metals. A half-wave-thick cell (length along the beam propagation axis L=426 nm) filled with Cs has been used in order to achieve sub-Doppler resolution which allows for separating the large number of atomic transitions that appear in the absorption spectrum when an external magnetic field is applied. For B > 3 kG the group of seven transitions Fg=3 - Fe=5 is completely resolved and is located at the high frequency wing of Fg=3 - Fe=2,3,4 transitions. The applied theoretical model very well describes the experimental curves.
Increasing ellipticity usually suppresses the recollision probability drastically. In contrast, we report on a recollision channel with large return energy and a substantial probability, regardless of the ellipticity. The laser envelope plays a dominant role in the energy gained by the electron, and in the conditions under which the electron comes back to the core. We show that this recollision channel eciently triggers multiple ionization with an elliptically polarized pulse.
We simultaneously trap ultracold lithium and cesium atoms in an optical dipole trap formed by the focus of a CO$_2$ laser and study the exchange of thermal energy between the gases. The cesium gas, which is optically cooled to $20 mu$K, efficiently decreases the temperature of the lithium gas through sympathetic cooling. The measured cross section for thermalizing $^{133}$Cs-$^7$Li collisions is $8 times 10^{-12}$ cm$^2$, for both species in their lowest hyperfine ground state. Besides thermalization, we observe evaporation of lithium purely through elastic cesium-lithium collisions (sympathetic evaporation).
We present temporal intensity correlation measurements of light scattered by a hot atomic vapor. Clear evidence of photon bunching is shown at very short time-scales (nanoseconds) imposed by the Doppler broadening of the hot vapor. Moreover, we demonstrate that relevant information about the scattering process, such as the ratio of single to multiple scattering, can be deduced from the measured intensity correlation function. These measurements confirm the interest of temporal intensity correlation to access non-trivial spectral features, with potential applications in astrophysics.
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