Search results for "physics.atom-ph"
showing 10 items of 395 documents
Domains of time-dependent density-potential mappings
2011
The key element in time-dependent density functional theory is the one-to-one correspondence between the one-particle density and the external potential. In most approaches this mapping is transformed into a certain type of Sturm-Liouville problem. Here we give conditions for existence and uniqueness of solutions and construct the weighted Sobolev space they lie in. As a result the class of v-representable densities is considerably widened with respect to previous work.
Sympathetic cooling of a trapped proton mediated by an LC circuit
2021
Efficient cooling of trapped charged particles is essential to many fundamental physics experiments1,2, to high-precision metrology3,4 and to quantum technology5,6. Until now, sympathetic cooling has required close-range Coulomb interactions7,8, but there has been a sustained desire to bring laser-cooling techniques to particles in macroscopically separated traps5,9,10, extending quantum control techniques to previously inaccessible particles such as highly charged ions, molecular ions and antimatter. Here we demonstrate sympathetic cooling of a single proton using laser-cooled Be+ ions in spatially separated Penning traps. The traps are connected by a superconducting LC circuit that enable…
Sympathetic cooling of protons and antiprotons with a common endcap Penning trap.
2017
We present an experiment to sympathetically cool protons and antiprotons in a Penning trap by resonantly coupling the particles to laser cooled beryllium ions using a common endcap technique. Our analysis shows that preparation of (anti)protons at mK temperatures on timescales of tens of seconds is feasible. Successful implementation of the technique will have immediate and significant impact on high-precision comparisons of the fundamental properties of protons and antiprotons. This in turn will provide some of the most stringent tests of the fundamental symmetries of the Standard Model.
Théorie des spectres rovibroniques des molécules octaédriques : Hamiltonien et moments de transition
2002
This thesis is devoted to the treatment of rovibronic couplings of octahedral species for which the Born-Oppenheimer approximation is broken down. By using the octahedral formalism, a full effective rovibronic model is extended from works about molecules in a non-degenerate electronic state. This effective model is dedicated to molecules with an odd or an even number of electrons and it has been successfully applied to V(CO)6 and ReF6. For both of them we have four interacting vibronic sublevels attributed to a dynamical Jahn-Teller effect and giving rise to very complicated spectra. This model is validated by the overall agreement between predicted and observed band profiles. Moreover, an …
Rubidium dimers in paraffin-coated cells
2010
Measurements were made to determine the density of rubidium dimer vapor in paraffin-coated cells. The number density of dimers and atoms in similar paraffin-coated and uncoated cells was measured by optical spectroscopy. Due to the relatively low melting point of paraffin, a limited temperature range of 43-80 deg C was explored, with the lower end corresponding to a dimer density of less than 10^7 cm^(-3). With one-minute integration time, a sensitivity to dimer number density of better than 10^6 cm^(-3) was achieved. No significant difference in dimer density was observed between the cells.
Simulating pump-probe photo-electron and absorption spectroscopy on the attosecond time-scale with time-dependent density-functional theory
2013
Molecular absorption and photoelectron spectra can be efficiently predicted with real-time time-dependent density functional theory. We show herein how these techniques can be easily extended to study time-resolved pump-probe experiments, in which a system response (absorption or electron emission) to a probe pulse is measured in an excited state. This simulation tool helps with the interpretation of fast-evolving attosecond time-resolved spectroscopic experiments, in which electronic motion must be followed at its natural timescale. We show how the extra degrees of freedom (pump-pulse duration, intensity, frequency, and time delay), which are absent in a conventional steady-state experimen…
Observation of laser-induced field-free permanent planar alignment of molecules
2011
International audience; Permanent planar alignment of gas-phase linear molecules is achieved by a pair of delayed perpendicularly polarized short laser pulses. The experiment is performed in a supersonic jet, ensuring a relatively high number density of molecules with moderately low rotational temperature. The effect is optically probed on a femtosecond time scale by the use of a third short pulse, enabling a time-resolved birefringence detection performed successively in two perpendicular planes of the laboratory frame. The technique allows for an unambiguous estimation of the molecular planar delocalization produced within the polarization plane of the pulse pair after the turn-off of the…
Hyperfine Paschen-Back regime realized in Rb nanocell
2012
A simple and efficient scheme based on one-dimensional nanometric thin cell filled with Rb and strong permanent ring magnets allowed direct observation of hyperfine Paschen-Back regime on D1 line in 0.5 - 0.7 T magnetic field. Experimental results are perfectly consistent with the theory. In particular, with sigma+ laser excitation, the slopes of B-field dependence of frequency shift for all the 10 individual transitions of 85,87Rb are the same and equal to 18.6 MHz/mT. Possible applications for magnetometry with submicron spatial resolution and tunable atomic frequency references are discussed.
Isotope Shifts of Radium Monofluoride Molecules
2021
Isotope shifts of $^{223-226,228}$Ra$^{19}$F were measured for different vibrational levels in the electronic transition $A^{2}{}{\Pi}_{1/2}\leftarrow X^{2}{}{\Sigma}^{+}$. The observed isotope shifts demonstrate the particularly high sensitivity of radium monofluoride to nuclear size effects, offering a stringent test of models describing the electronic density within the radium nucleus. Ab initio quantum chemical calculations are in excellent agreement with experimental observations. These results highlight some of the unique opportunities that short-lived molecules could offer in nuclear structure and in fundamental symmetry studies.
Alignement moléculaire sous impulsions laser ultracourtes
2006
Talk given by O. Faucher; National audience