Cold rubidium molecule formation through photoassociation: A spectroscopic study of the 0(g)(-) long-range state of Rb-87(2)

Year: 2001

Authors: Fioretti A., Amiot C., Dion C.M., Dulieu O., Mazzoni M., Smirne G., Gabbanini C.

Autors Affiliation: Istituto di Fisica Atomica e Molecolare del C.N.R., via Alfieri 1, 56010 Ghezzano, Pisa, Italy
Universita’ di Pisa, Dipartimento di Fisica, Unita’ INFM, piazza Torricelli 2, 56126 Pisa, Italy
Laboratoire Aimé Cotton, Université Paris-Sud, 91405 Orsay Cedex, France
Istituto di Elettronica Quantistica del C.N.R., via Panciatichi 56, 50127 Firenze, Italy

Abstract: We report the detailed analysis of translationally cold rubidium molecule formation through photoassociation. Cold molecules are formed after spontaneous decay of photoexcited molecules from a laser cooled atomic sample, and are detected by selective mass spectroscopy after two-photon ionization into Rb-2(+) ions. A spectroscopic study of the 0(g)(-)(5S + 5P(3/2)) pure long-range state of Rb-87(2) is performed by detecting the ion yield as a function of the photoassociation laser frequency the spectral data are theoretically analyzed within the semiclassical RKR approach. Molecular ionization is resonantly enhanced through either the 2(3) Pi (g), or the 2(3) Sigma (+)(g) intermediate molecular states. Some vibrational levels of the latter electronic state are observed and assigned here for the first time. Finally, cold molecules formation rates are calculated and compared to the experimentally measured ones, and the vibrational distribution of the formed molecules in the a(3) Sigma (+)(u) ground triplet state is discussed.

Journal/Review: EUROPEAN PHYSICAL JOURNAL D

Volume: 15 (2)      Pages from: 189  to: 198

KeyWords: ALKALI DIMERS; POTASSIUM MOLECULES; EXCITED-STATES; ATOMS; SPECTRUM; RB2
DOI: 10.1007/s100530170165

ImpactFactor: 1.583
Citations: 58
data from “WEB OF SCIENCE” (of Thomson Reuters) are update at: 2024-11-10
References taken from IsiWeb of Knowledge: (subscribers only)

Connecting to view paper tab on IsiWeb: Click here
Connecting to view citations from IsiWeb: Click here