Published November 2016 | Version v1
Journal article

Experimental study of the (4)0 short-range electronic state of the 85Rb133Cs molecule by high resolution photoassociation spectroscopy

  • 1. Collaborative Innovation Center of Extreme Optics, Shanxi University, Taiyuan, Shanxi 030006 (China)
  • 2. State Key Laboratory of Quantum Optics and Quantum Optics Devices, Institute of Laser Spectroscopy, Shanxi University, Taiyuan 030006 (China)
  • 3. Department of Physics, School of Applied Science, Taiyuan University of Science and Technology, Taiyuan 030024 (China)

Description

We present the formation of ultracold 85Rb133Cs molecules in the (4)0 short-range electronic state and the measurement of the permanent electric dipole moment by high resolution photoassociation spectroscopy. With the rotationally resolved photoassociation spectra via resonance-enhanced two-photon ionization, spectral data have been extended to more vibrational levels compared to previous observations. Precise electric dipole moments are obtained by using the DC Stark effect of the photoassociation spectrum. These studies containing previously unobserved electronic states are important to understand the molecular structure and discover transition pathways for transferring ultracold atoms to deeply bound rovibrational levels of the electronic ground state. - Highlights: • Ultracold 85RbCs molecules in (4)0 state are produced by PA and detected by RETPI. • More 6 resonances are presented, even with vibrational level down to v=2. • With the rotationally resolved PA spectra, rotational constants are determined. • Internuclear distance-dependent EDMs are compared with theoretical calculation.

Availability note (English)

Available from http://dx.doi.org/10.1016/j.jqsrt.2016.06.025

Additional details

Identifiers

DOI
10.1016/j.jqsrt.2016.06.025;
PII
S0022-4073(16)30062-0;

Publishing Information

Journal Title
Journal of Quantitative Spectroscopy and Radiative Transfer
Journal Volume
184
Journal Page Range
p. 8-13
ISSN
0022-4073
CODEN
JQSRAE

Optional Information

Copyright
Copyright (c) 2016 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.