Challenges
Datasets
Workspaces
Papers
Discussions
Leaderboard
Log inSign up
Challenges
Datasets
Workspaces
Papers
Discussions
Leaderboard
Blog
Job Board
Q3AS

© 2026 Aqora Quantum S.A.S.

TermsPrivacyLegal Notice

中国物理B：英文版

Precise measurement of the line width of the photoassociation spectra of ultracold molecules by using a frequency shifter

Jie Ma, Jie Ma, 姬中华, 张一驰, 李玉清, 汪丽蓉, 赵延霆, Liantuan Xiao, 贾锁堂

Published Jan 1, 2012• 0 citations
OpenAlex

Abstract

We propose a technique to precisely measure the line width of the photoassociation spectra of the excited cesium molecule by using a frequency shifter to generate two laser beams with a precise frequency difference. A series of photoassociation (PA) spectra are recorded with two laser beam induced molecular lines, whose peak separation serves as an accurate frequency ruler to measure the line width of the PA spectra. The full width half maximum line width was studied as a function of PA laser intensity. The extrapolated value at zero laser intensity is (34.84 ± 0.22) MHz. By analyzing other broadening mechanisms, a value of (32.02 ± 0.70) MHz was deduced. It is shown that this scheme is inexpensive, simple, robust, and is promising for applications in a variety of other atomic species.

Related papers

Precise measurement of the line width of the photoassociation spectra of ultracold molecules by using a frequency shifter

Jizhou Wu, Jie Ma, Zhonghua Ji +6 more

We propose a technique to precisely measure the line width of the photoassociation spectra of the excited cesium molecule by using a frequency shifter to generate two laser beams with a precise frequency difference. A series of photoassociation (PA) spectra are recorded with two laser beam induced molecular lines, whose peak separation serves as an accurate frequency ruler to measure the line width of the PA spectra. The full width half maximum line width was studied as a function of PA laser intensity. The extrapolated value at zero laser intensity is (34.84 ± 0.22) MHz. By analyzing other broadening mechanisms, a value of (32.02 ± 0.70) MHz was deduced. It is shown that this scheme is inexpensive, simple, robust, and is promising for applications in a variety of other atomic species.

Chinese Physics B•Sep 1, 2012•10 citations

High sensitive determination of laser-induced frequency shifts of ultracold cesium molecules

Jizhou Wu, Zhonghua Ji, Yichi Zhang +5 more

We experimentally present a technique for sensitively determining the laser-induced frequency shifts of the long-range molecular vibrational and rotational levels. The scheme relies on an optical frequency shifter, leading to two laser beams with a precise and adjustable frequency interval. A series of photoassociation spectra are recorded with both beams inducing molecular lines, whose peak separation provides an accurate frequency ruler to measure the frequency shifts of cesium molecular levels, which have not yet been observed in previous reports. The data are compared to theoretical predictions and show a good agreement.

Optics Letters•May 24, 2011•21 citations

Experimental observation and determination of the laser-induced frequency shift of hyperfine levels of ultracold polar molecules

Wenliang Liu, Xiaofeng Wang, Jizhou Wu +6 more

We report on the experimental observation and quantitative determination of the laser-induced frequency shift (LIFS) of the ultracold polar molecules formed by photoassociation (PA). The experiments are performed by detecting a series of double PA spectra with a molecular hyperfine structure, which are induced by two PA lasers with a precise and adjustable frequency reference. We find that the LIFS of the molecular hyperfine levels shows a linear dependence on PA laser intensity.

Physical Review A•Aug 2, 2017•13 citations

Control of laser-induced frequency shift in ultracold cesium molecules by an external magnetic field

Yuqing Li, Guosheng Feng, Wenliang Liu +4 more

We investigate an effective control of the laser-induced frequency shift of ultracold cesium molecules formed by photoassociation (PA) in a magnetically levitated crossed dipole trap via an external magnetic field. A series of molecular PA spectra have been measured with increasing the PA laser intensity at different bias fields. We find that the slope of laser-induced frequency shift is strongly dependent on the external magnetic field: the slope can be increased up to a maximum of ∼6 times compared with a slope without an external magnetic field. A qualitatively theoretical explanation has been offered by considering the external magnetic field that can be used to manipulate the interaction between ultracold atoms.

Optics Letters•May 4, 2015•11 citations

Direct measurement of laser-induced frequency shift rate of ultracold cesium molecules by analyzing losses of trapped atoms

Yichi Zhang, Jie Ma, Yuqing Li +7 more

We report on a quantitative experimental determination of the laser-induced frequency shift rate of the ultracold cesium molecules formed via photoassociation (PA) by means of the trap loss measurement of the losses of trapped atoms in a standard magneto-optical trap. The experiment was directly performed by varying the photoassociation laser intensity without any additional frequency monitor technologies. Our experimental method utilized dependences of the losses on the laser-induced frequency shift rate based on the conditions of the identified photoassociation spectral shape. We demonstrated that the method is sensitive enough to determine small frequency shifts of rovibrational levels of ultracold cesium molecules.

Applied Physics Letters•Sep 24, 2012•8 citations

Accurate determination of the rotational constants of ultracold molecules using double photoassociation spectroscopy

Jie Ma, Yuqing Li, Wenliang Liu +6 more

We report on an accurate determination of the rotational constants of the ultracold long-range Cesium molecules in near dissociation domain. The scheme relies on a precise reference of the frequency difference in a double photoassociation spectroscopy induced by two laser beams based on an acoustic-optical modulator. The rotational constants are obtained by fitting a non-rigid rotor model into the frequency intervals of the neighboring rotational levels deduced from the reference.

Optics Express•Feb 10, 2014•5 citations
We propose a technique to precisely measure the line width of the photoassociation spectra of the excited cesium molecule by using a frequency shifter to generate two laser beams with a precise frequency difference. A series of photoassociation (PA) spectra are recorded with two laser beam induced molecular lines, whose peak separation serves as an accurate frequency ruler to measure the line width of the PA spectra. The full width half maximum line width was studied as a function of PA laser intensity. The extrapolated value at zero laser intensity is (34.84 ± 0.22) MHz. By analyzing other broadening mechanisms, a value of (32.02 ± 0.70) MHz was deduced. It is shown that this scheme is inexpensive, simple, robust, and is promising for applications in a variety of other atomic species.
We propose a technique to precisely measure the line width of the photoassociation spectra of the excited cesium molecule by using a frequency shifter to generate two laser beams with a precise frequency difference. A series of photoassociation (PA) spectra are recorded with two laser beam induced molecular lines, whose peak separation serves as an accurate frequency ruler to measure the line width of the PA spectra. The full width half maximum line width was studied as a function of PA laser intensity. The extrapolated value at zero laser intensity is (34.84 ± 0.22) MHz. By analyzing other broadening mechanisms, a value of (32.02 ± 0.70) MHz was deduced. It is shown that this scheme is inexpensive, simple, robust, and is promising for applications in a variety of other atomic species.
We experimentally present a technique for sensitively determining the laser-induced frequency shifts of the long-range molecular vibrational and rotational levels. The scheme relies on an optical frequency shifter, leading to two laser beams with a precise and adjustable frequency interval. A series of photoassociation spectra are recorded with both beams inducing molecular lines, whose peak separation provides an accurate frequency ruler to measure the frequency shifts of cesium molecular levels, which have not yet been observed in previous reports. The data are compared to theoretical predictions and show a good agreement.
We investigate an effective control of the laser-induced frequency shift of ultracold cesium molecules formed by photoassociation (PA) in a magnetically levitated crossed dipole trap via an external magnetic field. A series of molecular PA spectra have been measured with increasing the PA laser intensity at different bias fields. We find that the slope of laser-induced frequency shift is strongly dependent on the external magnetic field: the slope can be increased up to a maximum of ∼6 times compared with a slope without an external magnetic field. A qualitatively theoretical explanation has been offered by considering the external magnetic field that can be used to manipulate the interaction between ultracold atoms.
We report on a quantitative experimental determination of the laser-induced frequency shift rate of the ultracold cesium molecules formed via photoassociation (PA) by means of the trap loss measurement of the losses of trapped atoms in a standard magneto-optical trap. The experiment was directly performed by varying the photoassociation laser intensity without any additional frequency monitor technologies. Our experimental method utilized dependences of the losses on the laser-induced frequency shift rate based on the conditions of the identified photoassociation spectral shape. We demonstrated that the method is sensitive enough to determine small frequency shifts of rovibrational levels of ultracold cesium molecules.