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

Applied Physics Letters

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

Yichi Zhang, Jie Ma, Yuqing Li, Jizhou Wu, Linjie Zhang, Gang Chen, Lirong Wang, Yanting Zhao, Liantuan Xiao, Suotang Jia

Published Sep 24, 2012• 8 citations
Publisher

Abstract

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.

DOI
10.1063/1.4756801

Related papers

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

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

Cold cesium molecules produced directly in a magneto—optical trap

Hongshan Zhang, Zhonghua Ji, Jinpeng Yuan +5 more

We report on the observation of ultracold ground electric-state cesium molecules produced directly in a magneto—optical trap with a good signal-to-noise ratio. These molecules arise from the photoassociation of magneto—optical trap lasers and they are detected by resonantly enhanced multiphoton ionization technology. The production rate of ultracold cesium molecules is up to 4×10 4 s −1 . We measure the characteristic time of the ground electric-state cesium molecules generated in the experiment and investigate the Cs 2 + molecular ion intensity as a function of the trapping laser intensity and the ionization pulse laser energy. We conclude that the production of cold cesium molecules may be enhanced by using appropriate experimental parameters, which is useful for future experiments involving the production and trapping of ultracold ground electric-state molecules.

Chinese Physics B•Dec 1, 2011•12 citations

[Experimental study of ultralow frequency modulation photoassociation spectrum].

Lirong Wang, Jie Ma, Yanting Zhao +2 more

In the present paper, ultracold cesium atoms were obtained in magnetic optical trap using the laser cooling technology. The number of ultracold atoms is 10(7). The temperature of ultracold atoms is about 200 μK and the diameter of the ultracold atoms cloud is about 400 μm. The ultracold cesium molecules of excited states were formed using the photoassociation of ultracold atoms. The resolution of vib-rotational spectrum was studied under different scan rates of photossociation laser in the experiment. The resolution of vib-rotational spectrum becomes high when the scan rate of photossociation laser becomes slow. The cold atoms fluorescence was obtained using the high sensitive avalanche photo detector and the high resolution vib-rotational spectrum of ultracold cesium molecule in its first excited state of with dissociation limit long range state was obtained. The ultracold ground molecule was formed by controlled Raman photoassociation and the photoassociation laser must be locked to atom-molecular hyperfine transitions. The ultracold atoms photoassociation spectrum was modulated using ultra-low frequency. The first-order differential signal was optimized by changing modulation amplitude and modulation frequency. It provides a feedback signal to correct error of the laser. The laser frequency satisfies experimental requirement to form ultracold ground molecules using the controlled Raman photoassociation. This work is important for studies of ultracold atoms and molecules in confined space.

•Dec 1, 2014•0 citations

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 +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.

中国物理B：英文版•Jan 1, 2012•0 citations
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.
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 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 report on the observation of ultracold ground electric-state cesium molecules produced directly in a magneto—optical trap with a good signal-to-noise ratio. These molecules arise from the photoassociation of magneto—optical trap lasers and they are detected by resonantly enhanced multiphoton ionization technology. The production rate of ultracold cesium molecules is up to 4×10 4 s −1 . We measure the characteristic time of the ground electric-state cesium molecules generated in the experiment and investigate the Cs 2 + molecular ion intensity as a function of the trapping laser intensity and the ionization pulse laser energy. We conclude that the production of cold cesium molecules may be enhanced by using appropriate experimental parameters, which is useful for future experiments involving the production and trapping of ultracold ground electric-state molecules.
In the present paper, ultracold cesium atoms were obtained in magnetic optical trap using the laser cooling technology. The number of ultracold atoms is 10(7). The temperature of ultracold atoms is about 200 μK and the diameter of the ultracold atoms cloud is about 400 μm. The ultracold cesium molecules of excited states were formed using the photoassociation of ultracold atoms. The resolution of vib-rotational spectrum was studied under different scan rates of photossociation laser in the experiment. The resolution of vib-rotational spectrum becomes high when the scan rate of photossociation laser becomes slow. The cold atoms fluorescence was obtained using the high sensitive avalanche photo detector and the high resolution vib-rotational spectrum of ultracold cesium molecule in its first excited state of with dissociation limit long range state was obtained. The ultracold ground molecule was formed by controlled Raman photoassociation and the photoassociation laser must be locked to atom-molecular hyperfine transitions. The ultracold atoms photoassociation spectrum was modulated using ultra-low frequency. The first-order differential signal was optimized by changing modulation amplitude and modulation frequency. It provides a feedback signal to correct error of the laser. The laser frequency satisfies experimental requirement to form ultracold ground molecules using the controlled Raman photoassociation. This work is important for studies of ultracold atoms and molecules in confined space.
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.