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

Chinese Physics B

Effect of pump-1 laser on Autler–Townes splitting in photoelectron spectrum of K 2 molecule

Wei Guo, Xingqiang Lu, Xin-Lin Wang, Hongbin Yao

Published Jan 1, 2015• 0 citations
Publisher

Abstract

We theoretically investigate the Autler–Townes (AT) splitting in the photoelectron spectrum of four-level ladder K 2 molecule driven by a pump 1-pump 2-probe pulse via employing the time-dependent wave packet approach. The effects of the pump-1 laser intensity and wavelength on AT splitting are studied for the first time. The magnitude of AT splitting increases with increasing the pump-1 laser intensity. The triple splitting with asymmetric profile occurs due to the nonresonant excitation. The triple structure is transformed into a double structure (near-resonant region), and then becomes a peak (far-off resonant region) progressively as the pump-1 laser is detuned from the resonance wavelength, which can be explained in terms of the asymmetric excitation/population of dressed states. The splitting between adjacent peaks and the splitting between the two sideband peaks in the triplet do not change with the pump-1 pulse wavelength. The three peaks shift toward lower energy with the same shift 1/4* Δ 1 as the pump-1 wavelength changes in near-resonant region. The asymptotic behaviors of AT splitting with the pump-1 laser intensity are interesting in the threshold points of the near-resonant region and the far-off resonant region.

DOI
10.1088/1674-1056/24/1/013302

Related papers

Effect of pump-1 laser on Autler Townes splitting in photoelectron spectrum of K2 molecule

郭玮, 路兴强, 王新林 +1 more

We theoretically investigate the Autler–Townes(AT)splitting in the photoelectron spectrum of four-level ladder K2molecule driven by a pump 1-pump 2-probe pulse via employing the time-dependent wave packet approach.The effects of the pump-1 laser intensity and wavelength on AT splitting are studied for the first time.The magnitude of AT splitting increases with increasing the pump-1 laser intensity.The triple splitting with asymmetric profile occurs due to the nonresonant excitation.The triple structure is transformed into a double structure(near-resonant region),and then becomes a peak(far-off resonant region)progressively as the pump-1 laser is detuned from the resonance wavelength,which can be explained in terms of the asymmetric excitation/population of dressed states.The splitting between adjacent peaks and the splitting between the two sideband peaks in the triplet do not change with the pump-1 pulse wavelength.The three peaks shift toward lower energy with the same shift 1/4*△1 as the pump-1 wavelength changes in near-resonant region.The asymptotic behaviors of AT splitting with the pump-1 laser intensity are interesting in the threshold points of the near-resonant region and the far-off resonant region.

中国物理B：英文版•Jan 1, 2015•0 citations

Field dependence of Autler-Townes splitting in pump/probe setup

Xingqiang Lu, Wei Guo, Xinlin Wang +1 more

We theoretically investigate the Autler-Townes (AT) splitting in the photoelectron spectra of threelevel ladder K 2 molecule driven by a pump-probe pulse via employing the time-dependent wave packet approach. The effect of the pump/probe laser intensity and wavelength on AT splitting is detailed studied. The magnitude of AT splitting increases with increasing the pump laser intensity, but does not vary with probe intensity. The double splitting with asymmetric profiles arises due to the nonresonant excitation. The double structure is transformed into one peak progressively as the pump is detuned from the resonance wavelength, which can be explained in terms of the asymmetric excitation/population of dressed states. The splitting between AT doublet changes with pump wavelength, but does not change with probe wavelength. The double peaks shift to lower energy with the different shift with increasing pump wavelength, but with the same shift with probe wavelength.

Russian Journal of Physical Chemistry A•Oct 12, 2015•0 citations

Wavelength dependence of Autler-Townes splitting in a four-level ladder molecular system

Wei Guo, Xingqiang Lu, Xinlin Wang +1 more

We theoretically investigated the Autler-Townes (AT) splitting in the photoelectron spectra of four-level ladder K-2 molecules in the presence of two control pump fields and one probe field by employing the time-dependent wave packet approach. The wavelength dependence of AT splitting on three laser pulses was studied in detail. The photoelectron spectra show triple splitting with symmetric profiles, but with asymmetric profiles when the wavelength is changed. The shifts of the absorption peaks are predicted by using an analytical fitting function when the wavelength of one of the three fields is changed, and the functional dependence appears to be linear. These novel results are of importance for the molecular spectroscopy, and may stimulate further theoretical studies analytically from the first principles. Copyright (C) EPLA, 2014

Europhysics Letters (EPL)•Dec 1, 2014•4 citations

Theoretical investigation of femtosecond-resolved photoelectron spectra of three-level ladder K2 molecules

Feng Xiao-Jing, Guo Wei, Lu Xing-Qiang +2 more

We investigate the effect of delay time, pulse width and pump wavelength on photoelectron spectra and wave packet forming process of the three-level K2 molecules via time-dependent wave packet approach. There is no Autler-Townes splitting for weaker pump intensity or shorter pulse width. Delay time and pump wavelength can affect peak structure, position, and relative height. The vibration period of wave packet does not vary with pump wavelength, while the oscillating amplitude decreases with increasing pulse width. Results may provide important basis for realizing the optical control of molecules experimentally.

Acta Physica Sinica•Jan 1, 2015•0 citations

Delay time dependence of wave packet motion and population transfer of four-level K2molecule in pump–pump–probe pulses

Zhiqiang Chang, Changming Li, Wei Guo +1 more

The effect of delay time on photoelectron spectra and state populations of a four-level ladder K 2 molecule is investigated by a pump1–pump2–probe pulse via the time-dependent wave packet approach. The periodical motion of the wave packet leads to the periodical change of the photoelectron spectra. The Autler–Townes triple splitting appears at zero delay time, double splitting appears at nonzero delay time between pump1 and pump2 pulses, and no splitting appears at nonzero delay time between pump2 and probe pulses. The periodical change of the state populations with the delay time may be due to the coupling effect between the two pulses. It is found that the selectivity of the state populations may be attained by regulating the delay time. The results can provide an important basis for realizing the optical control of molecules experimentally.

Chinese Physics B•May 1, 2018•2 citations

The delay time dependence of the photoelectron spectra and state populations of three-level ladder K2 molecule

Wei Guo, Xingqiang Lu, Xinlin Wang

The delay time dependence of photoelectron spectra and state populations of three-level ladder K 2 molecule is investigated by pump-probe pulses via time-dependent wave packet approach. The periodical motion of the wave packet with oscillating period 500 fs results in the periodical variation of photoelectron spectra. The photoelectron spectra show Autler-Townes double splitting at zero delay time, and no splitting at positive delay time. The periodical change of state populations with delay time can be ascribed to the coupling effect between the two pulses. It is found that the selectivity of the state populations may be attained by regulating the delay time. The results can provide some important basis for realizing the optical control of molecules experimentally.

Russian Journal of Physical Chemistry A•Feb 1, 2017•0 citations
We theoretically investigate the Autler–Townes (AT) splitting in the photoelectron spectrum of four-level ladder K 2 molecule driven by a pump 1-pump 2-probe pulse via employing the time-dependent wave packet approach. The effects of the pump-1 laser intensity and wavelength on AT splitting are studied for the first time. The magnitude of AT splitting increases with increasing the pump-1 laser intensity. The triple splitting with asymmetric profile occurs due to the nonresonant excitation. The triple structure is transformed into a double structure (near-resonant region), and then becomes a peak (far-off resonant region) progressively as the pump-1 laser is detuned from the resonance wavelength, which can be explained in terms of the asymmetric excitation/population of dressed states. The splitting between adjacent peaks and the splitting between the two sideband peaks in the triplet do not change with the pump-1 pulse wavelength. The three peaks shift toward lower energy with the same shift 1/4* Δ 1 as the pump-1 wavelength changes in near-resonant region. The asymptotic behaviors of AT splitting with the pump-1 laser intensity are interesting in the threshold points of the near-resonant region and the far-off resonant region.
We theoretically investigate the Autler–Townes(AT)splitting in the photoelectron spectrum of four-level ladder K2molecule driven by a pump 1-pump 2-probe pulse via employing the time-dependent wave packet approach.The effects of the pump-1 laser intensity and wavelength on AT splitting are studied for the first time.The magnitude of AT splitting increases with increasing the pump-1 laser intensity.The triple splitting with asymmetric profile occurs due to the nonresonant excitation.The triple structure is transformed into a double structure(near-resonant region),and then becomes a peak(far-off resonant region)progressively as the pump-1 laser is detuned from the resonance wavelength,which can be explained in terms of the asymmetric excitation/population of dressed states.The splitting between adjacent peaks and the splitting between the two sideband peaks in the triplet do not change with the pump-1 pulse wavelength.The three peaks shift toward lower energy with the same shift 1/4*△1 as the pump-1 wavelength changes in near-resonant region.The asymptotic behaviors of AT splitting with the pump-1 laser intensity are interesting in the threshold points of the near-resonant region and the far-off resonant region.
We theoretically investigate the Autler-Townes (AT) splitting in the photoelectron spectra of threelevel ladder K 2 molecule driven by a pump-probe pulse via employing the time-dependent wave packet approach. The effect of the pump/probe laser intensity and wavelength on AT splitting is detailed studied. The magnitude of AT splitting increases with increasing the pump laser intensity, but does not vary with probe intensity. The double splitting with asymmetric profiles arises due to the nonresonant excitation. The double structure is transformed into one peak progressively as the pump is detuned from the resonance wavelength, which can be explained in terms of the asymmetric excitation/population of dressed states. The splitting between AT doublet changes with pump wavelength, but does not change with probe wavelength. The double peaks shift to lower energy with the different shift with increasing pump wavelength, but with the same shift with probe wavelength.
We theoretically investigated the Autler-Townes (AT) splitting in the photoelectron spectra of four-level ladder K-2 molecules in the presence of two control pump fields and one probe field by employing the time-dependent wave packet approach. The wavelength dependence of AT splitting on three laser pulses was studied in detail. The photoelectron spectra show triple splitting with symmetric profiles, but with asymmetric profiles when the wavelength is changed. The shifts of the absorption peaks are predicted by using an analytical fitting function when the wavelength of one of the three fields is changed, and the functional dependence appears to be linear. These novel results are of importance for the molecular spectroscopy, and may stimulate further theoretical studies analytically from the first principles. Copyright (C) EPLA, 2014
We investigate the effect of delay time, pulse width and pump wavelength on photoelectron spectra and wave packet forming process of the three-level K2 molecules via time-dependent wave packet approach. There is no Autler-Townes splitting for weaker pump intensity or shorter pulse width. Delay time and pump wavelength can affect peak structure, position, and relative height. The vibration period of wave packet does not vary with pump wavelength, while the oscillating amplitude decreases with increasing pulse width. Results may provide important basis for realizing the optical control of molecules experimentally.
The effect of delay time on photoelectron spectra and state populations of a four-level ladder K 2 molecule is investigated by a pump1–pump2–probe pulse via the time-dependent wave packet approach. The periodical motion of the wave packet leads to the periodical change of the photoelectron spectra. The Autler–Townes triple splitting appears at zero delay time, double splitting appears at nonzero delay time between pump1 and pump2 pulses, and no splitting appears at nonzero delay time between pump2 and probe pulses. The periodical change of the state populations with the delay time may be due to the coupling effect between the two pulses. It is found that the selectivity of the state populations may be attained by regulating the delay time. The results can provide an important basis for realizing the optical control of molecules experimentally.
The delay time dependence of photoelectron spectra and state populations of three-level ladder K 2 molecule is investigated by pump-probe pulses via time-dependent wave packet approach. The periodical motion of the wave packet with oscillating period 500 fs results in the periodical variation of photoelectron spectra. The photoelectron spectra show Autler-Townes double splitting at zero delay time, and no splitting at positive delay time. The periodical change of state populations with delay time can be ascribed to the coupling effect between the two pulses. It is found that the selectivity of the state populations may be attained by regulating the delay time. The results can provide some important basis for realizing the optical control of molecules experimentally.