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Bulletin of the American Physical Society

Probing ultrafast electronic motions in atoms with the attosecond pump-probe

Lee A. Collins, S. X. Hu, Barry I. Schneider

Published Mar 15, 2006• 0 citations
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Using attosecond pulses to probe ultrafast electronic motions inside atoms

Lee A. Collins, S. X. Hu

Bulletin of the American Physical Society•May 17, 2006•0 citations

Attosecond Pump Probe: Exploring Ultrafast Electron Motion inside an Atom

S. X. Hu, Lee A. Collins

The attosecond pump probe, in close analogy to the standard femtosecond probing technique, has been proposed and theoretically demonstrated with its application to explore ultrafast electron motions inside atoms. We have performed realistic modeling for the full dynamics of both the femtosecond pumping and the attosecond probing processes. Our simulations have illustrated that an ultrashort oscillation period of 2.0 fs can be mapped out for a wave packet in low-lying excited states of the helium atom. This opens the prospect of a wealth of similar pump probe experiments to examine ultrafast electronic or atomic motions.

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Attosecond control of electron dynamics

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Research progress of the control and measurement of the atomic and molecular ultrafast electron dynamics using two-color field

Liu Can-Dong, Jia Zheng-Mao, Zheng Ying-Hui +3 more

The advent of the ultrafast laser pulse provides the powerful and efficient tool for probing the ultrafast electron dynamics in atoms and molecules. The various nonlinear process induced by the laser-matter interaction allows one to obtain the electron motion information on the sub-femtosecond time scale. A series of the ultrafast spectroscopic technique, such as attosecond streak camera, attosecond transient absorption spectrum, and etc., have been successfully applied to the probe of electron dynamics in atoms, molecules, and solids. Using two-color field is one of the significant methods to achieve the coherent control and exploring of the electron motion. This paper summarizes recent research activities in the field of the atomic and molecular ultrafast process investigated in State Key Laboratory of High Field Laser Physics, Shanghai Institute of Optics and Fine Mechanics, Chinese Academy of Sciences, including the detection of the electron dynamics of the multi-bound states, measurement of the carrier envelope phase (CEP) and the phase of the attosecond pulse, and the ultrafast electron control with the THz/UV and MIR/IR field. To measure the dynamics of the multi-bound states, a broadband attosecond pulse can be used to ionize the electrons after it is excited by the pump laser. By changing the delay between the pump laser and the attosecond pulse, the measured electrons ionized by the broadband xuv attosecond pulse can present the multi-bound states dynamics simultaneously. The XUV/IR scheme is popularly used in attosecond dynamics measurement. But usually, the IR field is not very strong. We find that, if the IR field is strong enough to induce the above threshold ionization (ATI), the interference between the ATI electron and the electron from XUV pulse can be used to measure the CEP of the attosecond XUV pulse. Besides, if the electron ionized by attosecond pulse can be pushed back to the nuclei, the emission from the recombination can be used to determine the spectral phase of the attosecond pulse, which is an all-optical measurement. We also investigate the two color scheme of THz/UV and MIR/IR fields. With THz/UV two color scheme, very high electron localization can be achieved duration molecular dissociation when we use the UV pulse to excite the electron and the THz pulse to control the following electron movement. When we use the MIR/IR field to control the electron motion during the high harmonic generation, the recollision can be greatly decreased and the single attosecond pulse can be produced with multi-cycle MIR laser field.

Acta Physica Sinica•Jan 1, 2016•1 citation

Attosecond light-pulse-induced photoassociation

P. Rivière, Camilo Ruíz, Jan Michael Rost

We explore stimulated photoassociation in the context of attosecond pump-probe schemes of atomic matter. An attosecond pulse---the probe---is used to induce photoassociation of an electronic wave packet which had been created before, typically with an attosecond pump pulse at an atomic center different from the one of photoassociation. We will show that the electron absorption is maximal for a certain delay between the pulses. Two ways of enhancing and controlling stimulated photoassociation are proposed, namely, using an additional infrared pulse to steer the electronic wave packet and using a train of attosecond pulses instead of a single pair. A direct application of ultrafast stimulated photoassociation is the measurement of atomic distances.

arXiv:0802.0122•Physical Review A•Mar 26, 2008•5 citations

Attosecond real-time observation of electron tunnelling and multi-electron dynamics in atoms

M. Schuttze, Matthias Uiberacker, Thorsten Uphues +15 more

•Jan 1, 2007•0 citations
The attosecond pump probe, in close analogy to the standard femtosecond probing technique, has been proposed and theoretically demonstrated with its application to explore ultrafast electron motions inside atoms. We have performed realistic modeling for the full dynamics of both the femtosecond pumping and the attosecond probing processes. Our simulations have illustrated that an ultrashort oscillation period of 2.0 fs can be mapped out for a wave packet in low-lying excited states of the helium atom. This opens the prospect of a wealth of similar pump probe experiments to examine ultrafast electronic or atomic motions.
The advent of the ultrafast laser pulse provides the powerful and efficient tool for probing the ultrafast electron dynamics in atoms and molecules. The various nonlinear process induced by the laser-matter interaction allows one to obtain the electron motion information on the sub-femtosecond time scale. A series of the ultrafast spectroscopic technique, such as attosecond streak camera, attosecond transient absorption spectrum, and etc., have been successfully applied to the probe of electron dynamics in atoms, molecules, and solids. Using two-color field is one of the significant methods to achieve the coherent control and exploring of the electron motion. This paper summarizes recent research activities in the field of the atomic and molecular ultrafast process investigated in State Key Laboratory of High Field Laser Physics, Shanghai Institute of Optics and Fine Mechanics, Chinese Academy of Sciences, including the detection of the electron dynamics of the multi-bound states, measurement of the carrier envelope phase (CEP) and the phase of the attosecond pulse, and the ultrafast electron control with the THz/UV and MIR/IR field. To measure the dynamics of the multi-bound states, a broadband attosecond pulse can be used to ionize the electrons after it is excited by the pump laser. By changing the delay between the pump laser and the attosecond pulse, the measured electrons ionized by the broadband xuv attosecond pulse can present the multi-bound states dynamics simultaneously. The XUV/IR scheme is popularly used in attosecond dynamics measurement. But usually, the IR field is not very strong. We find that, if the IR field is strong enough to induce the above threshold ionization (ATI), the interference between the ATI electron and the electron from XUV pulse can be used to measure the CEP of the attosecond XUV pulse. Besides, if the electron ionized by attosecond pulse can be pushed back to the nuclei, the emission from the recombination can be used to determine the spectral phase of the attosecond pulse, which is an all-optical measurement. We also investigate the two color scheme of THz/UV and MIR/IR fields. With THz/UV two color scheme, very high electron localization can be achieved duration molecular dissociation when we use the UV pulse to excite the electron and the THz pulse to control the following electron movement. When we use the MIR/IR field to control the electron motion during the high harmonic generation, the recollision can be greatly decreased and the single attosecond pulse can be produced with multi-cycle MIR laser field.
We explore stimulated photoassociation in the context of attosecond pump-probe schemes of atomic matter. An attosecond pulse---the probe---is used to induce photoassociation of an electronic wave packet which had been created before, typically with an attosecond pump pulse at an atomic center different from the one of photoassociation. We will show that the electron absorption is maximal for a certain delay between the pulses. Two ways of enhancing and controlling stimulated photoassociation are proposed, namely, using an additional infrared pulse to steer the electronic wave packet and using a train of attosecond pulses instead of a single pair. A direct application of ultrafast stimulated photoassociation is the measurement of atomic distances.