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

Springer eBooks

Optimal Control of Atomic, Molecular and Electron Dynamics with Tailored Femtosecond Laser Pulses

Tobias Brixner, Thomas Pfeifer, G. Gerber, M. Wollenhaupt, Thomas Baumert

Published Dec 11, 2005• 20 citations
Publisher
DOI
10.1007/0-387-23294-x_9

Related papers

Quantum Control of Atoms and Small Molecules with Intense Femtosecond Pulses

Adi Natan, Yaron R. Silberberg

•Jan 1, 2009•0 citations

Molecular Free Electron Vortices in Photoionization by Polarization-Tailored Ultrashort Laser Pulses

Tim Bayer, M. Wollenhaupt

Atomic and molecular free electron vortices (FEVs), characterized by their spiral-shaped momentum distribution, have recently attracted a great deal of attention due to their varied shapes and their unusual topological properties. Shortly after their theoretical prediction by the single-photon ionization (SPI) of He atoms using pairs of counterrotating circularly polarized attosecond pulses, FEVs have been demonstrated experimentally by the multiphoton ionization (MPI) of alkali atoms using single-color and bichromatic circularly polarized femtosecond pulse sequences. Recently, we reported on the analysis of the experimental results employing a numerical model based on the ab initio solution of the time-dependent Schrödinger equation (TDSE) for a two-dimensional (2D) atom interacting with a polarization-shaped ultrashort laser field. Here, we apply the 2D TDSE model to study molecular FEVs created by SPI and MPI of a diatomic molecule using polarization-tailored single-color and bichromatic femtosecond pulse sequences. We investigate the influence of the coupled electron-nuclear dynamics on the vortex formation dynamics and discuss the effect of CEP- and rotational averaging on the photoelectron momentum distribution. By analyzing how the molecular structure and dynamics is imprinted in the photoelectron spirals, we explore the potential of molecular FEVs for ultrafast spectroscopy.

Frontiers in Chemistry•Jun 2, 2022•10 citations

Controlling Quantum States of Atoms and Molecules by Ultrafast Femtosecond Laser Fields

罗嗣佐 Luo Sizuo, 陈洲 Chen Zhou, 李孝开 Li Xiaokai +2 more

Acta Optica Sinica•Jan 1, 2019•4 citations

Controlled rotational Raman echo recurrences and modulation of high-intensity ultrashort laser pulses by molecular rotations in the gas phase

И. В. Федотов, A. D. Savvin, Andrei B. Fedotov +1 more

We show that sequences of femtosecond laser pulses can control the rotational Raman response of a gas mixture, giving rise to a tunable manifold of echo recurrences in the retarded nonlinear-optical response of the gas. Tailored phase masks for high-intensity ultrashort laser pulses are experimentally demonstrated using molecular rotations in the gas phase driven by optimally time-ordered pulse sequences.

Optics Letters•Apr 17, 2007•15 citations

Coherent control of ultrafast bond making and subsequent molecular dynamics

Liat Levin, Daniel M. Reich, Moran Geva +3 more

Quantum coherent control of ultrafast bond making and the subsequent molecular dynamics is crucial for the realization of a new photochemistry, where a shaped laser field is actively driving the chemical system in a coherent way from the thermal initial state of the reactants to the final state of the desired products. We demonstrate here coherent control over the relative yields of Mg2 molecules that are generated via photoassociation and subsequently photodriven into different groups of final states. The strong-field process involves non-resonant multiphoton femtosecond photoassociation of a pair of thermally hot magnesium atoms into a bound Mg2 molecule and subsequent molecular dynamics on electronically excited states. The branching-ratio control is achieved with linearly chirped laser pulses, utilizing the different chirp dependence that various groups of final molecular states display for their post-pulse population. Our joint experimental and theoretical study establishes the feasibility of high degree coherent control over quantum molecular dynamics that is initiated by femtosecond photoassociation of thermal atoms.

•Jan 1, 2022•6 citations

Coherent Control and Manipulation of atoms using femtosecond pulses

Parvendra Kumar

•Jan 1, 2013•0 citations
Atomic and molecular free electron vortices (FEVs), characterized by their spiral-shaped momentum distribution, have recently attracted a great deal of attention due to their varied shapes and their unusual topological properties. Shortly after their theoretical prediction by the single-photon ionization (SPI) of He atoms using pairs of counterrotating circularly polarized attosecond pulses, FEVs have been demonstrated experimentally by the multiphoton ionization (MPI) of alkali atoms using single-color and bichromatic circularly polarized femtosecond pulse sequences. Recently, we reported on the analysis of the experimental results employing a numerical model based on the ab initio solution of the time-dependent Schrödinger equation (TDSE) for a two-dimensional (2D) atom interacting with a polarization-shaped ultrashort laser field. Here, we apply the 2D TDSE model to study molecular FEVs created by SPI and MPI of a diatomic molecule using polarization-tailored single-color and bichromatic femtosecond pulse sequences. We investigate the influence of the coupled electron-nuclear dynamics on the vortex formation dynamics and discuss the effect of CEP- and rotational averaging on the photoelectron momentum distribution. By analyzing how the molecular structure and dynamics is imprinted in the photoelectron spirals, we explore the potential of molecular FEVs for ultrafast spectroscopy.
Quantum coherent control of ultrafast bond making and the subsequent molecular dynamics is crucial for the realization of a new photochemistry, where a shaped laser field is actively driving the chemical system in a coherent way from the thermal initial state of the reactants to the final state of the desired products. We demonstrate here coherent control over the relative yields of Mg2 molecules that are generated via photoassociation and subsequently photodriven into different groups of final states. The strong-field process involves non-resonant multiphoton femtosecond photoassociation of a pair of thermally hot magnesium atoms into a bound Mg2 molecule and subsequent molecular dynamics on electronically excited states. The branching-ratio control is achieved with linearly chirped laser pulses, utilizing the different chirp dependence that various groups of final molecular states display for their post-pulse population. Our joint experimental and theoretical study establishes the feasibility of high degree coherent control over quantum molecular dynamics that is initiated by femtosecond photoassociation of thermal atoms.