Related Experiment Video
Updated: Sep 30, 2025

Direct Imaging of Laser-driven Ultrafast Molecular Rotation
Published on: February 4, 2017
Picosecond pulse-shaping for strong three-dimensional field-free alignment of generic asymmetric-top molecules
Terry Mullins1, Evangelos T Karamatskos1,2, Joss Wiese1,3,4
1Center for Free-Electron Laser Science, Deutsches Elektronen-Synchrotron DESY, Notkestraße 85, 22607, Hamburg, Germany.
Abstract:
Fixing molecules in space is a crucial step for the imaging of molecular structure and dynamics. Here, we demonstrate three-dimensional (3D) field-free alignment of the prototypical asymmetric top molecule indole using elliptically polarized, shaped, off-resonant laser pulses. A truncated laser pulse is produced using a combination of extreme linear chirping and controlled phase and amplitude shaping using a spatial-light-modulator (SLM) based pulse shaper of a broadband laser pulse. The angular confinement is detected through velocity-map imaging of H+ and C2+ fragments resulting from strong-field ionization and Coulomb explosion of the aligned molecules by intense femtosecond laser pulses. The achieved three-dimensional alignment is characterized by comparing the result of ion-velocity-map measurements for different alignment directions and for different times during and after the alignment laser pulse to accurate computational results. The achieved strong three-dimensional field-free alignment of [Formula: see text] demonstrates the feasibility of both, strong three-dimensional alignment of generic complex molecules and its quantitative characterization.
Related Concept Videos
NMR Spectrometers: Radiofrequency Pulses and Pulse Sequences
¹³C NMR: Distortionless Enhancement by Polarization Transfer (DEPT)
¹H NMR of Conformationally Flexible Molecules: Temporal Resolution
Double Resonance Techniques: Overview
Spin decoupling is usually achieved by...

