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Physics Faculty Research & Creative Works

Electron Diffraction

Publication Year

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Full-Text Articles in Physics

Influence Of Orbital Symmetry On Diffraction Imaging With Rescattering Electron Wave Packets, Michael G. Pullen, Benjamin Wolter, Anh-Thu Le, Matthias Baudisch, Michele Sclafani, Hugo Pires, Claus Dieter Schroeter, Joachim Ullrich, Robert Moshammer, Thomas Pfeifer, C. D. Lin, Jens Biegert Jun 2016

Influence Of Orbital Symmetry On Diffraction Imaging With Rescattering Electron Wave Packets, Michael G. Pullen, Benjamin Wolter, Anh-Thu Le, Matthias Baudisch, Michele Sclafani, Hugo Pires, Claus Dieter Schroeter, Joachim Ullrich, Robert Moshammer, Thomas Pfeifer, C. D. Lin, Jens Biegert

Physics Faculty Research & Creative Works

The ability to directly follow and time-resolve the rearrangement of the nuclei within molecules is a frontier of science that requires atomic spatial and few-femtosecond temporal resolutions. While laser-induced electron diffraction can meet these requirements, it was recently concluded that molecules with particular orbital symmetries (such as πg) cannot be imaged using purely backscattering electron wave packets without molecular alignment. Here, we demonstrate, in direct contradiction to these findings, that the orientation and shape of molecular orbitals presents no impediment for retrieving molecular structure with adequate sampling of the momentum transfer space. We overcome previous issues by showcasing …


Polyatomic Molecular Structure Retrieval Using Laser-Induced Electron Diffraction, Michael G. Pullen, Benjamin Wolter, Anh-Thu Le, Matthias Baudisch, Michael Hemmer, Arne Senftleben, M. Sclafani, Claus Dieter Schroeter, Joachim Ullrich, Robert Moshammer, C. D. Lin, Jens Biegert Sep 2015

Polyatomic Molecular Structure Retrieval Using Laser-Induced Electron Diffraction, Michael G. Pullen, Benjamin Wolter, Anh-Thu Le, Matthias Baudisch, Michael Hemmer, Arne Senftleben, M. Sclafani, Claus Dieter Schroeter, Joachim Ullrich, Robert Moshammer, C. D. Lin, Jens Biegert

Physics Faculty Research & Creative Works

Laser-induced electron diffraction is a developing dynamical imaging technique that is already able to probe molecular dynamics at few-femtosecond temporal resolutions and has the potential to reach the sub-femtosecond level. Here we provide the recipe for the extension of the technique to polyatomic molecules and we demonstrate the method by extracting the structure of aligned and anti-aligned acetylene (C₂H₂). We show that multiple bond lengths can be simultaneously imaged at high accuracy including elusive hydrogen containing bonds. Our results open the door to the investigation of larger complex molecules and the realization of a true molecular movie.


Imaging An Aligned Polyatomic Molecule With Laser-Induced Electron Diffraction, Michael G. Pullen, Benjamin Wolter, Anh-Thu Le, Matthias Baudisch, Michael Hemmer, Arne Senftleben, Claus Dieter Schroeter, Joachim Ullrich, Robert Moshammer, C. D. Lin, Jens Biegert Jun 2015

Imaging An Aligned Polyatomic Molecule With Laser-Induced Electron Diffraction, Michael G. Pullen, Benjamin Wolter, Anh-Thu Le, Matthias Baudisch, Michael Hemmer, Arne Senftleben, Claus Dieter Schroeter, Joachim Ullrich, Robert Moshammer, C. D. Lin, Jens Biegert

Physics Faculty Research & Creative Works

Laser-induced electron diffraction is an evolving tabletop method that aims to image ultrafast structural changes in gas-phase polyatomic molecules with sub-Ångström spatial and femtosecond temporal resolutions. Here we demonstrate the retrieval of multiple bond lengths from a polyatomic molecule by simultaneously measuring the C-C and C-H bond lengths in aligned acetylene. Our approach takes the method beyond the hitherto achieved imaging of simple diatomic molecules and is based on the combination of a 160kHz mid-infrared few-cycle laser source with full three-dimensional electron-ion coincidence detection. Our technique provides an accessible and robust route towards imaging ultrafast processes in complex gas-phase molecules …


Laser-Induced Electron Diffraction For Probing Rare Gas Atoms, Junliang Xu, Cosmin I. Blaga, Anthony D. Dichiara, Emily Sistrunk, Kaikai Zhang, Zhangjin Chen, Anh-Thu Le, Toru Morishita, C. D. Lin, Pierre Agostini, Louis F. Dimauro Dec 2012

Laser-Induced Electron Diffraction For Probing Rare Gas Atoms, Junliang Xu, Cosmin I. Blaga, Anthony D. Dichiara, Emily Sistrunk, Kaikai Zhang, Zhangjin Chen, Anh-Thu Le, Toru Morishita, C. D. Lin, Pierre Agostini, Louis F. Dimauro

Physics Faculty Research & Creative Works

Recently, using midinfrared laser-induced electron diffraction (LIED), snapshots of a vibrating diatomic molecule on a femtosecond time scale have been captured [C.I. Blaga et al., Nature (London) 483, 194 (2012)]. In this Letter, a comprehensive treatment for the atomic LIED response is reported, a critical step in generalizing this imaging method. Electron-ion differential cross sections (DCSs) of rare gas atoms are extracted from measured angular-resolved, high-energy electron momentum distributions generated by intense midinfrared lasers. Following strong-field ionization, the high-energy electrons result from elastic rescattering of a field-driven wave packet with the parent ion. For recollision energies [greater or equal] 100eV, …


Large-Angle Electron Diffraction Structure In Laser-Induced Rescattering From Rare Gases, D. Ray, B. Ulrich, I. Bocharova, C. Maharjan, P. Ranitovic, B. Gramkow, M. Magrakvelidze, S. De, I. V. Litvinyuk, Anh-Thu Le, Toru Morishita, C. D. Lin, G. G. Paulus, C. L. Cocke Apr 2008

Large-Angle Electron Diffraction Structure In Laser-Induced Rescattering From Rare Gases, D. Ray, B. Ulrich, I. Bocharova, C. Maharjan, P. Ranitovic, B. Gramkow, M. Magrakvelidze, S. De, I. V. Litvinyuk, Anh-Thu Le, Toru Morishita, C. D. Lin, G. G. Paulus, C. L. Cocke

Physics Faculty Research & Creative Works

We have measured full momentum images of electrons rescattered from Xe, Kr, and Ar following the liberation of the electrons from these atoms by short, intense laser pulses. At high momenta the spectra show angular structure (diffraction) which is very target dependent and in good agreement with calculated differential cross sections for the scattering of free electrons from the corresponding ionic cores.