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Authors
- Jie Yang, University of Nebraska-Lincoln
- Markus Guehr, Potsdam University, PotsdamFollow
- Xiaozhe Shen, SLAC National Accelerator LaboratoryFollow
- Renkai Li, SLAC National Accelerator LaboratoryFollow
- Theodore Vecchione, SLAC National Accelerator LaboratoryFollow
- Ryan Coffee, SLAC National Accelerator LaboratoryFollow
- Jeff Corbett, SLAC National Accelerator LaboratoryFollow
- Alan Fry, SLAC National Accelerator Laboratory,Follow
- Nick Hartmann, SLAC National Accelerator LaboratoryFollow
- Carsten Hast, SLAC National Accelerator LaboratoryFollow
- Kareem Hegazy, SLAC National Accelerator LaboratoryFollow
- Keith Jobe, SLAC National Accelerator LaboratoryFollow
- Igor Makasyuk, SLAC National Accelerator LaboratoryFollow
- Joseph Robinson, SLAC National Accelerator LaboratoryFollow
- Matthew S. Robinson, University of Nebraska-LincolnFollow
- Sharon Vetter, SLAC National Accelerator LaboratoryFollow
- Stephen Weathersby, SLAC National Accelerator LaboratoryFollow
- Charles Yoneda, SLAC National Accelerator LaboratoryFollow
- Xijie Wang, SLAC National Accelerator Laboratory, Menlo Park, CAFollow
- Martin Centurion, University of Nebraska-LincolnFollow
Date of this Version
10-7-2016
Citation
PHYSICAL REVIEW LETTERS 117, 153002 (2016)
DOI: 10.1103/PhysRevLett.117.153002
Abstract
Observing the motion of the nuclear wave packets during a molecular reaction, in both space and time, is crucial for understanding and controlling the outcome of photoinduced chemical reactions. We have imaged the motion of a vibrational wave packet in isolated iodine molecules using ultrafast electron diffraction with relativistic electrons. The time-varying interatomic distance was measured with a precision 0.07 Å and temporal resolution of 230 fs full width at half maximum. The method is not only sensitive to the position but also the shape of the nuclear wave packet.
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© 2016 American Physical Society. Used by permission.