| Literature DB >> 30822022 |
Harald Fuest1,2, Yu Hang Lai3, Cosmin I Blaga3, Kazuma Suzuki4, Junliang Xu3, Philipp Rupp1,2, Hui Li1,5,6, Pawel Wnuk1,2,7, Pierre Agostini3, Kaoru Yamazaki8, Manabu Kanno4, Hirohiko Kono4, Matthias F Kling1,2,5, Louis F DiMauro3.
Abstract
Theoretical studies indicated that C_{60} exposed to linearly polarized intense infrared pulses undergoes periodic cage structural distortions with typical periods around 100 fs (1 fs=10^{-15} s). Here, we use the laser-driven self-imaging electron diffraction technique, previously developed for atoms and small molecules, to measure laser-induced deformation of C_{60} in an intense 3.6 μm laser field. A prolate molecular elongation along the laser polarization axis is determined to be (6.1±1.4)% via both angular- and energy-resolved measurements of electrons that are released, driven back, and diffracted from the molecule within the same laser field. The observed deformation is confirmed by density functional theory simulations of nuclear dynamics on time-dependent adiabatic states and indicates a nonadiabatic excitation of the h_{g}(1) prolate-oblate mode. The results demonstrate the applicability of laser-driven electron diffraction methods for studying macromolecular structural dynamics in four dimensions with atomic time and spatial resolutions.Entities:
Year: 2019 PMID: 30822022 DOI: 10.1103/PhysRevLett.122.053002
Source DB: PubMed Journal: Phys Rev Lett ISSN: 0031-9007 Impact factor: 9.161