Ultrafast Proton Transfer Driven by a Femtosecond Strong-Field Laser Pulse
POSTER
Abstract
Kinetic energy distributions of protons ejected from a polyatomic molecule, anthraquinone, subjected to 60~fs, 800~nm laser pulses of intensity between 0.2 and 4.0x10\^{}14~W/cm\^{}2, reveal field-driven restructuring of the molecule (intramolecular proton migration) prior to its Coulomb explosion. Model calculations demonstrate that proton migrates into a field-dressed metastable potential energy minimum. Isomerization mediated by strong field is an important novel phenomenon in coupling of polyatomic molecules with intense laser pulses.