The dissociative ionization of ethanol C2H5OH in an intense laser field is investigated with a chirped laser pulse. From the sensitive dependence of the relative yields of the fragment ions on the absolute values of the linear chirp rate, it is shown that the light-dressed potential-energy surface (LDPES) at the singly charged stage governs the nuclear dynamics, and that the nuclear wave packet flow into the breaking of either of the C–C and C–O chemical bonds could be characterized by the holding time thold during which the LDPESs are maintained. It is also understood in term of the holding time that the enhanced ionization into the doubly charged stage followed by the Coulomb explosion at C–C or C–O proceeds when the nuclear wave packet at the singly charged stage reaches the critical distance for the further ionization.
Articles you may be interested inPhotodissociation dynamics of 3-bromo-1,1,1-trifluoro-2-propanol and 2-(bromomethyl) hexafluoro-2-propanol at 234 nm: Resonance-enhanced multiphoton ionization detection of Br (2 P j ) Metastable decomposition and hydrogen migration of ethane dication produced in an intense femtosecond nearinfrared laser field
Two-body Coulomb explosion with the C-O bond breaking of methanol induced by intense laser pulses with the duration of Delta t=7 and 21 fs is investigated by the coincidence momentum imaging method. When Delta t=7 fs, the angular distribution of recoil vectors of the fragment ions for the direct C-O bond breaking pathway, CH(3)OH(2+)-->CH(3) (+)+OH(+), exhibits a peak deflected from the laser polarization direction by 30 degrees -45 degrees , and the corresponding angular distribution for the migration pathway, CH(2)OH(2) (+)-->CH(2) (+)+H(2)O(+), in which one hydrogen migrates from the carbon site to the oxygen site prior to the C-O bond breaking, exhibits almost the same profile. When the laser pulse duration is stretched to Delta t=21 fs, the angular distributions for the direct and migration pathways exhibit a broad peak along the laser polarization direction probably due to the dynamical alignment and/or the change in the double ionization mechanism; that is, from the nonsequential double ionization to the sequential double ionization. However, the extent of the anisotropy in the migration pathway is smaller than that in the direct pathway, exhibiting a substantial effect of hydrogen atom migration in the dissociative ionization of methanol interacting with the linearly polarized intense laser field.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.