Перейти к основному содержанию
AkademIndex

Продукты

Для разработчиков

AkademBaseОткрытый API экосистемы
Статья

Nonadiabatic dynamics and multiphoton resonances in strong-field molecular ionization with few-cycle laser pulses

Vincent TagliamontiDepartment of Physics and Astronomy, Stony Brook University, Stony Brook, New York 11794-3800, USAPéter SándorDepartment of Physics and Astronomy, Stony Brook University, Stony Brook, New York 11794-3800, USAArthur ZhaoDepartment of Physics and Astronomy, Stony Brook University, Stony Brook, New York 11794-3800, USATamás RozgonyiInstitute of Materials and Environmental Chemistry, Research Centre for Natural Sciences, HAS, Budapest 1117 Magyar tudósok krt. 2, HungaryPhilipp MarquetandUniversity of Vienna, Faculty of Chemistry, Institute of Theoretical Chemistry, Währinger Straße 17, 1090 Wien, AustriaThomas WeinachtDepartment of Physics and Astronomy, Stony Brook University, Stony Brook, New York 11794-3800, USA
2016en
ABI

Аннотация

We study strong-field molecular ionization using few- (four to ten) cycle laser pulses. Employing a supercontinuum light source, we are able to tune the optical laser wavelength (photon energy) over a range of $\ensuremath{\sim}200$ nm (500 meV). We measure the photoelectron spectrum for a series of different molecules as a function of laser intensity, frequency, and bandwidth and illustrate how the ionization dynamics vary with these parameters. We find that multiphoton resonances and nonadiabatic dynamics (internal conversion) play an important role and result in ionization to different ionic continua. Interestingly, while nuclear dynamics can be ``frozen'' for sufficiently short laser pulses, we find that resonances strongly influence the photoelectron spectrum and final cationic state of the molecule regardless of pulse duration---even for pulses that are less than four cycles in duration.

Перевод пока недоступен

Идентификаторы

Цитирования и источники

Цитирований: 2Использованных источников: 0