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Light-induced deprotonation of molecules is an important process in photochemical reactions. Here, we theoretically investigate the tunneling deprotonation of H 2 + and its asymmetric isotopologues driven by circularly polarized THz laser pulses. The quasi-static picture shows that the field-dressed potential barrier is significantly lowered for the deprotonation channel when the mass asymmetry of the diatomic molecule increases. Our numerical simulations demonstrate that when the mass symmetry breaks, the tunneling deprotonation is significantly enhanced and the proton tunneling becomes the dominant dissociation channel in the THz driving fields. In addition, the simulated nuclear momentum distributions show that the emission of the proton is directed by the effective vector potential for the deprotonation channel and, meanwhile, the angular distribution of the emitting proton is affected by the alignment and rotation of the molecule induced by the rotating field. [ABSTRACT FROM AUTHOR]

We experimentally study two-body Coulomb explosions of CO2, O2, and CH3Cl molecules in intense femtosecond laser pulses. We observe an obvious variation in the ionic angular distribution of the fragments with respect to the kinetic energy releases (KERs). Using a classical model based on ab initio potential energy curves, we find that the dependence of the ionic angular distribution on the KER is relevant to the fact that the accurate potential energy deviates significantly from the value determined by applying the Coulomb interaction approximation at a relatively small internuclear distance of the molecule. We show that the KER-dependent ionic angular distribution provides an effective way to determine the critical internuclear distance at which the Coulomb interaction approximation holds or breaks down without relying on the knowledge of the accurate potential energy curves. [ABSTRACT FROM AUTHOR]

Using the classical ensemble method, we have investigated double ionization (DI) of diatomic molecules driven by circularly polarized laser pulses with different internuclear distances (R). The results show that the DI mechanism changes from sequential double ionization (SDI) to nonsequential double ionization (NSDI) as the internuclear distance increases. In SDI range, the structure of the electron momentum distribution changes seriously as R increases, which indicates the sensitive dependence of the release times of the two electrons on R. For NSDI, because of the circular polarization, the ionization of the second electron is not through the well-known recollision process but through a process where the first electron ionizes over the inner potential barrier of the molecule, moves directly towards the other nucleus, and kicks out the second electron. [ABSTRACT FROM AUTHOR]

Using the classical ensemble model, we systematically investigate strong-field nonsequential double ionization (NSDI) of Mg by intense elliptically polarized laser pulses with different wavelengths. Different from the noble atoms, NSDI occurs for Mg driven by elliptically and circularly polarized laser fields. Our results show that in elliptically and circularly polarized laser fields, the NSDI yield is sharply suppressed as the wavelength increases. Interestingly, the correlated behavior in the electron momentum spectra depends sensitively on the wavelengths. The corresponding electron dynamics is revealed by back tracing the classical trajectory.

With the classical ensemble model, we have investigated the pulse-duration dependence of nonsequential double ionization (NSDI) over a wide range of laser intensity. The correlated electron momentum distributions are distinctly different for the few-cycle and multiple cycle pulses, which agree well with the previous experiments. Based on this agreement, we analyzed the underlying process for the pulse-duration dependence of the electron correlation by tracing the classical trajectories. Counterintuitively, our analysis shows that the recollision-induced excited states of NSDI could resist ionization in the strong laser field for a time much longer than one optical cycle even at very high intensities. For the multiple-cycle pulses, NSDI events with such a long time delay have significant contribution to the total NSDI yields, which is responsible for the pulse-duration dependence of the observed correlated patterns in the electron momentum distributions.