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Register a new userIntensity-resolved ionization yileds of aniline with femtosecond laser pulses
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We present experimental results for the ionization of aniline and benzene molecules subjected to intense ultrashort laser pulses. Measured parent molecular ions yields were obtained using a recently developed technique capable of three-dimensional imaging of ion distributions within the focus of a laser beam. By selecting ions originating from the central region of the focus, where the spatial intensity distribution is nearly uniform, volumetric-free intensity-dependent ionization yields were obtained. The measured data revealed a previously unseen resonant-like multiphoton ionization process. Comparison of benzene, aniline and Xe ion yields demonstrate that the observed intensity dependent structures are not due to geometric artifacts in the focus. Finally we attribute the ionization of aniline to a stepwise process going through the pi-sigma^star state which sits 3 photons above the ground state and 2 photons below the continuum.
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A theoretical study of the intense-field single ionization of molecular hydrogen or deuterium oriented either parallel or perpendicular to a linear polarized laser pulse (400 nm) is performed for different internuclear separations and pulse lengths in an intensity range of $(2-13)times10^{13} $W cm$^{-2}$. The investigation is based on a non-perturbative treatment that solves the full time-dependent Schrodinger equation of both correlated electrons within the fixed-nuclei and the dipole approximation. The results for various internuclear separations are used to obtain the ionization yields of molecular hydrogen and deuterium in their ground vibrational states. An atomic model is used to identify the influence of the intrinsic diatomic two-center character of the problem.
Triple-differential cross sections for two-photon double ionization of molecular hydrogen are presented for a central photon energy of 30 eV. The calculations are based on a fully {it ab initio}, nonperturbative, approach to the time-dependent Schroedinger equation in prolate spheroidal coordinates, discretized by a finite-element discrete-variable-representation. The wave function is propagated in time for a few femtoseconds using the short, iterative Lanczos method to study the correlated response of the two photoelectrons to short, intense laser radiation. The current results often lie in between those of Colgan {it et al} [J. Phys. B {bf 41} (2008) 121002] and Morales {it et al} [J. Phys. B {bf 41} (2009) 134013]. However, we argue that these individual predictions should not be compared directly to each other, but preferably to experimental data generated under well-defined conditions.
We investigate the carrier-envelope phase and intensity dependence of the longitudinal momentum distribution of photoelectrons resulting from above-threshold ionization of argon by few-cycle laser pulses. The intensity of the pulses with a center wavelength of 750,nm is varied in a range between $0.7 times 10^{14}$ and $unit[5.5 times 10^{14}]{W/cm^2}$. Our measurements reveal a prominent maximum in the carrier-envelope phase-dependent asymmetry at photoelectron energies of 2,$U_mathrm{P}$ ($U_mathrm{P}$ being the ponderomotive potential), that is persistent over the entire intensity range. Further local maxima are observed at 0.3 and 0.8,$U_mathrm{P}$. The experimental results are in good agreement with theoretical results obtained by solving the three-dimensional time-dependent Schr{o}dinger equation (3D TDSE). We show that for few-cycle pulses, the carrier-envelope phase-dependent asymmetry amplitude provides a reliable measure for the peak intensity on target. Moreover, the measured asymmetry amplitude exhibits an intensity-dependent interference structure at low photoelectron energy, which could be used to benchmark model potentials for complex atoms.
Multiphoton ionization of sodium by femtosecond laser pulses of 800 nm wavelength in the range of laser peak intensities entering over-the-barrier ionization domain is studied. Photoelectron momentum distributions and the energy spectra are determined numerically by solving the time dependent Schroedinger equation for three values of the laser intensity from this domain. The calculated spectra agree well with the spectra obtained experimentally by Hart et al (Phys. Rev. A 2016 93 063426). A partial wave analysis of the spectral peaks related to Freeman resonances has shown that each peak is a superposition of the contributions of photoelectrons produced by the resonantly enhanced multiphoton ionization via different intermediate states. It is demonstrated that at specific laser intensities the selective ionization, which occurs predominantly through a single intermediate state, is possible.
We investigate molecular dynamics of multiple ionization in N2 through multiple core-level photoabsorption and subsequent Auger decay processes induced by intense, short X-ray free electron laser pulses. The timing dynamics of the photoabsorption and dissociation processes is mapped onto the kinetic energy of the fragments. Measurements of the latter allow us to map out the average internuclear separation for every molecular photoionization sequence step and obtain the average time interval between the photoabsorption events. Using multiphoton ionization as a tool of multiple-pulse pump-probe scheme, we demonstrate the modification of the ionization dynamics as we vary the x-ray laser pulse duration.
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