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Register a new userNuclear fission in intense laser fields
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Rapid-advancing intense laser technologies enable the possibility of a direct laser-nucleus coupling. In this paper the effect of intense laser fields on a series of nuclear fission processes, including proton decay, alpha decay, and cluster decay, is theoretically studied with the help of nuclear double folding potentials. The results show that the half-lives of these decay processes can be modified by non-negligible amounts, for example on the order of 0.01 or 0.1 percents in intense laser fields available in the forthcoming years. In addition to numerical results, an approximate analytical formula is derived to connect the laser-induced modification to the decay half-life and the decay energy.
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Application of a parallel-projection inversion technique to z-scan spectra of multiply charged xenon and krypton ions, obtained by non-resonant field ionization of neutral targets, has for the first time permitted the direct observation of intensity-dependent ionization probabilities. These ionization efficiency curves have highlighted the presence of structure in the tunnelling regime, previously unobserved under full-volume techniques.
In the semiclassical picture of photoionization process in intense laser fields, the ionization rate solely depends on the amplitude of the electric field and the final photoelectron momentum corresponds to the instant of ionization of the photoelectron, however, this picture has never been checked rigorously. Recently an attosecond angular streaking technique based on this semiclassical perspective has been widely applied to temporal measurement of the atomic and molecular dynamics in intense laser fields. We use a Wigner-distribution-like function to calculate the time-emission angle distribution, angular distribution and ionization time distribution for atomic ionization process in elliptically polarized few-cycle laser fields. By comparing with semiclassical calculations, we find that the two methods always show discrepancies except in some specific cases and the offset angles are generally not consistent with the offset times of the ionization time distributions obtained by the two methods even when the non-adiabatic effect is taken into account, indicating that the attoclock technique is in principle inaccurate. Moreover, calculations for linearly polarized laser fields also show similar discrepancies between two methods in the ionization time distribution. Our analysis indicates that the discrepancy between the semiclassical and quantum calculations can be attributed to correlation, i. e., temporal nonlocalization effect.
We report on tunnel ionization of Xe by 2-cycle, intense, infrared laser pulses and its dependence on carrier-envelope-phase (CEP). At low values of optical field ($E$), the ionization yield is maximum for cos-like pulses with the dependence becoming stronger for higher charge states. At higher $E$-values, the CEP dependence either washes out or flips. A simple phenomenological model is developed that predicts and confirms the observed results. CEP effects are seen to persist for 8-cycle pulses. Unexpectedly, electron rescattering plays an unimportant role in the observed CEP dependence. Our results provide fresh perspectives in ultrafast, strong-field ionization dynamics of multi-electron systems that lie at the core of attosecond science.
The ionization probability of N$_2$, O$_2$, and CO$_2$ in intense laser fields is studied theoretically as a function of the alignment angle by solving the time-dependent Schrodinger equation numerically assuming only the single-active-electron approximation. The results are compared to recent experimental data [D.~Pavi{v{c}}i{c} et al., Phys.,Rev.,Lett. {bf 98}, 243001 (2007)] and good agreement is found for N$_2$ and O$_2$. For CO$_2$ a possible explanation is provided for the failure of simplified single-active-electron models to reproduce the experimentally observed narrow ionization distribution. It is based on a field-induced coherent core-trapping effect.
In present paper we develop an analytic theory for the harmonic generation of symmetric diatomic molecular ions beyond two-level model, emphasizing the influence of charge-resonance (CR) states those are strongly coupled to electromagnetic fields for large internuclear distance. With taking into account the continuum states that is ignored in the two-level model and become important for intense laser case, our model is capable to produce spectrum for the whole range of harmonic orders consisting of a molecular plateau due to the CR transition and an atomic-like plateau for a long-wavelength excitation, and in good agreement with numerical results from directly solution of the Schrodinger equation. Our theory also identifies the crucial role of the CR states in the fine structure of harmonic spectrum and shows that the harmonic generation in molecular system can be effectively controlled by adjusting the internuclear distance.
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