Accurate in situ Measurement of Ellipticity Based on Subcycle Ionization Dynamics.

Elliptically polarized laser pulses (EPLPs) are widely applied in many fields of ultrafast sciences, but the ellipticity (ϵ) has never been in situ measured in the interaction zone of the laser focus. In this Letter, we propose and realize a robust scheme to retrieve the ϵ by temporally overlapping two identical counterrotating EPLPs. The combined linearly electric field is coherently controlled to ionize Xe atoms by varying the phase delay between the two EPLPs. The electron spectra of the above-threshold ionization and the ion yield are sensitively modulated by the phase delay. We demonstrate that these modulations can be used to accurately determine ϵ of the EPLP. We show that the present method is highly reliable and is applicable in a wide range of laser parameters. The accurate retrieval of ϵ offers a better characterization of a laser pulse, promising a more delicate and quantitative control of the subcycle dynamics in many strong field processes.

Proposal for Measuring Electron Displacement Induced by a Short Laser Pulse.

In laser-matter interaction, most previous studies have focused on the change of the electron momentum induced by the external fields. Here, we theoretically investigate the electron displacement induced by an ultrashort pulse, whose precise waveform is hard to determine experimentally. We propose and numerically demonstrate a scheme to accurately measure the electron displacement using a ruler formed by the interfering spirals in the photoelectron momentum distribution generated by two oppositely circularly polarized pulses. The scheme is robust against the focusing volume effects and the jitter of the carrier envelope phase of the two circular pulses. The ability to measure the electron displacement by an arbitrary pulse may pave the way to quantitative control of the charge migration in matter on the scale of Ångström.

Efficient time-sampling method in Coulomb-corrected strong-field approximation.

One of the main goals of strong-field physics is to understand the complex structures formed in the momentum plane of the photoelectron. For this purpose, different semiclassical methods have been developed to seek an intuitive picture of the underlying mechanism. The most popular ones are the quantum trajectory Monte Carlo (QTMC) method and the Coulomb-corrected strong-field approximation (CCSFA), both of which take the classical action into consideration and can describe the interference effect. The CCSFA is more widely applicable in a large range of laser parameters due to its nonadiabatic nature in treating the initial tunneling dynamics. However, the CCSFA is much more time consuming than the QTMC method because of the numerical solution to the saddle-point equations. In the present work, we present a time-sampling method to overcome this disadvantage. Our method is as efficient as the fast QTMC method and as accurate as the original treatment in CCSFA. The performance of our method is verified by comparing the results of these methods with that of the exact solution to the time-dependent Schrödinger equation.

Nonadiabatic Electron Dynamics in Orthogonal Two-Color Laser Fields with Comparable Intensities.

We theoretically investigate the nonadiabatic subcycle electron dynamics in orthogonally polarized two-color laser fields with comparable intensities. The photoelectron dynamics is simulated by exact solution to the 3D time-dependent Schrödinger equation, and also by two other semiclassical methods, i.e., the quantum trajectory Monte Carlo simulation and the Coulomb-corrected strong field approximation. Through these methods, we identify the underlying mechanisms of the subcycle electron dynamics and find that both the nonadiabatic effects and the Coulomb potential play very important roles. The contribution of the nonadiabatic effects manifest in two aspects, i.e., the nonadiabatic ionization rate and the nonzero initial velocities at the tunneling exit. The Coulomb potential has a different impact on the electrons' trajectories for different relative phases between the two pulses.