Search

Attosecond time-resolved electron tunneling dynamics have been investigated by using attosecond angular streaking spectroscopy, where a clock reference to the laser field vector is required in atomic strong-field ionization and the situation becomes complicated in molecules. Here we reveal a resonant ionization process via a transient state by developing an electron-tunneling-site-resolved molecular attoclock in Ar-Kr^{+}. Two distinct deflection angles are observed in the photoelectron angular distribution in the molecular frame, corresponding to the direct and resonant ionization pathways. We find the electron is temporally trapped in the Coulomb potential wells of the Ar-Kr^{+} before finally releasing into the continuum when the electron tunnels through the internal barrier. By utilizing the direct tunneling ionization as a self-referenced arm of the attoclock, the time delay of the electron trapped in the resonant state is revealed to be 3.50±0.04 fs. Our results give an impetus to exploring the ultrafast electron dynamics in complex systems and also endow a semiclassical presentation of the electron trapping dynamics in a quantum resonant state.

A recent ultrafast pump-probe technique has allowed measurement of time delays during photoemission in a variety of systems ranging from atoms and molecules to solids with unprecedented temporal resolution. However, identifying the underlying physics is still a challenge especially in complicated multichannel above-threshold ionization (ATI) experiments. Here we demonstrate that the time delays of different ionization pathways in ATI can be clearly resolved and extracted with a semiclassical statistical method. The remarkable phase shift of near threshold photoelectrons can be attributed to a temporary retrapping of a photoelectron by the atomic potential in a quasibound state after emerging in the continuum state. This continuum-bound-continuum scattering manifests as a new resonant effect in strong-field photoemission. Our results unify the seemingly opposing quantum Eisenbud-Wigner-Smith time delay and classical Coulomb-induced time delay by highlighting the same physical picture, which holds promise for an intuitive interpretation of time-resolved fundamental electronic processes in strong-field experiments and epistemological reexamination of the quantum-classical correspondence.

We theoretically investigate carrier-envelope phase dependence of few-cycle ultrashort laser pulse propagation in a polar molecule medium. Our results show that a soliton pulse can be generated during the two-photon resonant propagation of few-cycle pulse in the polar molecule medium. Moreover, the main features of the soliton pulse, such as pulse duration and intensity, depend crucially on the carrier-envelope phase of the incident pulse, which could be utilized to determine the carrier-envelope phase of a few-cycle ultrashort laser pulse from a mode-locked oscillator.