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Numerical attoclock is a theoretical model of attosecond angular streaking driven by a very short, nearly a single oscillation, circularly polarized laser pulse. The reading of such an attoclock is readily obtained from a numerical solution of the time-dependent Schrödinger equation as well as a semiclassical trajectory simulation. By comparing the two approaches, we highlight the essential physics behind the attoclock measurements. In addition, we analyze the predictions of the Keldysh-Rutherford model of the attoclock [A. W. Bray et al., Phys. Rev. Lett. 121, 123201 (2018)]. In molecular hydrogen, we highlight a strong dependence of the width of the attoclock angular peak on the molecular orientation and attribute it to the two-center electron interference. This effect is further exemplified in the weakly bound neon dimer.

Using classical arguments Wannier [Phys. Rev. 90, 817 (1953)PHRVAO0031-899X10.1103/PhysRev.90.817] proposed an electron-impact ionization cross section for neutral atoms to behave as E1.127, where E is the excess energy above threshold. Using similar arguments Klar [J. Phys. B 14, 4165 (1981)JPAMA40022-370010.1088/0022-3700/14/21/027] obtained E2.65 to be the corresponding threshold law for positron impact. Recently, Babij et al. [Phys. Rev. Lett. 120, 113401 (2018)PRLTAO0031-900710.1103/PhysRevLett.120.113401] measured near-threshold positron-impact breakup behavior to be similar to that expected for electrons. Using the convergent close-coupling method for the atomic hydrogen target, we examine cross sections at near-threshold energies for electron and positron impact. Contrary to the experiment, the calculated cross sections are found to behave differently for the two projectiles and consistently with the aforementioned threshold laws, despite the entirely quantum nature of these problems. For electron impact, the threshold behavior holds while the total electron spin asymmetry remains constant, whereas for positron scattering the threshold law holds for breakup while the positronium-formation component of the ionization cross section remains constant.

We demonstrate a clear similarity between attoclock offset angles and Rutherford scattering angles taking the Keldysh tunneling width as the impact parameter and the vector potential of the driving pulse as the asymptotic velocity. This simple model is tested against the solution of the time-dependent Schrodinger equation using hydrogenic and screened (Yukawa) potentials of equal binding energy. We observe a smooth transition from a hydrogenic to "hard-zero" intensity dependence of the offset angle with variation of the Yukawa screening parameter. Additionally, we make a comparison with the attoclock offset angles for various noble gases obtained with the classical-trajectory Monte Carlo method. In all cases we find a close correspondence between the model predictions and numerical calculations. This suggests a largely Coulombic origin of the attoclock offset angle and casts further doubt on its interpretation in terms of a finite tunneling time.

We report on a kinematically complete measurement of double ionization of helium by a single 1100 eV circularly polarized photon. By exploiting dipole selection rules in the two-electron continuum state, we observed the angular emission pattern of electrons originating from a pure quadrupole transition. Our fully differential experimental data and companion ab initio nonperturbative theory show the separation of dipole and quadrupole contributions to photo-double-ionization and provide new insight into the nature of the quasifree mechanism.

We consider photoemission from the 4 d shell of the free Xe and encapsulated Xe@ C 60 atoms by ionizing XUV and probing IR fields typical for a RABBITT (reconstruction of attosecond beating by interference of two-photon transitions) measurement.

We study the time delay in the primary photoemission channel near the opening of an additional channel and compare it with the Wigner time delay in elastic scattering of the photoelectron near the corresponding inelastic threshold. The photoemission time delay near threshold is significantly enhanced, to a measurable 40 as, in comparison to the corresponding elastic scattering delay. The enhancement is due to the different lowest order of interelectron interaction coupling the primary and additional photoemission channels. We illustrate these findings by considering photodetachment from the H− negative ion, and compare it with electron scattering on the hydrogen atom near the first excitation threshold. Other threshold processes of atomic photoionization and molecular photofragmentation, where photoemission time delay is enhanced, are identified. This opens the possibility of studying threshold behavior utilizing attosecond chronoscopy.