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Register a new userStrong chiral dichroism in above threshold ionization and ionization rates from locally-chiral light
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We derive here a new highly selective photoelectron-based chirality-sensing technique that utilizes locally-chiral laser pulses. We show that this approach results in strong chiral discrimination, where the standard forwards/backwards asymmetry of photoelectron circular dichroism (PECD) is lifted. The resulting dichroism is much larger and more robust than conventional PECD, is found in all hemispheres, and is not symmetric or antisymmetric with respect to any symmetry operator. Remarkably, a CD of up to 10% survives in the angularly-integrated above-threshold ionization (ATI) spectra, and of up to 5% in the total ionization rates. We demonstrate these results through ab-initio calculations in the chiral molecules Bromochlorofluoromethane, Limonene, Fenchone, and Camphor. We also explore the parameter-space of the locally-chiral field and show that the observed CD is strongly correlated to the degree of chirality of the light, validating it as a measure for chiral-interaction strengths. Our results pave the way for highly selective probing of ultrafast chirality in ATI, can potentially lead to all-optical enantio-separation, and motivate the use of locally-chiral light for enhancing ultrafast spectroscopies.
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We investigate the differential ionization probability of chiral molecules in the strong field regime as a function of the helicity of the incident light. To this end, we analyze the fourfold ionization of bromochlorofluoromethane (CHBrClF) with subsequent fragmentation into four charged fragments and different dissociation channels of the singly ionized methyloxirane. We observe a variation of the differential ionization probability in a range of several percent. Accordingly, we conclude that the helicity of light is a quantity that should be considered for the theoretical description of the strong field ionization rate of chiral molecules.
The role of Coulomb focusing in above-threshold ionization in an elliptically polarized mid-infrared strong laser field is investigated within a semiclassical model incorporating tunneling and Coulomb field effects. It is shown that Coulomb focusing up to moderate ellipticity values is dominated by multiple forward scattering of the ionized electron by the atomic core that creates a characteristic low-energy structure in the photoelectron spectrum and is responsible for the peculiar energy scaling of the ionization normalized yield along the major polarization axis. At higher ellipticities, the electron continuum dynamics is disturbed by the Coulomb field effect mostly at the exit of the ionization tunnel. Due to the latter, the normalized yield is found to be enhanced, with the enhancement factor being sharply pronounced at intermediate ellipticities.
Above-threshold ionization spectra from cesium are measured as a function of the carrier-envelope phase (CEP) using laser pulses centered at 3.1 $mu$m wavelength. The directional asymmetry in the energy spectra of backscattered electrons oscillates three times, rather than once, as the CEP is changed from $0$ to $2pi$. Using the improved strong-field approximation, we show that the unusual behavior arises from the interference of few quantum orbits. We discuss the conditions for observing the high-order CEP dependence, and draw an analogy with time-domain holography with electron wave packets.
Multiphoton ionization provides a clear window into the nature of electron correlations in the helium atom. In the present study, the final state energy range extends up to the region near the $N=2$ and $N=3$ ionization thresholds, where two-photon ionization proceeds via continuum intermediate states above the lowest threshold. Our calculations are performed using multichannel quantum defect theory (MQDT) and the streamlined R-matrix method. The sum and integration over all intermediate states in the two-photon ionization amplitude is evaluated using the inhomogeneous R-matrix method developed by Robicheaux and Gao. The seamless connection of that method with MQDT allows us to present high resolution spectra of the final state Rydberg resonances. Our analysis classifies the resonances above the $N=2$ threshold in terms of their group theory quantum numbers. Their dominant decay channels are found to obey the previously conjectured propensity rule far more weakly for these even parity states than was observed for the odd-parity states relevant to single photon ionization.
The yield of strong-field ionization, by a linearly polarized probe pulse, is studied experimentally and theoretically, as a function of the relative orientation between the laser field and the molecule. Experimentally, carbonyl sulfide, benzonitrile and naphthalene molecules are aligned in one or three dimensions before being singly ionized by a 30 fs laser pulse centered at 800 nm. Theoretically, we address the behaviour of these three molecules. We consider the degree of alignment and orientation and model the angular dependence of the total ionization yield by molecular tunneling theory accounting for the Stark shift of the energy level of the ionizing orbital. For naphthalene and benzonitrile the orientational dependence of the ionization yield agrees well with the calculated results, in particular the observation that ionization is maximized when the probe laser is polarized along the most polarizable axis. For OCS the observation of maximum ionization yield when the probe is perpendicular to the internuclear axis contrasts the theoretical results.
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