Rydberg-state excitation of atoms in strong infrared laser fields provides a new complementary aspect of the perspective of atom--strong field interactions. In this article, we perform an experimental and theoretical study on the corresponding process of diatomic molecules,
N2 and
O2. We show that neutral molecules can also survive strong 800-nm laser fields in high Rydberg states, while their behavior is remarkably different in comparison with their companion atoms, Ar and Xe. The Rydberg excitation of
N2 generally behaves similarly to Ar, while that of
O2 is more significantly suppressed than the ionization compared to Xe in a high intensity region, which can be understood in the frame of a semiclassical picture, together with their different structures of molecular orbitals. However, distinct quantum features in the Rydberg excitation processes that are apparently beyond the semiclassical picture have been identified, i.e., the less suppressed probability of
O2 at low intensity and the oscillation behavior of the ratio between
N2 and Ar, indicating that our understanding of the relevant physics is still far from complete.
Neutral Rydberg state excitation in strong UV laser fields of Xe atoms has been studied and compared with direct ionization. The yields of both strong-field excitation and ionization have been measured as a function of UV laser intensity and ellipticity. The underlying physical mechanism has been discussed based on the experimental results, indicating that the Rydberg states are populated via multi-photon resonance excitation in strong 400 nm laser fields. Finally, a comparative study of Xe and
O2 with similar ionization potentials have been performed, showing the suppressed excitation of molecules in strong UV laser fields.
Rydberg state excitations of neutral nitric oxide molecules are studied in strong ultraviolet (UV) and near-infra-red (IR) laser fields using a linear time-of-flight (TOF) mass spectrometer with the pulsed electronic field ionization method. The yield of Rydberg molecules is measured as a function of laser intensity and ellipticity, and the results in UV laser fields are compared with those in near-IR laser fields. The present study provides the first experimental evidence of neutral Rydberg molecules surviving in a strong laser field. The results indicate that a rescattering-after-tunneling process is the main contribution to the formation of Rydberg molecules in strong near-IR laser fields, while multi-photon excitation may play an important role in the strong UV laser fields.
Using field ionization combined with the direct detection of excited neutral atoms we measured the distribution of principal quantum number n of excited He Rydberg states after strong-field excitation at laser intensities well in the tunneling regime. Our results confirm theoretical predictions from semiclassical and quantum mechanical calculations and simultaneously underpin the validity of the semiclassical frustrated tunneling ionization model. Moreover, since our experimental detection scheme is spin sensitive in the case of He atoms, we show that strong-field excitation leads to strong population of triplet states. The origin of it lies in the fact that high angular momentum states are accessible in strong-field excitation. Thus, singlet-triplet transitions become possible due to the increased importance of spin-orbit interaction rather than due to direct laser induced spin-flip processes.
Electron capture cross sections for coherent elliptic Rydberg states have been measured as a function of eccentricity. The ion impact velocity was parallel to the minor axis of the associated, classical elliptic orbit and both clockwise and anticlockwise orbital motion of the electron were studied. The incoming ions were 2.5 keV 23 Na + and the Rydberg target, with principal quantum number n=25, was formed by laser excitation of Li atoms with subsequent adiabatic switching of crossed, external electric and magnetic fields. A strong dependence on eccentricity and sense of orbital motion was found.
We investigated the Rydberg-state excitation process of a hydrogen atom subjected to spatially homogeneous and inhomogeneous laser fields by means of ab initio calculations. It is found that, comparing with atoms exposed to spatially homogeneous laser fields, the excitation probability decreases and the electron tends to occupy the states with lower principal quantum numbers and angular quantum numbers for atoms in spatially inhomogeneous laser pulses. Furthermore, calculations of a quantum model without taking into account ionization of the electron after it is coherently captured by the Rydberg state are inconsistent with the above-stated findings by ab initio calculations. Analysis indicates that the aforementioned intriguing features can be attributed to the enhanced ionization of the Rydberg states by inhomogeneous laser fields since the distributions of Rydberg states of high principal quantum numbers and angular quantum numbers locate far away from the core where the inhomogeneous electric fields become significant.