Population of Doubly Excited States in Strong Laser Pulses

Joel Venzke, Brynn Reiff, Zetong Xue +3 more

Michael L. Bajema, Robert van Leeuwen, Elena Murgu +1 more

We have experimentally observed the time dependence of the population oscillation between a doubly excited state and singly excited Rydberg states subsequent to excitation by a short laser pulse. Specifically, we have examined the case in which the configuration interaction between a doubly excited state and a singly excited Rydberg series is weak. The data are quantitatively reproduced using a quantum defect theory calculation, and we contrast simple classical pictures of the population oscillation for weak and strong configuration interaction. We also observe significant, and unexpected, Raman redistribution by the final laser pulse, and we are able to demonstrate that it occurs primarily by Raman transitions via a lower state, not via the continuum.

Ioannis Liontos, S. Cohen, Agisilaos Bolovinos

We report on the single and double multiphoton ionization of ground state Sr atoms observed in an atomic beam experiment with laser pulses of ∼5 ns duration, maximum intensity ∼4 × 10 11 W cm −2 and within the 710–740 nm wavelength range. The Sr + spectrum consists of two strong lines originating from three-photon resonant four-photon ionization of bound states, a number of weak autoionizing resonances and a broad line due to four-photon excitation of the doubly excited 5p 2 1 S 0 state. The latter, along with a strong, broad and structured spectral feature, is also evident in the wavelength dependence of the doubly charged Sr 2+ ion. A weakly evident but reproducible inflection point ('knee' structure) appears in the intensity dependence of the Sr 2+ yield at the location of the 5p 2 1 S 0 resonance. A complementary fluorescence experiment revealed the accumulation of population in the 5p 1/2 , 3/2 , 6s 1/2 and 5d 3/2 , 5/2 excited Sr + states during the laser pulse. All fluorescence signals depend on laser wavelength in a manner similar to the recorded Sr + spectrum. The population accumulation in the 5p 1/2 , 3/2 ionic states unambiguously proves the absorption of two photons above the first 5s 1/2 atomic threshold while that of the 5d 3/2 , 5/2 and 6s 1/2 ones suggest the absorption of at least two more. Since under our laser pulse duration and intensity the absorption of such a number of photons in an unstructured continuum is highly improbable, it may be concluded that the process is mediated by dense manifolds of near- resonant doubly excited states, their role in the dynamics of laser–atom interaction under our conditions being far more crucial than in studies conducted using intense ultrashort pulses.

Constantine Mavroyannis

Constantine Mavroyannis

Z. Q. Yang, Difa Ye, Thomas Ding +2 more

In the present paper, we investigate the time-resolved transient absorption spectroscopy of doubly excited states of helium atoms by solving the time-dependent two-electron Schr\"odinger equation numerically based on a one-dimensional model. The helium atoms are subjected to an extreme ultraviolet (XUV) attosecond pulse and a time-delayed infrared (IR) few-cycle laser pulse. A superposition of doubly excited states populated by the XUV pulse is identified, which interferes with the direct ionization pathway leading to Fano resonance profiles in the photoabsorption spectrum. In the presence of an IR laser, however, the Fano line profiles are strongly modified: A shifting, splitting, and broadening of the original absorption lines is observed when the XUV attosecond pulse and infrared few-cycle laser pulse overlap in time, which is in good agreement with recent experimental results. At certain time delays, we observe symmetric Lorentz, inverted Fano profiles, and even negative absorption cross sections indicating that the XUV light can be amplified during the interaction with atoms. We further prove that the above pictures are general for different doubly excited states by suitably varying the frequency of the IR field to coherently couple the corresponding states.