Siegert pseudostate perturbation theory: one- and two-threshold cases

Perturbation theory for the Siegert pseudostates (SPS) [Phys.Rev.A 58, 2077 (1998) and Phys.Rev.A 67, 032714 (2003)] is studied for the case of two energetically separated thresholds. The perturbation formulas for the one-threshold case are derived as a limiting case whereby we reconstruct More's theory for the decaying states [Phys.Rev.A 3,1217(1971)] and amend an error. The perturbation formulas for the two-threshold case have additional terms due to the non-standard orthogonality relationship of the Siegert Pseudostates. We apply the theory to a 2-channel model problem, and find the rate of convergence of the perturbation expansion should be examined with the aide of the variance $D= ||E-\sum_{n}\lambda^n E^{(n)}||$ instead of the real and imaginary parts of the perturbation energy individually

Probing dipole-forbidden autoionizing states by isolated attosecond pulses

We propose a general technique to retrieve the information of dipole-forbidden resonances in the autoionizing region. In the simulation, a helium atom is pumped by an isolated attosecond pulse in the extreme ultraviolet (EUV) combined with a few-femtosecond laser pulse. The excited wave packet consists of the $^1S$, $^1P$, and $^1D$ states, including the background continua, near the $2s2p(^1P)$ doubly excited state. The resultant electron spectra with various laser intensities and time delays between the EUV and laser pulses are obtained by a multilevel model and an ab initio time-dependent Schr\"odinger equation calculation. By taking the ab initio calculation as a "virtual measurement", the dipole-forbidden resonances are characterized by the multilevel model. We found that in contrast to the common assumption, the nonresonant coupling between the continua plays a significant role in the time-delayed electron spectra, which shows the correlation effect between photoelectrons before they leave the core. This technique takes the advantages of ultrashort pulses uniquely and would be a timely test for the current attosecond technology.Comment: 10 pages, 6 figure

Accurate retrieval of structural information from laser-induced photoelectron and high-harmonic spectra by few-cycle laser pulses

By analyzing ``exact'' theoretical results from solving the time-dependent Schr\"odinger equation of atoms in few-cycle laser pulses, we established the general conclusion that differential elastic scattering and photo-recombination cross sections of the target ion with {\em free} electrons can be extracted accurately from laser-generated high-energy electron momentum spectra and high-order harmonic spectra, respectively. Since both electron scattering and photoionization (the inverse of photo-recombination) are the conventional means for interrogating the structure of atoms and molecules, this result shows that existing few-cycle infrared lasers can be implemented for ultrafast imaging of transient molecules with temporal resolution of a few femtoseconds.Comment: 4 pages, 4 figure

Retrieval of electron-atom scattering cross sections from laser-induced electron rescattering of atomic negative ions in intense laser fields

We investigated the two-dimensional electron momentum distributions of atomic negative ions in an intense laser field by solving the time-dependent Schrodinger equation (TDSE) and using the first- and 2nd-order strong-field approximations (SFA). We showed that photoelectron energy distributions and low-energy photoelectron momentum spectra predicted from SFA are in reasonable agreement with the solutions from the TDSE. More importantly, we showed that accurate electron-atom elastic scattering cross sections can be retrieved directly from high-energy electron momentum spectra of atomic negative ions in the laser field. This opens up the possibility of measuring electron-atom and electron-molecule scattering cross sections from the photodetachment of atomic and molecular negative ions by intense short lasers, respectively, with temporal resolutions in the order of femtoseconds.Comment: 6 papges, 5 figure

Effect of nuclear motion on tunneling ionization rates of molecules

ISSN:1094-1622ISSN:0556-2791ISSN:1050-294