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Physics Faculty Research & Creative Works

Molecules

2009

Articles 1 - 2 of 2

Full-Text Articles in Physical Sciences and Mathematics

Quantitative Rescattering Theory For High-Order Harmonic Generation From Molecules, Anh-Thu Le, R. R. Lucchese, S. Tonzani, Toru Morishita, C. D. Lin Jul 2009

Quantitative Rescattering Theory For High-Order Harmonic Generation From Molecules, Anh-Thu Le, R. R. Lucchese, S. Tonzani, Toru Morishita, C. D. Lin

Physics Faculty Research & Creative Works

The quantitative rescattering theory (QRS) for high-order harmonic generation (HHG) by intense laser pulses is presented. According to the QRS, HHG spectra can be expressed as a product of a returning electron wave packet and the photorecombination differential cross section of the laser-free continuum electron back to the initial bound state. We show that the shape of the returning electron wave packet is determined mostly by the laser. The returning electron wave packets can be obtained from the strong-field approximation or from the solution of the time-dependent Schrödinger equation (TDSE) for a reference atom. The validity of the QRS is …


Probing Molecular Frame Photoionization Via Laser Generated High-Order Harmonics From Aligned Molecules, Anh-Thu Le, R. R. Lucchese, M. T. Lee, C. D. Lin May 2009

Probing Molecular Frame Photoionization Via Laser Generated High-Order Harmonics From Aligned Molecules, Anh-Thu Le, R. R. Lucchese, M. T. Lee, C. D. Lin

Physics Faculty Research & Creative Works

Present experiments cannot measure molecular frame photoelectron angular distributions (MFPAD) for ionization from the outermost valence orbitals of molecules. We show that the details of MFPAD can be retrieved with high-order harmonics generated by infrared lasers from aligned molecules. Using accurately calculated photoionization transition dipole moments for fixed-in-space molecules, we show that the dependence of the magnitude and phase of the high-order harmonics on the alignment angle of the molecules observed in recent experiments can be quantitatively reproduced. This result provides the needed theoretical basis for ultrafast dynamic chemical imaging using infrared laser pulses.