Shifting nodal-plane suppressions in high-order-harmonic spectra from diatomic molecules in orthogonally polarized driving fields

Abstract

We analyze the imprint of nodal planes in high-order harmonic spectra from aligned diatomic molecules in intense laser fields whose components exhibit orthogonal polarizations. We show that the typical suppression in the spectra associated to nodal planes is distorted, and that this distortion can be employed to map the electron's angle of return to its parent ion. This investigation is performed semi-analytically at the single-molecule response and single-active orbital level, using the strong-field approximation and the steepest descent method. We show that the velocity form of the dipole operator is superior to the length form in providing information about this distortion. However, both forms introduce artifacts that are absent in the actual momentum-space wavefunction. Furthermore, elliptically polarized fields lead to larger distortions in comparison to two-color orthogonally polarized fields. These features are investigated in detail for O2, whose highest occupied molecular orbital provides two orthogonal nodal planes.

Two-color phase-of-the-phase spectroscopy in the multiphoton regime

“…A plethora of two-color studies have been performed recently, with different combinations of laser frequencies and polarizations [9][10][11][12][13][14][15][16][17][18][19][20][21][22][23][24][25]. Important foreseeable applications of two-color fields are the efficient generation of THz radiation from plasmas [13] or the control of strong-field phenomena by steering the electron emission [26], for instance.…”