T.T. Gorman [1], T.D. Scarborough [1], P.M. Abanador [2], F. Mauger [2], D. Kiesewetter [1], P. Sándor [3], S. Khatri [3], K. Lopata [4], K.J. Schafer [2], P. Agostini [1], M.B. Gaarde [2], and L.F. DiMauro [1]
[1] Department of Physics, The Ohio State University, Columbus, Ohio 43210, USA
[2] Department of Physics and Astronomy, Louisiana State University, Baton Rouge, Louisiana 70803, USA
[3] Department of Physics, University of Virginia, Charlottesville, Virginia 22904, USA
[4] Department of Chemistry, Louisiana State University, Baton Rouge, Louisiana 70803, USA
Abstract:We present molecular-frame measurements of the recombination dipole matrix element (RDME) in CO2, N2O, and carbonyl sulfide (OCS) molecules using high-harmonic spectroscopy. Both the amplitudes and phases of the RDMEs exhibit clear imprints of a two-center interference minimum, which moves in energy with the molecular alignment angle relative to the laser polarization. We find that whereas the angle dependence of this minimum is consistent with the molecular geometry in CO2 and N2O, it behaves very differently in OCS; in particular, the phase shift which accompanies the two-center minimum changes sign for different alignment angles. Our results suggest that two interfering structural features contribute to the OCS RDME, namely, (i) the geometrical two-center minimum and (ii) a Cooper-like, electronic-structure minimum associated with the sulfur end of the molecule. We compare our results to ab initio calculations using time-dependent density functional theory and present an empirical model that captures both the two-center and the Cooper-like interferences. We also show that the yield from unaligned samples of two-center molecules is, in general, reduced at high photon energies compared to aligned samples, due to the destructive interference between molecules with different alignments.
Status: Published, J. Chem. Phys. 150, 184308 (2019).
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