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High-order harmonic generation in polyatomic molecules generally involves multiple channels, each associated with a different orbital. Their unambiguous assignment remains a major challenge for high-harmonic spectroscopy. Here we present a multi-modal approach, using unaligned SF$_6$ molecules as an example, where we combine methods from extreme-ultraviolet spectroscopy, above-threshold ionization and attosecond metrology. Channel-resolved above-threshold ionization measurements reveal that strong-field ionization opens four channels. Two of them, identified by monitoring the ellipticity dependence of the high-harmonic emission, are found to dominate the harmonic signal. A switch from the HOMO-3 to the HOMO-1 channel at 26 eV is confirmed by a phase jump in the harmonic emission, and by the differing dynamical responses to molecular vibrations. This study demonstrates a modus operandi for extending high-harmonic spectroscopy to polyatomic molecules, where complex attosecond dynamics are expected.
High-order harmonic generation is a powerful and sensitive tool for probing atomic and molecular structures, combining in the same measurement an unprecedented attosecond temporal resolution with a high spatial resolution, of the order of the angstro
High-order harmonic generation by a bicircular field, which consists of two coplanar counter-rotating circularly polarized fields of frequency $romega$ and $somega$ ($r$ and $s$ are integers), is investigated for a polyatomic molecule. This field pos
We present an experimental technique using orbital angular momentum (OAM) in a fundamental laser field to drive High Harmonic Generation (HHG). The mixing of beams with different OAM allows to generate two laser foci tightly spaced to study the phase
We study theoretically and experimentally the electronic relaxation of NO2 molecules excited by absorption of one ~400 nm pump photon. Semi-classical simulations based on trajectory surface hopping calculations are performed. They predict fast oscill
An all-optical measurement of high-order fractional molecular echoes is demonstrated by using high-order harmonic generation (HHG). Excited by a pair of time-delayed short laser pulses, the signatures of full and high order fractional (1/2 and 1/3) a