To clarify the microscopic origin of chirality-induced optical effect, we develop an analytical method that extracts the chiral part of the Hamiltonian of molecular electronic states. We demonstrate this method in a model chiral molecule consisting of two helically stacked N-sided regular polygons, and compare it with numerical calculation for chiral discrimination via high harmonic generation (HHG) of the same molecule. The discrimination signal here is the Kuhn g factor, the difference between the harmonic intensity from the bicircular laser field and that from its reflected laser field normalized by their average. The g factor is a pseudoscalar quantity that reflects the chirality of the molecule. As a result, we find that the g factor becomes large over a wide range of harmonic orders making HHG suitable for chiral discrimination. We further find that to increase the difference of harmonic intensity from the above two fields, the unnormalized g factor, the increase of capacity to generate the longitudinal dipole moment is more advantageous than maximizing the transverse-to-longitudinal conversion efficiency via the optimization of molecular chirality. We speculate this criteria may be extended to other optical and current-induced processes relevant to the chiral molecules and materials.
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Kato et al. (2024) studied this question.
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