Using Time-Dependent Density Functional Theory (TDDFT) nonlinear nonperturbative response of the molecular system is studied for photoisomerization reaction. The 1,3-cyclohexadiene photoisomerization is probed by the high-harmonic generation (HHG) process induced by the ultrashort few femtosecond intense laser pulse. For each of the long-lived or stable isomers, we present results for HHG spectra and HHG ellipticities, as well as multi-photon ionization. Moreover, the laser-induced electronic excitations are calculated and the effect of excitations on HHG spectra is discussed. We describe the characteristic properties of the nonlinear response for each of the isomers that can be used for ultrafast detection of the isomers by tracking the specific changes in HHG response.
BT - Submitted N2 -Using Time-Dependent Density Functional Theory (TDDFT) nonlinear nonperturbative response of the molecular system is studied for photoisomerization reaction. The 1,3-cyclohexadiene photoisomerization is probed by the high-harmonic generation (HHG) process induced by the ultrashort few femtosecond intense laser pulse. For each of the long-lived or stable isomers, we present results for HHG spectra and HHG ellipticities, as well as multi-photon ionization. Moreover, the laser-induced electronic excitations are calculated and the effect of excitations on HHG spectra is discussed. We describe the characteristic properties of the nonlinear response for each of the isomers that can be used for ultrafast detection of the isomers by tracking the specific changes in HHG response.
PY - 2024 T2 - Submitted TI - High-order harmonic generation probing of a ring-opening reaction UR - https://arxiv.org/abs/2408.02216 ER -