Coherent electronic dynamics are of great significance in photo-induced processes and molecular magnetism. We theoretically investigate electronic dynamics of triatomic molecule H32+ by circularly polarized pulses, including electron density distributions,… Click to show full abstract
Coherent electronic dynamics are of great significance in photo-induced processes and molecular magnetism. We theoretically investigate electronic dynamics of triatomic molecule H32+ by circularly polarized pulses, including electron density distributions, induced electronic currents, and ultrafast magnetic field generation. By comparing the results of the coherent resonant excitation and direct ionization, we found that for the coherent resonant excitation, the electron is localized and the coherent electron wave packet moves periodically between three protons, which can be attributed to the coherent superposition of the ground A′ state and excited E+ state. Whereas, for the direct single-photon ionization, the induced electronic currents mainly come from the free electron in the continuum state. It is found that there are differences in the intensity, phase, and frequency of the induced current and the generated magnetic field. The scheme allows one to control the induced electronic current and the ultrafast magnetic field generation.
               
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