We design four linearly x-and y-polarized as well as circularly right (+) and left (−) polarized,
resonant π/2-laser pulses that prepare the model benzene molecule in four different …

Being motivated by the recent progress in attosecond laser technology, we theoretically
explore the strategy of inducing ultrafast electron dynamics inherent to aromatic molecules …

Recently, it was shown that a well-designed laser pulse may prepare an oriented linear
molecular ion in a specific superposition state of the electronic ground (g) and first excited …

Control of π-electrons in polycyclic aromatic hydrocarbons (PAHs) is one of the fundamental
issues in optoelectronics for ultrafast optical switching devices. We have proposed an …

In this work we quantitatively study the reliability of the frozen nuclei approximation for
ultrafast dynamics. Specifically we study laser excitation of HCCI+ from its ground state to …

We present results for quantum optimal control (QOC) of the coherent π electron ring
currents in polycyclic aromatic hydrocarbons (PAHs). Since PAHs consist of a number of …

Reducing decoherence is an essential step toward realizing general‐purpose quantum
computers beyond the present noisy intermediate‐scale quantum (NISQ) computers. To this …

Adiabatic attosecond charge migration (AACM) in a linear molecule or cation such as HCCI+
means that the system has been prepared in a superposition state eg of the electronic …

Electronic charge of molecules can move on time scales when the nuclei stand practically
still, from few hundreds of attoseconds to few femtoseconds. This ultrafast process is called" …

Coherent dynamics of localised π-electron rotations in an aromatic ring molecule may play
an important role in designing next generation photo-induced organic molecular devices. In …