Quantum unidirectional rotation directly imaged with molecules.

A gas-phase molecular ensemble coherently excited to have an oriented rotational angular momentum has recently emerged as an appropriate microscopic system to illustrate quantum mechanical behavior directly linked to classical rotational motion, which has a definite direction. To realize an intuitive visualization of such a unidirectional molecular rotation, we report high-resolution direct imaging of direction-controlled rotational wave packets in nitrogen molecules. The rotational direction was regulated by a pair of time-delayed, polarization-skewed laser pulses, introducing the dynamic chirality to the system.

Carrier-envelope phase-dependent high harmonic generation in the water window using few-cycle infrared pulses.

High harmonic generation (HHG) using waveform-controlled, few-cycle pulses from Ti:sapphire lasers has opened emerging researches in strong-field and attosecond physics. However, the maximum photon energy of attosecond pulses via HHG remains limited to the extreme ultraviolet region. Long-wavelength light sources with carrier-envelope phase stabilization are promising to extend the photon energy of attosecond pulses into the soft X-ray region.

Ultrafast angular momentum orientation by linearly polarized laser fields.

We theoretically show and experimentally verify that a pair of linearly polarized intense femtosecond pulses can create molecular ensembles with oriented rotational angular momentum on an ultrafast (approximately ps) time scale, when the delay and the mutual polarization between them are appropriately arranged. An asymmetric distribution for +M and -M sublevels relies on quantum interference between rotational wave packets created in stimulated Raman excitation by the first and second pulses. The present approach provides spatiotemporally propagating ensembles, of which the classical perspective is molecules rotating in a clockwise or counterclockwise direction.