Johannes Floß, Ilya Sh. Averbukh
We provide a detailed theoretical analysis of molecular rotational excitation by a chiral pulse train -- a sequence of linearly polarised pulses with the polarisation direction rotating from pulse to pulse by a controllable angle. Molecular rotation with a preferential rotational sense (clockwise or counter-clockwise) can be excited by this scheme. We show that the directionality of the rotation is caused by quantum interference of different excitation pathways. The chiral pulse train is capable of selective excitation of molecular isotopologues and nuclear spin isomers in a mixture. We demonstrate this using 14N2 and 15N2 as examples for isotopologues, and para- and ortho-nitrogen as examples for nuclear spin isomers.
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http://arxiv.org/abs/1210.8335
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