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Asymmetric molecules look different when viewed from one side or the other. This difference influences the electronic structure of the valence electrons, thereby giving stereo sensitivity to chemistry and biology. We show that attosecond and re-collision science provides a detailed and sensitive probe of electronic asymmetry. On each 1/2 cycle of an intense light pulse, laser-induced tunnelling extracts an electron wave packet from the molecule. When the electron wave packet recombines, alternately from one side of the molecule or the other, its amplitude and phase asymmetry determines the even and odd harmonics radiation that it generates. This harmonic spectrum encodes three manifestations of asymmetry; an amplitude and phase asymmetry in electron tunneling; an asymmetry in the phase that the electron wave packet accumulates relative to the ion between the moment of ionization and recombination; and an asymmetry in the amplitude and phase of the transition moment. We report the first measurement of high harmonics from oriented gas samples. We determine the phase asymmetry of the attosecond XUV pulses emitted when an electron recollides from opposite sides of the CO molecule, and the phase asymmetry of the recollision electron just before recombination. We discuss how the various contributions to asymmetry can be isolated in future experiments.
Using dynamical Hartree-Fock mean-field theory, we study the high-harmonic generation (HHG) in the fullerene molecules C$_{60}$ and C$_{70}$ under strong pump wave driving. We consider a strong-field regime and show that the output harmonic radiation
We show that the dependence of high-order harmonic generation (HHG) on the molecular orientation can be understood within a theoretical treatment that does not involve the strong field of the laser. The results for H_2 show excellent agreement with t
This paper has been withdrawn by the authors because the wave packet propagation used in the ion-dynamics calculation did not allow for electron-nuclei correlation. Hence, the conclusion that the ion-dynamics model is not in agreement with experiment is not substantiated.
We identify that both the dynamic core polarization and dynamic orbital deformation are important in the orientation-dependent high-harmonic generation of CO molecules subjected to intense few cycle laser fields. These polarization dynamics allow for
We develop the strong-field approximation for high-order harmonic generation in hydrogen molecules, including the vibrational motion and the laser-induced coupling of the lowest two Born-Oppenheimer states in the molecular ion that is created by the