Niikura Hiromichi, Corkum P B, Villeneuve D M
National Research Council of Canada, 100 Sussex Drive, Ottawa, Ontario, Canada K1A 0R6.
Phys Rev Lett. 2003 May 23;90(20):203601. doi: 10.1103/PhysRevLett.90.203601. Epub 2003 May 21.
Intense, nonresonant laser fields produce Stark shifts that strongly modify the potential energy surfaces of a molecule. A vibrational wave packet can be guided by this Stark shift if the laser field is appropriately modulated during the wave packet motion. We modulated a 70 fs laser pulse with a period on the time scale of the vibrational motion (approximately 10 fs) by mixing the signal and idler of an optical parametric amplifier. We used ionization of H2 or D2 to launch a vibrational wave packet on the ground state of H2(+) or D2(+). If the laser intensity was high as the wave packet reached its outer turning point, the Stark shift allowed the molecule to dissociate through bond softening. On the other hand, if the field was small at this critical time, little dissociation was measured. By changing the modulation period, we achieved control of the dissociation yield with a contrast of 90%.
强非共振激光场会产生斯塔克位移,这种位移会强烈改变分子的势能面。如果在波包运动过程中对激光场进行适当调制,振动波包就可以被这种斯塔克位移引导。我们通过混合光学参量放大器的信号光和闲频光,以振动运动时间尺度(约10飞秒)的周期对70飞秒激光脉冲进行调制。我们利用H2或D2的电离在H2(+)或D2(+)的基态上产生振动波包。当波包到达其外转折点时,如果激光强度很高,斯塔克位移会使分子通过键软化而解离。另一方面,如果在这个关键时间场强很小,则测得的解离很少。通过改变调制周期,我们实现了对解离产率的控制,对比度达到90%。