Department of Applied Physics, Nanjing University of Science and Technology, Nanjing 210094, P R China.
State Key Laboratory of Molecular Reaction Dynamics, Dalian Institute of Chemical Physics, Chinese Academy of Sciences, Dalian 116023, P R China.
Sci Rep. 2017 Feb 6;7:42086. doi: 10.1038/srep42086.
Using quantum mechanics calculations, we theoretically study the dissociation and ionization dynamics of the hydrogen-molecule ion in strong laser fields. Having prepared the nuclear wave packet of H in a specific vibrational state, a pump laser is used to produce a vibrational excitation, leading to quasi-periodical vibration without ionization. Then, a time-delayed few-cycle laser is applied to trigger the dissociation or ionization of H. Both the time delay and the intensity of the probe laser alter the competition between dissociation and ionization. We also explore the dependence of kinetic-energy release spectra of fragments on the time delay, showing that the channels of above-threshold dissociation and below-threshold dissociation are opened and closed periodically. Also, dissociation from different channels is influenced by nuclear motion. The dissociation mechanism has been described in detail using the Floquet picture. This work provides a useful method for steering the electronic and nuclear dynamics of diatomic molecules in intense laser fields.
我们运用量子力学计算,从理论上研究了强激光场中氢分子离子的离解和电离动力学。通过在特定振动态下制备氢的核波包,用泵浦激光产生振动激发,从而在不发生电离的情况下实现准周期性振动。然后,施加一个时滞的少周期激光来触发 H 的离解或电离。探测激光的时滞和强度都会改变离解和电离之间的竞争。我们还研究了碎片的动能释放谱对时滞的依赖性,表明阈上离解和阈下离解的通道是周期性地开启和关闭的。此外,不同通道的离解也受到核运动的影响。我们使用 Floquet 图像详细描述了离解机制。这项工作为在强激光场中控制双原子分子的电子和核动力学提供了一种有用的方法。