Department of Basic Science, The University of Tokyo, Komaba, 153-8902 Tokyo, Japan.
J Chem Phys. 2010 Jun 28;132(24):244102. doi: 10.1063/1.3439396.
We extend our formerly proposed theory for non-Born-Oppenheimer electronic and nuclear wavepacket dynamics within on-the-fly scheme [T. Yonehara, S. Takahashi, and K. Takatsuka, J. Chem. Phys. 130, 214113 (2009)] to a case of nonadiabatic dynamics under an intense laser field: electron wavepacket in a molecule is propagated in attosecond time-scale along non-Born-Oppenheimer nuclear paths that smoothly branch due to nonadiabatic coupling and/or optical interactions. Such branching paths are determined consistently with the motion of the electron wavepackets. Furthermore, these nuclear paths are quantized in terms of Gaussian wavepackets (action decomposed function), which can be applied to nonclassical paths. Both electronic wavepacket dynamics and quantization of non-Born-Oppenheimer paths are generalized so as to include the direct effects of the classical vector potential of electromagnetic fields. In the second half of this paper, we perform numerical studies to explore nonadiabatic dynamics in a laser field by examining two cases: one is a two-state model system having an avoided crossing, and the other is two-state dynamics in HF molecule on the two low lying ab initio potential curves. Both are placed in laser fields. With the former system, we survey some basic properties of the coupling of nonadiabatic dynamics and laser interaction varying the relevant coupling parameters such as the laser timing with respect to the incident of nonadiabatic transition. This investigation will set a foundation for the future studies of control of electronic states in realistic multidimensional molecular systems. Application to the latter system shows that non-Born-Oppenheimer quantum chemistry in laser fields is indeed useful in the study of dynamics in ab initio level. Through the comparison with full quantum data, we verify that the formalism and methodology developed here work accurately. Furthermore, we attain some basic insight about the characteristics of molecules in laser fields.
我们将之前提出的非玻恩-奥本海默电子和核波包动力学的实时方案[T. Yonehara、S. Takahashi 和 K. Takatsuka,J. Chem. Phys. 130, 214113(2009)]扩展到强激光场下的非绝热动力学情况:分子中的电子波包沿着非玻恩-奥本海默核路径在阿秒时间尺度上传播,这些核路径由于非绝热耦合和/或光相互作用而平滑分支。这些分支路径与电子波包的运动一致确定。此外,这些核路径在高斯波包(分解函数)的基础上量子化,这可以应用于非经典路径。非玻恩-奥本海默路径的电子波包动力学和量子化都被推广,以包括电磁场的经典矢量势的直接影响。在本文的后半部分,我们通过研究两个案例来进行数值研究,以探索激光场中的非绝热动力学:一个是具有避免交叉的两态模型系统,另一个是 HF 分子在两个低能从头算势能曲线上的两态动力学。这两个案例都置于激光场中。对于前一个系统,我们调查了非绝热动力学和激光相互作用的耦合的一些基本性质,通过改变相关的耦合参数,例如相对于非绝热跃迁的入射激光的定时,来改变激光的定时。这项研究将为在现实的多维分子系统中控制电子态的未来研究奠定基础。对于后一个系统的应用表明,激光场中非玻恩-奥本海默量子化学在从头算水平上的动力学研究中确实是有用的。通过与全量子数据的比较,我们验证了这里发展的形式和方法准确。此外,我们还获得了关于分子在激光场中的特性的一些基本见解。