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时间延迟双色飞秒激光中 H2+的解离动力学研究

王景哲 董福龙 刘杰

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时间延迟双色飞秒激光中 H2+的解离动力学研究

王景哲, 董福龙, 刘杰

Dissociation dynamic study of H2+ in time-delayed two-color femtosecond lasers

Wang JingZhe, Dong FuLong, Liu Jie
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  • 本文通过数值求解薛定谔方程,计算了具有时间延迟的泵浦及探测飞秒激光联合作用下氢分子离子解离的时间演化动力学.研究发现通过调节探测光的脉宽长度可以对解离过程进行有效的操控;同时,结合延迟时间依赖的离子解离动能谱,我们可以反演出解离过程中的电子与核的微观动力学行为.我们还基于能动量守恒发展了一个描述解离动力学的经典模型,该模型能够定性地预言延迟时间依赖的解离动能谱.利用离子动能谱对探测光频率的依赖关系,我们提出了一个重构离子核间距的含时演化的方案.
    In recent years, the rapid development of ultrashort pulse laser technology has made it possible to regulate the ionization and dissociation dynamics of atoms and molecules. Among them, the microscopic dynamics of molecular dissociation have always been a hot topic. The phenomenon of molecular dissociation caused by the interaction between femtosecond intense laser fields and H2+ molecules has attracted widespread attention. Previous theoretical studies on the dissociation of H2+ molecules mainly focused on studying its dissociation dynamics through numerical calculations, while there were relatively few theoretical models. This paper aims to establish a simple classical model to describe the dissociation dynamics. Firstly, this paper calculates the joint distribution of nuclear and electronic energies during the dissociation process of H2+ molecules under the action of pump lasers by numerically solving the Schrödinger equation, and proves that H2+ molecules initially in the ground state dissociate into H+ + H* after absorbing a pump photon in the pump light field. Next, this paper studies the dissociation dynamics of H2+ molecules in time-delayed two-color femtosecond lasers and finds that it closely depends on the specific forms of the pump light and the probe light. By utilizing the dependence of the dissociation kinetic energy release (KER) spectrum on the time delay of the two-color femtosecond lasers, we have retrieved the sub-attosecond microscopic dynamic behaviors of electrons and atomic nuclei during the dissociation process, and established a classical model based on the conservation of energy and momentum to describe the dissociation dynamics. This model can qualitatively predict the ion dissociation KER spectrum depending on the time delay of the two-color femtosecond lasers. In addition, by taking advantage of the dependence of the ion kinetic energy spectrum on the frequency of the probe laser (that is, the electronic resonant transition between the molecular ground state and the first excited state caused by the probe light will affect the ion kinetic energy spectrum during the dissociation process), we propose a scheme to reconstruct the evolution of the internuclear distance over time. Our reconstruction results can qualitatively predict the trend of the numerical simulation results, and this scheme may provide some theoretical guidance for experiments.
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