Zhang Jiaji, Borrelli Raffaele, Tanimura Yoshitaka
Department of Chemistry, Graduate School of Science, Kyoto University, Kyoto 606-8502, Japan.
DISAFA, University of Torino, Largo Paolo Braccini 2, I-10095 Grugliasco, Italy.
J Chem Phys. 2020 Jun 7;152(21):214114. doi: 10.1063/5.0010580.
We consider a proton transfer (PT) system described by a proton transfer reaction (PTR) coordinate and a rate promoting vibrational (RPV) coordinate interacting with a non-Markovian heat bath. While dynamics of PT processes has been widely discussed using two-dimensional potential energy surfaces, the role of the heat bath, in particular, in a realistic form of the system-bath interaction has not been well explored. Previous studies are largely based on a one-dimensional model and linear-linear system-bath interaction. In the present study, we introduce an exponential-linear (EL) system-bath interaction, which is derived from the analysis of a PTR-RPV system in a realistic situation. This interaction mainly causes vibrational dephasing in the PTR mode and population relaxation in the RPV mode. Numerical simulations were carried out using the hierarchical equations of motion approach. We analyze the role of the heat bath interaction in the chemical reaction rate as a function of the system-bath coupling strength at different temperatures and for different values of the bath correlation time. A prominent feature of the present result is that while the reaction rate predicted from classical and quantum Kramers theory increases as the temperature increases, the present EL interaction model exhibits opposite temperature dependence. The Kramers turn-over profile of the reaction rate as a function of the system-bath coupling is also suppressed in the present EL model, turning into a plateau-like curve for larger system-bath interaction strength. Such features arise from the interplay of the vibrational dephasing process in the PTR mode and the population relaxation process in the RPV mode.
我们考虑一个由质子转移反应(PTR)坐标和与非马尔可夫热浴相互作用的速率促进振动(RPV)坐标所描述的质子转移(PT)系统。虽然PT过程的动力学已通过二维势能面被广泛讨论,但热浴的作用,特别是在系统 - 浴相互作用的实际形式中,尚未得到充分探索。先前的研究主要基于一维模型和线性 - 线性系统 - 浴相互作用。在本研究中,我们引入了一种指数 - 线性(EL)系统 - 浴相互作用,它源自对实际情况下PTR - RPV系统的分析。这种相互作用主要导致PTR模式中的振动退相和RPV模式中的布居弛豫。使用运动方程的分层方法进行了数值模拟。我们分析了热浴相互作用在化学反应速率中的作用,它是不同温度下以及浴关联时间的不同值时系统 - 浴耦合强度的函数。本结果的一个突出特点是,虽然经典和量子克莱默斯理论预测的反应速率随温度升高而增加,但当前的EL相互作用模型表现出相反的温度依赖性。在当前的EL模型中,反应速率作为系统 - 浴耦合的函数的克莱默斯翻转曲线也受到抑制,对于较大的系统 - 浴相互作用强度变成类似平台的曲线。这些特征源于PTR模式中的振动退相过程和RPV模式中的布居弛豫过程的相互作用。