Non-linear correlation functions and zero-point energy flow in mixed quantum-classical semiclassical dynamics

被引:5
|
作者
Malpathak, Shreyas [1 ]
Ananth, Nandini [1 ]
机构
[1] Cornell Univ, Dept Chem & Chem Biol, Baker Lab, Ithaca, NY 14853 USA
来源
JOURNAL OF CHEMICAL PHYSICS | 2023年 / 158卷 / 10期
关键词
INITIAL-VALUE REPRESENTATION; CENTROID MOLECULAR-DYNAMICS; TIME-CORRELATION-FUNCTIONS; PHASE-SPACE; TRAJECTORY SIMULATIONS; NONADIABATIC DYNAMICS; VIBRATIONAL-ENERGY; PATH-INTEGRATION; RATE CONSTANTS; LONG-TIME;
D O I
10.1063/5.0133222
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Mixed quantum classical (MQC)-initial value representation (IVR) is a recently introduced semiclassical framework that allows for selective quantization of the modes of a complex system. In the quantum limit, MQC reproduces the semiclassical Double Herman-Kluk IVR results, accurately capturing nuclear quantum coherences and conserving zero-point energy. However, in the classical limit, although MQC mimics the Husimi-IVR for real-time correlation functions with linear operators, it is significantly less accurate for non-linear correlation functions with errors even at time zero. Here, we identify the origin of this discrepancy in the MQC formulation and propose a modification. We analytically show that the modified MQC approach is exact for all correlation functions at time zero, and in a study of zero-point energy (ZPE) flow, we numerically demonstrate that it correctly obtains the quantum and classical limits as a function of time. Interestingly, although classical-limit MQC simulations show the expected, unphysical ZPE leakage, we find that it is possible to predict and even modify the direction of ZPE flow through selective quantization of the system, with the quantum-limit modes accepting energy but preserving the minimum quantum mechanically required energy.
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页数:10
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