...
首页> 外文期刊>The Journal of Chemical Physics >An open-chain imaginary-time path-integral sampling approach to the calculation of approximate symmetrized quantum time correlation functions
【24h】

An open-chain imaginary-time path-integral sampling approach to the calculation of approximate symmetrized quantum time correlation functions

机译:近似对称量子时间相关函数计算的开放式虚构时间路径积分采样方法

获取原文
获取原文并翻译 | 示例
           

摘要

We introduce a scheme for approximating quantum time correlation functions numerically within the Feynman path integral formulation. Starting with the symmetrized version of the correlation function expressed as a discretized path integral, we introduce a change of integration variables often used in the derivation of trajectory-based semiclassical methods. In particular, we transform to sum and difference variables between forward and backward complex-time propagation paths. Once the transformation is performed, the potential energy is expanded in powers of the difference variables, which allows us to perform the integrals over these variables analytically. The manner in which this procedure is carried out results in an open-chain path integral (in the remaining sum variables) with a modified potential that is evaluated using imaginary-time path-integral sampling rather than requiring the generation of a large ensemble of trajectories. Consequently, any number of path integral sampling schemes can be employed to compute the remaining path integral, including Monte Carlo, path-integral molecular dynamics, or enhanced path-integral molecular dynamics. We believe that this approach constitutes a different perspective in semiclassical-type approximations to quantum time correlation functions. Importantly, we argue that our approximation can be systematically improved within a cumulant expansion formalism. We test this approximation on a set of one-dimensional problems that are commonly used to benchmark approximate quantum dynamical schemes. We show that the method is at least as accurate as the popular ring-polymer molecular dynamics technique and linearized semiclassical initial value representation for correlation functions of linear operators in most of these examples and improves the accuracy of correlation functions of nonlinear operators. Published by AIP Publishing.
机译:我们介绍一种用于在Feynman路径积分制构中数值上数值上近似量子时间相关函数的方案。从表现为离散化路径积分的相关函数的对称版本开始,我们引入了经常用于基于轨迹的半思法方法的推导中的集成变量的变化。特别是,我们转换到前向和向后复杂时间传播路径之间的总和和差异变量。一旦进行了变换,势能就差值的功率扩展,这允许我们分析地在这些变量上执行积分。执行该过程的方式导致开锁路径积分(在剩余和变量中),其使用虚数路径积分采样评估的修改电位,而不是要求生成轨迹的大型集合。因此,可以采用任何数量的路径积分采样方案来计算剩余的路径积分,包括蒙特卡罗,一体分子动力学或增强的路径积分分子动态。我们认为,这种方法在半定类型近似的不同视角构成了对量子时间相关函数的不同视角。重要的是,我们认为我们的近似可以在累积膨胀形式主义内系统地改善。我们在常用于近似量子动态方案的一组一维问题上测试该近似值。我们表明该方法至少与流行的环聚合物分子动力学技术一样准确,并且线性化的半导体初始值表示线性操作员在大多数这些示例中的相关函数,提高了非线性运算符的相关函数的准确性。通过AIP发布发布。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号