An exact imaginary-time path-integral phase-space formulation of multi-time correlation functions

Author:

Videla Pablo E.1ORCID,Batista Victor S.1ORCID

Affiliation:

1. Department of Chemistry, Yale Energy Sciences Institute and Yale Quantum Institute, Yale University , 225 Prospect Street, New Haven, Connecticut 06520, USA

Abstract

An exact representation of quantum mechanics using the language of phase-space variables provides a natural starting point to introduce and develop semiclassical approximations for the calculation of time correlation functions. Here, we introduce an exact path-integral formalism for calculations of multi-time quantum correlation functions as canonical averages over ring-polymer dynamics in imaginary time. The formulation provides a general formalism that exploits the symmetry of path integrals with respect to permutations in imaginary time, expressing correlations as products of imaginary-time-translation-invariant phase-space functions coupled through Poisson bracket operators. The method naturally recovers the classical limit of multi-time correlation functions and provides an interpretation of quantum dynamics in terms of “interfering trajectories” of the ring-polymer in phase space. The introduced phase-space formulation provides a rigorous framework for the future development of quantum dynamics methods that exploit the invariance of imaginary time path integrals to cyclic permutations.

Funder

Division of Chemistry

Publisher

AIP Publishing

Subject

Physical and Theoretical Chemistry,General Physics and Astronomy

Reference42 articles.

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