Environmental dynamics, correlations, and the emergence of noncanonical equilibrium states in open quantum systems

Jake Iles-Smith, Neill Lambert, Ahsan Nazir

Physical Review A · 2014 · 230 citations · 48 references

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TL;DR

Quantum systems are inherently open, evolving under environmental influences, yet standard methods discard environmental information to simplify dynamics. The study aims to embed a collective coordinate of the environment into the system Hamiltonian to enable experimental investigation of noncanonical steady states and deviations from canonical thermodynamics in molecular and solid‑state nanosystems. The authors embed a collective coordinate of the environment into the system Hamiltonian to retain environmental information. The theory reveals that strong, persistent system–environment correlations produce noncanonical equilibrium states, with environmental states becoming non‑Gaussian and the canonical steady state becoming inaccurate; the resulting equilibria are thermal states of the mapped system–collective coordinate Hamiltonian, markedly differing from standard perturbative predictions.

Abstract

Quantum systems are invariably open, evolving under surrounding influences rather than in isolation. Standard open quantum system methods eliminate all information on the environmental state to yield a tractable description of the system dynamics. By incorporating a collective coordinate of the environment into the system Hamiltonian, we circumvent this limitation. Our theory provides straightforward access to important environmental properties that would otherwise be obscured, allowing us to quantify the evolving system-environment correlations. As a direct result, we show that the generation of robust system-environment correlations that persist into equilibrium (heralded also by the emergence of non-Gaussian environmental states) renders the canonical system steady state almost always incorrect. The resulting equilibrium states deviate markedly from those predicted by standard perturbative techniques and are instead fully characterized by thermal states of the mapped system-collective coordinate Hamiltonian. We outline how noncanonical system states could be investigated experimentally to study deviations from canonical thermodynamics, with direct relevance to molecular and solid-state nanosystems.

References

48