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Updated: Dec 14, 2025

Synthesis of Cyclic Polymers and Characterization of Their Diffusive Motion in the Melt State at the Single Molecule Level
Published on: September 26, 2016
Reversal symmetries for cyclic paths away from thermodynamic equilibrium
John W Biddle1, Jeremy Gunawardena1
1Department of Systems Biology, Harvard Medical School, Boston, Massachusetts, United States.
Abstract:
If a system is at thermodynamic equilibrium, an observer cannot tell whether a film of it is being played forward or in reverse: any transition will occur with the same frequency in the forward as in the reverse direction. However, if expenditure of energy changes the rate of even a single transition to yield a nonequilibrium steady state, such time-reversal symmetry undergoes a widespread breakdown, far beyond the point at which the energy is expended. An explosion of interdependency also arises, with steady-state probabilities of system states depending in a complicated manner on the rate of every transition in the system. Nevertheless, in the midst of this global nonequilibrium complexity, we find that cyclic paths have reversibility properties that remain local, and which can exhibit symmetry, no matter how far the system is from thermodynamic equilibrium. Specifically, given any cycle of reversible transitions, the ratio of the frequencies with which the cycle occurs in one direction versus the other is determined, in the long-time limit, only by the thermodynamic force on the cycle itself, without requiring knowledge of transition rates elsewhere in the system. In particular, if there is no net energy expenditure on the cycle, then, over long times, the cycle occurrence frequencies are the same in either direction.
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