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Fluctuation theorem


Fluctuation theorem

The fluctuation theorem (FT), which originated from statistical mechanics, deals with the relative probability that the entropy of a system which is currently away from thermodynamic equilibrium (i.e., maximum entropy) will increase or decrease over a given amount of time. While the second law of thermodynamics predicts that the entropy of an isolated system should tend to increase until it reaches equilibrium, it became apparent after the discovery of statistical mechanics that the second law is only a statistical one, suggesting that there should always be some nonzero probability that the entropy of an isolated system might spontaneously decrease; the fluctuation theorem precisely quantifies this probability.


  • Statement of the fluctuation theorem 1
  • Second law inequality 2
  • Nonequilibrium partition identity 3
  • Dissipation function 4
  • The fluctuation theorem and Loschmidt's paradox 5
  • Summary 6
  • See also 7
  • Notes 8
  • References 9

Statement of the fluctuation theorem

Roughly, the fluctuation theorem relates to the probability distribution of the time-averaged irreversible entropy production [1], denoted \overline{\Sigma}_t. The theorem states that, in systems away from equilibrium over a finite time t, the ratio between the probability that \overline{\Sigma}_t takes on a value A and the probability that it takes the opposite value, −A, will be exponential in At. In other words, for a finite non-equilibrium system in a finite time, the FT gives a precise mathematical expression for the probability that entropy will flow in a direction opposite to that dictated by the second law of thermodynamics.

Mathematically, the FT is expressed as:


This means that as the time or system size increases (since \Sigma is extensive), the probability of observing an entropy production opposite to that dictated by the second law of thermodynamics decreases exponentially. The FT is one of the few expressions in non-equilibrium statistical mechanics that is valid far from equilibrium.

The FT was first proposed and tested using computer simulations, by Denis Evans, E.G.D. Cohen and Gary Morriss in 1993 in the journal Physical Review Letters. The first mathematical proof was given by Evans and Debra Searles in 1994. Since then, much mathematical and computational work has been done to show that the FT applies to a variety of statistical ensembles. The first laboratory experiment that verified the validity of the FT was carried out in 2002. In this experiment, a plastic bead was pulled through a solution by a laser. Fluctuations in the velocity were recorded that were opposite to what the second law of thermodynamics would dictate for macroscopic systems. See Wang et al. [Phys Rev Lett, 89, 050601(2002)] and later Carberry et al., [Phys Rev Lett, 92, 140601(2004)]. This work was widely reported in the press - Second law of thermodynamics "broken" (NewScientist, 19 July 2002); Nature July 23, 2002, .

Note that the FT does not state that the second law of thermodynamics is wrong or invalid. The second law of thermodynamics is a statement about macroscopic systems. The FT is more general. It can be applied to both microscopic and macroscopic systems. When applied to macroscopic systems, the FT is equivalent to the Second Law of Thermodynamics.

Second law inequality

A simple consequence of the fluctuation theorem given above is that if we carry out an arbitrarily large ensemble of experiments from some initial time t=0, and perform an ensemble average of time averages of the entropy production then an exact consequence of the FT is that the ensemble average cannot be negative for any value of the averaging time t:

\left\langle {\overline \Sigma _t } \right\rangle \ge 0,\quad \forall t.

This inequality is called the Second Law Inequality [Searles & Evans, Aust J Chem, 57, 1119 (2004)]. This inequality can be proved for systems with time dependent fields of arbitrary magnitude and arbitrary time dependence.

It is important to understand what the Second Law Inequality does not imply. It does not imply that the ensemble averaged entropy production is non-negative at all times. This is untrue, as consideration of the entropy production in a viscoelastic fluid subject to a sinusoidal time dependent shear rate shows. In this example the ensemble average of the time integral of the entropy production over one cycle is however nonnegative - as expected from the Second Law Inequality.

Nonequilibrium partition identity

Another remarkably simple and elegant consequence of the FT is the so-called "Nonequilibrium partition identity" (NPI):[1]

\left\langle {\exp [ - \overline \Sigma_t \; t ]} \right\rangle = 1,\quad \text{ for all } t .

Thus in spite of the Second Law Inequality which might lead you to expect that the average would decay exponentially with time, the exponential probability ratio given by the FT exactly cancels the negative exponential in the average above leading to an average which is unity for all time!

There are many important implications from the FT. One is that small machines (such as nanomachines or even mitochondria in a cell) will spend part of their time actually running in "reverse". What we mean with "reverse" is that it is possible to observe that these small molecular machines are able to generate work by taking heat from the environment. This is possible because there exist a symmetry relation in the work fluctuations associated with the forward and reverse changes a system undergoes as it is driven away from thermal equilibrium by the action of an external perturbation, which is a result predicted by the Crooks fluctuation theorem. For this molecular machines the environment itself continuously drive them away out of equilibrium and the fluctuations it generates over the system are very relevant, and the probability of observing an apparent violation of the second principle becomes significant. This is counterintuitive because, from a macroscopic point of view, it would imply for instance that if a jet engine were to run in "reverse" in this context, it would take in ambient heat and exhaust fumes to generate kerosene and oxygen. Nevertheless the size of such a system makes this observation almost impossible to occur. Such a process is possible to be observed microscopically because, as it has been stated above, the probability of observing a "reverse" trajectory depends on system size and is significant for molecular machines if an appropriate measurement instrument is available. This is the case with the development of new biophysical instruments such as the optical tweezers or the atomic force microscope. An example of verification of the Crook's theorem through RNA folding experiments can be found here.[2]

Dissipation function

Strictly speaking the fluctuation theorem refers to a quantity known as the dissipation function. In thermostatted nonequilibrium states that are close to equilibrium, the long time average of the dissipation function is equal to the average entropy production. However the FT refers to fluctuations rather than averages. The dissipation function is defined as,

\Omega _t (\Gamma ) = \int_0^t {ds\;\Omega (\Gamma ;s)} \equiv \ln \left[ {\frac} \right] + \frac{kT}

where k is Boltzmann's constant, f(\Gamma , 0) is the initial (t = 0) distribution of molecular states \Gamma , and \Gamma (t) is the molecular state arrived at after time t, under the exact time reversible equations of motion. f(\Gamma (t),0) is the INITIAL distribution of those time evolved states.

Note: in order for the FT to be valid we require that f(\Gamma (t),0) \ne 0,\;\forall \Gamma (0) . This condition is known as the condition of ergodic consistency. It is widely satisfied in common statistical ensembles - e.g. the canonical ensemble.

The system may be in contact with a large heat reservoir in order to thermostat the system of interest. If this is the case \Delta Q(t) is the heat lost to the reservoir over the time (0,t) and T is the absolute equilibrium temperature of the reservoir - see Williams et al., Phys Rev E70, 066113(2004). With this definition of the dissipation function the precise statement of the FT simply replaces entropy production with the dissipation function in each of the FT equations above.

Example: If one considers electrical conduction across an electrical resistor in contact with a large heat reservoir at temperature T, then the dissipation function is

\Omega = - JF_e V/{kT}\

the total electric current density J multiplied by the voltage drop across the circuit, F_e , and the system volume V, divided by the absolute temperature T, of the heat reservoir times Boltzmann's constant. Thus the dissipation function is easily recognised as the Ohmic work done on the system divided by the temperature of the reservoir. Close to equilibrium the long time average of this quantity is (to leading order in the voltage drop), equal to the average spontaneous entropy production per unit time - see de Groot and Mazur "Nonequilibrium Thermodynamics" (Dover), equation (61), page 348. However, the Fluctuation Theorem applies to systems arbitrarily far from equilibrium where the definition of the spontaneous entropy production is problematic.

The fluctuation theorem and Loschmidt's paradox

The second law of thermodynamics, which predicts that the entropy of an isolated system out of equilibrium should tend to increase rather than decrease or stay constant, stands in apparent contradiction with the time-reversible equations of motion for classical and quantum systems. The time reversal symmetry of the equations of motion show that if one films a given time dependent physical process, then playing the movie of that process backwards does not violate the laws of mechanics. It is often argued that for every forward trajectory in which entropy increases, there exists a time reversed anti trajectory where entropy decreases, thus if one picks an initial state randomly from the system's phase space and evolves it forward according to the laws governing the system, decreasing entropy should be just as likely as increasing entropy. It might seem that this is incompatible with the second law of thermodynamics which predicts that entropy tends to increase. The problem of deriving irreversible thermodynamics from time-symmetric fundamental laws is referred to as Loschmidt's paradox.

The mathematical proof of the Fluctuation Theorem and in particular the Second Law Inequality shows that, given a non-equilibrium starting state, the probability of seeing its entropy increase is greater than the probability of seeing its entropy decrease - see The Fluctuation Theorem from Advances in Physics 51: 1529. However, as noted in section 6 of that paper, one could also use the same laws of mechanics to extrapolate backwards from a later state to an earlier state, and in this case the same reasoning used in the proof of the FT would lead us to predict the entropy was likely to have been greater at earlier times than at later times. This second prediction would be frequently violated in the real world, since it is often true that a given nonequilibrium system was at an even lower entropy in the past (although the prediction would be correct if the nonequilibrium state were the result of a random fluctuation in entropy in an isolated system that had previously been at equilibrium - in this case, if you happen to observe the system in a lower-entropy state, it is most likely that you are seeing the minimum of the random dip in entropy, in which case entropy would be higher on either side of this minimum).

So, it seems that the problem of deriving time-asymmetric thermodynamic laws from time-symmetric laws cannot be solved by appealing to statistical derivations which show entropy is likely to increase when you start from a nonequilibrium state and project it forwards.[3] Many modern physicists believe the resolution to this puzzle lies in the low-entropy state of the universe shortly after the big bang,[4] although the explanation for this initial low entropy is still debated.[5]


The fluctuation theorem is of fundamental importance to non-equilibrium statistical mechanics. The FT (together with the Axiom of Causality) gives a generalisation of the second law of thermodynamics which includes as a special case, the conventional second law. It is then easy to prove the Second Law Inequality and the NonEquilibrium Partition Identity. When combined with the central limit theorem, the FT also implies the famous Green-Kubo relations for linear transport coefficients, close to equilibrium. The FT is however, more general than the Green-Kubo Relations because unlike them, the FT applies to fluctuations far from equilibrium. In spite of this fact, scientists have not yet been able to derive the equations for nonlinear response theory from the FT.

The FT does not imply or require that the distribution of time averaged dissipation be Gaussian. There are many examples known where the distribution of time averaged dissipation is non-Gaussian and yet the FT (of course) still correctly describes the probability ratios.

Lastly the theoretical constructs used to prove the FT can be applied to nonequilibrium transitions between two different equilibrium states. When this is done the so-called Jarzynski equality or nonequilibrium work relation, can be derived. This equality shows how equilibrium free energy differences can be computed or measured (in the laboratory), from nonequilibrium path integrals. Previously quasi-static (equilibrium) paths were required.

The reason why the fluctuation theorem is so fundamental is that its proof requires so little. It requires:

  • knowledge of the mathematical form of the initial distribution of molecular states,
  • that all time evolved final states at time t, must be present with nonzero probability in the distribution of initial states (t = 0) - the so-called condition of ergodic consistency and,
  • an assumption of time reversal symmetry.

In regard to the latter "assumption", all the equations of motion for either classical or quantum dynamics are in fact time reversible.

For an alternative view on the same subject see

See also


  1. ^ Carberry, D. M.; Williams, S. R.; Wang, G. M.; Sevick, E. M.; Evans, Denis J. (1 January 2004). "The Kawasaki identity and the Fluctuation Theorem". The Journal of Chemical Physics 121 (17): 8179–82.  
  2. ^ Collin, D.; Ritort, F., Jarzynski C., Smith, B., Tinoco Jr, I., Bustamante C. (8 September 2005). "Verification of Crooks fluctuation theorem and recovery of RNA folding free energies". Nature 437 (7056): 231–4.  
  3. ^  
  4. ^  
  5. ^ Carroll, S.M.; Chen, J. (2004), "Spontaneous Inflation and the Origin of the Arrow of Time, arXiv:hep-th/0410270v1


  • Denis J. Evans , E.G.D. Cohen & G.P. Morriss (1993). "Probability of second law violations in shearing steady states".  
  • Denis J. Evans & Debra J. Searles (1994). "Equilibrium microstates which generate second law violating steady states".  
  • G.M. Wang, E.M. Sevick, E. Mittag, D.J. Searles & Denis J. Evans (2002). "Experimental demonstration of violations of the Second Law of Thermodynamics for small systems and short time scales".  
  • Denis J. Evans & Debra J. Searles (2002). "The Fluctuation Theorem".  
  • N. Garnier & S. Ciliberto (2005). "Nonequilibrium fluctuations in a resistor".  
  • Marconi, Umberto Marini Bettolo; Puglisi, Andrea; Rondoni, Lamberto; Vulpiani, Angelo (2008). "Fluctuation-Dissipation: Response Theory in Statistical Physics".  
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