Fluctuation theorem

Fluctuation theorem

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

tatement of the fluctuation theorem (roughly)

The fluctuation theorem is a statement concerning 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:

: frac{Pr(overline{Sigma}_{t}=A)}{Pr(overline{Sigma}_{t}=-A)}=e^{At}.

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 - [http://www.newscientist.com/article.ns?id=dn2572 Second law of thermodynamics "broken" (NewScientist, 19 July 2002)] ; Nature July 23, 2002, http://www.nature.com/nsu/020722/020722-2.html .

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.

econd law inequality

A simple consequence of the fluctuation theorem given above is that if we carry out an 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:

: leftlangle {overline Sigma _t } ight angle ge 0,quad forall t

For rather obvious reasons 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 clearly untrue as consideration of the entropy production in a viscoelastic fluid subject to a sinusoidal time dependent shear rate clearly shows. In this example the ensemble average of the time integral of the entropy production is however non negative - 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):

: leftlangle {exp [ - overline Sigma_t ; t ] } ight angle = 1,quad forall t

see Carberry et al J Chem Phys 121, 8179(2004). 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". By "reverse", it is meant that they function so as to run in a way opposite to that for which they were presumably designed. As an example, consider a jet engine. 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.

Dissipation function

[1] 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 [ {fracf(Gamma ,0)f(Gamma (t),0)} ight] - fracDelta Q(Gamma ;t){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) e 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 arbitrariliy 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 [http://rsc.anu.edu.au/~evans/papers/Review_37_with_figs.pdf 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. [cite book | last = Greene | first = Brian | authorlink = Brian Greene | title = The Fabric of the Cosmos | publisher = Alfred A. Knopf | date = 2004 | pages = p. 161 | id = ISBN 0-375-41288-3 ] Many modern physicists believe the resolution to this puzzle lies in the low-entropy state of the universe shortly after the big bang, [cite book | last = Greene | first = Brian | authorlink = Brian Greene | title = The Fabric of the Cosmos | publisher = Alfred A. Knopf | date = 2004 | pages = p. 171 | id = ISBN 0-375-41288-3 ] although the explanation for this initial low entropy is still debated. [http://arxiv.org/pdf/hep-th/0410270v1]

ummary

The fluctuation theorem is of fundamental importance to nonequilibrium 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 been 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 http://www.scholarpedia.org/article/Fluctuation_theorem

ee also

*Linear response function
*Green's function (many-body theory)
*Loschmidt's paradox
* Le Chatelier's principle - a nineteenth century principle that defied a mathematical proof until the advent of the Fluctuation Theorem.
*Crooks fluctuation theorem - an example of transient fluctuation theorem relating the dissipated work in non equilibrium transformations to free energy differences.
*Jarzynski equality - another nonequilibrium equality closely related to the fluctuation theorem and to the second law of thermodynamics
*Green-Kubo relations - there is a deep connection between the fluctuation theorem and the Green-Kubo relations for linear transport coefficients - like shear viscosity or thermal conductivity
*Boltzmann
*Thermodynamics
* Brownian motor

References

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* "Fluctuation-Dissipation: Response Theory in Statistical Physics" by Umberto Marini Bettolo Marconi, Andrea Puglisi, Lamberto Rondoni, Angelo Vulpiani, [http://arxiv.org/abs/0803.0719]


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