Open main menu
Home
Random
Recent changes
Special pages
Community portal
Preferences
About Wikipedia
Disclaimers
Incubator escapee wiki
Search
User menu
Talk
Dark mode
Contributions
Create account
Log in
Editing
Fluctuation theorem
(section)
Warning:
You are not logged in. Your IP address will be publicly visible if you make any edits. If you
log in
or
create an account
, your edits will be attributed to your username, along with other benefits.
Anti-spam check. Do
not
fill this in!
== Dissipation function == Strictly speaking the fluctuation theorem refers to a quantity known as the dissipation function. In thermostatted nonequilibrium states{{clarify|date=February 2015}} 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 : <math> \Omega _t (\Gamma ) = \int_0^t {ds\;\Omega (\Gamma ;s)} \equiv \ln \left[ {\frac{{f(\Gamma ,0)}}{{f(\Gamma (t),0)}}} \right] + \frac{{\Delta Q(\Gamma ;t)}}{kT} </math> where ''k'' is the Boltzmann constant, <math>f(\Gamma , 0)</math> is the initial (t = 0) distribution of molecular states <math>\Gamma </math>, and <math> \Gamma (t) </math> is the molecular state arrived at after time t, under the exact time reversible equations of motion. <math> f(\Gamma (t),0) </math> is the INITIAL distribution of those time evolved states. Note: in order for the FT to be valid we require that <math>f(\Gamma (t),0) \ne 0,\;\forall \Gamma (0) </math>. This condition is known as the condition of ergodic consistency. It is widely satisfied in common [[statistical ensemble]]s - 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 <math> \Delta Q(t) </math> is the heat lost to the reservoir over the time (0,t) and T is the absolute equilibrium temperature of the reservoir.<ref>{{cite journal | url=https://journals.aps.org/pre/abstract/10.1103/PhysRevE.70.066113 | doi=10.1103/PhysRevE.70.066113 | title=Independence of the transient fluctuation theorem to thermostatting details | date=2004 | last1=Williams | first1=Stephen R. | last2=Searles | first2=Debra J. | last3=Evans | first3=Denis J. | journal=Physical Review E | volume=70 | issue=6 | page=066113 | pmid=15697440 | bibcode=2004PhRvE..70f6113W }}</ref> 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 : <math> \Omega = - JF_e V/{kT}\ </math> the total electric current density J multiplied by the voltage drop across the circuit, <math>F_e </math>, and the system volume V, divided by the absolute temperature T, of the heat reservoir times the Boltzmann 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|leading order]] in the voltage drop), equal to the average spontaneous entropy production per unit time.<ref>{{Cite book |last1=Groot |first1=S. R. De |url=https://books.google.com/books?id=mfFyG9jfaMYC |title=Non-Equilibrium Thermodynamics |last2=Mazur |first2=P. |date=2013-01-23 |publisher=Courier Corporation |isbn=978-0-486-15350-6 |pages=348 |quote=Equation (61)}}</ref> However, the fluctuation theorem applies to systems arbitrarily far from equilibrium where the definition of the spontaneous entropy production is problematic.
Edit summary
(Briefly describe your changes)
By publishing changes, you agree to the
Terms of Use
, and you irrevocably agree to release your contribution under the
CC BY-SA 4.0 License
and the
GFDL
. You agree that a hyperlink or URL is sufficient attribution under the Creative Commons license.
Cancel
Editing help
(opens in new window)