Ornstein-Zernike relation: Difference between revisions

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*<math>\Phi(r)</math> is the [[pair potential]] acting between pairs.
*<math>\Phi(r)</math> is the [[pair potential]] acting between pairs.
*<math>h(1,2)</math> is the [[total correlation function]] <math>h(1,2) \equiv  g(r) -1</math>.
*<math>h(1,2)</math> is the [[total correlation function]] <math>h(1,2) \equiv  g(r) -1</math>.
*$c(1,2)$ is the {\bf direct} correlation function.
*<math>c(1,2)</math> is the [[direct correlation function]].
*$\gamma (r)$ is the {\bf indirect} (or {\bf series} or  {\bf chain}) correlation function $\gamma ({\bf r}) \equiv  h({\bf r}) - c({\bf r})$.
*<math>\gamma (r)</math> is the [[indirect correlation function | indirect]] (or ''series'' or  ''chain'') correlation function <math>\gamma (r) \equiv  h(r) - c(r)</math>.
*$y(r_{12})$ is the {\bf cavity} correlation function $y(r)  \equiv g(r) /e^{-\beta \Phi(r)}$.
*<math>y(r_{12})</math> is the [[cavity correlation function]]<math>y(r)  \equiv g(r) /e^{-\beta \Phi(r)}</math>
*$B(r)$ is the {\bf bridge} function.
*<math>B(r)</math> is the [[Closures | bridge]] function.
*$\omega(r)$ is the {\bf thermal potential}, $\omega(r) \equiv \gamma(r) + B(r)$.
*<math>\omega(r)</math> is the [[thermal potential]], <math>\omega(r) \equiv \gamma(r) + B(r)</math>.
*$f(r)$ is the {\bf Mayer} $f$-function, defined as $f(r) \equiv  e^{-\beta \Phi(r)} -1$.
*<math>f(r)</math> is the [[Mayer <math>f</math>-function]], defined as <math>f(r) \equiv  e^{-\beta \Phi(r)} -1</math>.




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<math>\gamma ({\bf r}) \equiv  h({\bf r}) - c({\bf r}) = \rho \int  h({\bf r'})~c(|{\bf r} - {\bf r'}|) {\rm d}{\bf r'}</math>
<math>\gamma ({\bf r}) \equiv  h({\bf r}) - c({\bf r}) = \rho \int  h({\bf r'})~c(|{\bf r} - {\bf r'}|) {\rm d}{\bf r'}</math>
In words, this equation (Hansen \& McDonald \S 5.2 p. 107)
In words, this equation (Hansen \& McDonald \S 5.2 p. 107)
  ``...describes the fact that the {\it total} correlation between particles 1 and 2, represented by $h(1,2)$, is due in part to the ''direct''       correlation between 1 and 2, represented by <math>c(1,2)</math>, but also to the ''indirect'' correlation, <math>\gamma (r)</math>, propagated via increasingly large numbers of intermediate particles."
  ``...describes the fact that the ''total'' correlation between particles 1 and 2, represented by <math>h(1,2)</math>,  
is due in part to the ''direct'' correlation between 1 and 2, represented by <math>c(1,2)</math>, but also to the ''indirect'' correlation,
<math>\gamma (r)</math>, propagated via increasingly large numbers of intermediate particles."
 
Notice that this equation is basically a convolution, ''i.e.''
<math>h  \equiv c  + \rho h\otimes c </math>


Notice that this equation is basically a convolution, {\it i.e.}
\begin{equation}
h  \equiv c  + \rho h\otimes c
\end{equation}
(Note: the convolution operation written here as $ \otimes$ is more frequently written as $*$)\\
(Note: the convolution operation written here as $ \otimes$ is more frequently written as $*$)\\
This can be seen by expanding the integral in terms of $h({\bf r})$
This can be seen by expanding the integral in terms of $h({\bf r})$

Revision as of 16:11, 20 February 2007

Notation:

  • is the pair distribution function.
  • is the pair potential acting between pairs.
  • is the total correlation function .
  • is the direct correlation function.
  • is the indirect (or series or chain) correlation function .
  • is the cavity correlation function
  • is the bridge function.
  • is the thermal potential, .
  • is the [[Mayer -function]], defined as .


The Ornstein-Zernike relation (OZ) integral equation is

where denotes a functional of . This relation is exact. This is complemented by the closure relation

Note that depends on , and depends on . Because of this must be determined self-consistently. This need for self-consistency is characteristic of all many-body problems. (Hansen \& McDonald \S 5.2 p. 106) For a system in an external field, the OZ has the form (5.2.7)

If the system is both homogeneous and isotropic, the OZ relation becomes (\cite{KNAW_1914_17_0793} Eq. 6)

In words, this equation (Hansen \& McDonald \S 5.2 p. 107)

``...describes the fact that the total correlation between particles 1 and 2, represented by , 
is due in part to the direct correlation between 1 and 2, represented by , but also to the indirect correlation,  
, propagated via increasingly large numbers of intermediate particles."

Notice that this equation is basically a convolution, i.e.

(Note: the convolution operation written here as $ \otimes$ is more frequently written as $*$)\\ This can be seen by expanding the integral in terms of $h({\bf r})$ (here truncated at the fourth iteration): \begin{eqnarray*} h({\bf r}) = c({\bf r}) &+& \rho \int c(|{\bf r} - {\bf r'}|) c({\bf r'}) {\rm d}{\bf r'} \\ &+& \rho^2 \int \int c(|{\bf r} - {\bf r'}|) c(|{\bf r'} - {\bf r}|) c({\bf r}) {\rm d}{\bf r}{\rm d}{\bf r'} \\ &+& \rho^3 \int\int\int c(|{\bf r} - {\bf r'}|) c(|{\bf r'} - {\bf r}|) c(|{\bf r} - {\bf r'}|) c({\bf r}) {\rm d}{\bf r}{\rm d}{\bf r}{\rm d}{\bf r'}\\ &+& \rho^4 \int \int\int\int c(|{\bf r} - {\bf r'}|) c(|{\bf r'} - {\bf r}|) c(|{\bf r} - {\bf r}|) c(|{\bf r} - {\bf r'}|) h({\bf r'}) {\rm d}{\bf r'} {\rm d}{\bf r}{\rm d}{\bf r}{\rm d}{\bf r'} \end{eqnarray*} {\it etc.}\\ Diagrammatically this expression can be written as \cite{PRA_1992_45_000816}: \begin{figure}[H] \begin{center} \includegraphics[clip,height=30pt,width=350pt]{oz_diag.eps} \end{center} \end{figure} \noindent where the bold lines connecting root points denote $c$ functions, the blobs denote $h$ functions. An arrow pointing from left to right indicates an uphill path from one root point to another. An `uphill path' is a sequence of Mayer bonds passing through increasing particle labels.\\ The OZ relation can be derived by performing a functional differentiation of the grand canonical distribution function (HM check this).