Ornstein-Zernike relation: Difference between revisions

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If the system is both homogeneous and isotropic, the OZ relation becomes (Ref. 1Eq. 6)
If the system is both homogeneous and isotropic, the OZ relation becomes (Ref. 1Eq. 6)


<math>\gamma (r) \equiv  h(r) - c(r) = \rho \int  h(r')~c(|r - r'|) dr'</math>
:<math>\gamma (r) \equiv  h(r) - c(r) = \rho \int  h(r')~c(|r - r'|) dr'</math>


In words, this equation (Hansen and McDonald, section 5.2 p. 107)
In words, this equation (Hansen and McDonald, section 5.2 p. 107)
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(here truncated at the fourth iteration):
(here truncated at the fourth iteration):


<math>h(r) = c(r)  + \rho \int c(|r - r'|)  c(r')  dr'  
:<math>h(r) = c(r)  + \rho \int c(|r - r'|)  c(r')  dr'  
+ \rho^2  \int \int  c(|r - r'|)  c(|r' - r''|)  c(r'')  dr''dr'   
+ \rho^2  \int \int  c(|r - r'|)  c(|r' - r''|)  c(r'')  dr''dr'   
+ \rho^3 \int\int\int  c(|r - r'|) c(|r' - r''|) c(|r'' - r'''|) c(r''')  dr'''dr''dr'
+ \rho^3 \int\int\int  c(|r - r'|) c(|r' - r''|) c(|r'' - r'''|) c(r''')  dr'''dr''dr'

Revision as of 11:45, 23 February 2007

Notation:


The Ornstein-Zernike relation (OZ) integral equation is

h=h[c]

where h[c] denotes a functional of c. This relation is exact. This is complemented by the closure relation

c=c[h]

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

h(1,2)=c(1,2)+∫ρ(1)(3)c(1,3)h(3,2)d3

If the system is both homogeneous and isotropic, the OZ relation becomes (Ref. 1Eq. 6)

γ(r)≡h(r)−c(r)=ρ∫h(r′)c(|r−r′|)dr′

In words, this equation (Hansen and McDonald, section 5.2 p. 107)

``...describes the fact that the 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 c(1,2), but also to the indirect correlation,  
γ(r), propagated via increasingly large numbers of intermediate particles."

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

h≡c+ρh⊗c

(Note: the convolution operation written here as ⊗ is more frequently written as *) This can be seen by expanding the integral in terms of h(r) (here truncated at the fourth iteration):

h(r)=c(r)+ρ∫c(|r−r′|)c(r′)dr′+ρ2∫∫c(|r−r′|)c(|r′−r″|)c(r″)dr″dr′+ρ3∫∫∫c(|r−r′|)c(|r′−r″|)c(|r″−r‴|)c(r‴)dr‴dr″dr′+ρ4∫∫∫∫c(|r−r′|)c(|r′−r″|)c(|r″−r‴|)c(|r‴−r⁗|)h(r⁗)dr⁗dr‴dr″dr′

etc. Diagrammatically this expression can be written as (Ref. 2):

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).

OZ equation in Fourier space

The OZ equation may be written in Fourier space as (Eq. 5 in Ref. 3):

γ^=(I−ρc^)−1c^ρc^

The carets denote the three-dimensional Fourier transformed quantities which reduce explicitly to:

γ^(k)=4πk∫0∞rsin(kr)γ(r)dr


γ(r)=12π2r∫0∞ksin(kr)γ^(r)dk

Note:

h^(0)=∫h(r)dr


c^(0)=∫c(r)dr

References

  1. [L. S. Ornstein and F. Zernike "Accidental deviations of density and opalescence at the critical point of a single substance", Koninklijke Nederlandse Akademie van Wetenschappen Amsterdam Proc. Sec. Sci. 17 pp. 793- (1914)]
  2. James A. Given "Liquid-state methods for random media: Random sequential adsorption", Physical Review A 45 pp. 816 - 824 (1992)
  3. Der-Ming Duh and A. D. J. Haymet "Integral equation theory for uncharged liquids: The Lennard-Jones fluid and the bridge function", Journal of Chemical Physics 103 pp. 2625-2633 (1995)
  4. [Hansen and MacDonald "Theory of Simple Liquids"]