The density of states in dilute solid solutions

The difference in the density of states in energy in a dilute solid solution, relative to its value in the pure solvent, is derived. It is shown to be simply related to the energy level shift induced by virtual electron scattering off the solute ions and to the density of states in the pure solvent. The result, which follows from a brief physical argument, is shown to be completely equivalent to that obtained from a far more laborious derivation by means of Green function techniques. An application to the determination of the specific heat of dilute metallic solid solutions is given and a former incomplete result, as derived by Jones from an approximate evaluation of the Green function method, is amended.

1970 ◽  
Vol 8 (13) ◽  
pp. 1069-1071 ◽  
Author(s):  
F. Flores ◽  
F. Garcia-Moliner ◽  
J. Rubio

1996 ◽  
Vol 03 (02) ◽  
pp. 1253-1257 ◽  
Author(s):  
HUI ZHANG ◽  
SHULIN CONG

The Green function method and the chemisorption theory of Einstein and Schrieffer are used to calculate the chemisorption energies of O and CO on the multilayer segregated Ni-Cu disordered binary alloy within the many-coupled self-consistent coherent potential approximation. In general cases, the chemisorption-induced surface segregation can change the surface component and the chemisorption property to varying degrees. When the mutual influence of chemisorption and multilayer segregation is considered, the changes appear slightly mild. The chemisorption energy for O/Ni-Cu (CO/Ni-Cu) depends sensitively on O(CO) coverage θ, and decreases with increasing θ.


2013 ◽  
Vol 2013 ◽  
pp. 1-15
Author(s):  
Sami Boudieb ◽  
Lyazid Chetouani

The Green function for a Dirac particle moving in a non-Abelian field and having a particular form is exactly determined by the path integral approach. The wave functions were deduced from the residues of Green’s function. It is shown that the classical paths contributed mainly to the determination of the Green function.


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