DIELECTRIC THEORY OF PLASMA OSCILLATIONS AND ITS EXTENSION TO THE EXCITON PROBLEM

1963 ◽  
Vol 41 (9) ◽  
pp. 1470-1481
Author(s):  
C. Horie

A new form of the microscopic expression for the dielectric constant is derived and used to obtain the dispersion relation for plasma modes. It is found that the usual dispersion relation for plasma modes derived using the random phase approximation contains higher-order correlation effects than is usually believed. The dielectric approach to the plasma problem is extended to the exciton problem by introducing a nonlocal charge density instead of the local charge density appearing in the case of the plasma modes. The same equation determining the energy of the exciton states as derived in a previous paper is obtained.

2005 ◽  
Vol 3 (2) ◽  
pp. 141-149 ◽  
Author(s):  
M.R. Nikolic ◽  
Aleksandar Tancic

In this paper, we present our calculation for the elastic scattering of the slow positron from atoms. The calculation is performed for He, Ne, Xe and Kr. In the calculations we used Random phase approximation. By slowing Dyson equation we take into account the correlation effects. Our results are consistent with experimental and other theoretical results.


2009 ◽  
Vol 51 (12) ◽  
pp. 2557-2560 ◽  
Author(s):  
R. F. Akhmet’yanov ◽  
E. S. Shikhovtseva ◽  
G. S. Lomakin

2020 ◽  
Vol 62 (1) ◽  
pp. 153
Author(s):  
Е.И. Кухарь ◽  
С.В. Крючков

Dispersion relation for plasma waves in graphene bilayer has been investigated. Influence of the bias voltage on the dispersion curve for plasmon in bigraphene has been studied within random phase approximation. The possibility of controlling of energy and group velocity for plasmon by changing of bias voltage has been shown. The dependence of plasmon energy on the bias voltage has been predicted to have the nonmonotonous character. Effect of the temperature on the plasmon dispersion has been analyzed.


1995 ◽  
Vol 60 (10) ◽  
pp. 1641-1652 ◽  
Author(s):  
Henri C. Benoît ◽  
Claude Strazielle

It has been shown that in light scattering experiments with polymers replacement of a solvent by a solvent mixture causes problems due to preferential adsorption of one of the solvents. The present paper extends this theory to be applicable to any angle of observation and any concentration by using the random phase approximation theory proposed by de Gennes. The corresponding formulas provide expressions for molecular weight, gyration radius, and the second virial coefficient, which enables measurements of these quantities provided enough information on molecular and thermodynamic quantities is available.


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