Theory of the Electron–Phonon Interaction

1974 ◽  
Vol 52 (14) ◽  
pp. 1304-1314 ◽  
Author(s):  
R. A. Moore ◽  
J. P. Perdew ◽  
S. H. Vosko

An exact solution to the self-consistent field screening problem is presented in terms of Bloch-state matrix elements of the bare perturbation. This solution is equivalent to one given by Sham and Ziman in terms of Fourier transforms of the bare perturbation, but unlike the latter it avoids the convergence problem in momentum space that arises in the screening of the electron–phonon interaction because of the 'deep' part of the ionic potential. The new form of the solution converts naturally into a pseudopotential formalism. At the same time it provides a framework in which to discuss and extend the two most common calculation schemes for the electron–phonon matrix element, the rigid Schrödinger potential model and the diffraction model. The inverse dielectric tensor is evaluated to first-order in the pseudopotential. Local field effects cause the Q → 0 limit of the electron–phonon interaction to deviate from its conventional value.

1974 ◽  
Vol 52 (14) ◽  
pp. 1315-1321 ◽  
Author(s):  
J. P. Perdew ◽  
S. H. Vosko ◽  
R. A. Moore

The exact solution to the self-consistent field screening problem presented in a previous paper (Moore et al.), reduces in the weak pseudopotential limit to the diffraction model for the electron–phonon matrix element, and in particular to Animalu's expression for the screening of a nonlocal pseudopotential. Systematic corrections to the diffraction model, including local field effects, are presented for a pseudopotential of moderate strength; these corrections are particularly simple when the pseudopotential is local. Local pseudopotential calculations of the anisotropic electron–phonon form factors indicate that corrections to the diffraction model are small in sodium but substantial in lithium.


Molecules ◽  
2020 ◽  
Vol 25 (20) ◽  
pp. 4791
Author(s):  
Robert Ponec ◽  
David L. Cooper ◽  
Peter B. Karadakov

Systematic scrutiny is carried out of the ability of multicentre bond indices and the NOEL-based similarity index dAB to serve as excited-state aromaticity criteria. These indices were calculated using state-optimized complete active-space self-consistent field wavefunctions for several low-lying singlet and triplet states of the paradigmatic molecules of benzene and square cyclobutadiene and the inorganic ring S2N2. The comparison of the excited-state indices with aromaticity trends for individual excited states suggested by the values of magnetic aromaticity criteria show that whereas the indices work well for aromaticity reversals between the ground singlet and first triplet electronic states, addressed by Baird’s rule, there are no straightforward parallels between the two sets of data for singlet excited states. The problems experienced while applying multicentre bond indices and dAB to singlet excited states are explained by the loss of the information inherently present in wavefunctions and/or pair densities when calculating the first-order density matrix.


1992 ◽  
Vol 97 (10) ◽  
pp. 7573-7584 ◽  
Author(s):  
Keld Lars Bak ◽  
Poul Jo/rgensen ◽  
Hans Jo/rgen Aa. Jensen ◽  
Jeppe Olsen ◽  
Trygve Helgaker

1957 ◽  
Vol 53 (2) ◽  
pp. 508-513 ◽  
Author(s):  
I. C. Pyle

ABSTRACTSecond-order perturbation theory, in conjunction with the usual treatment of electron-phonon interaction, allows us to calculate the correction to the first-order result for the scattering of phonons by electrons. It is shown that the second-order term is much smaller, and therefore negligible. This justifies the use of the first-order theory in the treatment of the interaction in metals and semi-conductors.


1996 ◽  
Vol 452 ◽  
Author(s):  
S. L. Fang ◽  
L. Grigorian ◽  
A. M. Rao ◽  
P. C. Eklund ◽  
G. Dresselhaus ◽  
...  

AbstractRoom temperature Raman scattering spectra are reported for the type II superconductors MxBaySi46 (M-Na, K) which were recently shown to exhibit Tc's ∼ 3.5 K. The spectra are compared to those of other Si46-clathrates which exhibit normal metallic behavior down to 2K. Thirteen of the twenty first-order Raman frequencies predicted by group theory have been detected, and the frequencies are found to be sensitive to the particular dopants. The Raman linewidths observed for the MxBaySi46 system are comparable to those observed for Na8Si46 and K7Si46. The data, taken collectively, suggest that the line broadening in the metallic Si-clathrates is due to important contributions from both the electron-phonon interaction as well as to a random filling of the Si cages.


1997 ◽  
Vol 7 (C2) ◽  
pp. C2-515-C2-516
Author(s):  
H. Agren ◽  
L. G.M. Pettersson ◽  
V. Carravetta ◽  
Y. Luo ◽  
L. Yang ◽  
...  

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