scholarly journals Influence of strong-coupling and retardation effects on superconducting state in YB6 compound

2018 ◽  
Vol 546 ◽  
pp. 44-48
Author(s):  
A.M. Bujak ◽  
K.A. Szewczyk ◽  
M. Kostrzewa ◽  
K.M. Szczȩśniak ◽  
M.A. Sowińska
2000 ◽  
Vol 69 (7) ◽  
pp. 2240-2249 ◽  
Author(s):  
Takanobu Jujo ◽  
Youichi Yanase ◽  
Kosaku Yamada

2019 ◽  
Vol 33 (16) ◽  
pp. 1950169 ◽  
Author(s):  
Tomasz P. Zemła ◽  
Klaudia M. Szczȩśniak ◽  
Adam Z. Kaczmarek ◽  
Svitlana V. Turchuk

At present, hydrogen-based compounds constitute one of the most promising classes of materials for applications as phonon-mediated high-temperature superconductors. Herein, the behavior of the superconducting phase in tellurium hydride (HTe) at high pressure (p = 300 GPa) is analyzed in detail, by using the isotropic Migdal–Eliashberg equations. The chosen pressure conditions are considered here as a case study which corresponds to the highest critical temperature value [Formula: see text] in the analyzed material, as determined within recent density functional theory simulations. It is found that the Migdal–Eliashberg formalism, which constitutes a strong-coupling generalization of the Bardeen–Cooper–Schrieffer (BCS) theory, predicts that the critical temperature value ([Formula: see text] K) is higher than previous estimates of the McMillan formula. Further investigations show that the characteristic dimensionless ratios for the thermodynamic critical field, the specific heat for the superconducting state, and the superconducting band gap exceed the limits of the BCS theory. In this context, also the effective electron mass is not equal to the bare electron mass as provided by the BCS theory. On the basis of these findings it is predicted that the strong-coupling and retardation effects play pivotal role in the superconducting phase of HTe at 300 GPa, in agreement with similar theoretical estimates for the sibling hydrogen and hydrogen-based compounds. Hence, it is suggested that the superconducting state in HTe cannot be properly described within the mean-field picture of the BCS theory.


1984 ◽  
Vol 51 (5) ◽  
pp. 339-342 ◽  
Author(s):  
V.Z. Kresin ◽  
H. Gutfreund ◽  
W.A. Little

2010 ◽  
Vol 105 (2) ◽  
Author(s):  
P. Popovich ◽  
A. V. Boris ◽  
O. V. Dolgov ◽  
A. A. Golubov ◽  
D. L. Sun ◽  
...  

Author(s):  
M. A. Kirk ◽  
M. C. Baker ◽  
B. J. Kestel ◽  
H. W. Weber

It is well known that a number of compound superconductors with the A15 structure undergo a martensite transformation when cooled to the superconducting state. Nb3Sn is one of those compounds that transforms, at least partially, from a cubic to tetragonal structure near 43 K. To our knowledge this transformation in Nb3Sn has not been studied by TEM. In fact, the only low temperature TEM study of an A15 material, V3Si, was performed by Goringe and Valdre over 20 years ago. They found the martensite structure in some foil areas at temperatures between 11 and 29 K, accompanied by faults that consisted of coherent twin boundaries on {110} planes. In pursuing our studies of irradiation defects in superconductors, we are the first to observe by TEM a similar martensite structure in Nb3Sn.Samples of Nb3Sn suitable for TEM studies have been produced by both a liquid solute diffusion reaction and by sputter deposition of thin films.


2019 ◽  
Author(s):  
S. Giarrusso ◽  
Paola Gori-Giorgi

We analyze in depth two widely used definitions (from the theory of conditional probablity amplitudes and from the adiabatic connection formalism) of the exchange-correlation energy density and of the response potential of Kohn-Sham density functional theory. We introduce a local form of the coupling-constant-dependent Hohenberg-Kohn functional, showing that the difference between the two definitions is due to a corresponding local first-order term in the coupling constant, which disappears globally (when integrated over all space), but not locally. We also design an analytic representation for the response potential in the strong-coupling limit of density functional theory for a model single stretched bond.<br>


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