Reformulation of pairing theory

1988 ◽  
Vol 02 (05) ◽  
pp. 1101-1105 ◽  
Author(s):  
Miklos GULACSI ◽  
Zsolt GULACSI

The original Cooper pairing theory is reformulated for electrons confined in a layer. This analysis is motivated by the quasi-two-dimensional character of the oxidic superconductors, in case of which the extension of the initial (3D) Cooper framework is practically impossible. By considering the electrons moving in a flat box, due to quantum size effect the properties of these oxidic superconductors can be explained in a natural way. In this short communication we will concentrate to the variation of the critical transition temperature due to the layer thickness and to the number of conduction (Cu-O) planes. The results are confirmed by the experiment. This being an evidence for the presence of the charge confinement effect in the oxidic superconductors.

2008 ◽  
Vol 63 (11-12) ◽  
pp. 1372-1375 ◽  
Author(s):  
H.P. Roeser ◽  
F. Hetfleisch ◽  
F.M. Huber ◽  
M.F. von Schoenermark ◽  
M. Stepper ◽  
...  

2008 ◽  
Vol 62 (12) ◽  
pp. 733-736 ◽  
Author(s):  
H.P. Roeser ◽  
F. Hetfleisch ◽  
F.M. Huber ◽  
M.F. von Schoenermark ◽  
M. Stepper ◽  
...  

1986 ◽  
Vol 77 ◽  
Author(s):  
Feng Xiaomei ◽  
Liu Hsiangna ◽  
Wang Zhichao ◽  
Qiu Shuye ◽  
He Yuliang

ABSTRACTPhotoacoustic (PAS) and optical transmission spectra were measured on a-Si:H/a-SiNx:H superlattices. The absorption coefficient ∝ in the range 102∼104 cm-1 was obtained by converting the PAS signal to ∝. The enhancement of the PAS peak intensity Qs and the increase in the width of the Urbach edge with decreasing a-Si:H layer thickness are explained as results of quantum size effect in the superlattice structure.


2011 ◽  
Vol 319-320 ◽  
pp. 161-166 ◽  
Author(s):  
Morsy M.A. Sekkina ◽  
M. El-Hofy ◽  
Khaled M. Elsabawy ◽  
M. Bediwy

BSCCO 2212 superconducting samples, doped Tellurium, with the chemical formula Bi2-xTexSr2CaCu2O8, were prepared by the conventional solid state reaction technique. The prepared samples were studied utilizing XRD, DC-electrical conductivity and SEM. XRD spectra indicated that 2212 with tetragonal structure is the major phase, whereas Bi-2201 and CaTeO4 are minor phases. At higher Te-additions x, traces from some other semi conducting phases were detected. The critical transition temperature Tcoffset was found to decrease non-linearly with x, which attributed to the hole filling caused by the liberated electrons of Te4+ ions. For x–values in the range 0.1 ≤ x ≤ 0.4, the steepness of (ρ vs T) relationship increases abruptly around 150 K; this was attributed to change in the oxygen vacancy feature (phase-like transition). SEM photographs revealed that as Te-content increases the compactness of the surface and the connectivity of the grains decreases, while pores and voids increase as a result of decreasing the amount of Bi and presence of multiple-phases in the sample.


2015 ◽  
Vol 2015 ◽  
pp. 1-5
Author(s):  
Gang Mu ◽  
Bo Gao ◽  
Xiaoming Xie ◽  
Yoichi Tanabe ◽  
Jingtao Xu ◽  
...  

Low-temperature specific heat (SH) is measured on the postannealed Ba(Fe1−xNix)2As2single crystal withx= 0.058 under different magnetic fields. The sample locates on the overdoped sides and the critical transition temperatureTcis determined to be 14.8 K by both the magnetization and SH measurements. A simple and reliable analysis shows that, besides the phonon and normal electronic contributions, a clearT2term emerges in the low temperature SH data. Our observation is similar to that observed in the Co-doped system in our previous work and is consistent with the theoretical prediction for a superconductor with line nodes in the energy gap.


2005 ◽  
Vol 19 (16) ◽  
pp. 771-778 ◽  
Author(s):  
R. B. SAXENA ◽  
RAJIV GIRI ◽  
V. P. S. AWANA ◽  
H. K. SINGH ◽  
M. A. ANSARI ◽  
...  

Samples of series Bi 1.6 Pb 0.4 Sr 2 Ca 2 Cu 3-x Zn x O 10-δ with x = 0.0, 0.015, 0.03, 0.06, 0.09 and 0.12 are synthesized by solid-state reaction route. All the samples crystallize in tetragonal structure with majority (> 90%) of Bi -2223( Bi 2 Sr 2 Ca 2 Cu 3 O 10) phase (c-lattice parameter ~ 36 Å). The proportion of Bi -2223 phase decreases slightly with an increase in x. The lattice parameters a and c of main phase ( Bi -2223) do not change significantly with increasing x. Superconducting critical transition temperature (Tc) decreases with x as evidenced by both resistivity [ρ(T)] and ac magnetic susceptibility [χ(T)] measurements. Interestingly the decrement of Tc is not monotonic and the same saturates at around 96 K for x > 0.06. In fact Tc decreases fast (~ 10 K/at%) for x = 0.015 and 0.03 samples and later nearly saturates for higher x values. Present results of Zn doping in Bi -2223 system are compared with other Zn -doped HTSC (high temperature superconducting) systems, namely the RE -123 ( REBa 2 Cu 3 O 7) and La -214 (( La, Sr )2 CuO 4).


2007 ◽  
Vol 1044 ◽  
Author(s):  
Yuki Nakanishi ◽  
Hiromichi Ohta ◽  
Teruyasu Mizoguchi ◽  
Yuichi Ikuhara ◽  
Kunihito Koumoto

AbstractVery recently, we have found that the high density 2DEG (ne ∼1021 cm−3), which is confined within a unit cell layer thickness of SrTiO3, exhibits unusually large Seebeck coefficient (S2DEG/Sbulk ∼5)[1]. In the optimum, extremely high ZT2DEG of ∼2.4 can be obtained at room temperature, while the effective ZTeff. was only ∼0.24 because 9 unit cells of electrically insulating SrTiO3 layers were used to fabricate the 2DEG structure. Thus, high ZTeff can be realized if the insulating layer thickness is reduced significantly. We selected BaTiO3∼SrTiO3:Nb superlattice to reduce insulating layer thickness because dielectric constant of BaTiO3 is one order of magnitude large (∼3,000) as compared to that of SrTiO3 (∼300). We expected that the conduction electrons can be confined much strongly in the SrTiO3:Nb layer by sandwiching between highly dielectric BaTiO3 layers. As a result, we clarified that the critical BaTiO3 layer thickness is 1.2 nm, significantly small as compared to SrTiO3 layer (4 nm). The BaTiO3/SrTiO3:Nb superlattice films were fabricated by a pulsed laser deposition (PLD) method on (001)-face of LaAlO3 single crystal substrate at 900°C. During the film growth, we monitored RHEED intensity oscillation to control layer thickness precisely. Out-of-plane high-resolution X-ray diffraction measurements and cross sectional HAADF-STEM observations revealed that the resultant films were high quality BaTiO3/SrTiO3:Nb superlattice. Hall mobility of the SrTiO3:Nb layer was 0.4 cm2·V−1·s−1, while that of superlattice decreased gradually with increasing BaTiO3 layer thickness most likely due to that intra layer diffusion of Ba2+ ion occurred between BaTiO3 and SrTiO3:Nb layers[2], which was clearly observed by the EELS mapping. Seebeck coefficient |S|300K of SrTiO3:Nb layer was 57 μV·K−1, which corresponds carrier concentration ne of 5×1021 cm−3. The |S|300K value became large with decreasing the SrTiO3:Nb layer thickness (dSrTiO3:Nb) and it reached 305 μV·K−1, which is approximately 5 times larger than that of SrTiO3:Nb bulk. The slope of log |S|- log dSrTiO3:Nb plots was 1/2, suggesting that quantum size effect occurred. Critical BaTiO3 layer thickness for the quantum confinement of the electrons was 1.2 nm (3 unit cells of BaTiO3), which is significantly small as compared to SrTiO3 (4 nm). Thus, BaTiO3/SrTiO3:Nb superlattice would be a promising candidate to realize high ZTeff.


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