A Novel Antiferromagnetic Organic Superconductor κ-(BETS)2FeBr4[Where BETS = Bis(ethylenedithio)tetraselenafulvalene]

2001 ◽  
Vol 123 (2) ◽  
pp. 306-314 ◽  
Author(s):  
Hideki Fujiwara ◽  
Emiko Fujiwara ◽  
Yasuhiro Nakazawa ◽  
Bakhyt Zh. Narymbetov ◽  
Kiyonori Kato ◽  
...  
1993 ◽  
Vol 3 (3) ◽  
pp. 871-885 ◽  
Author(s):  
P. Auban-Senzier ◽  
C. Bourbonnais ◽  
D. Jérome ◽  
C. Lenoir ◽  
P. Batail ◽  
...  

1983 ◽  
Vol 44 (C3) ◽  
pp. C3-893-C3-901 ◽  
Author(s):  
M. Miljak ◽  
J. R. Cooper ◽  
K. Bechgaard

Crystals ◽  
2021 ◽  
Vol 11 (1) ◽  
pp. 72
Author(s):  
Kaushal K. Kesharpu ◽  
Vladislav D. Kochev ◽  
Pavel D. Grigoriev

In highly anisotropic organic superconductor (TMTSF)2ClO4, superconducting (SC) phase coexists with metallic and spin-density wave phases in the form of domains. Using the Maxwell-Garnett approximation (MGA), we calculate the volume ratio and estimate the shape of these embedded SC domains from resistivity data at various temperature and anion disorder, controlled by the cooling rate or annealing time of (TMTSF)2ClO4 samples. We found that the variation of cooling rate and of annealing time affect differently the shape of SC domains. In all cases the SC domains have oblate shape, being the shortest along the interlayer z-axis. This contradicts the widely assumed filamentary superconductivity along the z-axis, used to explain the anisotropic superconductivity onset. We show that anisotropic resistivity drop at the SC onset can be described by the analytical MGA theory with anisotropic background resistance, while the anisotropic Tc can be explained by considering a finite size and flat shape of the samples. Due to a flat/needle sample shape, the probability of percolation via SC domains is the highest along the shortest sample dimension (z-axis), and the lowest along the sample length (x-axis). Our theory can be applied to other heterogeneous superconductors, where the size d of SC domains is much larger than the SC coherence length ξ, e.g., cuprates, iron-based or organic superconductors. It is also applicable when the spin/charge-density wave domains are embedded inside a metallic background, or vice versa.


1991 ◽  
Vol 30 (12) ◽  
pp. 2586-2588 ◽  
Author(s):  
Urs. Geiser ◽  
Hau H. Wang ◽  
K. Douglas. Carlson ◽  
Jack M. Williams ◽  
Henry A. Charlier ◽  
...  

1981 ◽  
Vol 42 (19) ◽  
pp. 445-449 ◽  
Author(s):  
A. Fournel ◽  
C. More ◽  
G. Roger ◽  
J.P. Sorbier ◽  
J.M. Delrieu ◽  
...  

1992 ◽  
Vol 247 ◽  
Author(s):  
H. Hau Wang ◽  
K. D. Carlson ◽  
U. Geiser ◽  
A. M. Kini ◽  
A. J. Schultz ◽  
...  

ABSTRACTThe syntheses and physical properties of K-(ET)2CU[N(CN)2]X (X = Br and Cl) are summarized. The K-(ET)2Cu [N(CN)2] Br salt is the highest Tc radical-cation based ambient pressure organic superconductor (Tc = 11.6 K), and the K-(ET)2CU [N(CN)2] C1 salt becomes a superconductor at even higher Tc under 0.3 kbar hydrostatic pressure (Tc = 12.8 K). The similarities and differences between K-(ET)2Cu[N(CN)2]Br and K-(ET)2CU(NCS)2 (TC = 10.4 K) are presented. The X-ray structures at 127 K reveal that the S-S contacts shorten between ET dimers in the former compound while the S-S contacts shorten within dimers in the latter. The differences in their ESR linewidth behavior is also explained in terms of the structural differences. A semiconducting compound, (ET)Cu[N(CN)2]2, isolated during K-(ET)2Cu[N(CN)2]Cl synthesis is also reported. The ESR measurements of the K-(ET)2Cu[N(CN)2]Cl salt indicate that the phase transition near 40 K is similar to the spin density wave transition in (TMTSF)2SbF6. A new class of organic superconductors, K-(ET)2CU2(CN)3 and K-(ET)2Cu2(CN)3.δBrδ, is reported with Tc's of 2.8 K (1.5 kbar) and 2.6 K (1 kbar), respectively.


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