Author
Listed:
- S. Uji
(National Research Institute for Metals)
- H. Shinagawa
(National Research Institute for Metals)
- T. Terashima
(National Research Institute for Metals)
- T. Yakabe
(National Research Institute for Metals)
- Y. Terai
(National Research Institute for Metals)
- M. Tokumoto
(Electrotechnical laboratory)
- A. Kobayashi
(Research Centre for Spectrochemistry, Graduate School of Science, The University of Tokyo)
- H. Tanaka
(Institute for Molecular Science)
- H. Kobayashi
(Institute for Molecular Science)
Abstract
The application of a sufficiently strong magnetic field to a superconductor will, in general, destroy the superconducting state. Two mechanisms are responsible for this. The first is the Zeeman effect1,2, which breaks apart the paired electrons if they are in a spin-singlet (but not a spin-triplet) state. The second is the so-called ‘orbital’ effect, whereby the vortices penetrate into the superconductors and the energy gain due to the formation of the paired electrons is lost3. For the case of layered, two-dimensional superconductors, such as the high-Tc copper oxides, the orbital effect is reduced when the applied magnetic field is parallel to the conducting layers4. Here we report resistance and magnetic-torque experiments on single crystals of the quasi-two-dimensional organic conductor λ-(BETS)2FeCl4, where BETS is bis(ethylenedithio)tetraselenafulvalene5,6,7,8. We find that for magnetic fields applied exactly parallel to the conducting layers of the crystals, superconductivity is induced for fields above 17 T at a temperature of 0.1 K. The resulting phase diagram indicates that the transition temperature increases with magnetic field, that is, the superconducting state is further stabilized with magnetic field.
Suggested Citation
S. Uji & H. Shinagawa & T. Terashima & T. Yakabe & Y. Terai & M. Tokumoto & A. Kobayashi & H. Tanaka & H. Kobayashi, 2001.
"Magnetic-field-induced superconductivity in a two-dimensional organic conductor,"
Nature, Nature, vol. 410(6831), pages 908-910, April.
Handle:
RePEc:nat:nature:v:410:y:2001:i:6831:d:10.1038_35073531
DOI: 10.1038/35073531
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