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Pressure-induced superconductivity in Bi 4 (I 1−x Br x ) 4 crystals grown by chemical vapor transport and flux methods
Achieving superconductivity in topological materials is thought as a promising route for realizing topological superconductivity, which may provide potential applications to quantum computation. Previously, rich superconducting phases have been reported in the pressurized Bi 4 I 4 and Bi 4 Br 4 crys...
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Published in: | Superconductor science & technology 2023-08, Vol.36 (8), p.85010 |
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Main Authors: | , , , , , , , , , , , |
Format: | Article |
Language: | English |
Citations: | Items that this one cites |
Online Access: | Get full text |
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Summary: | Achieving superconductivity in topological materials is thought as a promising route for realizing topological superconductivity, which may provide potential applications to quantum computation. Previously, rich superconducting phases have been reported in the pressurized Bi
4
I
4
and Bi
4
Br
4
crystals which belong to an interesting quasi-one-dimensional topological system. In this work, we have performed a high-pressure study on some Bi
4
(I
1−
x
Br
x
)
4
crystals grown by two different methods. Remarkably, crystals grown by the chemical vapor transport (CVT) method and the self-flux method show clearly different pressure effects. In the CVT-grown crystals, only one superconducting transition is observed, while three superconducting transitions can be detected in crystals grown by the flux method. Through comparisons of the pressure-dependent phase diagrams and the upper critical field behaviors in the two kinds of crystals, the higher superconducting transition (>6 K) in the flux-grown crystals is suggested to come from the residual Bi. High-pressure Raman spectroscopy measurements on both kinds of crystals have confirmed the occurrence of a similar structural transition around 10 GPa in Br-doped samples. Overall, our data could be helpful for identifying the intrinsic pressure-induced superconductivity in various Bi-based materials. |
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ISSN: | 0953-2048 1361-6668 |
DOI: | 10.1088/1361-6668/ace086 |