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Extremely Overdoped Superconducting Cuprates via High Pressure Oxygenation Methods

Linda SederholmDepartment of Chemistry and Materials Science, Aalto University, 00076 Aalto, FinlandSteven D. ConradsonDepartment of Chemistry, Washington State University, Pullman, WA 90164, USAT. H. GeballeDepartment of Applied Physics, Stanford University, Stanford, CA 94305, USAChangqing JinInstitute of Physics, Chinese Academy of Sciences, Beijing 100190, ChinaAndrea GauzziIMPMC, CNRS, IRD and MNHN, Sorbonne University, 75005 Paris, FranceE. GilioliCNR, Institute of Materials for Electronics and Magnetism, A-43124 Parma, ItalyMaarit KarppinenDepartment of Chemistry and Materials Science, Aalto University, 00076 Aalto, FinlandGianguido BaldinozziCNRS CentraleSupélec, Université Paris-Saclay, 91192 Gif-sur-Yvette, France
2021en
ABI

Annotatsiya

Within the cuprate constellation, one fixed star has been the superconducting dome in the quantum phase diagram of transition temperature vs. the excess charge on the Cu in the CuO2-planes, p, resulting from O-doping or cation substitution. However, a more extensive search of the literature shows that the loss of the superconductivity in favor of a normal Fermi liquid on the overdoped side should not be assumed. Many experimental results from cuprates prepared by high-pressure oxygenation show Tc converging to a fixed value or continuing to slowly increase past the upper limit of the dome of p = 0.26–0.27, up to the maximum amounts of excess oxygen corresponding to p values of 0.3 to > 0.6. These reports have been met with disinterest or disregard. Our review shows that dome-breaking trends for Tc are, in fact, the result of careful, accurate experimental work on a large number of compounds. This behavior most likely mandates a revision of the theoretical basis for high-temperature superconductivity. That excess O atoms located in specific, metastable sites in the crystal, attainable only with extreme O chemical activity under HPO conditions, cause such a radical extension of the superconductivity points to a much more substantial role for the lattice in terms of internal chemistry and bonding.

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