Articolo in rivista, 2017, ENG, 10.1209/0295-5075/118/37003
Mazziotti, Maria Vittoria; Valletta, Antonio; Campi, Gaetano; Innocenti, Davide; Perali, Andrea; Bianconi, Antonio
Rome Int Ctr Mat Sci Superstripes; CNR; CNR; Univ Liverpool; Univ Camerino; Natl Res Nucl Univ; Latvian Acad Sci
Recent experiments have reported the emergence of high-temperature superconductivity with critical temperature T-c between 43K and 123K in a potassium-doped aromatic hydrocarbon para-Terphenyl or p-Terphenyl. This achievement provides the record for the highest T-c in an organic superconductor overcoming the previous record of T-c = 38K in Cs3C60 fulleride. Here we propose that the driving mechanism is the quantum resonance between superconducting gaps near a Lifshitz transition which belongs to the class of Fano resonances called shape resonances. For the case of p-Terphenyl our numerical solutions of the multigap equation shows that high T-c is driven by tuning the chemical potential by K doping and it appears only in a narrow energy range near a Lifshitz transition. At the maximum critical temperature, T-c = 123 K, the condensate in the appearing new small Fermi surface pocket is in the BCS-BEC crossover while the T-c drops below 0.3K where it is in the BEC regime. Finally, we predict the experimental results which can support or falsify our proposed mechanism: a) the variation of the isotope coefficient as a function of the critical temperature and b) the variation of the gaps and their ratios 2 Delta/T-c as a function of T-c. Copyright (C) EPLA, 2017
Europhysics letters (Print) 118 (3), pp. 37003-p1–37003-p7
Organic superconductors, Theories and models of superconducting state, Occurrence, potential candidates
Valletta Antonio, Campi Gaetano
IC – Istituto di cristallografia, IMM – Istituto per la microelettronica e microsistemi
ID: 380446
Year: 2017
Type: Articolo in rivista
Creation: 2017-12-15 19:06:05.000
Last update: 2021-05-06 22:16:42.000
CNR authors
External IDs
CNR OAI-PMH: oai:it.cnr:prodotti:380446
DOI: 10.1209/0295-5075/118/37003
ISI Web of Science (WOS): 000407226300018
Scopus: 2-s2.0-85024112790