Charge fluctuations, phonons, and superconductivity in multilayer graphene
Ziyan Li, Xueheng Kuang, Alejandro Jimeno-Pozo, Héctor Sainz-Cruz, Zhen Zhan, Shengjun Yuan, Francisco Guinea
DOI 10.1103/PhysRevB.108.045404 · Physical Review B
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Abstract
Motivated by the recent experimental detection of superconductivity in Bernal bilayer (AB) and rhombohedral trilayer (ABC) graphene, we study the emergence of superconductivity in multilayer graphene based on a Kohn-Luttinger (KL) -like mechanism in which the pairing glue is the screened Coulomb interaction. We find that electronic interactions alone can drive superconductivity in AB bilayer graphene and ABC trilayer graphene with the critical temperatures in good agreement with the experimentally observed ones, allowing us to further predict superconductivity from electronic interactions in Bernal ABA trilayer, ABAB tetralayer, and rhombohedral ABCA tetralayer graphene. By comparing the critical temperatures (Tc) of these five nontwisted graphene stacks, we find that the ABC trilayer graphene possesses the highest Tc∼100 mK. After considering the enhancement of superconductivity due to Ising spin-orbit coupling, we observe that the AB bilayer graphene has the largest enhancement in the critical temperature, increasing from 23 to 143 mK. The superconducting behaviors in these nontwisted graphene stacks could be explained by the order parameters (OPs). The OPs of Bernal stacks preserve intravalley C3 symmetry, whereas rhombohedral stacks break it. In all stacks, the OPs have zeros and change sign between valleys, which means that these multilayers of graphene are nodal spin-triplet superconductors. Moreover, dressing the purely electronic interaction with acoustic phonons, we observe minor changes of the critical temperatures in these five stacks. We adopt the KL-like mechanism to investigate the tendency of superconductivity in multilayer graphene without fitting parameters, which could provide guidance to future experiments exploring superconductivity in nontwisted graphene.
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