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Pierre A. Pantaleón

Researcher at IMDEA Nanoscience

Publications -  6
Citations -  124

Pierre A. Pantaleón is an academic researcher from IMDEA Nanoscience. The author has contributed to research in topics: Bilayer graphene & Graphene. The author has an hindex of 3, co-authored 6 publications receiving 34 citations.

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Band structure of twisted bilayer graphene on hexagonal boron nitride

TL;DR: In this article, the effect of hexagonal boron nitride (hBN) layer closely aligned with twisted bilayer graphene (TBG) was studied. And they found that for a realistic combination of the twist angle in the TBG and the twisted angle between the hBN and the graphene layer, the system can be described using a single moir\'e unit cell.
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Tunable large Berry dipole in strained twisted bilayer graphene

TL;DR: In this article, the authors show that the nonlinear effects of the Berry dipole can exceed the linear response for moderate applied fields, and the dependence of these effects on applied strain, coupling to the substrate, density of carriers, and temperature, makes them highly tunable.
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Band structure and superconductivity in twisted trilayer graphene

TL;DR: In this article, the role of long-range electron-electron interactions near the first magic angle was analyzed in the band structure of twisted trilayer graphene, and superconducting phases with either spin-singlet/valley-triplet or spin-triplets/valleyssinglet symmetry were found with critical temperatures up to a few Kelvin.
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High transmission in twisted bilayer graphene with angle disorder

TL;DR: In this paper, the local density of states and the Landauer-Buttiker transmission through an angle disorder barrier with a width comparable to the moir\'e period were computed using a decimation technique based on real-space description.
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Narrow bands, electrostatic interactions and band topology in graphene stacks

TL;DR: In this paper, the effect of Coulomb interaction on twisted bilayer graphene was investigated, treated within the self-consistent Hartree-Fock approximation, and it was shown that the on-site part of the Fock potential strongly modifies the band structure at charge neutrality.