Condensed Matter Theory

Abstract:

Luttinger’s theorem is a fundamental result in the theory of interacting Fermi systems: it states that the volume inside the Fermi surface is left invariant by interactions, if the number of particles is held fixed. Although this is traditionally justified in terms of analytic properties of Green’s functions, it can be viewed as arising from a momentum balance argument that examines the response of the ground state to the insertion of a single flux quantum [M. Oshikawa, Phys. Rev. Lett. 84, 3370 (2000)]. This reveals that the Fermi volume is a topologically protected quantity, whose change requires a phase transition. However, this sheds no light on the stability or lack thereof of interacting semimetals, that either lack a Fermi surface, or have perfectly compensated electron and hole pockets and hence vanishing net Fermi volume. Here, I show that semimetallic phases in non-symmorphic crystals possess additional topological ‘Luttinger invariants’ that can be nonzero even though the Fermi volume vanishes. The existence of these invariants is linked to the inability of non-symmorphic crystals to host band insulating ground states except at special fillings. I exemplify the use of these new invariants by showing that they distinguish various classes of twoand three-dimensional semimetals.

Abstract:

We use the oxDNA coarse-grained model to provide a detailed characterization of the fundamental structural properties of DNA origami, focussing on archetypal 2D and 3D origami. The model reproduces well the characteristic pattern of helix bending in a 2D origami, showing that it stems from the intrinsic tendency of anti-parallel four-way junctions to splay apart, a tendency that is enhanced both by less screened electrostatic interactions and by increased thermal motion. We also compare to the structure of a 3D origami whose structure has been determined by cryo-electron microscopy. The oxDNA average structure has a root-mean-square deviation from the experimental structure of 8.4 Å, which is of the order of the experimental resolution. These results illustrate that the oxDNA model is capable of providing detailed and accurate insights into the structure of DNA origami, and has the potential to be used to routinely pre-screen putative origami designs and to investigate the molecular mechanisms that regulate the properties of DNA origami.