Motivated by the vast string landscape, we consider the shear viscosity to entropy density ratio in conformal field theories dual to Einstein gravity with curvature square corrections. After field redefinitions these theories reduce to Gauss-Bonnet gravity, which has special properties that allow us to compute the shear viscosity nonperturbatively in the Gauss-Bonnet coupling. By tuning of the coupling, the value of the shear viscosity to entropy density ratio can be adjusted to any positive value from infinity down to zero, thus violating the conjectured viscosity bound. At linear order in the coupling, we also check consistency of four different methods to calculate the shear viscosity, and we find that all of them agree. We search for possible pathologies associated with this class of theories violating the viscosity bound.

In recent work we showed that, for a class of conformal field theories (CFT) with Gauss-Bonnet gravity dual, the shear viscosity to entropy density ratio, eta/s, could violate the conjectured Kovtun-Starinets-Son viscosity bound, eta/s > or = 1/4 pi. In this Letter we argue, in the context of the same model, that tuning eta/s below (16/25)(1/4 pi) induces microcausality violation in the CFT, rendering the theory inconsistent. This is a concrete example in which inconsistency of a theory and a lower bound on viscosity are correlated, supporting the idea of a possible universal lower bound on eta/s for all consistent theories.

Liquids relax extremely slowly on approaching the glass state. One explanation is that an entropy crisis, because of the rarefaction of available states, makes it increasingly arduous to reach equilibrium in that regime. Validating this scenario is challenging, because experiments offer limited resolution, while numerical studies lag more than eight orders of magnitude behind experimentally relevant timescales. In this work, we not only close the colossal gap between experiments and simulations but manage to create in silico configurations that have no experimental analog yet. Deploying a range of computational tools, we obtain four estimates of their configurational entropy. These measurements consistently confirm that the steep entropy decrease observed in experiments is also found in simulations, even beyond the experimental glass transition. Our numerical results thus extend the observational window into the physics of glasses and reinforce the relevance of an entropy crisis for understanding their formation.

We holographically engineer a periodic lattice of localized fermionic impurities within a plasma medium by putting an array of probe D5-branes in the background produced by N D3-branes. Thermodynamic quantities are computed in the large N limit via the holographic dictionary. We then dope the lattice by replacing some of the D5-branes by anti-D5-branes. In the large N limit, we determine the critical temperature below which the system dimerizes with bond ordering. Finally, we argue that for the special case of a square lattice our system is glassy at large but finite N , with the low temperature physics dominated by a huge collection of metastable dimerized configurations without long-range order, connected only through tunneling events.

Liquids cooled towards the glass transition temperature transform into amorphous solids that have a wide range of applications. While the nature of this transformation is understood rigorously in the mean-field limit of infinite spatial dimensions, the problem remains wide open in physical dimensions. Nontrivial finite-dimensional fluctuations are hard to control analytically, and experiments fail to provide conclusive evidence regarding the nature of the glass transition. Here, we develop Monte Carlo methods for two-dimensional glass-forming liquids that allow us to access equilibrium states at sufficiently low temperatures to directly probe the glass transition in a regime inaccessible to experiments. We find that the liquid state terminates at a thermodynamic glass transition which occurs at zero temperature and is associated with an entropy crisis and a diverging static correlation length. Our results thus demonstrate that a thermodynamic glass transition can occur in finite dimensional glass-formers.