Scaling behavior of crystalline membranes: an ϵ\epsilon-expansion approach

We study the scaling behavior of two-dimensional (2D) crystalline membranes in the flat phase by a renormalization group (RG) method and an $\epsilon$-expansion. Generalization of the problem to non-integer dimensions, necessary to control the $\epsilon$-expansion, is achieved by dimensional continuation of a well-known effective theory describing out-of-plane fluctuations coupled to phonon-mediated interactions via a scalar composite field, equivalent for small deformations to the local Gaussian curvature. The effective theory, which will be referred to as Gaussian curvature interaction (GCI) model, is equivalent to theories of elastic $D$-dimensional manifolds fluctuating in a $(D + d_{c})$-dimensional embedding space in the physical case $D = 2$ for arbitrary $d_{c}$. For $D\neq 2$, instead, the GCI model is not equivalent to a direct dimensional continuation of elastic membrane theory and it defines an alternative generalization to generic internal dimension $D$. We calculate explicitly RG functions at two-loop order and determine the exponent $\eta$ characterizing the long-wavelength scaling of correlation functions to order $\epsilon^{2}$ in an $\epsilon=(4-D)$-expansion. The self-consistent screening approximation (SCSA) for the GCI model is shown to be exact to O($\epsilon^{2}$). For $d_{c} = 1$, the O($\epsilon^{2}$) correction is suppressed by a small numerical prefactor. As a result, despite the large value of $\epsilon = 2$, extrapolation of the first and second order results to $D = 2$ leads to very close numbers, $\eta = 0.8$ and $\eta \simeq 0.795$. The calculated exponent values are close to earlier reference results obtained by non-perturbative RG, the SCSA and numerical simulations. These indications suggest that a perturbative analysis of the GCI model could provide an useful framework for accurate quantitative predictions of the scaling exponent even at $D = 2$.Comment: 15 pages, 4 figure

Effect of dimensionality on the charge-density-wave in few-layers 2H-NbSe2_2

We investigate the charge density wave (CDW) instability in single and double layers, as well as in the bulk 2H-NbSe$_{2}$. We demonstrate that the density functional theory correctly describes the metallic CDW state in the bulk 2H-NbSe$_{2}$. We predict that both mono- and bilayer NbSe$_{2}$ undergo a CDW instability. However, while in the bulk the instability occurs at a momentum $\mathbf{q}_{CDW}\approx{2/3}\mathbf{\Gamma M}$, in free-standing layers it occurs at $\mathbf{q}_{CDW}\approx{1/2}\mathbf{\Gamma M}$. Furthermore, while in the bulk the CDW leads to a metallic state, in a monolayer the ground state becomes semimetallic, in agreement with recent experimental data. We elucidate the key role that an enhancement of the electron-phonon matrix element at $\mathbf{q}\approx\mathbf{q}_{CDW}$ plays in forming the CDW ground state.Comment: 4 pages 5 figure

Effects of magnetism and doping on the electron-phonon coupling in BaFe2_{2}As2_{2}

We calculate the effect of local magnetic moments on the electron-phonon coupling in BaFe$_{2}$As$_{2}+\delta$ using the density functional perturbation theory. We show that the magnetism enhances the total electron-phonon coupling by $\sim 50$, up to $\lambda \lesssim 0.35$, still not enough to explain the high critical temperature, but strong enough to have a non-negligible effect on superconductivity, for instance, by frustrating the coupling with spin fluctuations and inducing order parameter nodes. The enhancement comes mostly from a renormalization of the electron-phonon matrix elements. We also investigate, in the rigid band approximation, the effect of doping, and find that $\lambda$ versus doping does not mirror the behavior of the density of states; while the latter decreases upon electron doping, the former does not, and even increases slightly.Comment: 4 pages, 3 figure