Heavy Fermion Quantum Criticality

During the last few years, investigations of Rare-Earth materials have made clear that not only the heavy fermion phase in these systems provides interesting physics, but the quantum criticality where such a phase dies exhibits novel phase transition physics not fully understood. Moreover, attempts to study the critical point numerically face the infamous fermion sign problem, which limits their accuracy. Effective action techniques and Callan-Symanzik equations have been very popular in high energy physics, where they enjoy a good record of success. Yet, they have been little exploited for fermionic systems in condensed matter physics. In this work, we apply the RG effective action and Callan-Symanzik techiques to the heavy fermion problem. We write for the first time the effective action describing the low energy physics of the system. The f-fermions are replaced by a dynamical scalar field whose nonzero expected value corresponds to the heavy fermion phase. This removes the fermion sign problem, making the effective action amenable to numerical studies as the effective theory is bosonic. Renormalization group studies of the effective action can be performed to extract approximations to nonperturbative effects at the transition. By performing one-loop renormalizations, resummed via Callan-Symanzik methods, we describe the heavy fermion criticality and predict the heavy fermion critical dynamical susceptibility and critical specific heat. The specific heat coefficient exponent we obtain (0.39) is in excellent agreement with the experimental result at low temperatures (0.4).Comment: 5 pages. In the replacement, the numerical value for the specific heat coefficient exponent has been included explicitly in decimal form, and has been compared with the experimental result

Dynamical instability and loss of p-band bosons in optical lattices

We study how the bosonic atoms on the excited p-band of an optical lattice are coupled to the lowest s-band and the 2nd excited d-band. We find that in some parameter regimes the atom-atom interactions can cause a dynamical instability of the p-band atoms towards decay to the s- and d-bands. Furthermore, even when dynamical instability is not expected s- and d-bands can become substantially populated.Comment: 7 figures, minor changes to the earlier versio

Superfluid Helium On-Orbit Transfer (SHOOT) operatons

The in-flight tests and the operational sequences of the Superfluid Helium On-Orbit Transfer (SHOOT) experiment are outlined. These tests include the transfer of superfluid helium at a variety of rates, the transfer into cold and warm receivers, the operation of an extravehicular activity coupling, and tests of a liquid acquisition device. A variety of different types of instrumentation will be required for these tests. These include pressure sensors and liquid flow meters that must operate in liquid helium, accurate thermometry, two types of quantity gauges, and liquid-vapor sensors

Magnetic moment and magnetic anisotropy of linear and zigzag 4{\it d} and 5{\it d} transition metal nanowires: First-principles calculations

An extensive {\it ab initio} study of the physical properties of both linear and zigzag atomic chains of all 4$d$ and 5$d$ transition metals (TM) within the GGA by using the accurate PAW method, has been carried out. All the TM linear chains are found to be unstable against the corresponding zigzag structures. All the TM chains, except Nb, Ag and La, have a stable (or metastable) magnetic state in either the linear or zigzag or both structures. Magnetic states appear also in the sufficiently stretched Nb and La linear chains and in the largely compressed Y and La chains. The spin magnetic moments in the Mo, Tc, Ru, Rh, W, Re chains could be large ($\geq$1.0 $\mu_B$/atom). Structural transformation from the linear to zigzag chains could suppress the magnetism already in the linear chain, induce the magnetism in the zigzag structure, and also cause a change of the magnetic state (ferromagnetic to antiferroamgetic or vice verse). The calculations including the spin-orbit coupling reveal that the orbital moments in the Zr, Tc, Ru, Rh, Pd, Hf, Ta, W, Re, Os, Ir and Pt chains could be rather large ($\geq$0.1 $\mu_B$/atom). Importantly, large magnetic anisotropy energy ($\geq$1.0 meV/atom) is found in most of the magnetic TM chains, suggesting that these nanowires could have fascinating applications in ultrahigh density magnetic memories and hard disks. In particular, giant magnetic anisotropy energy ($\geq$10.0 meV/atom) could appear in the Ru, Re, Rh, and Ir chains. Furthermore, the magnetic anisotropy energy in several elongated linear chains could be as large as 40.0 meV/atom. A spin-reorientation transition occurs in the Ru, Ir, Ta, Zr, La and Zr, Ru, La, Ta and Ir linear chains when they are elongated. Remarkably, all the 5$d$ as well as Tc and Pd chains show the colossal magnetic anisotropy (i.e., it is impossible to rotate magnetization into certain directions). Finally, the electronic band structure and density of states of the nanowires have also been calculated in order to understand the electronic origin of the large magnetic anisotropy and orbital magnetic moment as well as to estimate the conduction electron spin polarization.Comment: To appear in Phys. Rev.

Spontaneous magnetization and structure formation in a spin-1 ferromagnetic Bose-Einstein condensate

Motivated by recent experiments involving the non-destructive imaging of magnetization of a spin-1 87Rb Bose gas (Higbie et al., cond-mat/0502517), we address the question of how the spontaneous magnetization of a ferromagnetic BEC occurs in a spin-conserving system. Due to competition between the ferromagnetic interaction and the total spin conservation, various spin structures such as staggered magnetic domains, and helical and concentric ring structures are formed, depending on the geometry of the trapping potential.Comment: 8 pages, 5 figure

Quantized Lattice Dynamic Effects on the Spin-Peierls Transition

The density matrix renormalization group method is used to investigate the spin-Peierls transition for Heisenberg spins coupled to quantized phonons. We use a phonon spectrum that interpolates between a gapped, dispersionless (Einstein) limit to a gapless, dispersive (Debye) limit. A variety of theoretical probes are used to determine the quantum phase transition, including energy gap crossing, a finite size scaling analysis, bond order auto-correlation functions, and bipartite quantum entanglement. All these probes indicate that in the antiadiabatic phonon limit a quantum phase transition of the Berezinskii-Kosterlitz-Thouless type is observed at a non-zero spin-phonon coupling, $g_{\text c}$. An extrapolation from the Einstein limit to the Debye limit is accompanied by an increase in $g_{\text c}$ for a fixed optical ($q=\pi$) phonon gap. We therefore conclude that the dimerized ground state is more unstable with respect to Debye phonons, with the introduction of phonon dispersion renormalizing the effective spin-lattice coupling for the Peierls-active mode. We also show that the staggered spin-spin and phonon displacement order parameters are unreliable means of determining the transition.Comment: To be published in Phys. Rev.

Doping of graphene by a Au(111) substrate: Calculation strategy within the local density approximation and a semiempirical van der Waals approach

We have performed a density functional study of graphene adsorbed on Au(111) surface using both a local density approximation and a semiempirical van der Waals approach proposed by Grimme, known as the DFT-D2 method. Graphene physisorbed on metal has the linear dispersion preserved in the band-structure, but the Fermi level of the system is shifted with respect to the conical points which results in a doping effect. We show that the type and amount of doping depends not only on the choice of the exchange-correlation functional used in the calculations, but also on the supercell geometry that models the physical system. We analyzed how the factors such as the in-plane cell parameter and interlayer spacing in gold influence the Fermi level shift and we found that even a small variation in these parameters may cause a transition from p-type to n-type doping. We have selected a reasonable set of model parameters and obtained that graphene is either undoped or at most slightly p-type doped on the clean Au(111) surface, which seems to be in line with experimental findings. On the other hand, modifications of the substrate lattice may induce larger doping up to 0.30-0.40 eV depending on the graphene-metal adsorption distance. The sensitivity of the graphene-gold interface to the structural parameters may allow to tune doping across the samples which could lead to possible applications in graphene-based electronic devices. We believe that the present remarks can be also useful for other studies based on the periodic DFT