Unitary Fermi Gas in a Harmonic Trap

We present an {\it ab initio} calculation of small numbers of trapped, strongly interacting fermions using the Green's Function Monte Carlo method (GFMC). The ground state energy, density profile and pairing gap are calculated for particle numbers $N = 2 \sim 22$ using the parameter-free "unitary" interaction. Trial wave functions are taken of the form of correlated pairs in a harmonic oscillator basis. We find that the lowest energies are obtained with a minimum explicit pair correlation beyond that needed to exploit the degeneracy of oscillator states. We find that energies can be well fitted by the expression $a_{TF} E_{TF} + \Delta {\rm mod}(N,2)$ where $E_{TF}$ is the Thomas-Fermi energy of a noninteracting gas in the trap and $\Delta$ is a pairing gap. There is no evidence of a shell correction energy in the systematics, but the density distributions show pronounced shell effects. We find the value $\Delta= 0.7\pm 0.2\omega$ for the pairing gap. This is smaller than the value found for the uniform gas at a density corresponding to the central density of the trapped gas.Comment: 2 figures, 2 table

Thermal buckling analysis for stiffened orthotropic cylindrical shells

Structural analysis of thermal buckling of orthotropic, multilayered, stiffened cylindrical shell using finite differences and determinant plotting or modal iteratio

Valley-dependent Brewster angles and Goos-Hanchen effect in strained graphene

We demonstrate theoretically how local strains in graphene can be tailored to generate a valley polarized current. By suitable engineering of local strain profiles, we find that electrons in opposite valleys (K or K') show different Brewster-like angles and Goos-H\"anchen shifts, exhibiting a close analogy with light propagating behavior. In a strain-induced waveguide, electrons in K and K' valleys have different group velocities, which can be used to construct a valley filter in graphene without the need for any external fields.Comment: 5 pages, 4 figure

A systematic study of Rayleigh-Brillouin scattering in air, N2 and O2 gases

Spontaneous Rayleigh-Brillouin scattering experiments in air, N2 and O2 have been performed for a wide range of temperatures and pressures at a wavelength of 403 nm and at a 90 degrees scattering angle. Measurements of the Rayleigh-Brillouin spectral scattering profile were conducted at high signal-to-noise ratio for all three species, yielding high-quality spectra unambiguously showing the small differences between scattering in air, and its constituents N2 and O2. Comparison of the experimental spectra with calculations using the Tenti S6 model, developed in 1970s based on linearized kinetic equations for molecular gases, demonstrates that this model is valid to high accuracy. After previous measurements performed at 366 nm, the Tenti S6 model is here verified for a second wavelength of 403 nm. Values for the bulk viscosity for the gases are derived by optimizing the model to the measurements. It is verified that the bulk viscosity parameters obtained from previous experiments at 366 nm, are valid for wavelengths of 403 nm. Also for air, which is treated as a single-component gas with effective gas transport coefficients, the Tenti S6 treatment is validated for 403 nm as for the previously used wavelength of 366 nm, yielding an accurate model description of the scattering profiles for a range of temperatures and pressures, including those of relevance for atmospheric studies. It is concluded that the Tenti S6 model, further verified in the present study, is applicable to LIDAR applications for exploring the wind velocity and the temperature profile distributions of the Earth's atmosphere. Based on the present findings, predictions can be made on the spectral profiles for a typical LIDAR backscatter geometry, which deviate by some 7 percent from purely Gaussian profiles at realistic sub-atmospheric pressures occurring at 3-5 km altitude in the Earth's atmosphere

Resonant Tunneling through S- and U-shaped Graphene Nanoribbons

We theoretically investigate resonant tunneling through S- and U-shaped nanostructured graphene nanoribbons. A rich structure of resonant tunneling peaks are found eminating from different quasi-bound states in the middle region. The tunneling current can be turned on and off by varying the Fermi energy. Tunability of resonant tunneling is realized by changing the width of the left and/or right leads and without the use of any external gates.Comment: 6 pages, 7 figure

Ab initio study of a mechanically gated molecule: From weak to strong correlation

The electronic spectrum of a chemically contacted molecule in the junction of a scanning tunneling microscope can be modified by tip retraction. We analyze this effect by a combination of density functional, many-body perturbation and numerical renormalization group theory, taking into account both the non-locality and the dynamics of electronic correlation. Our findings, in particular the evolution from a broad quasiparticle resonance below to a narrow Kondo resonance at the Fermi energy, correspond to the experimental observations.Comment: 4 pages, 3 figure