Theory of integer quantum Hall effect in insulating bilayer graphene

A variational ground state for insulating bilayer graphene (BLG), subject to quantizing magnetic fields, is proposed. Due to the Zeeman coupling, the layer anti-ferromagnet (LAF) order parameter in fully gapped BLG gets projected onto the spin easy plane, and simultaneously a ferromagnet order, which can further be enhanced by exchange interaction, develops in the direction of the magnetic field. The activation gap for the $\nu=0$ Hall state then displays a crossover from quadratic to linear scaling with the magnetic field, as it gets stronger, and I obtain excellent agreement with a number of recent experiments with realistic strengths for the ferromagnetic interaction. A component of the LAF order, parallel to the external magnetic field, gives birth to additional incompressible Hall states at filling $\nu=\pm 2$, whereas the remote hopping in BLG yields $\nu=\pm 1$ Hall states. Evolution of the LAF order in tilted magnetic fields, scaling of the gap at $\nu=2$, the effect of external electric fields on various Hall plateaus, and different possible hierarchies of fractional quantum Hall states are highlighted.Comment: Published version: 5 pages, 2 figures (Supplementary: 6 pages, 2 figures); New references, typos correcte

RF analysis of aggressively scaled pHEMTs

No abstract avaliable

The pale evidence for treatment of iron-deficiency anaemia in older people

Funding The authors have received funding to carry out a pilot RCT on management of IDA in older people from the Chief Scientist Office, Scotland.Peer reviewedPostprin

New nonlinear coherent states and some of their nonclassical properties

We construct a displacement operator type nonlinear coherent state and examine some of its properties. In particular it is shown that this nonlinear coherent state exhibits nonclassical properties like squeezing and sub-Poissonian behaviour.Comment: 3 eps figures. to appear in J.Opt

Characterization of nanodimensional Ni-Zn ferrite prepared by mechanochemical and thermal methods.

Nickel zinc ferrite nanoparticles, Ni1−xZnxFe2O4 (x = 0, 0.2, 0.5, 0.8, 1.0), with dimensions below 10 nm have been prepared by combining chemical precipitation with high-energy ball milling. For comparison, their analogues obtained by thermal synthesis have also been studied. Mössbauer spectroscopy, X-ray diffraction, and magnetic measurements are used for the characterization of the obtained materials. X-ray diffraction shows that after 3h of mechanical treatment ferrites containing zinc are formed, while 6h of treatment is needed to obtain NiFe2O4. The magnetic properties of the samples exhibit a strong dependence on the phase composition, particle size and preparation method

Quantum-fluid-dynamics approach for strong-field processes: Application to the study of multiphoton ionization and high-order harmonic generation of He and Ne atoms in intense laser fields

This is the published version, also available here: http://dx.doi.org/10.1103/PhysRevA.65.043402.We explore the feasibility of extending the quantum-fluid dynamics (QFD) approach for quantitative investigation of nonlinear optical processes of many-electron quantum systems in intense laser fields. Through the amalgamation of the QFD and density-functional theory (DFT), a single time-dependent hydrodynamical equation of motion can be derived. This equation has the form of a generalized nonlinear Schrödinger equation (GNLSE) but includes the many-body effects through a local time-dependent exchange-correlation potential. The time-dependent generalized pseudospectral method is extended to the solution of the GNLSE in spherical coordinates, allowing nonuniform spatial discretization and efficient, accurate solution of the hydrodynamical density and wave function in space and time. The procedure is applied to the study of multiphoton ionization (MPI) and high-order harmonic generation (HHG) of He and Ne atoms in intense laser fields. Excellent agreement with other recent self-interaction-free time-dependent DFT calculations is obtained for He, while for Ne, good agreement is achieved. Four different exchange-correlation energy functionals are used in the study with an aim to explore the roles of exchange and correlation on MPI/HHG processes in details. The method offers a conceptually appealing and computationally practical approach for nonperturbative treatment of strong-field processes of many-electron systems beyond the time-dependent Hartree-Fock level

Density-functional calculations on singly and doubly excited Rydberg states of many-electron atoms

This is the published version, also available here: http://dx.doi.org/10.1103/PhysRevA.65.052508.Nearly 100 low-, moderately high-, and high-lying singly and doubly excited states of He, Li, and Be have been calculated using a nonvariational, work-function-based exchange potential within the nonrelativistic Hohenberg-Kohn-Sham density-functional theory (DFT). The nonlinear gradient included in the Lee-Yang-Parr correlation functional is used to incorporate the correlation potential. The generalized pseudospectral method is used for nonuniform and optimal spatial grid discretization and solution of the Kohn-Sham equation to obtain accurate eigenvalues, expectation values, and radial densities for both ground and excited states. The results are compared with the available theoretical and experimental data. The discrepancy in the calculated singly excited state energies is within about 0.01% for He (for other atoms, it is less than 0.2%), while that for the doubly excited states of He is well within 3.6%. The deviations in the calculated single- and double-excitation energies for 31 selected states are in the error ranges 0.009–0.632 % and 0.085–1.600 %, respectively. The overall agreement of the present results is quite gratifying, especially in the light of DFT’s difficulties in dealing with excited states. The exchange-only results are practically of Hartree-Fock quality, and the correlation-included results are usually slightly overestimated. The present method offers a simple, computationally efficient and general scheme for accurate calculation of multiply excited Rydberg states within DFT

Failure of Intravenous Morphine to Serve as an Effective Instrumental Reinforcer in Dopamine D2 Receptor Knock-Out Mice

The rewarding effects of opiates are thought to be mediated through dopaminergic mechanisms in the ventral tegmental area, dopamine-independent mechanisms in the nucleus accumbens, or both. The purpose of the present study was to explore the contribution of dopamine to opiate-reinforced behavior using D2 receptor knock-out mice. Wild-type, heterozygous, and D2 knock-out mice were first trained to lever press for water reinforcement and then implanted with intravenous catheters. The ability of intravenously delivered morphine to maintain lever pressing in these mice was studied under two schedules of reinforcement: a fixed ratio 4 (FR4) schedule (saline, 0.1, 0.3, or 1.0 mg/kg, per injection) and a progressive ratio (PR) schedule (1.0 mg/kg, per injection). In the wild-type and heterozygous mice, FR4 behavior maintained by morphine injections was significantly greater than behavior maintained by vehicle injections. Response rate was inversely related to injection dose and increased significantly in the wild-type and heterozygous mice when the animals were placed on the PR schedule. In contrast, the knock-out mice did not respond more for morphine than for saline and did not respond more when increased ratios were required by the PR schedule. Thus, morphine served as a positive reinforcer in the wild-type and heterozygous mice but failed to do so in the knock-out mice. Under this range of doses and response requirements, the rewarding effects of morphine appear to depend critically on an intact D2 receptor systemFil: Elmer, Greg I.. University of Maryland; Estados UnidosFil: Pieper, Jeanne O.. National Institutes of Health; Estados UnidosFil: Rubinstein, Marcelo. Consejo Nacional de Investigaciones Científicas y Técnicas. Instituto de Investigaciones en Ingeniería Genética y Biología Molecular "Dr. Héctor N. Torres"; ArgentinaFil: Low, Malcolm J.. Oregon Health and Sciences University; Estados UnidosFil: Grandy, David K.. Oregon Health and Sciences University; Estados UnidosFil: Wise, Roy A.. National Institutes of Health; Estados Unido