arXiv subjects

F. Wang

Publications and source records attributed to F. Wang.

At least 91 records · Page 5Linked to original sources

arXiv2013

Hydrogen lines in LAMOST low resolution spectra of RR Lyrae stars

The LAMOST spectroscopic survey for Galactic structure and evolution has been in operation since October 2012, following a one-year pilot survey. The pilot survey produced a data release containing over 600,000 stellar spectra. By cross-checking with a large time series photometric database of RR Lyrae stars in high Galactic latitude regions, we found a total number of 157 stars that have been observed with LAMOST. In this sample, we successfully captured three RR Lyrae stars in the fast expansion phase, all of them showing significant hypersonic shock wave features in the spectra. By fitting the Hα line shape, we determine that the emission features seen within the broader Hα absorption line suggest hypersonic relative motions in the atmospheres of these three objects. With a further LAMOST survey of millions of stars, we will capture a large sample of RR Lyrae stars in their hypersonic expansion phase, and therefore provide a large database for the study of the internal structure and pulsation mechanism of RR Lyrae stars.

astro-ph.SR↗

arXiv2013

Magnetoelectric coupling in the paramagnetic state of a metal-organic framework

Although the magnetoelectric effects - the mutual control of electric polarization by magnetic fields and magnetism by electric fields, have been intensively studied in a large number of inorganic compounds and heterostructures, they have been rarely observed in organic materials. Here we demonstrate magnetoelectric coupling in a metal-organic framework [(CH3)2NH2]Mn(HCOO)3 which exhibits an order-disorder type of ferroelectricity below 185 K. The magnetic susceptibility starts to deviate from the Curie-Weiss law at the paraelectric-ferroelectric transition temperature, suggesting an enhancement of short-range magnetic correlation in the ferroelectric state. Electron spin resonance study further confirms that the magnetic state indeed changes following the ferroelectric phase transition. Inversely, the ferroelectric polarization can be improved by applying high magnetic fields. We interpret the magnetoelectric coupling in the paramagnetic state in the metal-organic framework as a consequence of the magnetoelastic effect that modifies both the superexchange interaction and the hydrogen bonding.

cond-mat.mtrl-sci↗

arXiv2013

Adsorption of cytosine and aza derivatives of cytidine on Au single crystal surfaces

The adsorption of cytosine on the Au(111) and Au(110) surfaces has been studied using both aqueous deposition and evaporation in vacuum to prepare the samples. Soft X-ray photoelectron spectroscopy (XPS) and near edge X-ray absorption fine structure spectroscopy (NEXAFS) were used to determine the electronic structure and orientation of the adsorbates. In addition, three derivatives of cytosine, 6-azacytosine, 6-azacytidine and 5- azacytidine, were studied. Monolayer films of the latter three samples were adsorbed on Au(111) from aqueous solution, and the nature of bonding was determined. Spectra have been interpreted in the light of published calculations of free cytosine molecules and new ab initio calculations of the other compounds. Surface core level shifts of Au 4f imply that all of these compounds are chemisorbed. Cytosine adsorbs as a single tautomer, but in two chemical states with different surface-molecule bonding. For deposition in vacuum, a flat-lying molecular state bonded through the N(3) atom of the pyrimidine ring dominates, but a second state is also present. For deposition from solution, the second state dominates, with the molecular plane no longer parallel to the surface. This state also bonds through the N(3) atom, but in addition interacts with the surface via the amino group. Two tautomers of 6-azacytosine were observed, and they and 6-azacytidine adsorb with similar geometries, chemically bonding via the azacytosine ring. The ribose ring does not appear to perturb the adsorption of azacytidine compared with azacytosine. The azacytosine ring is nearly but not perfectly parallel to the surface, like 5-azacytidine, which adsorbs as an imino tautomer. ...

physics.chem-ph↗

arXiv2013

Experimental Distillation of Quantum Nonlocality

We report the first experimental demonstration of distillation of quantum nonlocality, confirming the recent theoretical protocol [\textit{Phys. Rev. Lett. 102, 120401 (2009)}]. Quantum nonlocality is described by a correlation box with binary inputs and outputs, and the nonlocal boxes are realized through appropriate measurements on polarization entangled photon pairs. We demonstrate that nonlocality is amplified by connecting two nonlocal boxes into a composite one through local operations and four-photon coincidence measurements.

quant-ph↗

arXiv2013

Photoemission Spectroscopy and the Unusually Robust One Dimensional Physics of Lithium Purple Bronze

Temperature dependent photoemission spectroscopy in Li0.9Mo6O17 contributes to evidence for one dimensional physics that is unusually robust. Three generic characteristics of the Luttinger liquid are observed, power law behavior of the k-integrated spectral function down to temperatures just above the superconducting transition, k-resolved lineshapes that show holon and spinon features, and quantum critical (QC) scaling in the lineshapes. Departures of the lineshapes and the scaling from expectations in the Tomonaga Luttinger model can be partially described by a phenomenological momentum broadening that is presented and discussed. The possibility that some form of 1d physics obtains even down to the superconducting transition temperature is assessed.

cond-mat.str-el↗

arXiv2012

A wide band gap metal-semiconductor-metal nanostructure made entirely from graphene

A blueprint for producing scalable digital graphene electronics has remained elusive. Current methods to produce semiconducting-metallic graphene networks all suffer from either stringent lithographic demands that prevent reproducibility, process-induced disorder in the graphene, or scalability issues. Using angle resolved photoemission, we have discovered a unique one dimensional metallic-semiconducting-metallic junction made entirely from graphene, and produced without chemical functionalization or finite size patterning. The junction is produced by taking advantage of the inherent, atomically ordered, substrate-graphene interaction when it is grown on SiC, in this case when graphene is forced to grow over patterned SiC steps. This scalable bottomup approach allows us to produce a semiconducting graphene strip whose width is precisely defined within a few graphene lattice constants, a level of precision entirely outside modern lithographic limits. The architecture demonstrated in this work is so robust that variations in the average electronic band structure of thousands of these patterned ribbons have little variation over length scales tens of microns long. The semiconducting graphene has a topologically defined few nanometer wide region with an energy gap greater than 0.5 eV in an otherwise continuous metallic graphene sheet. This work demonstrates how the graphene-substrate interaction can be used as a powerful tool to scalably modify graphene's electronic structure and opens a new direction in graphene electronics research.

cond-mat.mes-hall↗

arXiv2012

Dynamical study of the light scalar mesons below 1 GeV in a flux-tube model

The light scalar mesons below 1 GeV as tetraquark states are studied in the framework of the flux-tube model, the multi-body confinement instead of the additive two-body confinement is used. From the calculated results, we find that the light scalar mesons, $σ$, $κ$ could be well accommodated in the diquark-antidiquark tetraquark picture in the flux-tube model and they could be color confinement resonances. The mass of the first radial excited state of $[ud][\bar{u}\bar{d}]$ is 1019 MeV, which is close to the mass of $f_0(980)$. Whereas $a_0(980)$ can not be fitted in this interpretation.

hep-ph↗

arXiv2012

Tm-doped fiber laser mode-locked by graphene-polymer composite

We demonstrate mode-locking of a thulium-doped fiber laser operating at 1.94μm, using a graphene-based saturable absorber. The laser outputs 3.6ps pulses, with~0.4nJ energy and an amplitude fluctuation~0.5%, at 6.46MHz. This is a simple, low-cost, stable and convenient laser oscillator for applications where eye-safe and low-photon-energy light sources are required, such as sensing and biomedical diagnostics

cond-mat.mes-hall↗

arXiv2012

Infrared conductivity of hole accumulation and depletion layers in (Ga,Mn)As- and (Ga,Be)As-based electric field-effect devices

We have fabricated electric double-layer field-effect devices to electrostatically dope our active materials, either $x$=0.015 Ga$_{1-x}$Mn$_x$As or $x$=3.2$\times10^{-4}$ Ga$_{1-x}$Be$_x$As. The devices are tailored for interrogation of electric field induced changes to the frequency dependent conductivity in the accumulation or depletions layers of the active material via infrared (IR) spectroscopy. The spectra of the (Ga,Be)As-based device reveal electric field induced changes to the IR conductivity consistent with an enhancement or reduction of the Drude response in the accumulation and depletion polarities, respectively. The spectroscopic features of this device are all indicative of metallic conduction within the GaAs host valence band (VB). For the (Ga,Mn)As-based device, the spectra show enhancement of the far-IR itinerant carrier response and broad mid-IR resonance upon hole accumulation, with a decrease of these features in the depletion polarity. These later spectral features demonstrate that conduction in ferromagnetic (FM) Ga$_{1-x}$Mn$_x$As is distinct from genuine metallic behavior due to extended states in the host VB. Furthermore, these data support the notion that a Mn-induced impurity band plays a vital role in the electron dynamics of FM Ga$_{1-x}$Mn$_x$As. We add, a sum-rule analysis of the spectra of our devices suggests that the Mn or Be doping does not lead to a substantial renormalization of the GaAs host VB.

cond-mat.mtrl-sci↗

arXiv2012

Effect of positron-atom interactions on the annihilation gamma spectra of molecules

Calculations of gamma spectra for positron annihilation on a selection of molecules, including methane and its fluoro-substitutes, ethane, propane, butane and benzene are presented. The annihilation gamma spectra characterise the momentum distribution of the electron-positron pair at the instant of annihilation. The contribution to the gamma spectra from individual molecular orbitals is obtained from electron momentum densities calculated using modern computational quantum chemistry density functional theory tools. The calculation, in its simplest form, effectively treats the low-energy (thermalised, room-temperature) positron as a plane wave and gives annihilation gamma spectra that are about 40% broader than experiment, although the main chemical trends are reproduced. We show that this effective "narrowing" of the experimental spectra is due to the action of the molecular potential on the positron, chiefly, due to the positron repulsion from the nuclei. It leads to a suppression of the contribution of small positron-nuclear separations where the electron momentum is large. To investigate the effect of the nuclear repulsion, as well as that of short-range electron-positron and positron-molecule correlations, a linear combination of atomic orbital description of the molecular orbitals is employed. It facilitates the incorporation of correction factors which can be calculated from atomic many-body theory and account for the repulsion and correlations. Their inclusion in the calculation gives gamma spectrum linewidths that are in much better agreement with experiment. Furthermore, it is shown that the effective distortion of the electron momentum density, when it is observed through positron annihilation gamma spectra, can be approximated by a relatively simple scaling factor.

physics.atom-ph↗

arXiv2011

Scientific Productivity, Research Funding, Race and Ethnicity

In a recent study by Ginther et al., the probability of receiving a U.S. National Institutes of Health (NIH) RO1 award was related to the applicant's race/ethnicity. The results indicate black/African-American applicants were 10% less likely than white peers to receive an award, after controlling for background and qualifications. It has generated a widespread debate regarding the unfairness of the NIH grant review process and its correction. In this paper, the work by Ginther et al. was augmented by pairing analysis, axiomatically-individualized productivity and normalized funding success measurement. Although there are racial differences in R01 grant success rates, normalized figures of merit for funding success explain the discrepancy. The suggested "leverage points for policy intervention" are in question and require deeper and more thorough investigations. Further adjustments in policies to remove racial disparity should be made more systematically for equal opportunity, rather than being limited to the NIH review process.

stat.AP↗

arXiv2011

Silicon intercalation into the graphene-SiC interface

In this work we use LEEM, XPEEM and XPS to study how the excess Si at the graphene-vacuum interface reorders itself at high temperatures. We show that silicon deposited at room temperature onto multilayer graphene films grown on the SiC(000[`1]) rapidly diffuses to the graphene-SiC interface when heated to temperatures above 1020. In a sequence of depositions, we have been able to intercalate ~ 6 ML of Si into the graphene-SiC interface.

cond-mat.mes-hall↗

arXiv2010

Symmetry breaking in commensurate graphene rotational stacking; a comparison of theory and experiment

Graphene stacked in a Bernal configuration (60 degrees relative rotations between sheets) differs electronically from isolated graphene due to the broken symmetry introduced by interlayer bonds forming between only one of the two graphene unit cell atoms. A variety of experiments have shown that non-Bernal rotations restore this broken symmetry; consequently, these stacking varieties have been the subject of intensive theoretical interest. Most theories predict substantial changes in the band structure ranging from the development of a Van Hove singularity and an angle dependent electron localization that causes the Fermi velocity to go to zero as the relative rotation angle between sheets goes to zero. In this work we show by direct measurement that non-Bernal rotations preserve the graphene symmetry with only a small perturbation due to weak effective interlayer coupling. We detect neither a Van Hove singularity nor any significant change in the Fermi velocity. These results suggest significant problems in our current theoretical understanding of the origins of the band structure of this material.

cond-mat.mes-hall↗

arXiv2010

Graphene Q-switched, tunable fiber laser

We demonstrate a wideband-tunable Q-switched fiber laser exploiting a graphene saturable absorber. We get ~2us pulses, tunable between 1522 and 1555nm with up to~40nJ energy. This is a simple and low-cost light source for metrology, environmental sensing and biomedical diagnostics.

cond-mat.mes-hall↗

arXiv2010

Sub 200fs pulse generation from a graphene mode-locked fiber laser

Ultrafast fiber lasers with short pulses and broad bandwidth are in great demand for a variety of applications, such as spectroscopy, biomedical diagnosis and optical communications. In particular sub-200fs pulses are required for ultrafast spectroscopy with high temporal resolution. Graphene is an ideal ultra-wide-band saturable absorber. We report the generation of 174fs pulses from a graphene-based fiber laser

cond-mat.mes-hall↗

arXiv2010

Wideband tunable, graphene-mode locked, ultrafast laser

We report a tunable ultrafast fiber laser mode-locked with a graphene saturable absorber. The linear dispersions of the Dirac electrons in graphene enable wideband tunability. We get ~1ps pulses, tunable between 1525 and 1559nm, demonstrating graphene as a broadband saturable absorber.

cond-mat.other↗

arXiv2009

Instability of two dimensional graphene: Breaking sp2 bonds with soft X-rays

We study the stability of various kinds of graphene samples under soft X-ray irradiation. Our results show that in single layer exfoliated graphene (a closer analogue to two dimensional material), the in-plane carbon-carbon bonds are unstable under X-ray irradiation, resulting in nanocrystalline structures. As the interaction along the third dimension increases by increasing the number of graphene layers or through the interaction with the substrate (epitaxial graphene), the effect of X-ray irradiation decreases and eventually becomes negligible for graphite and epitaxial graphene. Our results demonstrate the importance of the interaction along the third dimension in stabilizing the long range in-plane carbon-carbon bonding, and suggest the possibility of using X-ray to pattern graphene nanostructures in exfoliated graphene.

cond-mat.mtrl-sci↗

arXiv2009

Graphene Mode-Locked Ultrafast Laser

Graphene is at the center of a significant research effort. Near-ballistic transport at room temperature and high mobility make it a potential material for nanoelectronics. Its electronic and mechanical properties are also ideal for micro and nanomechanical systems, thin-film transistors and transparent and conductive composites and electrodes. Here we exploit the optoelectronic properties of graphene to realize an ultrafast laser. A graphene-polymer composite is fabricated using wet-chemistry techniques. Pauli blocking following intense illumination results in saturable absorption, independent of wavelength. This is used to passively mode-lock an Erbium-doped fibre laser working at 1559nm, with a 5.24nm spectral bandwidth and ~460fs pulse duration, paving the way to graphene-based photonics.

cond-mat.mtrl-sci↗