The Luminosity - E_p Relation within Gamma--Ray Bursts and Implications for Fireball Models

Using a sample of 2408 time-resolved spectra for 91 BATSE gamma-ray bursts (GRBs) presented by Preece et al., we show that the relation between the isotropic-equivalent luminosity (L_iso) and the spectral peak energy (E_p) in the cosmological rest frame, L_iso \propto E_p^2, not only holds within these bursts, but also holds among these GRBs, assuming that the burst rate as a function of redshift is proportional to the star formation rate. The possible implications of this relation for the emission models of GRBs are discussed. We suggest that both the kinetic-energy-dominated internal shock model and the magnetic-dissipation-dominated external shock model can well interpret this relation. We constrain the parameters for these two models, and find that they are in a good agreement with the parameters from the fittings to the afterglow data (abridged).Comment: 3 pages plus 5 figures, emulateapj style, accepted for publication in ApJ Letter

Photoluminescence and x-ray diffraction studies of the diffusion behavior of lattice matched InGaAs/InP heterostructures

Copyright (2003) American Institute of Physics. This article may be downloaded for personal use only. Any other use requires prior permission of the author and the American Institute of Physics. The following article appeared in (F. Bollet and W. P. Gillin, J. Appl. Phys. 94, 988 (2003) and may be found at http://link.aip.org/link/?jap/94/988

Effect of Native Defects on Optical Properties of InxGa1-xN Alloys

The energy position of the optical absorption edge and the free carrier populations in InxGa1-xN ternary alloys can be controlled using high energy 4He+ irradiation. The blue shift of the absorption edge after irradiation in In-rich material (x > 0.34) is attributed to the band-filling effect (Burstein-Moss shift) due to the native donors introduced by the irradiation. In Ga-rich material, optical absorption measurements show that the irradiation-introduced native defects are inside the bandgap, where they are incorporated as acceptors. The observed irradiation-produced changes in the optical absorption edge and the carrier populations in InxGa1-xN are in excellent agreement with the predictions of the amphoteric defect model

Direct extraction of the Eliashberg function for electron-phonon coupling: A case study of Be(1010)

We propose a systematic procedure to directly extract the Eliashberg function for electron-phonon coupling from high-resolution angle-resolved photoemission data. The procedure is successfully applied to the Be(1010) surface, providing new insights to electron-phonon coupling at this surface. The method is shown to be robust against imperfections in experimental data and suitable for wider applications.Comment: 4 pages, 4 figures. More details concerning the procedure are include

Structure-Induced Reversible Anionic Redox Activity in Na Layered Oxide Cathode

Anionic redox reaction (ARR) in lithium- and sodium-ion batteries is under hot discussion, mainly regarding how oxygen anion participates and to what extent oxygen can be reversibly oxidized and reduced. Here, a P3-type Na0.6[Li0.2Mn0.8]O2 with reversible capacity from pure ARR was studied. The interlayer O-O distance (peroxo-like O-O dimer, 2.506(3) Å), associated with oxidization of oxygen anions, was directly detected by using a neutron total scattering technique. Different from Li2RuO3 or Li2IrO3 with strong metal-oxygen (M-O) bonding, for P3-type Na0.6[Li0.2Mn0.8]O2 with relatively weak Mn-O covalent bonding, crystal structure factors might play an even more important role in stabilizing the oxidized species, as both Li and Mn ions are immobile in the structure and thus may inhibit the irreversible transformation of the oxidized species to O2 gas. Utilization of anionic redox reaction (ARR) on oxygen has been considered as an effective way to promote the charge-discharge capacity of the layered oxide cathodes for lithium- or sodium-ion batteries. The detailed mechanism of ARR, in particular how crystal structure affects and coordinates with the ARR, is not yet well understood. In the present work, a combination of X-ray and neutron total scattering measurements has been performed to study the structure of the prototype P3-type layered Na0.6[Li0.2Mn0.8]O2 with pure ARR. Unique structural characteristics, rather than prevailing knowledge of covalency of metal-oxygen, enable the stabilization of the crystal structure of Na0.6[Li0.2Mn0.8]O2 along with the ARR. This work suggests that reversible ARR can be manipulated by proper structure designs, thus to achieve high lithium or sodium storage in layered oxide cathodes. For P3-type Na0.6[Li0.2Mn0.8]O2 with relatively weak Mn-O covalent bonding, crystal structure factors play an important role in stabilizing the oxidized species, inhibiting the irreversible transformation of the oxidized species to O2 gas. The finding is important for better design of layered oxide positive materials with higher reversible capacity via the introduction of a reversible anionic redox reaction

Hawking Radiation of Dirac Particles in an Arbitrarily Accelerating Kinnersley Black Hole

Quantum thermal effect of Dirac particles in an arbitrarily accelerating Kinnersley black hole is investigated by using the method of generalized tortoise coordinate transformation. Both the location and the temperature of the event horizon depend on the advanced time and the angles. The Hawking thermal radiation spectrum of Dirac particles contains a new term which represents the interaction between particles with spin and black holes with acceleration. This spin-acceleration coupling effect is absent from the thermal radiation spectrum of scalar particles.Comment: Revtex, 12pt, 16 pages, no figure, to appear in Gen. Rel. Grav. 34 (2002) N0.