Coulomb interaction and electron-hole asymmetry in cyclotron resonance of bilayer graphene in high magnetic field

Inter-Landau-level transitions in the bilayer graphene at high perpendicular magnetic field at the filling-factor v<<1 have been studied. The next-nearest-neighbor transitions, energy difference between dimer and non-dimer sites and layer asymmetry are included. The influence of Coulomb interaction is taken into account. The magnetoplasmon excitations in bilayer graphene at small momenta are considered in the frame of the Hartree-Fock approximation. It is shown that asymmetry in cyclotron resonance of clean bilayer graphene depends on magnetic field. At lower magnetic fields the energy splitting in the spectrum is due to electron-hole one-particle asymmetry, at higher magnetic fields the energy splitting in the spectrum is due to Coulomb interaction. For the fullsymmetric case with half-filled zero-energy levels the energy splitting proportional to the energy of Coulomb interaction is found both for bilayer and monolayer graphene.Comment: 6 pages, 2 figure

Coherent spin dynamics of an interwell excitonic gas in GaAs/AlGaAs coupled quantum wells

The spin dynamics of an interwell excitons gas has been investigated in n-i-n GaAs/AlGaAs coupled quantum wells (CQWs). In these heterostructures the electron and the hole are spatially separated in neighboring quantum wells by a narrow AlAs barrier, when an electric field is applied. The time evolution kinetics of the interwell exciton photoluminescence has been measured under resonant excitation of the 1sHH intrawell exciton, using a pulsed tunable laser. The formation of a collective exciton phase in time and the temperature dependence of its spin relaxation rate have been studied. The spin relaxation rate of the interwell excitons is strongly reduced in the collective phase. This observation provides evidence for the coherence of the indirect excitons collective phase at temperatures below a critical $T_c$.Comment: 8 pages, 9 figure

Reduced Graphene Oxide: fundamentals and applications

In this paper we report our recent studies on the fundamental physical/chemical properties of supported reduced Graphene Oxide (rGO) obtained either via standard thermal annealing or under extreme-UV (EUV) light exposure alongside with investigations on its possible technological applications. rGO has been studied by X-ray Photoelectron Spectroscopy (XPS), micro-Raman Spectroscopy (μRS), and Optical Microscopy. rGO reduction degree has been calibrated on the basis of its color contrast (CC) providing a handy tool to quantitatively determine the fraction of sp The original choice of using EUV instead of UV light to photo-reduce supported GO is not only advantageous in terms of reduction efficiency but it also allows to introduce the concept of EUV photolithography (today limited to the silicon technology only) for the processing of graphene-based materials. Here we demonstrate resistless sub-micrometer GO photo-patterning over large areas ( 10 mm 2 ) This result is a relevant upgrade for the graphene-based technology that can take advantage, in this way, from the entire know-how of the EUV-based technology in view of an eco-sustainable all-carbon technology

Proton Transfer, Hydrogen Bonding, and Disorder: Nitrogen Near-Edge X-ray Absorption Fine Structure and X-ray Photoelectron Spectroscopy of Bipyridine-Acid Salts and Co-crystals

The sensitivity of near-edge X-ray absorption fine structure (NEXAFS) spectroscopy to Brønsted donation and the protonation state of nitrogen in the solid state is investigated through a series of multicomponent bipyridine–acid systems alongside X-ray photoelectron spectroscopy (XPS) data. A large shift to high energy occurs for the 1s → 1π* resonance in the nitrogen K-edge NEXAFS with proton transfer from the acid to the bipyridine base molecule and allows assignment as a salt (C═NH+), with the peak ratio providing the stoichiometry of the types of nitrogen species present. A corresponding binding energy shift for C═NH+ is observed in the nitrogen XPS, clearly identifying protonation and formation of a salt. The similar magnitude shifts observed with both techniques relative to the unprotonated nitrogen of co-crystals (C═N) suggest that the chemical state (initial-state) effects dominate. Results from both techniques reveal the sensitivity to identify proton transfer, hydrogen bond disorder, and even the potential to distinguish variations in hydrogen bond length to nitrogen

Iron Behaving Badly: Inappropriate Iron Chelation as a Major Contributor to the Aetiology of Vascular and Other Progressive Inflammatory and Degenerative Diseases

The production of peroxide and superoxide is an inevitable consequence of aerobic metabolism, and while these particular "reactive oxygen species" (ROSs) can exhibit a number of biological effects, they are not of themselves excessively reactive and thus they are not especially damaging at physiological concentrations. However, their reactions with poorly liganded iron species can lead to the catalytic production of the very reactive and dangerous hydroxyl radical, which is exceptionally damaging, and a major cause of chronic inflammation. We review the considerable and wide-ranging evidence for the involvement of this combination of (su)peroxide and poorly liganded iron in a large number of physiological and indeed pathological processes and inflammatory disorders, especially those involving the progressive degradation of cellular and organismal performance. These diseases share a great many similarities and thus might be considered to have a common cause (i.e. iron-catalysed free radical and especially hydroxyl radical generation). The studies reviewed include those focused on a series of cardiovascular, metabolic and neurological diseases, where iron can be found at the sites of plaques and lesions, as well as studies showing the significance of iron to aging and longevity. The effective chelation of iron by natural or synthetic ligands is thus of major physiological (and potentially therapeutic) importance. As systems properties, we need to recognise that physiological observables have multiple molecular causes, and studying them in isolation leads to inconsistent patterns of apparent causality when it is the simultaneous combination of multiple factors that is responsible. This explains, for instance, the decidedly mixed effects of antioxidants that have been observed, etc...Comment: 159 pages, including 9 Figs and 2184 reference

Intersubband collective excitations in a quasi-two-dimensional electron system in external magnetic field

The spectrum of collective excitations in a quasi-two- dimensional electron system was studied by the method of Raman scattering spectroscopy. In an applied magnetic field, such systems exhibit collective excitations related to the electron transitions between dimensionally quantized subbands with a change in the Landau level index (intersubband Bernstein modes). It is shown that these modes interact with the fundamental intersubband excitations of the charge and spin densities, the interaction energy being determined by the excitation quasimomentum. Interaction of the intersubband Bernstein modes and the fundamental intersubband excitations with quasi-two-dimensional LO phonons was studied. Behavior of the new branches of collective excitations in a quasi-two- dimensional electron system possessing more than one occupied Landau level was studied and the nature of these branches was determined. (C) 2002 MAIK "Nauka / Interperiodica"