Natural orbits of atomic Cooper pairs in a nonuniform Fermi gas

We examine the basic mode structure of atomic Cooper pairs in an inhomogeneous Fermi gas. Based on the properties of Bogoliubov quasi-particle vacuum, the single particle density matrix and the anomalous density matrix share the same set of eigenfunctions. These eigenfunctions correspond to natural pairing orbits associated with the BCS ground state. We investigate these orbits for a Fermi gas in a spherical harmonic trap, and construct the wave function of a Cooper pair in the form of Schmidt decomposition. The issue of spatial quantum entanglement between constituent atoms in a pair is addressed.Comment: 14 pages, 4 figures, submitted to Phys. Rev.

Effect of oxygen stoichiometry on microstructural and magnetic properties of FePt/TaOx bilayer fabricated by ion-beam-bombardment deposition

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X-ray absorption spectroscopy studies of Ba1-xCaxTiO3

[[abstract]]We report x-ray absorption near edge spectroscopy (XANES) of Ca and O K-edges of Ba1-xCaxTiO3 (x = 0, 0.01, 0.08, 1) and understand the spectral features related to the electronic structure of these perovskites. The XANES spectra of Ca K-edge possess a pre-edge peak similar to other 3d transition metals like Ti, Ni when present in perovskite structure and provides information about p-type or hole doping. Presence of considerable amount of 3d states justifies the reason to consider it as a light 3d transition metal. The O K-edge spectra display characteristic spectral features assigned as eg and t2g and show strong dependence on concentration.[[notice]]補正完畢[[journaltype]]國外[[booktype]]紙本[[booktype]]電子版[[countrycodes]]US

Structural transition in epitaxial Co/Cr multilayers as studied by X-ray absorption spectroscopy

[[abstract]]We have performed Cr and Co K-edge x-ray-absorption measurements to investigate the dependence of local electronic and atomic structures on the Cr-layer thickness in epitaxial Co (40A)/Ct (t~) (t~ = 2, 3, 5, 7, and 9A) multilayers. The Cr K x-ray absorption near edge structure (XANES) spectra of Co/Cr multilayers indicate an abrupt transition of the Cr layer from a bcc structure to a hcp structure when the thickness of the Cr layer is decreased down to -5A or three atomic layers. The structural transition and bond-length distortion in Cr and Co layers observed in the extended x-ray absorption fine structure (EXAFS) measurements are consistent with the XANES results.[[notice]]補正完畢[[journaltype]]國外[[booktype]]紙本[[booktype]]電子版[[countrycodes]]US

Nitrogen-Functionalized Graphene Nanoflakes (GNFs:N): Tunable Photoluminescence and Electronic Structures

This study investigates the strong photoluminescence (PL) and X-ray excited optical luminescence observed in nitrogen-functionalized 2D graphene nanoflakes (GNFs:N), which arise from the significantly enhanced density of states in the region of {\pi} states and the gap between {\pi} and {\pi}* states. The increase in the number of the sp2 clusters in the form of pyridine-like N-C, graphite-N-like, and the C=O bonding and the resonant energy transfer from the N and O atoms to the sp2 clusters were found to be responsible for the blue shift and the enhancement of the main PL emission feature. The enhanced PL is strongly related to the induced changes of the electronic structures and bonding properties, which were revealed by the X-ray absorption near-edge structure, X-ray emission spectroscopy, and resonance inelastic X-ray scattering. The study demonstrates that PL emission can be tailored through appropriate tuning of the nitrogen and oxygen contents in GNFs and pave the way for new optoelectronic devices.Comment: 8 pages, 6 figures (including toc figure

X-ray absorption spectroscopy study of diluted magnetic semiconductors: Zn1-xMxSe (M = Mn, Fe, Co) and Zn1-xMnxY (Y = Se, Te)

We have investigated 3d electronic states of doped transition metals in II-VI diluted magnetic semiconductors, Zn1-xMxSe (M = Mn, Fe, Co) and Zn1-xMnxY (Y = Se, Te), using the transition-metal L2,3-edge X-ray absorption spectroscopy (XAS) measurements. In order to explain the XAS spectra, we employed a tetragonal cluster model calculation, which includes not only the full ionic multiplet structure but also configuration interaction (CI). The results show that CI is essential to describe the experimental spectra adequately, indicating the strong hybridization between the transition metal 3d and the ligand p orbitals. In the study of Zn1-xMnxY (Y = Se, Te), we also found considerable spectral change in the Mn L2,3-edge XAS spectra for different ligands, confirming the importance of the hybridization effects in these materials.Comment: This paper consists of 22 pages including 4 figures. This paper is submitted to Physical Review