SCOOTER: A compact and scalable dynamic labeling scheme for XML updates

Although dynamic labeling schemes for XML have been the focus of recent research activity, there are significant challenges still to be overcome. In particular, though there are labeling schemes that ensure a compact label representation when creating an XML document, when the document is subject to repeated and arbitrary deletions and insertions, the labels grow rapidly and consequently have a significant impact on query and update performance. We review the outstanding issues todate and in this paper we propose SCOOTER - a new dynamic labeling scheme for XML. The new labeling scheme can completely avoid relabeling existing labels. In particular, SCOOTER can handle frequently skewed insertions gracefully. Theoretical analysis and experimental results confirm the scalability, compact representation, efficient growth rate and performance of SCOOTER in comparison to existing dynamic labeling schemes

Dirac Cosmology and the Acceleration of the Contemporary Universe

A model is suggested to unify the Einstein GR and Dirac Cosmology. There is one adjusted parameter $b_2$ in our model. After adjusting the parameter $b_2$ in the model by using the supernova data, we have calculated the gravitational constant $\bar G$ and the physical quantities of $a(t)$, $q(t)$ and $\rho_r(t)/ \rho_b(t)$ by using the present day quantities as the initial conditions and found that the equation of state parameter $w_{\theta}$ equals to -0.83, the ratio of the density of the addition creation $\Omega_{\Lambda}=0.8$ and the ratio of the density of the matter including multiplication creation, radiation and normal matter $\Omega_m =0.2$ at present. The results are self-consistent and in good agreement with present knowledge in cosmology. These results suggest that the addition creation and multiplication creation in Dirac cosmology play the role of the dark energy and dark matter.Comment: 13 pages, 8 figure

Antiferromagnetism in the Exact Ground State of the Half Filled Hubbard Model on the Complete-Bipartite Graph

As a prototype model of antiferromagnetism, we propose a repulsive Hubbard Hamiltonian defined on a graph \L={\cal A}\cup{\cal B} with ${\cal A}\cap {\cal B}=\emptyset$ and bonds connecting any element of ${\cal A}$ with all the elements of ${\cal B}$. Since all the hopping matrix elements associated with each bond are equal, the model is invariant under an arbitrary permutation of the ${\cal A}$-sites and/or of the ${\cal B}$-sites. This is the Hubbard model defined on the so called $(N_{A},N_{B})$-complete-bipartite graph, $N_{A}$ ($N_{B}$) being the number of elements in ${\cal A}$ (${\cal B}$). In this paper we analytically find the {\it exact} ground state for $N_{A}=N_{B}=N$ at half filling for any $N$; the repulsion has a maximum at a critical $N$-dependent value of the on-site Hubbard $U$. The wave function and the energy of the unique, singlet ground state assume a particularly elegant form for N \ra \inf. We also calculate the spin-spin correlation function and show that the ground state exhibits an antiferromagnetic order for any non-zero $U$ even in the thermodynamic limit. We are aware of no previous explicit analytic example of an antiferromagnetic ground state in a Hubbard-like model of itinerant electrons. The kinetic term induces non-trivial correlations among the particles and an antiparallel spin configuration in the two sublattices comes to be energetically favoured at zero Temperature. On the other hand, if the thermodynamic limit is taken and then zero Temperature is approached, a paramagnetic behavior results. The thermodynamic limit does not commute with the zero-Temperature limit, and this fact can be made explicit by the analytic solutions.Comment: 19 pages, 5 figures .ep

Janus monolayers of transition metal dichalcogenides.

Structural symmetry-breaking plays a crucial role in determining the electronic band structures of two-dimensional materials. Tremendous efforts have been devoted to breaking the in-plane symmetry of graphene with electric fields on AB-stacked bilayers or stacked van der Waals heterostructures. In contrast, transition metal dichalcogenide monolayers are semiconductors with intrinsic in-plane asymmetry, leading to direct electronic bandgaps, distinctive optical properties and great potential in optoelectronics. Apart from their in-plane inversion asymmetry, an additional degree of freedom allowing spin manipulation can be induced by breaking the out-of-plane mirror symmetry with external electric fields or, as theoretically proposed, with an asymmetric out-of-plane structural configuration. Here, we report a synthetic strategy to grow Janus monolayers of transition metal dichalcogenides breaking the out-of-plane structural symmetry. In particular, based on a MoS2 monolayer, we fully replace the top-layer S with Se atoms. We confirm the Janus structure of MoSSe directly by means of scanning transmission electron microscopy and energy-dependent X-ray photoelectron spectroscopy, and prove the existence of vertical dipoles by second harmonic generation and piezoresponse force microscopy measurements

A time-domain control signal detection technique for OFDM

Transmission of system-critical control information plays a key role in efficient management of limited wireless network resources and successful reception of payload data information. This paper uses an orthogonal frequency division multiplexing (OFDM) architecture to investigate the detection performance of a time-domain approach used to detect deterministic control signalling information. It considers a type of control information chosen from a finite set of information, which is known at both transmitting and receiving wireless terminals. Unlike the maximum likelihood (ML) estimation method, which is often used, the time-domain detection technique requires no channel estimation and no pilots as it uses a form of time-domain correlation as the means of detection. Results show that when compared with the ML method, the time-domain approach improves detection performance even in the presence of synchronisation error caused by carrier frequency offset

Non-collinear magnetic structure and anisotropic magnetoelastic coupling in cobalt pyrovanadate Co2V2O7

The Co2V2O7 is recently reported to exhibit amazing magnetic field-induced magnetization plateaus and ferroelectricity, but its magnetic ground state remains ambiguous due to its structural complexity. Magnetometry measurements, and time-of-flight neutron powder diffraction (NPD) have been employed to study the structural and magnetic properties of Co2V2O7, which consists of two non-equivalent Co sites. Upon cooling below the Ne\'el temperature TN = 6.3 K, we observe magnetic Bragg peaks at 2K in NPD which indicated the formation of long range magnetic order of Co2+ moments. After symmetry analysis and magnetic structure refinement, we demonstrate that Co2V2O7 possesses a complicated non-collinear magnetic ground state with Co moments mainly located in b-c plane and forming a non-collinear spin-chain-like structure along the c-axis. The ab initio calculations demonstrate that the non-collinear magnetic structure is more stable than various ferromagnetic states at low temperature. The non-collinear magnetic structure with canted up-up-down-down spin configuration is considered as the origin of magnetoelectric coupling in Co2V2O7 because the inequivalent exchange striction induced by the spin-exchange interaction between the neighboring spins is the driving force of ferroelectricity. Besides, it is found that the deviation of lattice parameters a and b is opposite below TN, while the lattice parameter c and stay almost constant below TN, evidencing the anisotropic magnetoelastic coupling in Co2V2O7.Comment: 9 pages, 8 figure

Characterization of InGaN/GaN multi-quantum-well blue-light-emitting diodes grown by metal organic chemical vapor deposition

The structural,surface morphology, and the temperature dependence photoluminescence of InGaN(3 nm)/GaN(7 nm) 5 period multi-quantum-well blue-light-emitting diode (LED)structures grown by metal organic chemical vapor deposition(MOCVD) have been studied. Quantum dot-likestructures and strain contrast evident by black lumps were observed in the quantum wells using high-resolution transmission electron microscopy(HRTEM) analysis. Double-crystal high-resolution x-ray diffraction (HRXRD) spectra of blue LED were simulated using kinematical theory method, to obtain composition, and period thickness of well and barrier. The “S” shape character shift as red–blue–redshift of the quantum-well emission line, i.e., blue emission peak 2.667 eV at 10 K, was observed with variation of temperature in the photoluminescence (PL) spectra. The shift is assigned to the potential fluctuations due to alloy inhomogeneous distribution in the quantum wells. The In composition in the quantum wells obtained by two independent techniques, namely HRXRD and PL, was 8% and 19%, respectively. The reason for this large difference in composition is explained in this letter

Carbon Nanotubes by a CVD Method. Part II: Formation of Nanotubes from (Mg, Fe)O Catalysts

The aim of this paper is to study the formation of carbon nanotubes (CNTs) from different Fe/MgO oxide powders that were prepared by combustion synthesis and characterized in detail in a companion paper. Depending on the synthesis conditions, several iron species are present in the starting oxides including Fe2+ ions, octahedral Fe3+ ions, Fe3+ clusters, and MgFe2O4-like nanoparticles. Upon reduction during heating at 5 °C/min up to 1000 °C in H2/CH4 of the oxide powders, the octahedral Fe3+ ions tend to form Fe2+ ions, which are not likely to be reduced to metallic iron whereas the MgFe2O4-like particles are directly reduced to metallic iron. The reduced phases are R-Fe, Fe3C, and ç-Fe-C. Fe3C appears as the postreaction phase involved in the formation of carbon filaments (CNTs and thick carbon nanofibers). Thick carbon nanofibers are formed from catalyst particles originating from poorly dispersed species (Fe3+ clusters and MgFe2O4-like particles). The nanofiber outer diameter is determined by the particle size. The reduction of the iron ions and clusters that are well dispersed in the MgO lattice leads to small catalytic particles (<5 nm), which tend to form SWNTS and DWNTs with an inner diameter close to 2 nm. Well-dispersed MgFe2O4-like particles can also be reduced to small metal particles with a narrow size distribution, producing SWNTs and DWNTs. The present results will help in tailoring oxide precursors for the controlled formation of CNTs