Na2C monolayer: a novel 2p Dirac half-metal with multiple symmetry-protected Dirac cones.

A Dirac half-metal material, which has a gapped band structure in one spin channel but Dirac cones in the other, combines two intriguing properties of 100% spin polarization and massless Dirac fermions and has recently started to attract increasing attention. In this work, using first-principles calculations we predict that the disodium carbide (Na2C) monolayer is an intrinsic 2p Dirac half-metal material with 12 fully spin-polarized and symmetry-protected Dirac cones, and a slightly gapped (53 meV) spin-polarized nodal line coexisting in one spin channel, leaving the other spin channel insulated with a gap of 1.9 eV. There are two kinds of Dirac cones in Na2C, protected by different crystalline symmetries, both of which are robust against biaxial strains (±5%) and spin-orbit coupling effects, with Fermi velocities of up to 5.2 × 105 m s-1. Ferromagnetism is mainly contributed to by the unpaired 2p electrons in the carbon, with a Curie temperature estimated to be 382 K, and the origin of the 2p magnetism could be explained by the superexchange mechanism between C2- anions with the Na+ cation as a bridge. Our results not only indicate a promising candidate for high-speed spintronic devices, but also reveal the hidden mechanism of the origin of symmetric protection and ferromagnetic exchange interactions in a Dirac semi-metal, which would provide a feasible strategy for the design of Dirac materials.

Robust Room-Temperature Quantum Spin Hall Effect in Methyl-functionalized InBi honeycomb film.

Two-dimensional (2D) group-III-V honeycomb films have attracted significant interest for their potential application in fields of quantum computing and nanoelectronics. Searching for 2D III-V films with high structural stability and large-gap are crucial for the realizations of dissipationless transport edge states using quantum spin Hall (QSH) effect. Based on first-principles calculations, we predict that the methyl-functionalized InBi monolayer (InBiCH3) has no dynamic instability, and hosts QSH state with a band gap as large as 0.29 eV, exhibiting an interesting electronic behavior viable for room-temperature applications. The topological characteristic is confirmed by s-pxy band inversion, topological invariant Z2 number, and the time-reversal symmetry protected helical edge states. Noticeably, the QSH states are tunable and robust against the mechanical strain, electric field and different levels of methyl coverages. We also find that InBiCH3 supported on h-BN substrate maintains a nontrivial QSH state, which harbors the edge states lying within the band gap of substrate. These findings demonstrate that the methyl-functionalized III-V films may be a good QSH platform for device design and fabrication in spintronics.

Unexpected Giant-Gap Quantum Spin Hall Insulator in Chemically Decorated Plumbene Monolayer.

Quantum spin Hall (QSH) effect of two-dimensional (2D) materials features edge states that are topologically protected from backscattering by time-reversal symmetry. However, the major obstacles to the application for QSH effect are the lack of suitable QSH insulators with a large bulk gap. Here, we predict a novel class of 2D QSH insulators in X-decorated plumbene monolayers (PbX; X = H, F, Cl, Br, I) with extraordinarily giant bulk gaps from 1.03 eV to a record value of 1.34 eV. The topological characteristic of PbX mainly originates from s-p(x,y) band inversion related to the lattice symmetry, while the effect of spin-orbital coupling (SOC) is only to open up a giant gap. Their QSH states are identified by nontrivial topological invariant Z2 = 1, as well as a single pair of topologically protected helical edge states locating inside the bulk gap. Noticeably, the QSH gaps of PbX are tunable and robust via external strain. We also propose high-dielectric-constant BN as an ideal substrate for the experimental realization of PbX, maintaining its nontrivial topology. These novel QSH insulators with giant gaps are a promising platform to enrich topological phenomena and expand potential applications at high temperature.

[Rash and fever illness caused by herpes simplex virus type 1 needs to be distinguished from hand, foot and mouth disease].

An epidemic of rash and fever illnesses suspected of hand, foot and mouth disease (HFMD) occurred in Gansu Province of China in 2008, laboratory tests were performed in order to identify the pathogen that caused this epidemic. Eight clinical specimens collected from the 4 patients (each patient has throat swab and herpes fluid specimens) with rash and febrile illness, were inoculated onto RD and HEp-2 cells for virus isolation, and the viral nucleic acid was then extracted with the positive virus isolates, the dual-channel real-time reverse transcript-polymerase chain reaction (RT-PCR) was performed to detect the nucleic acid of human enterovirus (HEV) in the viral isolates at the same time. For the viral isolates with the negative results of HEV, a sequence independent single primer amplification technique (SISPA) was used for "unknown pathogen" identification. Totally, 6 viral isolates were identified as herpes simplex virus type 1 (HSV-1). Comprehensive analyses results of the clinical manifestations of the patients, epidemiological findings and laboratory test indicated that this epidemic of rash and febrile illness was caused by HSV-1. The differences among the gG region of 6 HSV-1 isolates at nucleotide level and amino acid level were all small, and the identities were up to 98. 8% and 97.9%, respectively, showing that this outbreak was caused by only one viral transmission chain of HSV-1. HSV-1 and other viruses that cause rash and febrile illnesses need differential diagnosis with HFMD. The etiology of rash and febrile illness is sometimes difficult to distinguish from the clinical symptoms and epidemiological data, the laboratory diagnosis is therefore critical.

[Crystallography orientation by molecular spectrum of structural hydroxide in pyroxene megacryst].

Crystal can be crystallographically oriented by molecular spectrum with the change in band shift, band intensity, and band shape. The three groups of band shift of augite are different between vertical to c-axis and parallel to c-axis: the first peak value 3 629-3 633 red shifts to 3 601-3 616; the same as the second peak value 3 514-3 543; on the contrary, the third peak value 3 460-3 465 is blue shift. The intensity of the first band is equivalent in two directions, while the second and the third parallel to c-axis are much stronger than the vertical. The wave shape is not quite different. The intensity of the Raman spectra vertical to c-axis is stronger than that parallel to c-axis in general, while the band shift and the shape show little difference. It was indicated that the geological tectonic environment can be reflected by the spectra of structural hydroxide with different crystal directions.

[Raman spectra of pyroxene].

By testing the Raman spectra of megacryst pyroxene, enstatite and diopside in terms of location, shape and intensity, the symmetries of the main spectral band of pyroxene and the vibration modes of Raman shift were identified. The spectral bands of corresponding ionic groups such as non-bridge oxygen Si-O- and bridge oxygen Si-O0, O-Si-O and M-O were assigned for vibrational mode. Through the change in the intensity of the spectral band in different section direction and the deficiency of some spectral bands, the orientation problem in mineral crystallography was preliminarily studied.

[Quantitative determination of glass content in monazite glass-ceramics by IR technique].

Monazite glass-ceramics consist of both monazite and metaphoshate glass phases. The absorption bands of both phases do not overlap each other, and the absorption intensities of bands 1,275 and 616 cm-1 vary with the glass contents. The correlation coefficient between logarithmic absorbance ratio of the two bands and glass contents was r = 0.9975 and its regression equation was y = 48.356 + 25.93x. The absorbance ratio of bands 952 and 616 cm-1 also varied with different ratios of Ce2O3/La2O3 in synthetic monazites, with r = 0.9917 and a regression equation y = 0.2211 exp (0.0221x). High correlation coefficients show that the IR technique could find new application in the quantitative analysis of glass content in phosphate glass-ceramics.