ABSTRACT
We performed angle-resolved photoemission spectroscopy studies on a series of FeTe1-xSex monolayer films grown on SrTiO3. The superconductivity of the films is robust and rather insensitive to the variations of the band position and effective mass caused by the substitution of Se by Te. However, the band gap between the electron- and hole-like bands at the Brillouin zone center decreases towards band inversion and parity exchange, which drive the system to a nontrivial topological state predicted by theoretical calculations. Our results provide a clear experimental indication that the FeTe1-xSex monolayer materials are high-temperature connate topological superconductors in which band topology and superconductivity are integrated intrinsically.
ABSTRACT
We have systematically investigated the wideband slow light in two-dimensional material graphene, revealing that graphene exhibits much larger slow light capability than other materials. The slow light performances including material dispersion, bandwidth, dynamic control ability, delay-bandwidth product, propagation loss, and group-velocity dispersion are studied, proving graphene exhibits significant advantages in these performances. A large delay-bandwidth product has been obtained in a simple yet functional grating waveguide with slow down factor c/v(g) at 163 and slow light bandwidth Δω at 94.4 nm centered at 10.38 µm, which is several orders of magnitude larger than previous results. Physical explanation of the enhanced slow light in graphene is given. Our results indicate graphene is an excellent platform for slow light applications, promoting various future slow light devices based on graphene.
ABSTRACT
A cDNA fragment locating at the putative envelop protein 2(E2) region of GBV-C/HGV fused with Schistosoma japonicum, glutathione S-transferase(GST) was amplified with PCR from plasmid pGEX-E2. The amplified DNA fragment was inserted into plasmid pGEX-5X-1, at the downstream of the coding sequences of GST, in the same reading frame with the gene of GST. The fusion gene fragment of GST-E2 was amplified with PCR, using the recombinant plasmid pGEX-5X-1-E2 as the template. The amplified 1324 bp DNA fragment of GST-E2 was inserted into Pichia pastoris expression vector pPIC9K in reading frame with alpha-factor secreting signal peptide. The plasmid pPIC9K-GST-E2 was transformed into Pichia pastoris GS115 with electroporation. The transformants (His+ Muts) were selected and induced to express the 54kD GST-E2 fusion protein, which could be specially recognized by both the antisera directed against E2 and against GST. The GST-E2 fusion protein was purified with Sepharose 4B glutathione affinity chromatography to a purity of 95%. The expression was optimized to achieve the highest expression level of GST-E2 fusion protein which was accumulated up to 50% of total proteins in the culture supernatant. The GST-E2 protein derived from the recombinant Pichia pastoris was proved possessing antigenicity and high specificity by ELISA, probed with sera from the patients infected by GBV-C/HGV.
