Graphitic carbon nitrides (g-C3N4) with unique physicochemical properties are promising candidates for photocatalysis applications. However, pristine g-C3N4 often suffers from narrow absorption ranges and high carrier recombination rates, which result...

BackgroundDucks (Anas platyrhynchos) an economically important waterfowl for meat, eggs and feathers; is also a natural reservoir for influenza A viruses. The emergence of novel viruses is attributed to the status of co-existence of multiple types and subtypes of viruses in the reservoir hosts. For effective prediction of future viral epidemic or pandemic an in-depth understanding of the virome status in the key reservoir species is highly essential.MethodsTo obtain an unbiased measure of viral diversity in the enteric tract of ducks by viral metagenomic approach, we deep sequenced the viral nucleic acid extracted from cloacal swabs collected from the flock of 23 ducks which shared the water bodies with wild migratory birds.ResultIn total 7,455,180 reads with average length of 146 bases were generated of which 7,354,300 reads were de novo assembled into 24,945 contigs with an average length of 220 bases and the remaining 100,880 reads were singletons. The duck virome were identified by sequence similarity comparisons of contigs and singletons (BLASTx E score, <10−3) against viral reference database. Numerous duck virome sequences were homologous to the animal virus of the Papillomaviridae family; and phages of the Caudovirales, Inoviridae, Tectiviridae, Microviridae families and unclassified phages. Further, several duck virome sequences had homologous with the insect viruses of the Poxviridae, Alphatetraviridae, Baculoviridae, Densovirinae, Iflaviridae and Dicistroviridae families; and plant viruses of the Secoviridae, Virgaviridae, Tombusviridae and Partitiviridae families, which reflects the diet and habitation of ducks.ConclusionThis study increases our understanding of the viral diversity and expands the knowledge about the spectrum of viruses harboured in the enteric tract of ducks.

Transition-metal nitrides have attracted significant attention because of their unique electronic and surface properties and superior chemical and mechanical stability. Although various metal nitrides nanostructures have been realized, it remains challenging to introduce porosity and the high specific surface in these nanostructures, but they are required to expand the application possibility of these materials in energy storage and conversion. Here, we report the preparation of nanoporous titanium carbonitride using a high-nitrogen-containing mesoporous carbon nitride, C3N6 (MCN-4), as a reactive template and titanium tetrachloride as the titanium source. Nitrogen adsorption and microscopic results reveal that the prepared samples are highly nanoporous in nature, and the optimized sample exhibits a specific surface area of 700 m2/g and a high specific pore volume of 1.3 cm3/g. With the slight variation of the amount of MCN-4 in the synthesis mixture, the composition and the crystal structure of the nanoporous titanium carbonitride can be finely controlled. Near-edge X-ray absorption fine structure and Raman spectroscopic analyses of these samples confirm that the titanium atoms are strongly bonded with both carbon and nitrogen. The electrochemical hydrogen evolution reaction measurements of the optimized nanoporous titanium carbonitride loaded with 5 wt % of platinum in acidic medium reveal a high electrocatalytic performance with the overpotential of 27 mV at the current density of 10 mA cm–2, which is similar to that of commercially available Pt/C which contains 20 wt % of Pt. The combination of nanoporous structure together with the highly conducting carbon matrix in these metal carbonitride samples really helps to enhance the electrocatalytic activity. This research reveals a great opportunity for the design of porous metal nitride-based nanostructures with different composition and the potential for these materials to be used in energy storage and conversion technologies.

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