Nanjing University of Science and Technology

About: Nanjing University of Science and Technology is a education organization based out in Nanjing, China. It is known for research contribution in the topics: Control theory & Catalysis. The organization has 31581 authors who have published 36390 publications receiving 525474 citations. The organization is also known as: Nánjīng Lǐgōng Dàxué & Nánlǐgōng.

Synthesis and characterization of the pentazolate anion cyclo-N5ˉ in (N5)6(H3O)3(NH4)4Cl

Abstract: The flip side of the robust stability of N2 is the instability of any larger molecules composed exclusively of nitrogen. These molecules nonetheless remain enticing targets for explosive and propellant applications. Zhang et al. successfully prepared the pentazolate ion, a negatively charged ring of five nitrogens, by oxidative cleavage of a C–N bond in an aryl-substituted precursor (see the Perspective by Christe). The molecule was stabilized and isolated in the solid state as a hydrated ammonium chloride salt. Spectroscopic and crystallographic characterization confirmed the ring's planar geometry. Science , this issue p. [374][1]; see also p. [351][2] [1]: /lookup/doi/10.1126/science.aah3840 [2]: /lookup/doi/10.1126/science.aal5057

Organic-Inorganic Hybrid Passivation Enables Perovskite QLEDs with an EQE of 16.48.

Abstract: Perovskite quantum dots (QDs) with high photoluminescence quantum yields (PLQYs) and narrow emission peak hold promise for next-generation flexible and high-definition displays. However, perovskite QD films often suffer from low PLQYs due to the dynamic characteristics between the QD's surface and organic ligands and inefficient electrical transportation resulting from long hydrocarbon organic ligands as highly insulating barrier, which impair the ensuing device performance. Here, a general organic-inorganic hybrid ligand (OIHL) strategy is reported on to passivate perovskite QDs for highly efficient electroluminescent devices. Films based on QDs through OIHLs exhibit enhanced radiative recombination and effective electrical transportation properties compared to the primal QDs. After the OIHL passivation, QD-based light-emitting diodes (QLEDs) exhibit a maximum peak external quantum efficiency (EQE) of 16.48%, which is the most efficient electroluminescent device in the field of perovskite-based LEDs up to date. The proposed OIHL passivation strategy positions perovskite QDs as an extremely promising prospect in future applications of high-definition displays, high-quality lightings, as well as solar cells.

High-content ductile coherent nanoprecipitates achieve ultrastrong high-entropy alloys

Abstract: Precipitation-hardening high-entropy alloys (PH-HEAs) with good strength−ductility balances are a promising candidate for advanced structural applications. However, current HEAs emphasize near-equiatomic initial compositions, which limit the increase of intermetallic precipitates that are closely related to the alloy strength. Here we present a strategy to design ultrastrong HEAs with high-content nanoprecipitates by phase separation, which can generate a near-equiatomic matrix in situ while forming strengthening phases, producing a PH-HEA regardless of the initial atomic ratio. Accordingly, we develop a non-equiatomic alloy that utilizes spinodal decomposition to create a low-misfit coherent nanostructure combining a near-equiatomic disordered face-centered-cubic (FCC) matrix with high-content ductile Ni3Al-type ordered nanoprecipitates. We find that this spinodal order–disorder nanostructure contributes to a strength increase of ~1.5 GPa (>560%) relative to the HEA without precipitation, achieving one of the highest tensile strength (1.9 GPa) among all bulk HEAs reported previously while retaining good ductility (>9%). High entropy alloys usually emphasize equiatomic compositions, which restrict the compositions available to induce strengthening via precipitation. Here the authors use spinodal decomposition in a five-element alloy to obtain high content nanophases and the highest tensile strength reported to date.

One step synthesis of oxygen doped porous graphitic carbon nitride with remarkable improvement of photo-oxidation activity: Role of oxygen on visible light photocatalytic activity

Abstract: A novel metal-free oxygen doped porous graphitic carbon nitride (OA-g-C3N4) was synthesized by condensation of oxalic acid and urea. The 40% OA-g-C3N4 catalyst can degrade bisphenol A (15 mg L−1) in 240 min with a mineralization rate as high as 56%. The markedly higher visible-light-driven oxidation activity of OA-g-C3N4 is attributed to the porous morphology and unique electrical structure. The porous structure of OA-g-C3N4 provides more active sites for adsorption and degradation of pollutants. Moreover, oxygen atoms in the tri-s-triazine units help to extend sufficient light absorption range up to 700 nm, improve the separation of charge-carriers and alter the position of valence band (VB) and conduction band (CB). The VB edge shifts from 1.95 eV to 2.46 eV due to the incorporation of O atoms, which leads to the change of active species in the photocatalytic reaction. Trapping experiment shows that superoxide radicals play the major role in the photocatalytic degradation of BPA on g-C3N4, while hydroxyl radical is the dominant active species in the photocatalytic degradation process over 40% OA-g-C3N4. This study presents a simple, economical and environment-friendly method to synthesized oxygen doped porous graphitic carbon nitride.