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Photocatalytic nitrogen fixation has become a hot topic in recent years due to its mild and sustainable advantages. Selleck 1-Methylnicotinamide While modifying the photocatalyst to enhance its electron separation, light absorption and nitrogen reduction abilities, the role of the active sites in the catalytic reaction cannot be ignored because the N[triple bond, length as m-dash]N nitrogen bond is too strong to activate. This review summarizes the recent research on nitrogen fixation, focusing on the active sites for N2 on the catalyst surface, classifying common active sites, explaining the main role and additional role of the active sites in catalytic reactions, and discussing the methods to increase the number of active sites and their activation ability. Finally, the outlook for future research is presented. It is hoped this review could help researchers understand more about the activation of the nitrogen molecules and lead more efforts into research on nitrogen fixation photocatalysts.The high specific capacity, low cost and environmental friendliness make manganese dioxide materials promising cathode materials for zinc-ion batteries (ZIBs). In order to understand the difference between the electrochemical behavior of manganese dioxide materials with different valence states, i.e., Mn(iii) and Mn(iv), we investigated and compared the electrochemical properties of pure MnO2 and Mn2O3 as ZIB cathodes via a combined experimental and computational approach. The MnO2 electrode showed a higher discharging capacity (270.4 mA h g-1 at 0.1 A g-1) and a superior rate performance (125.7 mA h g-1 at 3 A g-1) than the Mn2O3 electrode (188.2 mA h g-1 at 0.1 A g-1 and 87 mA h g-1 at 3 A g-1, respectively). The superior performance of the MnO2 electrode was ascribed to its higher specific surface area, higher electronic conductivity and lower diffusion barrier of Zn2+ compared to the Mn2O3 electrode. This study provides a detailed picture of the diversity of manganese dioxide electrodes as ZIB cathodes.A comb-like amphiphilic polymer (PBTF), composed of hydrophobic backbones and hydrophilic side chains, was employed to grow honeycomb coating layers in situ on a filter paper via directly casting a polymer solution and by the subsequent dynamic breath figure (BF) method. Through regulating the hydrophilic polymer side chain density and the solution concentration, a continuous honeycomb coating layer contouring to the filter paper surface profile, in addition to possessing a water contact angle (WCA) as high as 146°, was successfully fabricated. The present study also finds that increasing the hydrophilic side chain density will turn PBTF into a surfactant-like polymer, and thus, endow the PBTF solution with the capacity of numerous micro-nano-sized water droplets, rather than simply stabilizing the ordered water droplet arrays on the surface of the solution. With vast nano-sized water droplets in it, the once transparent PBTF solution changed into a translucent nano-emulsion, which demonstrates a strong Tyndall effect. While casting such nano-emulsion on a filter paper and then subjecting to the BF process, the polymeric solute takes both nano-emulsion intrinsic nano-sized water droplets and solvent evaporation-induced water droplets as templates and self-assembles into a bird-nest-like three-dimensional porous microstructure, which possesses micro-nano-sized communicating pores. By regulating the water content in the nano-emulsion, the bird-nest-like structure can be uniformly formed on the surface of the filter paper, which revealed a WCA of 152°. The coated filter papers possess selective wettability, and meanwhile, maintain the inherent permeability of the substrates, which therefore can be directly utilized as oil/water separation materials.Sunscreen lotions and creams are arguably the most popular products used to protect the skin against harmful UV radiation. Several studies have been conducted to untangle the internal microstructure of creams and lotions. However, the effect of UV filters and other materials such as preservatives, on the internal microstructure and the aesthetics of these products is not yet fully understood. Using small-angle neutron scattering (SANS), we were able to investigate the effect of adding the commonly used organic UV filters (avobenzone (AVB), ethylhexyl methoxycinnamate (EMC), ethylhexyl triazone (EHT) and bemotrizinol (BMT)) and the water soluble preservatives (1,5-pentanediol (1,5-PD) and 1,2-hexanediol (1,2-HD)), on the internal architecture and microstructure of an oil-in-water (o/w) based sunscreen lotion. Our findings highlight the complexities of these formulations, and how the introduction of different additives could influence their structure and possibly their performance.Fraxin (FX) (7-hydroxy-6-methoxycoumarin 8-glucoside) is a typical natural product of the coumarin family. This compound was shown to protect endothelial cells from oxidative stress; however, the nature of its antioxidant properties is still ambiguous. In this study, we report on a systematic evaluation of the radical scavenging activity of FX using a two-tier protocol based on thermodynamic and kinetic calculations. The results show that FX has moderate activity in the aqueous physiological environment against a range of radicals including HO˙, CCl3O˙, CCl3OO˙, NO2, , and HOO˙. The latter was examined in detail due to the prevalence of HOO˙ as a source of oxidative stress in biological systems. HOO˙ scavenging activity was promising in the gas phase but low in physiological environments with k overall = 1.57 × 106, 3.13 × 102 and 2.68 × 103 M-1 s-1 in the gas phase, pentyl ethanoate and water solvents, respectively. The formal hydrogen transfer mechanism at the O7-H bond dominates the hydroperoxyl radical scavenging of FX in the nonpolar media, whereas, in the polar environment, the activity is exerted by the single electron transfer mechanism of the anion state. This activity falls behind typical antioxidants such as Trolox, ascorbic acid, and trans-resveratrol under the studied conditions. Thus FX may have multiple health benefits, but it is not an outstanding natural antioxidant.An efficient, green, one-pot, and three-component protocol has been reported for the stereoselective synthesis of a new class of spiro thiazolidines. A series of spiro-heterocycle derivatives were produced stereoselectively in high yields by the reaction of 5-arylidene thiazolidine-2,4-diones, isatin, and secondary amino acids in the presence of MnCoCuFe2O4@l-proline (MCCFe2O4@l-proline) magnetic nanorods as a novel nanocatalyst. The synthesized catalyst was fully characterized for thermal stability, magnetic properties, and other physicochemical properties via numerous techniques. It was applied as an efficient and reusable catalyst for the synthesis of endo-isomers of spirocyclic pyrrolidine/pyrrolizidine/pyrrolothiazolidine derivatives in high yield. The regioselectivity and stereochemistry of these heterocyclic spiro-compounds were established by 1H, 13C, HMBC, HSQC, and COSY NMR spectroscopy techniques. The main attractive characteristics of the presented protocol are high yield, high level of diastereoselectivity, and easy recovery of catalyst without significant loss of its catalytic activity.In this work, electrospun polyacrylonitrile/reduced graphene oxide-amino-halloysite/bimetallic metal-organic framework (PAN/rGO-amino-HNT/Co0.5Zn0.5(MeIm)2) nanofiber film was synthesized and investigated as a novel adsorbent for the ultrasonic-assisted thin-film microextraction (UA-TFME) of fatty acid methyl esters (FAMEs), including palmitic methyl ester (PAME), oleic methyl ester (OAME), stearic methyl ester (SAME), and linoleic methyl ester (LAME), from dairy products. The hybrid nanocomposite was obtained via bonding halloysite nanotubes to reduced graphene oxide, followed by loading with bimetallic metal-organic frameworks. The determination of FAMEs with nanofiber film was performed in two stages of desorption and absorption where, initially, the analytes were adsorbed onto the nanofiber film and then desorbed with organic solvent. In this study, ultrasound was used for both the adsorption and desorption stages. The advantages of ultrasonication are extensive, overcoming the shortcomings of conventionacid methyl esters in dairy products (milk, yogurt, cheese, yogurt soda and butter samples) for the first time. The fatty acids were transesterified using standard procedures and were subjected to UA-TFME treatment prior to GC-FID determination. The developed method possesses the advantages of simplicity, rapidity, cost-effectiveness, sensitivity, and non-invasiveness.(Ba0.95Ca0.05)1-x (Ti0.8Sn0.2)1-x Na x Nb x O3 (BCNTSNO3) lead-free ceramics with compositions (x = 0.75, 0.8 and 0.85) were synthesized through the traditional solid-state reaction method. X-ray powder diffraction analysis showed the formation of a single phase compound crystallized in tetragonal space group P4mm. The evolution of Raman spectra displayed a disorder introduced into the structure, which favors a ferroelectric relaxor behavior. The dependence of the dielectric properties on temperature exhibited two composition ranges with different behaviors. Ferroelectric relaxor properties were observed for the compositions x less then 0.85 and the classical ferroelectric behavior for x = 0.85. Lead free (Ba0.95Ca0.05)1-x (Ti0.8Sn0.2)1-x Na x Nb x O3 ceramics exhibited larger dielectric constants than those of parent crystal NaNbO3, suggesting that it is a good candidate for lead-free ceramics in several industrial applications. Using UV-Vis spectroscopy, the optical band gap energy of ceramics (Ba0.95Ca0.05)1-x (Ti0.8Sn0.2)1-x Na x Nb x O3 is found at 2.89, 2.92, and 3.05 eV for x = 0.75, 0.8 and 0.85, respectively.Unlike rigid microparticles, soft and deformable elastomer (rubber) microspheres were found to exhibit a non-close-packed arrangement on solid substrates after the evaporation of water from their dispersions. The microscopic observation revealed that individual microspheres are ordered in regular intervals at the air/water interface of a sessile droplet and remain fixed on the substrate without being affected by the capillary forces during evaporation due to their deformability. Moreover, using the Langmuir-Blodgett method, thin films of non-close-packed structures could be successfully generated over large areas. Our findings may potentially help to control the arranged structures of elastomer microspheres, which can be expected to improve the nano-science and technology for the precise control for e.g. surface patterning.The heterocyclic donor molecule 2,4,7,9-tetramethyl-1,6-dithiapyrene (TMDTP) has been synthesized in five steps. Oxidation of TMDTP is facile (E 1 1/2 = 0.27 V and E 2 1/2 = 0.79 V vs. SCE). The charge-transfer complex, TMDTP-TCNQ, has been prepared and the salt, (TMDTP)3(PF6)2·2THF, obtained by electrocrystallization. The structure of TMDTP, TMDTP-TCNQ and (TMDTP)3(PF6)2·2THF has been characterized by X-ray crystallography and computationally.It is of vital importance to develop probes to monitor hypochlorous acid (HClO) in biological systems as HClO is associated with many important physiological and pathological processes. Metal nanoclusters (NCs) are promising luminescent nanomaterials for highly reactive oxygen species (hROS) detection on the basis of their strong reaction ability with hROS. However, metal NCs typically can respond to most common hROS and are susceptible to etching by biothiols, hindering their application in the construction of effective HClO probes. Herein, we proposed a strategy to develop a nanoprobe based on Au NCs for highly sensitive and selective detection of HClO. We synthesized luminescent benzyl mercaptan-stabilized Au NCs and encapsulated them with an amphiphilic polymer (DSPE-PEG). After encapsulation, an obvious emission enhancement and good resistance to the etching by biothiols for Au NCs were achieved. More importantly, the DSPE-PEG encapsulated Au NCs can be used as a nanoprobe for detection of HClO with good performance.