Publications by authors named "Baoshan Wu"

Ammonia (NH) synthesis via the nitrate reduction reaction (NORR) offers a competitive strategy for nitrogen cycling and carbon neutrality; however, this is hindered by the poor NORR performance under high current density. Herein, it is shown that boron-doped TiCT MXene nanosheets can highly efficiently catalyze the conversion of NORR-to-NH at ambient conditions, showing a maximal NH Faradic efficiency of 91% with a peak yield rate of 26.2 mgh mg , and robust durability over ten consecutive cycles, all of them are comparable to the best-reported results and exceed those of pristine TiCT MXene.

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  • * The study involved heating water samples to different temperatures to analyze radon retention, revealing that radon levels decreased between 25 and 70 °C, stabilized from 70 to 85 °C, and then gradually declined.
  • * Using a computational model, researchers calculated the radiation doses from radon exposure during typical situations like drinking water and showering, concluding that normal water consumption does not pose a significant
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As one of the drinking water quality parameters, natural radioactivity parameters are recommended to prevent a potential health threat to the public. In this study, the gross-α and gross-β activity concentrations in 15 different brands of commercial bottled mineral water consumed in China were analyzed to evaluate the quality and corresponding health impact on the population. The activity concentrations of gross-α and gross-β in different samples varied from 4.

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The structure-dependent thermal stability of fullerene electron transport layers (ETLs) and its impact on device stability have been underrated for years. Based on cocrystallographic understanding, herein, we develop a thermally stable ETL comprising a hybrid layer of [6,6]-phenyl-C-butyric acid methyl ester (PCBM) and [6,6]-phenyl-C-propylbenzene (PCPB). By tuning the weight ratios of PCBM and PCPB to influence the noncovalent intermolecular interactions and packing of fullerene derivatives, we obtained a champion device based on the 20PCPB (20 wt % addition of PCPB into the mixture of PCBM/PCPB) ETL and excellent thermal stability of 500 h under 85 °C thermal aging in a N atmosphere in the dark.

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A bimetallic Pt-Co/KL catalyst was fabricated via the atomic layer deposition (ALD) method and demonstrated to be highly active and stable for the aromatization of n-heptane at a low temperature (420 °C), which is due to the restructured Pt-Co clusters providing unique catalytic sites and the enhanced electron-donating properties of the catalyst.

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  • The conversion of straight-chain paraffins to aromatics is important yet difficult in oil refining, highlighting the need for effective catalysts.
  • A new strategy involves using Fe-modified KL zeolites to enhance platinum (Pt) catalysts' efficiency by supporting high dispersion of single-atom Pt and Pt clusters within zeolite channels.
  • The developed PtFe-1/KL catalyst shows impressive performance with 90.1% selectivity for aromatics from -heptane and improved stability at lower temperatures, suggesting a significant advancement in catalyst design for this process.*
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Although some kinds of semiconductor metal oxides (SMOs) have been applied as electron selective layers (ESLs) for planar perovskite solar cells (PSCs), electron transfer is still limited by low electron mobility and defect film formation of SMO ESLs fabricated via low-temperature solution process. Herein, the C interlayer between TiO and (HC(NH)PbI)(CHNHPbCl) is prepared by spin-coating and low-temperature annealing for planar n-i-p PSCs. The resultant TiO/C ESL shows good surface morphology, efficient electron extraction, and facilitation of high-quality perovskite film formation, which can be attributed to the suitable nanosize and the superior electronic property of C molecules.

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Free-standing activated carbon nanofibers (ACNF) were prepared through electrospinning combining with CO2 activation and then used for nonaqueous Li-O2 battery cathodes. As-prepared ACNF based cathode was loosely packed with carbon nanofibers complicatedly overlapped. Owing to some micrometer-sized pores between individual nanofibers, relatively high permeability of O2 across the cathode becomes feasible.

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The lithium-sulfur primary batteries, as seldom reported in the previous literatures, were developed in this work. In order to maximize its practical energy density, a novel cauliflower-like hierarchical porous C/S cathode was designed, for facilitating the lithium-ions transport and sulfur accommodation. This kind of cathode could release about 1300 mAh g(-1) (S) capacity at sulfur loading of 6 ~ 14 mg cm(-2), and showed excellent shelf stability during a month test at room temperature.

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Although various kinds of catalysts have been developed for aprotic Li-O2 battery application, the carbon-based cathodes are still vulnerable to attacks from the discharge intermediates or products, as well as the accompanying electrolyte decomposition. To ameliorate this problem, the free-standing and carbon-free CoO nanowire array cathode was purposely designed for Li-O2 batteries. The single CoO nanowire formed as a special mesoporous structure, owing even comparable specific surface area and pore volume to the typical Super-P carbon particles.

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The genomic DNA from Ephedra glauca was randomly transferred to Saccharomyces cerevisiae and Hansenula anomala by argon and nitrogen ion implantation. Through repeated subculturing and using reversed phase high-performance liquid chromatography analysis to quantify the concentrations of the secondary metabolites, l-ephedrine and d-pseudoephedrine, 12 recombinant strains of genetically stable yeast were obtained, each using glucose as a carbon source, NaNO3 as a nitrogen source and producing l-ephedrine and/or d-pseudoephedrine. After culturing in liquid medium for 72 h, extracellular l-ephedrine and d-pseudoephedrine concentrations of 18.

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