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  • Lane Langhoff posted an update 8 hours, 44 minutes ago

    Charge-trapping memory devices based on two-dimensional (2D) material heterostructures possess an atomically thin structure and excellent charge transport capability, making them promising candidates for next-generation flash memories to achieve miniaturized size, high storage capacity, fast switch speed, and low power consumption. Here, we report a nonvolatile floating-gate memory device based on an ReS2/boron nitride/graphene heterostructure. selleck inhibitor The implemented ReS2 memory device displays a large memory window exceeding 100 V, leading to an ultrahigh current ratio over 108 between programming and erasing states. The ReS2 memory device also exhibits an ultrafast switch speed of 1 μs. In addition, the device can endure hundreds of switching cycles and shows stable retention characteristics with ∼40% charge remaining after 10 years. More importantly, taking advantage of its anisotropic electrical properties, a single ReS2 flake can achieve direction-sensitive multi-level data storage to enhance the data storage density. On the basis of these characteristics, the proposed ReS2 memory device is potentially able to serve the entire memory device hierarchy, meeting the need for scalability, capacity, speed, retention, and endurance at each level.A series of chiral fluorescent helicene-BODIPY conjugates was prepared by the regioselective formylation of aza[4]helicene precursors and then an efficient one-pot two-step BODIPY synthesis (13 examples, 28-82%). Fused conjugates exhibit absorption and fluorescence properties (ΦF 30-45%) in the red visible domain, and a CPL signature could be measured at 605 nm (glum ±5 × 10-4). Photophysical and electronic properties were investigated and rationalized through first principles.Noble-metal aerogels (NMAs) including silver aerogels have drawn increasing attention because of their highly conductive networks, large surface areas, and abundant optically/catalytically active sites. However, the current approaches of fabricating silver aerogels are tedious and time-consuming. In this regard, it is highly desirable to develop a simple and effective method for preparing silver aerogels. Herein, we report a facile strategy to fabricate silver gels via the in situ synthesis of silver nanowires (AgNWs). The obtained AgNW aerogels show superior electrical conductivity, ultralow density, and good mechanical robustness. AgNW aerogels with a density of 24.3 mg cm-3 display a conductivity of 2.1 × 105 S m-1 and a Young’s modulus of 38.7 kPa. Furthermore, using an infiltration-air-drying-crosslinking technique, polydimethylsiloxane (PDMS) was introduced into 3 dimensional (3D) AgNW networks for preparing silver aerogel/elastomer composite materials. The obtained AgNW/PDMS aerogel composite exhibits outstanding elasticity while retaining excellent electrical conductivity. The fast piezoresistive response proves that the aerogel composite has a potential application for vibration sensors.Developing a low cost, sustainable and high-performance precious-metal free catalyst to replace platinum (Pt)-based catalysts for the oxygen reduction reaction (ORR) in fuel cells has recently attracted significant attention. It is crucial to produce more abundant and more uniformly dispersed ORR active sites for improving the ORR performance of the catalyst. Herein, we synthesized tri-(Fe/F/N)-doped porous carbons as high-efficiency electrocatalysts for the ORR by using Fe-zeolitic imidazolate framework-8 (Fe-ZIF-8) and ammonium fluoride as precursors. The results indicate that the as-prepared FeFNC-5 catalysts exhibit superior ORR activity, methanol tolerance, and long-term stability compared to commercial 20 wt% Pt/C in both alkaline and acidic media because of the abundant and dispersed Fe-Nx and pyridinic-N active sites, high specific surface area, and hierarchical porous structure. This work provides a new method and insights into the synthesis of Fe, F, and N triple-doped porous carbons as high-efficiency ORR electrocatalysts.The naturally occurring spermine (Spm), as one of the many cationic polyamines, plays a key role in biological processes and is involved in a variety of diseases. The very similar structures among biogenic polyamines present a major challenge to achieve discriminative testing among them. In this contribution, using arbitrary ssDNA-coated Au@PtNPs as the probe, we demonstrated that a dual-mode strategy via a gas pressure and colorimetric signal readout can be used for the sensitive and specific detection of Spm, due to the target-responsive aggregation of the Au@PtNPs leading to the inhibition of the catalyzed gas-generation reaction and the colorimetric change of the Au@PtNP solution. The proposed pressure-based signaling strategy has a detection limit of 9.6 nM, and can be used not only in the laboratory but also in the point-of-care setting. Meanwhile, the colorimetric assay displays the advantage of being easily discerned with the naked eye. Compared with the traditional methods of chromatography and capillary electrophoresis combined with chemical derivatization, the strategy described here would provide a convenient new alternative for the specific detection of Spm in biological samples.A catalytically active conjugated microporous polymer (SP-CMP-Cu) was facilely constructed with condensation polymerization of salen-Cu (salen = N,N’-bis(3-tertbutyl-5-formylsalicylidene) ethylenediamine) and pyrrole. The as-synthesized SP-CMP-Cu was completely characterized by powder X-ray diffraction (PXRD), Fourier transform infrared (FT-IR) spectroscopy, thermogravimetric analysis (TGA), X-ray photoelectron spectroscopy (XPS), and energy-dispersive X-ray (EDX) analysis. The morphological features of SP-CMP-Cu were revealed by scanning electron microscopy (SEM) and transmission electron microscopy (TEM). According to the N2 adsorption/desorption isotherm, the Brunauer-Emmett-Teller (BET) surface area of SP-CMP-Cu was calculated to be 252 m2 g-1 with a total pore volume of 0.178 cm3 g-1. SP-CMP-Cu exhibited an outstanding catalytic performance for the Henry reaction in aqueous solutions with excellent conversion and good selectivity. Moreover, SP-CMP-Cu can be reused for up to five consecutive runs without any significant loss in its catalytic efficiency.

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