Bilayer graphene formed by passage of current through graphite: evidence for a three-dimensional structure

The passage of an electric current through graphite or few-layer graphene can result in a striking structural transformation, but there is disagreement about the precise nature of this process. Some workers have interpreted the phenomenon in terms of the sublimation and edge reconstruction of essentially flat graphitic structures. An alternative explanation is that the transformation actually involves a change from a flat to a three-dimensional structure. Here we describe detailed studies of carbon produced by the passage of a current through graphite which provide strong evidence that the transformed carbon is indeed three-dimensional. The evidence comes primarily from images obtained in the scanning transmission electron microscope using the technique of high-angle annular dark-field imaging, and from a detailed analysis of electron energy loss spectra. We discuss the possible mechanism of the transformation, and consider potential applications of “three-dimensional bilayer graphene”

Sub‐nanometer thick gold nanosheets as highly efficient catalysts

2D metal nanomaterials offer exciting prospects in terms of their properties and functions. However, the ambient aqueous synthesis of atomically‐thin, 2D metallic nanomaterials represents a significant challenge. Herein, freestanding and atomically‐thin gold nanosheets with a thickness of only 0.47 nm (two atomic layers thick) are synthesized via a one‐step aqueous approach at 20 °C, using methyl orange as a confining agent. Owing to the high surface‐area‐to‐volume ratio, abundance of unsaturated atoms exposed on the surface and large interfacial areas arising from their ultrathin 2D nature, the as‐prepared Au nanosheets demonstrate excellent catalysis performance in the model reaction of 4‐nitrophenol reduction, and remarkable peroxidase‐mimicking activity, which enables a highly sensitive colorimetric sensing of H2O2 with a detection limit of 0.11 × 10−6 m. This work represents the first fabrication of freestanding 2D gold with a sub‐nanometer thickness, opens up an innovative pathway toward atomically‐thin metal nanomaterials that can serve as model systems for inspiring fundamental advances in materials science, and holds potential across a wide region of applications

Sub‐nanometer thick gold nanosheets: sub‐nanometer thick gold nanosheets as highly efficient catalysts (Adv. Sci. 21/2019)

In article number 1900911, Stephen D. Evans and co‐workers develop an ambient aqueous synthesis for preparing atomically‐thin gold nanosheets (termed gold nanoseaweed, AuNSW, because of its morphology, color and aqueous growth). These AuNSWs represent the first free‐standing 2D gold with a sub‐nanometer thickness (0.47 nm, e.g., two atomic layers thick), and exhibit excellent catalysis performance in the model reaction of 4‐nitrophenol reduction, as well as remarkable peroxidase‐mimicking activity

Sub‐nanometer thick gold nanosheets: sub‐nanometer thick gold nanosheets as highly efficient catalysts (Adv. Sci. 21/2019)

In article number 1900911, Stephen D. Evans and co‐workers develop an ambient aqueous synthesis for preparing atomically‐thin gold nanosheets (termed gold nanoseaweed, AuNSW, because of its morphology, color and aqueous growth). These AuNSWs represent the first free‐standing 2D gold with a sub‐nanometer thickness (0.47 nm, e.g., two atomic layers thick), and exhibit excellent catalysis performance in the model reaction of 4‐nitrophenol reduction, as well as remarkable peroxidase‐mimicking activity

Homogeneous coating of photonic macroporous oxides with inorganic nanocrystals

A simple method to obtain homogeneous sub-monolayer coverage of metal oxide and chalcogenide nanocrystals onto porous oxide supports is described. Quantitative nanoparticle coverage was probed using photonic macroporous oxide supports. Composites of nanocrystals of TiO2, Fe3O 4 or CdS dispersed onto macroporous SiO2 or ZrO 2 all show a predictable linear shift in the photonic stop band position

Nanoparticle vesicle encoding for imaging and tracking cell populations.

For phenotypic behavior to be understood in the context of cell lineage and local environment, properties of individual cells must be measured relative to population-wide traits. However, the inability to accurately identify, track and measure thousands of single cells via high-throughput microscopy has impeded dynamic studies of cell populations. We demonstrate unique labeling of cells, driven by the heterogeneous random uptake of fluorescent nanoparticles of different emission colors. By sequentially exposing a cell population to different particles, we generated a large number of unique digital codes, which corresponded to the cell-specific number of nanoparticle-loaded vesicles and were visible within a given fluorescence channel. When three colors are used, the assay can self-generate over 17,000 individual codes identifiable using a typical fluorescence microscope. The color-codes provided immediate visualization of cell identity and allowed us to track human cells with a success rate of 78% across image frames separated by 8 h

A substoichiometric tungsten oxide catalyst provides a sustainable and efficient counter electrode for dye-sensitized solar cells

Development of Pt-free catalyst materials for the counter electrode (CE) in dye-sensitized solar cells (DSSCs) has been regarded as one of the crucial steps to improving energy conversion efficiency and cost effectiveness of DSSCs. In this work, low cost tungsten oxide (WO3-x) counter electrodes, prepared by annealing tungsten metal sheets under an Ar and low O2atmosphere, exhibited high catalytic activity and energy conversion efficiency. The highest efficiency achieved here for DSSCs with WO3-xcounter electrodes, was 5.25%, obtained from a 500 °C annealed tungsten sheet. TEM and XPS analysis suggested the formation of sub-stoichiometric tungsten oxide layer (∼WO2.6) with the presence of W6+, W5+and W4+oxidation states at the tungsten metal surface after the 500 °C annealing. Only W6+and W5+oxidation states were detected after a 600 °C annealing indicating the formation of a more stoichiometric tungsten oxide layer (∼WO2.8) and resulting in a drop in efficiency of the DSSC. We suggest that mixed valence tungsten states account for the excellent catalytic activity and good electrical conductivity as evidenced by the highest cyclic voltammetry response of 0.76 mA/cm2and the lowest impedance value of 44.33 Ω, respectively

Pore confinement effects and stabilization of carbon nitride oligomers in macroporous silica for photocatalytic hydrogen production

An ordered macroporous host (mac-SiO2) has been used to prevent aggregation of layered photocatalysts based on carbon nitride. Using typical carbon nitride synthesis conditions, cyanamide was condensed at 550 °C in the presence and absence of mac-SiO2. Condensation in the absence of mac-SiO2 results in materials with structural characteristics consistent with the carbon nitride, melon, accompanied by ca. 2 wt% carbonization. For mac-SiO2 supported materials, condensation occurs with greater carbonization (ca. 6 wt%). On addition of 3 wt% Pt cocatalyst photocatalytic hydrogen production under visible light is found to be up to 10 times greater for the supported composites. Time-resolved photoluminescence spectroscopy shows that excited state relaxation is more rapid for the mac-SiO2 supported materials suggesting faster electron-hole recombination and that supported carbon nitride does not exhibit improved charge separation. CO2 temperature programmed desorption indicates that enhanced photoactivity of supported carbon nitride is attributable to an increased surface area compared to bulk carbon nitride and an increase in the concentration of weakly basic catalytic sites, consistent with carbon nitride oligomers