A one-step method was developed to fabricate conductive graphene/SnO2 (GS) nanocomposites in acidic solution. Graphite oxides were reduced by SnCl2 to graphene sheets in the presence of HCl and urea. The reducing process was accompanied by generation of SnO2 nanoparticles. The structure and composition of GS nanocomposites were confirmed by means of transmission electron microscopy, x-ray photoelectron and Raman spectroscopy. Moreover, the ultracapacitor characteristics of GS nanocomposites were studied by cyclic voltammograms (CVs) and electrical impedance spectroscopy (EIS). The CVs of GS nanocomposites are nearly rectangular in shape and the specific capacitance degrades slightly as the voltage scan rate is increased. The EIS of GS nanocomposites presents a phase angle close to pi/2 at low frequency, indicating a good capacitive behavior. In addition, the GS nanocomposites could be promisingly applied in many fields such as nanoelectronics, ultracapacitors, sensors, nanocomposites, batteries and gas storage.

AgBr nanoparticles supported on graphitic-C3N4-decorated nitrogen-doped graphene intercorrelated ternary superhybrid composites (ACNNG-x) acting as a novel visible-light driven photocatalyst are reported. Because of the fast interfacial charge separation and photoelectrochemical performance, the representative of ACNNG-50 superhybrid structure achieves high efficiency and stable photocatalytic capability for organic contaminant degradation and CO2 reduction.

No abstract

Graphene sheets are used for the first time to fabricate a new type of solid-contact ion-selective electrode (SC-ISE) as the intermediate layer between an ionophore-doped solvent polymeric membrane and a glassy carbon electrode. The new transducing layer was characterized by transmission electron microscopy, scanning electron microscopy, cyclic voltammetry and electrochemical impedance spectroscopy. The performance of the new K(+-)selective electrodes was examined by a potentiometric water layer test, potentiometric measurements, and current reversal chronopotentiometry. The obtained potentiometric sensors were characterized with a calibration line of slope close to Nernstian (59.2 mV/decade) within the activity from 10(-4.5) to 0.1 M. The high capacitance of the graphene solid contacts results in a signal that is stable over one week. The short response time is less than 10 s for activities higher than 10(-5) M. The potential drift of the electrodes was calculated from the slope of the curves at longer times (ΔE/Δt = 1.2 × 10(-5) V s(-1) (I = 1 nA) and ΔE/Δt = 5.5 × 10(-5) V s(-1) (I = 5 nA)). All the results indicate that graphene is a promising material for use as a transducer layer for SC-ISEs.

3D AgX/graphene aerogel (GA) composites (X = Br, Cl) are synthesized. Not only is the photocatalytic performance increased in comparison with pristine AgX, but also the photocatalytic cycling process is facilitated just using tweezers Thus, the comprehensive performance of the AgX/GA composites provides robust support for future industrial applications of the photocatalyst.

The upgrading of biomass into sustainable and valuable fine chemicals is an alternative to the use of state-of-the-art petrochemicals. The conversion of 5-hydroxymethylfurfural (HMF) biomass derivative into 2,5-furandicarboxylic acid (FDCA) has been recognized as an economical and green approach to replace the current polyethylene terephthalate based plastic industry. However, this reaction mostly relies on noble-metal-based catalysts for the sluggish aerobic oxidation of alcohol groups. In this work, we report a series of hierarchical Ni-Co-based transition metal oxide catalysts for HMF oxidation by electrocatalysis. Comprehensive material characterization and electrochemical evaluation have been performed. A 90 % FDCA yield, nearly 100 % Faradaic efficiency, and robust stability were achieved for NiCo O nanowires. As non-precious-metal catalysts, Ni-Co-based transition metal oxides may open up new potential materials for highly efficient electrochemical biomass upgrading.

To greatly improve the hydrogen evolution reaction (HER) performance, it is the key approach to expose as many active edges of MoS2 as possible. This target is the research hotspot and difficulty of MoS2 which is a promising HER catalyst. In this work, we realized the active-edges control of MoS2 nanosheets on carbon cloth (CC) by growth control during the synthesis procedure. Moreover, MoS2 nanosheets vertically grown on carbon cloth (MoS2⊥CC) was confirmed to be the best morphology with maximum active edges exposed. Multifactors structure control resulted in abundant active-edges exposure and effective electron delivery, thus excellent HER activity. This three-dimensional cathode, MoS2⊥CC, can reach a great current density of 200 mA/cm(2) at a small overpotential of 205 mV. The preeminent HER performance can rival the best MoS2-based catalyst ever reported.

No abstract