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The transition metal-based nitride (TMN) holds great promise as catalysts with high efficiency for energy-related technologies. Herein, on the basis of global structure search and density functional theory calculations, a novel two-dimensional (2D) TMN was identified: RuN 2 monolayer with tetracoordinated Ru atoms and isolated N═N dimers, which is revealed to possess high thermal, dynamic, and chemical stabilities as well as metallic nature, thus providing great feasibility for its practical application in electrochemical reactions. Remarkably, we found that the predicted RuN 2 monolayer exhibits superior catalytic performance for the oxygen reduction reaction (ORR) with a rather high limiting potential (0.99 V) and an overwhelming four-electron reduction pathway selectivity. Thus, our results suggested the robust applicability of RuN 2 monolayer as a novel non-Pt catalyst due to its excellent catalytic efficiency and outstanding selectivity for ORR, which not only proposes a new member to the hypercoordinate 2D TMN with novel properties, but also provides a feasible strategy to further develop novel TMN-based nanomaterials for electrocatalytic energy conversion.

Cellular-structured graphene foam (GF)/epoxy composites are prepared based on a three-step fabrication process involving infiltration of epoxy into the porous GF. The three-dimensional (3D) GF is grown on a Ni foam template via chemical vapor deposition. The 3D interconnected graphene network serves as fast channels for charge carriers, giving rise to a remarkable electrical conductivity of the composite, 3 S/cm, with only 0.2 wt % GF. The corresponding flexural modulus and strength increase by 53 and 38%, respectively, whereas the glass transition temperature increases by a notable 31 °C, compared to the solid neat epoxy. The GF/epoxy composites with 0.1 wt % GF also deliver an excellent fracture toughness of 1.78 MPa·m(1/2), 34 and 70% enhancements against their "porous" epoxy and solid epoxy counterparts, respectively. These observations signify the unrivalled effectiveness of 3D GF relative to 1D carbon nanotubes or 2D functionalized graphene sheets as reinforcement for polymer composites without issues of nanofiller dispersion and functionalization prior to incorporation into the polymer.

We report a graphene oxide (GO)-based fluorescent sensor for Hg(2+) detection in aqueous solutions by using hybridization chain reactions (HCRs). GO is used as an adsorption material for capturing single-stranded DNA and an efficient fluorescence quencher for reducing the background signal. In the detection strategy, two hairpin probes and a helper DNA are employed. Without Hg(2+), they are adsorbed by the GO and the fluorescence of one of the hairpin probes is quenched. In the presence of Hg(2+), the HCRs between the two hairpin probes are initiated by Hg(2+) with the aid of the helper DNA through T-Hg(2+)-T coordination chemistry. The double-stranded DNA products of the HCRs are released by the GO and the fluorescence is recovered. The detection limit of the sensing method is 0.3 nM, which is sufficiently sensitive for practical applications. The sensing system also exhibits high selectivity against other divalent metal ions, and the application of the sensor for drinking water shows that the proposed method works well for real samples.

A facile method was developed for preparing uniform silver nanoparticles with small particle sizes of less than 10 nm at high concentrations, in which aniline was used to reduce silver nitrate (AgNO(3)) to silver nanoparticles in the presence of dodecylbenzenesulfonic acid (DBSA) as a stabilizer. Upon the addition of excess NaOH to the DBSA-aniline-AgNO(3) (DAA) system, the formation of silver nanoparticles was almost complete in just 2 min at 90 °C (in 94% yield). The average size of those resultant silver nanoparticles was 8.9 ± 1.1 nm, and the colloids were stable for more than 1 year at ambient temperature. A possible mechanism for the formation of silver nanoparticles was proposed to be related to two factors: one was the mesoscopic structures of the DAA system in which silver ions were restricted in the dispersed phases composed of DBSA and aniline; the other was Ag(2)O nanocrystallites generated in situ that could be readily reduced by aniline to small silver nanoparticles at high concentrations., (© 2011 American Chemical Society)