Recent Advances in Noble Metal (Pt, Ru, and Ir)-Based Electrocatalysts for Efficient Hydrogen Evolution Reaction

Noble metal (Pt, Ru, and Ir)-based electrocatalysts are currently considered the most active materials for the hydrogen evolution reaction (HER). Although they have been associated with high cost, easy agglomeration, and poor stability during the HER reaction, recent efforts to intentionally tailor noble-metal-based catalysts have led to promising improvements, with lower cost and superior activity, which are critical to achieving large-scale production of pure hydrogen. In this mini-review, we focus on the recent advances in noble-metal-based HER electrocatalysts. In particular, the synthesis strategies to enhance cost-effectiveness and the catalytic activity for HER are highlighted

A solvent-free Diels-Alder reaction of graphite into functionalized graphene nanosheets

A solvent-free Diels-Alder reaction was carried out by heating a mixture of graphite and a typical dienophile, maleic anhydride (MA) or maleimide (MI), in a sealed glass ampoule of argon. The functionalization of graphite with dienophiles was confirmed by various characterization techniques, suggesting the efficient functionalization and delamination of graphite into a few layers of graphitic nanosheets.close0

Nanocomposites Derived from Polymers and Inorganic Nanoparticles

Polymers are considered to be good hosting matrices for composite materials because they can easily be tailored to yield a variety of bulk physical properties. Moreover, organic polymers generally have long-term stability and good processability. Inorganic nanoparticles possess outstanding optical, catalytic, electronic and magnetic properties, which are significantly different their bulk states. By combining the attractive functionalities of both components, nanocomposites derived from organic polymers and inorganic nanoparticles are expected to display synergistically improved properties. The potential applications of the resultant nanocomposites are various, e.g. automotive, aerospace, opto-electronics, etc. Here, we review recent progress in polymer-based inorganic nanoparticle composites.open565

In situ Polymerization of Multi-Walled Carbon Nanotube/Nylon-6 Nanocomposites and Their Electrospun Nanofibers

Multiwalled carbon nanotube/nylon-6 nanocomposites (MWNT/nylon-6) were prepared by in situ polymerization, whereby functionalized MWNTs (F-MWNTs) and pristine MWNTs (P-MWNTs) were used as reinforcing materials. The F-MWNTs were functionalized by Friedel-Crafts acylation, which introduced aromatic amine (COC6H4-NH2) groups onto the side wall. Scanning electron microscopy (SEM) images obtained from the fractured surfaces of the nanocomposites showed that the F-MWNTs in the nylon-6 matrix were well dispersed as compared to those of the P-MWNTs. Both nanocomposites could be electrospun into nanofibers in which the MWNTs were embedded and oriented along the nanofiber axis, as confirmed by transmission electron microscopy. The specific strength and modulus of the MWNTs-reinforced nanofibers increased as compared to those of the neat nylon-6 nanofibers. The crystal structure of the nylon-6 in the MWNT/nylon-6 nanofibers was mostly γ-phase, although that of the MWNT/nylon-6 films, which were prepared by hot-pressing the pellets between two aluminum plates and then quenching them in icy water, was mostly α-phase, indicating that the shear force during electrospinning might favor the γ-phase, similarly to the conventional fiber spinning

Hyperbranched macromolecules: From synthesis to applications

Hyperbranched macromolecules (HMs, also called hyperbranched polymers) are highly branched three-dimensional (3D) structures in which all bonds converge to a focal point or core, and which have a multiplicity of reactive chain-ends. This review summarizes major types of synthetic strategies exploited to produce HMs, including the step-growth polycondensation, the self-condensing vinyl polymerization and ring opening polymerization. Compared to linear analogues, the globular and dendritic architectures of HMs endow new characteristics, such as abundant functional groups, intramolecular cavities, low viscosity, and high solubility. After discussing the general concepts, synthesis, and properties, various applications of HMs are also covered. HMs continue being materials for topical interest, and thus this review offers both concise summary for those new to the topic and for those with more experience in the field of HMs

Ruthenium anchored on carbon nanotube electrocatalyst for hydrogen production with enhanced Faradaic efficiency

Developing efficient and stable electrocatalysts is crucial for the electrochemical production of pure and clean hydrogen. For practical applications, an economical and facile method of producing catalysts for the hydrogen evolution reaction (HER) is essential. Here, we report ruthenium (Ru) nanoparticles uniformly deposited on multi-walled carbon nanotubes (MWCNTs) as an efficient HER catalyst. The catalyst exhibits the small overpotentials of 13 and 17 mV at a current density of 10 mA cm(-2) in 0.5M aq. H2SO4 and 1.0M aq. KOH, respectively, surpassing the commercial Pt/C (16 mV and 33 mV). Moreover, the catalyst has excellent stability in both media, showing almost "zeroloss" during cycling. In a real device, the catalyst produces 15.4% more hydrogen per power consumed, and shows a higher Faradaic efficiency (92.28%) than the benchmark Pt/C (85.97%). Density functional theory calculations suggest that Ru-C bonding is the most plausible active site for the HER

"Direct" grafting of linear macromolecular "wedges" to the edge of pristine graphite to prepare edge-functionalized graphene-based polymer composites

The edges of pristine graphite were covalently grafted with para-poly(ether-ketone) (pPEK) in a mildly acidic polyphosphoric acid (PPA)/phosphorus pentoxide (P(2)O(5)) medium. The resulting pPEK grafted graphite (pPEK-g-graphite) showed that the pristine graphite had been exfoliated into a few layers of graphene platelets (graphene-like sheets), which were uniformly dispersed into a pPEK matrix. As a result, the tensile properties of pPEK-g-graphite films were greatly improved compared to those of controlled pPEK films. The origins of these enhanced mechanical properties were deduced from scanning electron microscope (SEM) images of fracture surfaces. Upon tracing wide-angle X-ray scattering (WAXS) patterns of the film under strain, the graphene-like sheets were further exfoliated by an applied shear force, suggesting that a toughening mechanism for the pPEK-g-graphite film occurred. This approach envisions that the "direct'' edge grafting of pristine graphite without pre-treatments such as corrosive oxidation and/or destructive sonication is a simple and efficient method to prepare graphene-based polymer composites with enhanced mechanical properties.close161

Strain-induced delamination of edge-grafted graphite

Edge-selectively grafted graphite (EGG) with poly(ether-ketone) was prepared by the Friedel-Crafts acylation in a mild polyphosphoric acid (PPA)-phosphorous pentoxide (P2O5) mixture. The homogeneous reaction dope was coagulated in air moisture at different temperatures. The morphology of expanded EGG was changed from balls, balls/rods and rods with respect to coagulation temperatures of 80, 60, 40 and 25 degrees C, respectively.close1