Revealing the atomic structure of the buffer layer between SiC(0001) and epitaxial graphene

On the SiC(0001) surface (the silicon face of SiC), epitaxial graphene is obtained by sublimation of Si from the substrate. The graphene film is separated from the bulk by a carbon-rich interface layer (hereafter called the buffer layer) which in part covalently binds to the substrate. Its structural and electronic properties are currently under debate. In the present work we report scanning tunneling microscopy (STM) studies of the buffer layer and of quasi-free-standing monolayer graphene (QFMLG) that is obtained by decoupling the buffer layer from the SiC(0001) substrate by means of hydrogen intercalation. Atomic resolution STM images of the buffer layer reveal that, within the periodic structural corrugation of this interfacial layer, the arrangement of atoms is topologically identical to that of graphene. After hydrogen intercalation, we show that the resulting QFMLG is relieved from the periodic corrugation and presents no detectable defect sites

A topological approach to non-Archimedean Mathematics

Non-Archimedean mathematics (in particular, nonstandard analysis) allows to construct some useful models to study certain phenomena arising in PDE's; for example, it allows to construct generalized solutions of differential equations and variational problems that have no classical solution. In this paper we introduce certain notions of non-Archimedean mathematics (in particular, of nonstandard analysis) by means of an elementary topological approach; in particular, we construct non-Archimedean extensions of the reals as appropriate topological completions of $\mathbb{R}$. Our approach is based on the notion of $\Lambda$-limit for real functions, and it is called $\Lambda$-theory. It can be seen as a topological generalization of the $\alpha$-theory presented in \cite{BDN2003}, and as an alternative topological presentation of the ultrapower construction of nonstandard extensions (in the sense of \cite{keisler}). To motivate the use of $\Lambda$-theory for applications we show how to use it to solve a minimization problem of calculus of variations (that does not have classical solutions) by means of a particular family of generalized functions, called ultrafunctions.Comment: 22 page

NEW SECONDARY METABOLITES IN THE AMPHINOMID FIREWORM HERMODICE CARUNCULATA

Eight betaine-derived novel compounds were found in extracts of the Mediterranean stinging fireworm Hermodice carunculata. The identification of their structures relies on 1D and 2D NMR (Fig. 1-3) and HPLC-ESI/HRMS spectra. Two types of terminal ammonium portions A and B and a series of different alkyl chains were identified (Fig. 4a,b). Their matching provides the structures of uncharacterized secondary metabolites, named carunculines, and their related isomers. These molecules differ from already known trimethylammonium inflammatory compounds (i.e. complanines) isolated from another amphinomid species, for the structures of the terminal ammonium groups (Fig. 4c) [1]. Carunculine anatomical distribution within H. carunculata was assessed by screening through HPLC-ESI/HRMS (Fig. 5, Table 1): their occurrence was revealed in all the body parts analyzed, both involved in predator-prey interactions [2], and mainly in the digestive apparatus. The results achieved reveal an array of different novel compounds from a chemically unknown species, improving knowledge on Marine Animal Products with chemical and biological potential for bioprospection [3]. Overall, these data reinforce the necessity of studying poorly-investigated taxa to expand knowledge on animal venom biology, their mechanisms of action and exploitation as promising source of drug molecule

Effects of the modification of gas diffusion electrodes by organic redox catalysts for hydrogen peroxide electrosynthesis

This paper reports a comparative study of the electrochemical performance of in situ hydrogen peroxide electrogeneration on gas diffusion electrodes modified by organic redox catalysts 2-ethylanthraquinone, 2-terc-butylanthraquinone and azobenzene in medium of 0.1 mol L-1 H2SO4 plus 0.1 mol L-1 K2SO4, pH = 1. Hydrogen peroxide generation proved strongly dependent on the applied potential and on the concentration of added catalysts. Electrode modifications led to a significant increase in H2O2 yield (30%) reaching 850 mg L-1, and the overpotential for oxygen reduction shifted to less negative values (400 mV vs Ag/AgCl for electrodes modified by quinones and 300 mV vs Ag/AgCl for electrodes modified by azobenzene) compared to noncatalyzed gas diffusion electrodes, resulting in reduced energy consumption of 596.5 to 232.4 kWh kg-1. The results indicated that the best electrode for H2O2 electrogeneration is the gas diffusion electrode modified with 10% of 2-ethylanthraquinone, offering the best cost to benefit ratio.Este trabalho apresenta um estudo comparativo da eficiência eletroquímica na eletrogeração de peróxido de hidrogênio in situ usando eletrodos da difusão gasosa modificados com os catalisadores orgânicos redox: 2-etilantraquinona, 2-terc-butilantraquinona e azobenzeno em meio de 0,1 mol L-1 H2SO4 + 0,1 mol L-1 K2SO4, pH = 1. A produção de peróxido de hidrogênio está diretamente relacionada ao potencial aplicado e a concentração dos catalisadores adicionados. A modificação dos eletrodos resultou em um aumento significativo no rendimento de H2O2 (30%) alcançando 850 mg L-1 e o sobrepotencial da reação de redução do oxigênio foi deslocado para valores menos negativos (400 mV vs Ag/AgCl para os eletrodos modificados com quinonas e 300 mV vs. Ag/AgCl para os eletrodos modificados com azobenzeno) comparado ao eletrodo de difusão gasosa não modificado, reduzindo o consumo de energia de 596,5 para 232,4 kWh kg-1. Os resultados indicaram que o melhor eletrodo para a eletrogeração do H2O2 é o eletrodo de difusão gasosa modificado com 10% de 2-etilantraquinona, o qual apresentou a melhor relação custo/benefício.643650Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP

Polymerizable deep eutectic solvents: Convenient reactive dispersion media for the preparation of novel multi-walled carbon nanotubes-based functional materials

A new straightforward and green approach for the covalent functionalization of multi-walled carbon nanotubes (MWCNTs) was developed. This carbon nanostructure was efficiently derivatized by polymerizing proper deep eutectic monomers (DEM), a subclass of deep eutectic solvents (DES), based on a series of mono- and bis-vinyl imidazolium salts endowed with different functional groups (–OH, –NH2, –NH3+Br–) in the side chain or in the spacer. Herein, DEM systems played a triple role as convenient dispersion media for MWCNTs, efficient reactive systems, and also as structure-directing agents for the radical-initiated polymerization process onto the surface of MWCNTs. In addition, the new methodology allowed obtaining highly functionalized hybrid materials, as shown by thermogravimetric analyses, in short reaction times (<1h). Transmission electron microscopy (TEM) revealed that the polymeric network orderly develops along the surface of the nanotubes, which act as templating agent for both mono- and bis-vinyl imidazolium salts, despite the random nature of the polymerization process for the latter species. This new functionalization strategy of MWCNTs stands out for its environmentally friendly and time-saving nature leading to the formation of materials with significant potential for applications in a plethora of research fields. As a proof of their possible application, we tested these new hybrid materials as recoverable and recyclable catalysts for the conversion of CO2 into cyclic carbonates under solvent-free conditions, showing good catalytic performances, even in the absence of additional co-catalysts