Electro-optical interfacial effects on a graphene/?-conjugated organic semiconductor hybrid system.

The influence of graphene and retinoic acid (RA) ? a ?-conjugated organic semiconductor ? interface on their hybrid system is investigated. The physical properties of the interface are assessed via scanning probe microscopy, optical spectroscopy (photoluminescence and Raman) and ab initio calculations. The graphene/RA interaction induces the formation of a well-organized ?-conjugated self-assembled monolayer (SAM) at the interface. Such structural organization leads to the high optical emission efficiency of the RA SAM, even at room temperature. Additionally, photo-assisted electrical force microscopy, photo-assisted scanning Kelvin probe microscopy and Raman spectroscopy indicate a RA-induced graphene doping and photo-charge generation. Finally, the optical excitation of the RA monolayer generates surface potential changes on the hybrid system. In summary, interface-induced organized structures atop 2D materials may have an important impact on both design and operation of ?-conjugated nanomaterialbased hybrid systems

Raman evidence for pressure-induced formation of diamondene.

Despite the advanced stage of diamond thin-film technology, with applications ranging from superconductivity to biosensing, the realization of a stable and atomically thick two-dimensional diamond material, named here as diamondene, is still forthcoming. Adding to the outstanding properties of its bulk and thin-film counterparts, diamondene is predicted to be a ferromagnetic semiconductor with spin polarized bands. Here, we provide spectroscopic evidence for the formation of diamondene by performing Raman spectroscopy of double-layer graphene under high pressure. The results are explained in terms of a breakdown in the Kohn anomaly associated with the finite size of the remaining graphene sites surrounded by the diamondene matrix. Ab initio calculations and molecular dynamics simulations are employed to clarify the mechanism of diamondene formation, which requires two or more layers of graphene subjected to high pressures in the presence of specific chemical groups such as hydroxyl groups or hydrogens

Gypsum : an environment-friendly, inexpensive and robust height calibration standard at nanometer-scale for atomic force microscopy.

Gypsum is an Earth-abundant mineral with enormous applications in agriculture and civil engineering. Here, we show it is also an excellent height calibration standard alternative for atomic force microscopy (AFM). Using plain water as etchant, gypsum flakes readily review 0.75 nm tall terraces which are easy to image (lateral dimensions from tens to hundreds of nanometers) and robust against time in ambient conditions. Therefore, the present work demonstrates a new height standard alternative which is easily-available for all AFM microscopists around the world

Corrosion, wear and wear–corrosion behavior of graphite-like a-C:H films deposited on bare and nitrided titanium alloy.

This work presents a comparative wear, corrosion and wear–corrosion (the last one in a simulated physiological solution) study of graphite-like a-C:H (GLCH) films deposited on bare and nitrided Ti6Al4V alloy. Films, deposited by r.f. PACVD, presented low porosity and promoted high corrosion resistance. The friction coefficient of the films was very lowwith appreciablewear resistance at roomconditions. However, due to the simultaneous action of both load and the corrosive environment in wear–corrosion tests a marked reduction in the coating lifetime was observed. Unexpectedly, films deposited on the nitrided alloy presented a lifetime at least ten times shorter than that of films on bare alloy. We explain such a result in terms of film/substrate interaction. The weak GLCH/nitride alloy interaction facilitates fluid penetration between the film and the substratewhich leads to a fast film delamination. Such an interpretation is supported by force curve measurements, which show that the interaction between GLCH and nitrided alloy is four times weaker than that between GLCH and bare alloy

Characterization of metal oxide-based gas nanosensors and microsensors fabricated via local anodic oxidation using atomic force microscopy

Thiswork reports on nanoscale and microscalemetal oxide gas sensors, consisting ofmetal-semiconductor-metal barriers designed via scanning probe microscopy. Two distinctmetal oxides, molybdenum and titaniumoxides, were tested at different temperatures using CO2 and H2 as test gases. Sensitivities down to ppm levels are demonstrated, and the influence of dry and humid working atmospheres on these metal oxide conductivities was studied. Furthermore, the activation energy was evaluated and analyzed within working sensor temperature range. Finally, full morphological, chemical, and structural analyses of the oxides composites are provided allowing their identification as MoO3 and TiO2−x

Mapping the local dielectric constant of a biological nanostructured system

The aim of this work is to determine the varying dielectric constant of a biological nanostructured system via electrostatic force microscopy (EFM) and to show how this method is useful to study natural photonic crystals. We mapped the dielectric constant of the cross section of the posterior wing of the damselfly Chalcopteryx rutilans with nanometric resolution. We obtained structural information on its constitutive nanolayers and the absolute values of their dielectric constant. By relating the measured profile of the static dielectric constant to the profile of the refractive index in the visible range, combined with optical reflectance measurements and simulation, we were able to describe the origin of the strongly iridescent wing colors of this Amazonian rainforest damselfly. The method we demonstrate here should be useful for the study of other biological nanostructured systems

Study of controlled release of PMMA-g-PEG copolymer and derivatives incorporated with the indomethacin drug.

Synthetic polymers are made up of repeated monomeric units, and this gives them a very versatile appearance, making them useful in many areas of science. One is the pharmaceutical, which correlates the properties of the polymer with the active principle, so they can be used as an excipient or in the controlled release system. The PMMA?g?PEG4000 has characteristics derived from its precursors, that are pharmacologically active. When we incorporate drugs into this structure, the polymer can act on the controlled release, lessening the toxic character of the drug and producing fewer side effects. In this work, incorporations of the drug indomethacin were made in the PMMA?g?PEG copolymer and derivatives (PMMA?g?PEG4000 ETIL and PMMA?g?PEG4000 ACET). The samples were characterized by infrared spectroscopy (FTIR), Scanning Electron Microscopy (SEM), thermogravimetric analysis (TGA), and atomic force microscopy (AFM) measurements. For each sample, the controlled release was performed in a total time of 4?h and the efficiency of the modified structures was verified

Universal deformation pathways and flexural hardening of nanoscale 2D-material standing folds.

In the present work, we use atomic force microscopy nanomanipulation of 2D-material standing folds to investigate their mechanical deformation. Using graphene, h-BN and talc nanoscale wrinkles as testbeds, universal force?strain pathways are clearly uncovered and well-accounted for by an analytical model. Such universality further enables the investigation of each fold bending stiffness ? as a function of its characteristic height h 0. We observe a more than tenfold increase of ? as h 0 increases in the 10?100 nm range, with power-law behaviors of ? versus h 0 with exponents larger than unity for the three materials. This implies anomalous scaling of the mechanical responses of nano-objects made from these materials

Charge transfer between carbon nanotubes on surfaces.

The charge transfer between neighboring single-walled carbon nanotubes (SWNTs) on a silicon oxide surface was investigated as a function of both the SWNT nature (metallic or semiconducting) and the anode/cathode distance using scanning probe techniques. Two main mechanisms were observed: a direct electron tunneling described by the typical Fowler?Nordheim model, and indirect electron transfer (hopping) mediated by functional groups on the supporting surface. Both mechanisms depend on the SWNT nature and on the anode/cathode separation: direct electron tunneling dominates the charge transfer process for metallic SWNTs, especially for large distances, while both mechanisms compete with each other for semiconducting SWNTs, prevailing one over the other depending on the anode/cathode separation. These mechanisms may significantly influence the design and operation of SWNT-based electronic devices