Luca Artiglia

Activation energy paths for graphene nucleation and growth on Cu.

The synthesis of wafer-scale single crystal graphene remains a challenge toward the utilization of its intrinsic properties in electronics. Until now, the large-area chemical vapor deposition of graphene has yielded a polycrystalline material, where grain boundaries are detrimental to its electrical properties. Here, we study the physicochemical mechanisms underlying the nucleation and growth kinetics of graphene on copper, providing new insights necessary for the engineering synthesis of wafer-scale single crystals. Graphene arises from the crystallization of a supersaturated fraction of carbon-adatom species, and its nucleation density is the result of competition between the mobility of the carbon-adatom species and their desorption rate. As the energetics of these phenomena varies with temperature, the nucleation activation energies can span over a wide range (1-3 eV) leading to a rational prediction of the individual nuclei size and density distribution. The growth-limiting step was found to be the attachment of carbon-adatom species to the graphene edges, which was independent of the Cu crystalline orientation.

Partially oxidized graphene as a precursor to graphene

Solution exfoliation of graphite holds promise for large-scale bulk synthesis of graphene. Non-covalent exfoliation is attractive because the electronic structure of graphene is preserved but the yield is low and the lateral dimensions of the sheets are small. Chemical exfoliation via formation of graphite oxide is a highly versatile and scalable route but the covalent functionalization of graphene with oxygen significantly alters the properties. Here, we report a new method for large-scale facile synthesis of micron-sized partially oxidized graphene (POG) sheets with dramatically improved electronic properties compared to other solution-phase exfoliated graphene. Due to low initial oxygen content (∼12%), POG requires only mild annealing (<300 °C) to achieve a sheet resistance of 28 kΩ sq−1 at the neutrality point, only a factor of ∼4 larger than the intrinsic sheet resistance of pristine graphene (∼6 kΩ sq−1) and substantially lower than graphene exfoliated by other methods. Such a partial oxidation approach opens up new promising routes to solution based high-performance, low temperature, transparent and conducting graphene-based flexible electronics.

TiO2@CeOx core-shell nanoparticles as artificial enzymes with peroxidase-like activity.

The Ce4+↔Ce3+ redox switch is at the basis of an all-inorganic catalytic cycle that is capable of mimicking the activity of several natural redox enzymes. The efficiency of these artificial enzymes (nanozymes) strongly depends on the Ce4+/Ce3+ ratio. By capitalizing on the results obtained on oxide/oxide model systems, we implemented a simple and effective procedure to obtain conformal TiO2@CeOx core-shell nanoparticles whose thickness is controlled with single-layer precision. Since the Ce3+ species are stabilized only at the interface by the electronic hybridization with the TiO2 states, the modulation of the shell thickness offers a simple method to tailor the Ce4+/Ce3+ ratio and therefore the catalytic properties. The activity of these nanoparticles as artificial peroxidase-like enzymes was tested, showing exceptional performances, even better than natural horseradish peroxidase enzyme. The main advantage with respect to other oxide/oxide nanozymes is that our nanoparticles, having a tunable Ce4+/Ce3+ ratio, are efficient already at low H2O2 concentrations.

Atomic Structure and Special Reactivity Toward Methanol Oxidation of Vanadia Nanoclusters on TiO2(110)

We have grown highly controlled VOx nanoclusters on rutile TiO2(110). The combination of photoemission and photoelectron diffraction techniques based on synchrotron radiation with DFT calculations has allowed identifying these nanostructures as exotic V4O6 nanoclusters, which hold vanadyl groups, even if vanadium oxidation state is formally +3. Our theoretical investigation also indicates that on the surface of titania, vanadia mononuclear species, with oxidation states ranging from +2 to +4, can be strongly stabilized by aggregation into tetramers that are characterized by a charge transfer to the titania substrate and a consequent decrease of the electron density in the vanadium 3d levels. We then performed temperature programmed desorption experiments using methanol as probe molecule to understand the impact of these unusual electronic and structural properties on the chemical reactivity, obtaining that the V4O6 nanoclusters can selectively convert methanol to formaldehyde at an unprecedented low temperature (300 K).

Towards an improved process for hydrogen production: the chemical-loop reforming of ethanol

M-modified ferrospinels with the formula M0.6Fe2.4Oy (M = Co, Mn or Co/Mn) were employed as ionic oxygen and electron carrier materials for an alternative sustainable route to produce hydrogen via chemical-loop reforming of ethanol. The new materials were tested in terms of both redox properties and catalytic activity to generate hydrogen by oxidation with steam, after a reductive step carried out with ethanol. In addition, the research includes in situ DRIFTS and in situ XPS studies that allowed the extraction of information at the molecular level and following surface changes within the reduction/re-oxidation processes during ethanol chemical-loop reforming. It was found that Co(II)-incorporation in spinels effectively improves decomposition/oxidation of ethanol, however a greater amount of coke is accumulated. On the other hand, addition of Mn(II) into the system helps to significantly reduce the amount of coke and hence to avoid fast deactivation of the material. Thus, the behavior of Co0.3Mn0.3Fe2.4Oy was shown to be the most promising one, as this material forms less coke during the reduction step, and consequently less COx is generated during the re-oxidation step with water, nevertheless a high hydrogen yield is maintained.

Xylene sensing properties of aryl-bridged polysilsesquioxane thin films coupled to gold nanoparticles

Surface plasmon resonance gas sensors based on organic–inorganic hybrid thin films coupled to gold nanoparticles were fabricated and tested against the detection of xylene at the concentration of 30 ppm. Such nanocomposites are prepared either by dispersing Au nanoparticles inside an aryl-bridged polysilsesquioxane system, synthesized via a sol–gel process, or by depositing an aryl-bridged polysilsesquioxane film on Au nanoparticle sub-monolayers. Ultra-high-vacuum temperature programmed desorption of xylene on both the aryl-bridged polysilsesquioxane films and the nanocomposite Au/hybrid system was investigated, resulting in an interaction energy between the sensitive film and the gas molecules in the 38–139 kJ mol−1 range. The functional activity of the nanostructured composites as xylene gas optical sensors was tested monitoring gold localized surface plasmon resonance, and was shown to be reversible. The detection sensitivity was calculated in 0.1 ppb through a calibration procedure in the 16–30 ppm range, and a threshold limit of detection of 265 ppb xylene was estimated as three standard deviations of the baseline noise. Typical response and regeneration times are of one min and about one ten of minutes, respectively.

Unraveling the Multiple Effects Originating the Increased Oxidative Photoactivity of {001}-Facet Enriched Anatase TiO2

Crystal shape control on a series of anatase photocatalysts was achieved by varying the amount of HF employed as a capping agent in their hydrothermal synthesis. A systematic comparison between their physicochemical properties, determined by several complementary surface and bulk techniques before and after thermal treatment at 500 °C, allowed one to discern the influence of the relative amount of exposed {001} crystal facets among a series of effects simultaneously affecting their oxidative photocatalytic activity. The results of both formic acid and terephthalic acid photo-oxidation test reactions point to the primary role played by calcination in making {001} facets effectively photoactive. Annealing not only removes most of the residual fluorine capping agent from the photocatalyst surface, thus favoring substrate adsorption, but also produces morphological modifications to a crystal packing that makes accessible a larger portion of surface {001} facets due to the unpiling of platelike crystals. The photocatalyst bearing the highest amount of exposed {001} facets (60%) shows the highest photoactivity in both the direct and the (•)OH-radical-mediated photocatalytic test reaction.

Au nanoparticles on a templating TiOx/Pt(111) ultrathin polar film: a photoemission and photoelectron diffraction study

We present an in-depth investigation of Au nanoparticles self-assembled on a zigzag-like TiO(x)/Pt(111) ultrathin polar film, whose structure is known in great detail. The peculiar pattern of defects (picoholes) templates a linear array of size-selected (ca. 1 nm) Au nanoparticles without disruption of the titania layer, as observed by scanning tunneling microscopy. Their structure and electronic properties have been investigated by several large-area spectroscopic tools, i.e. high-resolution core and valence level photoemission and angle-scanned and energy-scanned photoelectron diffraction. The comparison between experimental data and density functional theoretical calculations indicates that the Au atoms landing on the oxide film are rather mobile, and that the picoholes can act as effective trapping and nucleation centers for the growth of the Au nanoparticles. All the experimental results are in concord in indicating that the Au NPs are flat islands with a maximum thickness of 2-3 layers exposing the (111) surface.

Silver nanoprism arrays coupled to functional hybrid films for localized surface plasmon resonance-based detection of aromatic hydrocarbons.

We report the achievement of sensitive gas detection using periodic silver nanoprisms fabricated by a simple and low-cost lithographic technique. The presence of sharp tips combined with the periodic arrangement of the nanoprisms allowed the excitement of isolated and interacting localized surface plasmon resonances. Specific sensing capabilities with respect to aromatic hydrocarbons were achieved when the metal nanoprism arrays were coupled in the near field with functional hybrid films, providing a real-time, label-free, and reversible methodology. Ultra-high-vacuum temperature-programmed desorption measurements demonstrated an interaction energy between the sensitive film and analytes in the range of 55-71 kJ/mol. The far-field optical properties and the detection sensitivity of the sensors, modeled using a finite element method, were correlated to experimental data from gas sensing tests. An absorbance variation of 1.2% could be observed and associated with a theoretical increase in the functional film refractive index of ∼0.001, as a consequence to the interaction with 30 ppm xylene. The possibility of detecting such a small variation in the refractive index suggests the highly promising sensing capabilities of the presented technique.

Introducing Time Resolution to Detect Ce3+ Catalytically Active Sites at the Pt/CeO2 Interface through Ambient Pressure X-ray Photoelectron Spectroscopy

X-ray photoelectron spectroscopy has been employed for the qualitative and quantitative characterization of both model and real catalytic surfaces. Recent progress in the detection of photoelectrons has enabled the acquisition of spectra at pressures up to a few tens of millibars. Although reducing the pressure gap represents a remarkable advantage for catalysis, active sites may be short-lived or hidden in the majority of spectator species. Time-resolved experiments, conducted under transient conditions, are a suitable strategy for discriminating between active sites and spectators. In the present work, we characterized the surface of a Pt/CeO2 powder catalyst at 1.0 mbar of a reacting mixture of carbon monoxide and oxygen and, by means of time resolution, identified short-lived active species. We replaced oxygen with nitrogen in the reaction mixture while fast-detecting the core level peaks of cerium. The results indicate that active Ce3+ sites form transiently at the surface when the oxygen is switched off. Analysis of the depth profile shows that Ce3+ ions are located at the ceria surface. The same experiment, performed on platinum-free ceria, reveals negligible reduction, indicating that platinum boosts the formation of Ce3+ active sites at the interface.