In recent years there has been a growing interest in sp-carbon chains as possible novel nanostructures. An example of sp-carbon chains are the so-called polyynes, characterized by the alternation of...
Ag(4)O(4) (i.e. silver(I)-silver(III) oxide) thin films with tailored structure and morphology at the nanoscale have been grown by reactive pulsed laser deposition (PLD) in an oxygen-containing atmosphere and they are shown to exhibit a very strong antibacterial activity towards Gram-negative bacteria (E. coli) and to completely inhibit the growth of Gram-positive bacteria (S. aureus). The formation of this particular high-valence silver oxide is explained in terms of the reactions occurring during the expansion of the ablated species in the reactive atmosphere, leading to the formation of low-stability Ag-O dimers and atomic oxygen, providing reactive species at the substrate where the film grows. PLD is shown to allow control of the structure (i.e. crystallinity and grain size) and of the morphology of the films, from compact and columnar to foam-like, thus allowing the deposition of nanocrystalline films with increased porosity and surface area. The antibacterial action towards E. coli is demonstrated and is shown to be superior to that of nanostructured Ag-based medical products. This can be related to the release of Ag ions with high oxidation number, which are known to be very reactive towards bacteria, and to the peculiar morphology at the nanoscale resulting in a large effective surface area.
sp-Hybridized carbon atomic wires are appealing systems with large property tunability. In particular, their electronic properties are intimately related to length, structure, and type of functional end-groups as well as to other effects such as the intermolecular charge transfer with metal nanoparticles. Here, by a combined Raman, Surface Enhanced Raman Scattering (SERS) investigation and first principles calculations of different N,N-dimethylanilino-terminated polyynes, we suggest that, upon charge transfer interaction with silver nanoparticles, the function of sp-carbon atomic wire can change from electron donor to electron acceptor by increasing the wire length. In addition, the insertion into the wire of a strong electrophilic group (1,1,4,4-tetracyanobuta-1,3-diene-2,3-diyl) changes the electron-accepting molecular regions involved in this intermolecular charge transfer. Our results indicate that carbon atomic wires could display a tunable charge transfer between the sp-wire and the metal, and hold promise as active materials in organic optoelectronics and photovoltaics.
In this work, we describe self-assembled surfaces with a peculiar multiscale organization, from the nanoscale to the microscale, exhibiting the Cassie-Baxter wetting regime with extremely low water adhesion: floating drops regime with roll-off angles < 5°. These surfaces comprise bundles of hierarchical, quasi-one-dimensional (1D) TiO2 nanostructures functionalized with a fluorinated molecule (PFNA). While the hierarchical nanostructures are the result of a gas-phase self-assembly process, their bundles are the result of the capillary forces acting between them when the PFNA solvent evaporates. Nanometric features are found to influence the hydrophobic behavior of the surface, which is enhanced by the micrometric structures up to the achievement of the superhydrophobic Cassie-Baxter state (contact angle (CA) ≫ 150°). Thanks to their high total and diffuse transmittance and their self-cleaning properties, these surfaces could be interesting for several applications such as smart windows and photovoltaics where light management and surface cleanliness play a crucial role. Moreover, the multiscale analysis performed in this work contributes to the understanding of the basic mechanisms behind extreme wetting behaviors.
Polyynes, linear sp-carbon chains of finite length, can be synthesised by submerged arc discharge in liquid, which so far, has been mainly exploited in organic solvents.In this work, we investigated the technique in water as a cheap and non-toxic solvent to produce polyynes. After optimisation of the process parameters, hydrogen-terminated polyynes (CnH2: n=6-16) were identified by high-performance liquid chromatography with the support of theoretical calculations. Size-selected polyynes were separately analysed by surface-enhanced Raman spectroscopy allowing to assign the bands of mixed polyynes solution to specific wire lengths. Stabilisation strategies for hydrogen-capped polyynes were also studied, obtaining promising results.
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