Targeting the Antifungal Activity of Carbon Dots against Candida albicans Biofilm Formation by Tailoring Their Surface Functional Groups.

Carbon dots (CDs) are an emerging class of carbon nanoparticles, which for their characteristics have found applications in many fields such as catalysis, materials and biomedicine. Within this context, the application of CDs as antibacterial agents has received much attention in very recent years, while their use as antifungal nanoparticles has been scarcely investigated. Here we report a systematic investigation of the surface functional groups of CDs to study their influence on these nanoparticles' against Candida albicans. Three classes of CDs have been synthesised and fully characterized. A thorough in vitro and in vivo biological screening against C. albicans was performed to test their antifungal, antiadhesion and antibiofilm formation activities. Moreover, the interaction with C. albicans cells was investigated by microscopic analysis. Our results evidence how the presence of a positively polarised surface results crucial for the internalization into COS-7 cells. Positively charged nanoparticles were also able to inhibit adhesion and biofilm formation, to interact with the cellular membrane of C. albicans, and to increase the survival of G. mellonella infected larvae after the injection with positive nanoparticles. The antifungal activity of CDs and their extremely low toxicity may represent a new strategy to combat infections sustained by C.albicans.

Decomposition of Deep Eutectic Solvent Aids Metals Extraction in Lithium-Ion Batteries Recycling.

The application of deep eutectic solvents (DESs) to dissolve metal oxides in lithium-ion batteries (LIBs) recycling represents a green technological alternative to the mineral acids employed in hydrometallurgical recycling processes. However, DESs are much more expensive than mineral acids and must be reused to ensure economic feasibility of LIB recycling. To evaluate DES reusability, the role of the choline chloride-ethylene glycol DES decomposition products on metal oxides dissolution was investigated. The temperatures generally applied to carry on this DES leaching induced the formation of decomposition products that ultimately improved the ability to dissolve LIB metal oxides. The characterization of DES decomposition products revealed that the improved metal dissolution was mainly determined by the formation of Cl3 - , which was proposed to play a pivotal role in the oxidative dissolution of LIB metal oxides.

Molecular and electronic properties transferred to Silicon via wet-chemistry surface nanofunctionalization: ethynylferrocene on Si(100).

In the frame of our research activity on covalent anchoring of functional molecules on Si oriented surfaces, we report here on the hybrid species resulting from the reaction of ethynylferrocene with H-Si(100) either in a single, direct step, or after production of a self-assembled alpha,omega-bifunctional alkyl monolayer. In the former approach, a short Si-C covalent bond is established through visible-light activation of the unsaturated side arm of ethynylferrocene via an extra-mild approach. In the latter case, an azide-alkyne Huisgen cycloaddition reaction ("click" chemistry) is induced between the C[triple bond]C group of the molecule and the -N3 terminations of undecyl hydrocarbon chains pre-assembled onto H-Si(100). These two routes lead to electroactive monolayers wherein the ferrocene head groups are respectively located close to or far from the Si surface. This allows for a fine tuning of the properties of the resulting hybrids on Si, in terms of distinct redox potentials, electron transfer rate constants, oxidation resistance. The different reaction steps have been monitored with X-ray Photoelectron Spectroscopy (XPS), in order to evaluate the presence and the chemical nature of the anchored species, while electrochemical measurements have evidenced reversible redox responses of the resulting SAMs.