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Sepiolite clay is a natural filler particularly suitable to be used with polysaccharide matrices (e.g., in starch-based bio-nanocomposites), increasing their attractiveness for a wide range of applications, such as packaging. Herein, the effect of the processing (i.e., starch gelatinization, addition of glycerol as plasticizer, casting to obtain films) and of the sepiolite filler amount on the microstructure of starch-based nanocomposites was investigated by SS-NMR (solid-state nuclear magnetic resonance), XRD (X-ray diffraction) and FTIR (Fourier-transform infrared) spectroscopy. Morphology, transparency and thermal stability were then assessed by SEM (scanning electron microscope), TGA (thermogravimetric analysis) and UV–visible spectroscopy. It was demonstrated that the processing method allowed to disrupt the rigid lattice structure of semicrystalline starch and thus obtain amorphous flexible films, with high transparency and good thermal resistance. Moreover, the microstructure of the bio-nanocomposites was found to intrinsically depend on complex interactions among sepiolite, glycerol and starch chains, which are also supposed to affect the final properties of the starch–sepiolite composite materials.

The incorporation of silica nanoparticles (Si-NPs) into the polymer matrix is a growing area of interest research to produce high-performance polymer nanocomposites (NCs) across a wide range of nanotechnology applications. This improvement is due to the Si-NPs capability to self-assembly giving rise to specific well-organized structures with both short- and long-range order across a hierarchy of spatial scales, determined by both NP-NP and NP-matrix interactions, involving a careful balance among attractive driving forces, repulsive forces, and directional forces. Respect to this, the aim of the present paper is to systematically review the use of Si-NPs in polymer NCs and on the role of NPs self-assembly in determining the final material properties. Firstly, we explored the synthesis and modification of both isotropic and anisotropic Si-NPs in relation with use in NC materials, focusing on NPs dispersion and distribution, as well as on the functionalization strategies of Si-NPs. Besides Si-NPs functionalization with conventional small organic molecules, a large section is devoted to an emerging class of functionalized Si-NPs with macromolecules, namely silica hairy NPs (Si-HNPs), able to give rise a rich variety of complex assemblies and materials with new structures and functionalities. Successively, NCs materials containing Si-NPs and Si-HNPs have been explored in terms of synthetic preparation and properties. The self-organization of Si-NPs and Si-HNPs in polymer matrices has been reported and its effect on the functional materials properties have been evaluated with a critical point of view on the results, limits, and future perspectives. Our review can be considered a tutorial work, aiming at providing useful insights to researchers in the field of nanotechnology and nanoscience, taking into consideration the fundamental role of NPs self-assembly processes in determining the functional material properties.

The interaction between activators (ZnO) and co-activators (stearic acid, SA) represents a key step in the vulcanization process, to generate Zn(II) intermediate complexes that enhance the reaction kinetic and promote the shortening of sulfur bridges, leading to highly cross-linked materials. To understand the influence of the structural, morphological and surface properties of ZnO in the reactivity with SA, in this work, pure ZnO nanoparticles (NPs) and ZnO NPs anchored on SiO2 (ZnO/SiO2) were prepared through soft chemistry techniques. Tailoring of morphology and surface features was accomplished through a fine control of the synthetic parameters, as demonstrated by the careful characterization of the activators. Then, the interaction of pure ZnO and ZnO/SiO2 activators with SA in the absence of rubber was investigated by using Differential Scanning Calorimetry (DSC). The occurrence of Zn(II)-SA complexes with different thermal stability and structural properties was assessed by a comprehensive thermogravimetric and spectroscopic survey. The generation and the chemical structure of these specific vulcanization intermediates was related to the peculiar characteristics of the ZnO/SiO2 systems and, in turn, to their ability in imparting faster kinetics and higher curing efficiency to isoprene rubber nanocomposites, compared to bare ZnO. These results, besides proposing a valid benchmark for achieving further insights on the interaction of stearic acid with activators, pave the way to provide specific protocols for a better design and implementation of ZnO-based materials able to effectively enhance the rubber vulcanization process, with significant economic and environmental advantages.

I nanocompositi di gomma mostrano generalmente una scarsa conduttività termica, che può essere parzialmente migliorata dall'aggiunta di riempitivi termicamente conduttivi, ad esempio grafite, nerofumo, fibre di carbonio, particelle di ceramica o di metallo. Per raggiungere questo obiettivo sono in genere necessari concentrazioni di riempimento elevate; tuttavia, ciò altera notevolmente il comportamento meccanico e la densità di reticolazione dei materiali finali. Inoltre, i sistemi di riempimento attualmente impiegati non sono in grado di soddisfare contemporaneamente i requisiti chiave di elevata conducibilità termica e prestazioni meccaniche. In questo contesto, l'attività di ricerca del dottorato mira a progettare nuovi riempitivi adatti allo sviluppo di nanocompositi di gomma con elevata conducibilità termica e prestazioni meccaniche soddisfacenti. Sarà condotta un'indagine su diversi nano-riempitivi termicamente conduttivi, studiando in profondità le correlazioni tra struttura, morfologia, dispersione e distribuzione delle nanoparticelle nella matrice polimerica e proprietà finali dei compositi. Le migliori formulazioni verranno selezionate ed eventualmente scalate al fine di fornire reali applicazioni tecnologiche., Rubber nanocomposites generally exhibit poor thermal conductivity, which has been partially enhanced by the addition of thermally conductive fillers, i.e. graphite, carbon black, carbon fibres, ceramic or metal particles. High filler loadings are typically necessary to achieve this target; however, this dramatically alters the mechanical behaviour and the cross-linking density of the final materials. Further, the filler systems currently employed are not able to fulfil the key requirements of high thermal conductivity and remarkable performances, simultaneously. In this context, the PhD research activity aims at design novel fillers suitable for developing rubber nanocomposites with high thermal conductivity and satisfactory mechanical performances. A survey of different conductive nanofillers will be carried out, by investigating in depth the correlations between nanoparticles structure, morphology, dispersion and distribution in the polymer matrix, and final composites properties. The best formulations will be selected and possibly up-scaled in order to provide real technological applications.

The occurrence of uncontrolled electrostatic discharge (ESD) is among the major causes of damage in unprotected electronic components during industrial processes. To counteract this undesired phenomenon, ESD composites showing static-dissipative and antistatic responses are developed. In particular, static-dissipative materials are able to slow down the flow of electric charges, whereas antistatic materials directly suppress the initial charges induced by undesired charging by properly dispersing conductive fillers within an insulant matrix and thus forming a conductive filler network. In this context, the purpose of this review is to provide a useful resume of the main fundamentals of the technology necessary for facing electrostatic charging. The formation mechanisms of electrostatic charges at the material surface were described, providing a classification of ESD composites and useful characterization methods. Furthermore, we reported a deep analysis of the role of conductive fillers in the formation of filler networks to allow electric charge movements, along with an overview of the different classes of inorganic conductive fillers exploitable in ESD composites, evidencing pros/cons and criticalities of each category of inorganic fillers.

The present study reports on the synthesis of a new alkoxysilane-bearing light-responsive cinnamyl group and its application as a surface functionalization agent for the development of SiO2 nanoparticles (NPs) with photoreversible tails. In detail, cinnamic acid (CINN) was activated with N-hydroxysuccinimide (NHS) to obtain the corresponding NHS-ester (CINN-NHS). Subsequently, the amine group of 3-aminopropyltriethoxysilane (APTES) was acylated with CINN-NHS leading to the generation of a novel organosilane, CINN-APTES, which was then exploited for decorating SiO2 NPs. The covalent bond to the silica surface was confirmed by solid state NMR, whereas thermogravimetric analysis unveiled a functionalization degree much higher compared to that achieved by a conventional double-step post-grafting procedure. In light of these intriguing results, the strategy was successfully extended to naturally occurring sepiolite fibers, widely employed as fillers in technological applications. Finally, a preliminary proof of concept of the photoreversibility of the obtained SiO2@CINN-APTES system has been carried out through UV diffuse reflectance. The overall outcomes prove the consistency and the versatility of the methodological protocol adopted, which appears promising for the design of hybrid NPs to be employed as building blocks for photoresponsive materials with the ability to change their molecular structure and subsequent properties when exposed to different light stimuli.

The development of hybrid nanoscintillators is hunted for the implementation of modern detection technologies, like in high energy physics, homeland security, radioactive gas sensing, and medical imaging, as well as of the established therapies in radiation oncology, such as in X-ray activated photodynamic therapy. Engineering of the physico-chemical properties of nanoparticles (NPs) enables the manufacture of hybrids in which the conjugation of inorganic/organic components leads to increased multifunctionality and performance. However, the optimization of the properties of nanoparticles in combination with the use of ionizing radiation is not trivial: a complete knowledge on the structure, composition, physico-chemical features, and scintillation property relationships in hybrid nanomaterials is pivotal for any applications exploiting X-rays. In this paper, the design of hybrid nanoscintillators based on ZnO grown onto porous SiO2 substrates (ZnO/SiO2) has been performed in the view to create nanosystems potentially suitable in X-ray activated photodynamic therapy. Indeed, cytotoxic porphyrin dyes with increasing concentrations have been anchored on ZnO/SiO2 nanoparticles through amino-silane moieties. Chemical and structural analyses correlated with photoluminescence reveal that radiative energy transfer between ZnO and porphyrins is the principal mechanism prompting the excitation of photosensitizers. The use of soft X-ray excitation results in a further sensitization of the porphyrin emission, due to augmented energy deposition promoted by ZnO in the surroundings of the chemically bound porphyrin. This finding unveils the cruciality of the design of hybrid nanoparticles in ruling the efficacy of the interaction between ionizing radiation and inorganic/organic moieties, and thus of the final nanomaterial performances towards the foreseen application.

Lithium metal batteries (LMBs) will be a breakthrough in automotive applications, but they require the development of next-generation solid-state electrolytes (SSEs) to stabilize the anode interface. Polymer-in-ceramic PEO/TiO2 nanocomposite SSEs show outstanding properties, allowing unprecedented LMBs durability and self-healing capabilities. However, the mechanism underlying the inhibition/delay of dendrite growth is not well understood. In fact, the inorganic phase could act as both a chemical and a mechanical barrier to dendrite propagation. Combining advanced in situ and ex situ experimental techniques, we demonstrate that oligo(ethylene oxide)-capped TiO2, although chemically inert toward lithium metal, imparts SSE with mechanical and dynamical properties particularly favorable for application. The self-healing characteristics are due to the interplay between mechanical robustness and high local polymer mobility which promotes the disruption of the electric continuity of the lithium dendrites (razor effect).

The coupling of ZnO-based nanomaterials with organic photosensitizers (PS) is potentially interesting for cancer treatment under X-ray. In these conditions, ZnO nanoparticles (NPs) convert the X-ray into UV-Vis emission, promoting the PS excitation and producing reactive oxygen species (ROS). Main advantages for in vivo applications are ZnO photostability and biocompatibility, even if its efficient coupling with different PS (typically porphyrin) is still a controversial issue, as both a high ZnO luminescence yield and a good overlapping of ZnO emission-PS absorption spectra are necessary, along with a suitable energy transfer between ZnO and PS. In this perspective, the aim is the investigation of the optical properties of an ad-hoc system composed of porphyrin functionalized ZnO NPs anchored on SiO2 NPs (ZnO/SiO2). The goal is the understanding of the optimal conditions for a good energy transfer efficiency of ZnO-porphyrin structures, including the role of ZnO-PS proximity, to promote their application in anti-cancer therapies and imaging with ionizing radiations. First, amorphous ZnO NPs of 5-6 nm were anchored onto SiO2 NPs (~80 nm); then, ZnO/SiO2 was functionalized with different porphyrin contents (tetrakis(4-carboxyphenyl)porphyrin, TCPP, 0.3 – 3.0 wt%) by exploiting a silane grafting agent (3-aminopropyl)triethoxysilane. The structural characterization demonstrated that increasing TCPP amounts were bonded to SiO2 depending on the TCPP loading. The optical properties were preliminary tested in dimethylformamide, used as solvent reaction for TCPP anchoring on SiO2. The Photoluminescence Analysis (PL) revealed a high luminescence of ZnO NPs and the occurrence of a radiative energy transfer between ZnO and TCPP, that was not visible in a mechanical mixing of ZnO and TCCP, highlighting their optical interaction upon functionalization. Besides, TCPP emission was hugely enhanced under X-ray in the Radioluminescence (RL), whereas no enhancement was detectable in t

Composite materials based on hybrid filler systems can be a promising approach to produce advanced rubber nanocomposites (NCs). Recently, the positive effect of the combined use of silica and sepiolite on NCs mechanical properties has been reported, compared to those of compounds reinforced with the same amount of the only silica filler. In this context, the present work aims at studying the possible synergistic self-assembly of nanosilica and sepiolite in the generation of a cooperative hybrid filler network in rubber-based NCs, in connection with material performance for tires application. In detail, the influence of the introduction of a secondary anisotropic filler in conjunction with isotropic nanosilica on their dispersion and interaction with the rubber matrix has been comprehensively investigated, in order to define the best formulation ensuring low rolling resistance and significant fuel saving. NCs, containing simultaneously silica and sepiolite, either pristine (Sep) or chemically modified (mSep) by an acid treatment, were prepared by combining latex compounding technique (LCT) and melt blending. Rheological and dynamic-mechanical analyses highlighted that the use of a double white filler, constituted by particles with different aspect ratio, affords a good balance between efficient reinforcement and low Payne effect. Tansmission electron microscope (TEM) analysis evidenced the formation, within the rubber matrix, of cooperative superstructures due to the self-assembly of sepiolite and silica nanoparticles containing occluded rubber, when the secondary filler is mSep. The peculiar characteristics of mSep, characterized by fibers shorter than Sep and higher surface silanol bonding sites, bring about significant interactions between mSep and silica, which promote self-assembly of the two fillers in a collaborative hybrid network, improving dynamic-mechanical performances. These results, even if related to sepiolite/silica NCs, demonstrate the effective role