Structural colors have drawn wide attention for their potential as a future printing technology for various applications, ranging from biomimetic tissues to adaptive camouflage materials. However, an efficient approach to realize robust colors with a scalable fabrication technique is still lacking, hampering the realization of practical applications with this platform. Here, we develop a new approach based on large-scale network metamaterials that combine dealloyed subwavelength structures at the nanoscale with lossless, ultra-thin dielectric coatings. By using theory and experiments, we show how subwavelength dielectric coatings control a mechanism of resonant light coupling with epsilon-near-zero regions generated in the metallic network, generating the formation of saturated structural colors that cover a wide portion of the spectrum. Ellipsometry measurements support the efficient observation of these colors, even at angles of 70°. The network-like architecture of these nanomaterials allows for high mechanical resistance, which is quantified in a series of nano-scratch tests. With such remarkable properties, these metastructures represent a robust design technology for real-world, large-scale commercial applications.

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Surfaces with water contact angles above 150° are regarded as superhydrophobic. In this study the use of atmospheric pressure plasma jet system called PlasmaStreamTM to deposit superhydrophobic coatings is investigated. The coatings were deposited from the following liquid precursors: hexamethyldisiloxane (HMDSO), tetramethyl cyclotetrasiloxane (Tomcats) and a mixture of Tomcats and fluorosiloxane. The objective of the study is to investigate how precursor type and deposition conditions, influences the morphology and mechanical performance of the deposited superhydrophobic coatings. Optical profilometry, AFM, SEM, Ellipsometry, XPS, Water contact angle and FTIR techniques were used to evaluate the surface roughness, morphology, thickness and chemical functionality of the deposited coatings. The mechanical properties were evaluated using the Nano Tribometer, Nano Scratch, Ultra Nanoindentation and ultrasonic abrasion tests. Superhydrophobic coatings deposited from a precursor mixture of Tomcats and fluorosiloxane yielded a substantial enhancement in coating adhesion and mechanical durability compared to the superhydrophobic coatings obtained with either Tomcats or HMDSO precursors alone.

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In the last decades, the combination of high mechanical performances and low production costs increased the industrial interest on ductile cast irons. These grades are often used for applications where the fatigue resistance can be a critical issue (eg, machine frames for the wind‐power industry or crankshaft used in trucks) and the investigation of the main damaging mechanisms during both the crack initiation and the crack propagation stage could offer new perspectives about these alloys. Ductile cast irons can be considered as a natural composite, being characterized by graphite elements (nodules) embedded in a more or less ductile matrix (ranging from fully ferritic to pearlitic, from martensitic to austempered). In this work, the fatigue crack initiation mechanisms were investigated considering different matrix microstructure and the presence of a mechanical properties gradient in the graphite nodules.

Most advantages of organic electronic materials are enabled by mechanical deformability, as flexible (and stretchable) devices made from these materials must be able to withstand roll-to-roll printing and survive mechanical insults from the external environment. Cohesion and adhesion are two properties that dictate the mechanical reliability of a flexible organic electronic device. In this paper, progressive-load scratch tests are used for the first time to correlate the cohesive and adhesive behavior of poly(3-alkylthiophenes) (P3ATs) with respect to two molecular parameters: length of the alkyl side chain and molecular weight. In contrast to metrological techniques based on buckling or pull testing of pseudofreestanding films, scratch tests reveal information about both the cohesive and adhesive properties of thin polymeric films from a single procedure. Our data show a decrease in cohesion and adhesion, that is, a decrease in overall mechanical robustness, with increasing length of the side chain. This behavior is likely due to increases in free volume and concomitant decreases in the glass transition temperature. In contrast, we observe increases in both the cohesion and adhesion with increasing molecular weight. This behavior is attributed to an increased density of entanglements with high molecular weight, which manifests as increased extensibility. These observations are consistent with the results of molecular dynamics simulations. Interestingly, the normal (applied) forces associated with cohesive and adhesive failure are directly proportional to the average degree of polymerization, as opposed to simply the molecular weight, as the length of the alkyl side chain increases the molecular weight without increasing the degree of polymerization.