The understanding of adhesion and survival behavior of bacterial pathogens on implant surfaces are critical to control and reduce implant-associated infections. Herein, the authors investigate the interactions of Staphylococcus aureus, one of the most prevalent causes of implant infections, with Mg–4Zn–0.5Ca implants. It was found that within 60 min of exposure, 99.1% of adherent bacteria were inactivated. The combination of unique mechanical properties, biodegradation kinetics, and antimicrobial characteristics of Mg–4Zn–0.5Ca alloy makes it a promising candidate for future implant applications.

Molecular semiconductors synergize a variety of uniquely advantageous properties such as excellent absorption and emission properties, soft and deformable mechanical properties, and mixed ionic and electrical conduction. Over the past two decades, this outstanding set of features has put molecular semiconductors in the spotlight for a variety of optoelectronics and sensing applications. When it comes to mass-market adaptation, however, a challenge in these soft and van der Waals-bonded materials remains their electrical as well as environmental stability and degradation. This Prospective will summarize some of our current understanding of why organic semiconductors degrade with a strong emphasis put on the quintessential role played by water in this process. Furthermore, it will be revisited by which mechanisms water-related stability shortcomings might be addressed in the future and how these lessons can be translated to relevant hybrid systems such as perovskites and carbon nanotubes. Throughout this discussion, some parallels and key differences between organic and hybrid materials will be highlighted, and it will be elaborated on how this affects the associated device stability.

The stiffness of conjugated polymers should lead to chain alignment near buried interfaces, even if the polymer film is nominally amorphous. Although simulations predict that this alignment layer is approximately 1.5 times the persistence length, chain alignment at buried interfaces of amorphous polymers has not been experimentally measured. Using Mueller matrix spectroscopy, the optical response of regiorandom poly(3-hexylthiophene-2,5-diyl) (P3HT) was modeled in order to extract the aligned layer thickness. By approximating the optical properties of the aligned layer as that of regioregular P3HT, the data can be effectively modeled. When the film is thicker than 150 nm, optical properties are best described with a 4-nm aligned layer, which is quantitatively consistent with previous predictions.

The dendrite morphologies of the cast nickel-based superalloy CMSX-4® (CMSX-4® is registered trademarks of the Cannon-Muskegon Corporation) and the austenitic stainless steel HP microalloy have been obtained via an automated serial-sectioning process which allows three-dimensional (3D) microstructural characterization. The dendrite arm spacing, volume fraction of segregation, and fraction of porosity have been determined. This technique not only increases the depth, scope, and level of detailed microstructural characterization but also delivers microstructural data for modeling and simulation.

Our recent exploration into the use of biodegradable metals and surface treatments resulting in sufficient strength for skeletal reconstruction applications has led to the need to test these devices’ cytotoxicity. More specifically, our group has developed a resorbable magnesium alloy, Mg–1.2Zn–0.5Ca–0.5Mn, that can be strengthened by heat treatment and coated with a ceramic layer offering time-certain resorption of a medical device. This in vitro study shows that these treatments do not result in cytotoxicity. Both heat-treated (HT) and HT + ceramic-coated (sol–gel) coupons demonstrated more than 70% viability. Thus, these processing steps are likely to be useful in producing biocompatible, resorbable implants that incorporate our Mg–1.2Zn–0.5Ca–0.5Mn alloy.

Obtaining a good statistical representation of material microstructures is crucial for establishing robust process–structure–property linkages and machine learning techniques can bridge this gap. One major difficulty in leveraging recent advances in deep learning for this purpose is the scarcity of good quality data with enough metadata. In machine learning, similarity metric learning using Siamese networks has been used to deal with sparse data. Inspired by this, the authors propose a Siamese architecture to learn microstructure representations. The authors show that analysis tasks such as the classification of microstructures can be done more efficiently in the learned representation space.

This work studies phase-separated fibers in the CaO–SiO2 and NiO–SiO2 systems. The nature of the phase-separated microstructures and underlying phase equilibria are discussed, including dimensionality, composition, and phase formation as well as the realization of ferrimagnetic behavior in the NiO–SiO2 fibers based on the formation of metallic Ni inclusions. In addition to understanding the composition/processing relationships in these systems, the work represents a step forward toward novel magneto-optic fibers. It is important to understand the underlying materials science in order to advance the properties of novel optical fibers possessing engineered heterogeneities in the core.

Planet–satellite-type supracolloidal clusters represent a comparably young class of nanomaterials, which are unique with regard to structural order. In this prospective article, different approaches for their synthesis are discussed and compared. These synthetic methods enable the engineering of supracolloidal structural and adaptive properties, which in turn enables different emerging applications, such as in sensing and catalysis. These possibilities are explored on the basis of selected recent examples. A perspective about possible future developments is given at the end of this article.

This research investigates a novel composite of encapsulated paraffin in boron nitride nanotube (BNNT) which is more thermally and chemically stable than carbon nanotube. This composite can achieve high thermal conductivity and, meanwhile, have thermal energy storage capability for efficient thermal management under extreme conditions. Equilibrium molecular dynamics simulations were conducted to study self-diffusion coefficient, thermal conductivity, and specific heat of encapsulated paraffin. The simulation results indicated that the self-diffusion coefficient and thermal conductivity of paraffin could be increased by up to 10 and 7 times, respectively, while specific heat was reduced after encapsulating into BNNT.

The development of thermoelectric measurement technology at nanoscale is a challenging task. Here, a novel MEMS-based dual temperature control (DTC) measurement method for thermoelectric properties of individual nanowires was proposed. Different from conventional thermal bridge testing devices, this DTC thermoelectric testing device can obtain the thermoelectric properties by independently control ambient temperature and temperature difference between two ends of the nanowires through two separate resistance thermometers without auxiliary heating devices. The reliability of the model and the testing accuracy were verified by accurately measuring the thermal conductivity, electrical conductivity, and the absolute value of the Seebeck coefficient of VO2 nanowires.

In this work, a facile superhydrophobic coating for 2024-T3 aluminum alloy is developed and characterized. The corrosion resistance of the coating was analyzed. The results showed that the coating has high polarization resistance and a low corrosion rate. Furthermore, a micro/nanoscale investigation about the interaction between substrates and the corrosive environment was carried out using the in situ atomic force microscope technique. The change in surface topography was monitored for both the bare aluminum alloy substrate and the superhydrophobic aluminum alloy. The results showed that the coating retained surface features indicated that the coating has excellent corrosion resistance.

Quantitative Fe content determination of powders by Mössbauer spectroscopy is described. In this method, powder samples and internal standard are combined homogeneously in a plastic film ensuring a thin absorber. This method was verified by quantifying the Fe content of a series of samples and independently confirming by inductively coupled plasma optical emission spectroscopic analysis. Additionally, for the first time, Fe contamination in ball-milled Si as a function of milling time was quantified. It was found that Fe contamination increased with time but surprisingly became steady state at 1.12 ± 0.04 at.% Fe after grain size reduction.

When the Cassie–Baxter and Wenzel states coexist for a liquid droplet on a micropatterned surface, the Cassie-to-Wenzel transition takes place if the energy barrier is overcome. Although multiple metastable states coexist due to the micropattern, this paper presents a simple Cassie-to-Wenzel transition of a 2 µL water droplet on a particular micropillared surface: When the droplet is gently deposited above the surface, it equalizes to the Cassie state at zero gravity; however, it transitions to the Wenzel state at the terrestrial gravity, in which the gravitational potential energy overcomes the energy barrier between the Cassie and Wenzel states.

In this paper, the Lewis base character of 3-aminopropyltrimethoxysilane (3-APTMS), an imine derivative of siloxane, and an indole monomer were shown to enable the reduction of gold cations in acetone. The Lewis acid–base adduct of indole monomers and gold formed a polyindole–gold nanoparticle sol. Similarly, the Lewis acid–base adduct of 3-APTMS and gold enabled the formation of gold nanoparticles in the presence of acetone. The polyindole–gold nanoparticle sol and siloxane–gold nanoparticles underwent self-assembly into a polymeric nanofluid that was suitable for casting membranes. The use of these membranes as a potentiometric ion sensor for both cations and anions was considered; a common nonspecific ion exchange molecule, sodium tetraphenylborate, and the polymeric nanofluid were used to prepare an anion sensor and a cation sensor.

The incorporation of small amounts of phenolic antioxidants, such as 2,6-di-tert-butyl-4-cresol and pentaerythritol tetrakis[3-(3,5-di-tert-butyl-4-hydroxyphenyl)propionate], into photovoltaic organo-lead halide perovskite layers significantly suppressed the degradation of the perovskite compounds via light irradiation in the presence of ambient oxygen. While the facile incorporation of the antioxidants did not decrease both the quality of the formed perovskite crystal grains and the photovoltaic conversion performance of the cells, it enhanced the antioxidizing property and water repellency of the perovskite layer owing to the elimination of superoxide anion radical and hydrophobic molecular structure and improved the durability of the cells.

Waterproof bioelectrodes enable long-term biological monitoring and the assessment of performances of athletes in water. Existing gel electrodes change their electrical properties even when covered with a waterproof film. Here, the authors present the poly(3,4-ethylene dioxythiophene):poly(styrene sulfonate) (PEDOT:PSS)/poly(styrene-butadiene-styrene) (SBS) bi-layer nanosheet and waterproof film for a comfortable waterproof bioelectrode. PEDOT:PSS/SBS is fully foldable with a conductivity loss of only 5%. This foldable nanosheet electrode provides a reliable electrical connection between the skin and the wire. The waterproof film-covered bioelectrode enables continuous monitoring of electrocardiograms in water, showing a signal-to-noise ratio of 21.5 dB for the R wave and 17.5 dB for the T wave, comparable to atmospheric measurements, and sensing a change in heart rate from 79 to 131 bpm during bathing.

In the present work, an efficient route has been further explored to achieve the batch synthesis of inorganic fullerene (IF)-WS2 nanoparticles, and the self-lubricating film is conveniently prepared by coating these nanoparticles on the surface of metal substrates. The as-synthesized IF-WS2 nanoparticles have a closed hollow structure with an average particle size of about 50 nm and are evenly distributed in the self-lubricating film. Further friction tests show that the film has excellent friction properties, with its lowest friction coefficient of approximately 0.008, which can be mainly attributed to the unique hollow cage structure and a smaller particle size of the IF-WS2 nanoparticles.

To overcome the steric effect of norbornene (NB), first-generation Grubbs’ catalyst (GC1) was used as the catalyst to graft NB onto the polypropylene (PP) chain by reactive extrusion. Instead of harsh reaction conditions, such as anhydrous, which was the general method to synthesize NB polymers, this convenient method would be easier to industrialize. The mechanism of grafting was studied by using Fourier Transform InfraRed spectra and differential scanning calorimetry. It was found that GC1 could initiate the ring-opening metathesis polymerization of NB to obtain short NB chain-grafted PP-g-NB. The rheological behavior showed that the grafted NB short chains on PP-g-NB increase the shear thinning of the polymers and decrease the system viscosity.

A hybrid graphene–gold nanomesh, realized through Au deposition on a patterned graphene nanomesh with a focused ion beam, is introduced and illustrated for enhanced light absorption in the visible spectrum. Numerical studies reveal that the hybrid nanomesh with dual resonances in the visible spectrum exhibit ~50% light absorption and enhancement factor as high as ~1 × 108. The simulations also show that the enhanced optical absorption is associated with the excitation of surface plasmons. This is confirmed through the localization of electric fields at the resonant wavelengths. Such a hybrid graphene–gold nanomesh exhibiting enhanced light-matter interactions paves the way toward plasmonics, surface-enhanced Raman scattering applications, etc.

The enhanced reducibility of the surface of ceria relative to the bulk has long been established. Several studies also show that ceria nanoparticles with different facets exhibit different catalytic activities. Despite consensus that the activity is correlated with the surface Ce3+ concentration, experimental measurements of this concentration as a function of termination are lacking. Here, X-ray absorption near-edge spectroscopy (XANES) is used to quantify the Ce3+ concentration in films with (001), (110), and (111) surface terminations under reaction relevant conditions. While an enhanced Ce3+ concentration is found at the surfaces, it is surprisingly insensitive to film orientation.