The safe and efficient capture of radioactive iodine is highly necessary, but still remains an ongoing challenge. Herein, because of its special layer structure, CuBi–CO3-layered double hydroxides (CuBi–CO3-LDHs) are used to serve as a generic platform, and 3D hierarchical flowerlike ZIF-67/CuBi–CO3-LDH composites are synthesized by a simple coprecipitation method. After immobilization, the flowerlike morphology of CuBi–CO3-LDHs can be completely preserved and proved by scanning electron microscope. Various affecting factors on adsorption performance are investigated, including adsorbent dose, initial concentration of iodine, and temperature. The experimental and modeling results manifest that iodine adsorption is accurately elucidated by pseudo-second-order model, and the equilibrium isotherm is accordant with the Freundlich model. Moreover, the regeneration experiment indicates that ZIF-67/CuBi–CO3-LDH composites possess good stability and reusability for the removal of iodine. The possible adsorption mechanisms of iodine on ZIF-67/CuBi–CO3-LDHs involve particular layer structure and the strong interaction between nitrogen of imidazole ring and iodine, which were investigated by X-ray diffraction, energy-dispersive X-ray, and X-ray photoelectron spectroscopy spectra. The good performance for the iodine adsorption indicates that ZIF-67/CuBi–CO3-LDHs may be identified as a promising adsorbent in the field of iodine capture.

Ta–W co-alloying was realized by double glow plasma surface metallurgy technology, and their effects on high-temperature oxidation behavior of γ-TiAl were studied. Ta–W co-alloying coating was composed of a deposited layer and interdiffusion layer. The results of isothermal oxidation experiment indicated that a compact mixed oxide film of Ta and W was formed on the sample. The interdiffusion layer reduced the oxygen intrusion that improved the high-temperature oxidation resistance of γ-TiAl. The effects of Ta–W co-alloying on oxygen adsorption energy and electronic structure of γ-TiAl(111) were analyzed by first-principle calculation. The results showed that the optimal adsorption sites of O atoms changed from fcc-Al to hcp-Ti and hcp-Al, indicating that Ta–W co-alloying inhibited the diffusion of O. The electronic structure analysis of γ-TiAl(111) after Ta–W alloying indicated the affinity of Ti and O was inhibited, which resulted in decreased TiO2 in the oxide film.

Modern electronics have been geared toward exploring novel electronic materials that can encompass a broad set of unusual functionalities absent in conventional platforms. In this regard, two-dimensional (2D) transition metal dichalcogenide (TMD) semiconductors are highly promising, owing to their large mechanical resilience coupled with superior transport properties and van der Waals (vdW) attraction-enabled relaxed assembly. Moreover, 2D TMD heterolayers based on chemically distinct constituent layers exhibit even more intriguing properties beyond their mono-component counterparts, which can materialize only when they are manufactured on a technologically practical wafer-scale. This mini-review provides a comprehensive overview of recent progress in exploring wafer-scale 2D TMD heterolayers of various kinds. It extensively surveys a variety of manufacturing strategies and discusses their scientific working principles, resulting 2D TMD heterolayers, their material properties, and device applications. Moreover, it offers extended discussion on remaining challenges and future outlooks toward further improving the material quality of 2D TMD heterolayers in both material and manufacturing aspects.

In this work, PbS and PbS/CdS core–shell quantum dots (QDs) were synthesized by a new photochemical approach. Prepared QDs were characterized by means of x-ray diffraction (XRD), field emission scanning electron microscopy (FESEM), energy dispersive x-ray analysis (EDAX), UV–Vis, and Z-scan analyses. Synthesized QDs were in a cubic phase with a spherical morphology, and the crystallite sizes are estimated using the strain–size method. A uniform shift of Bragg diffraction peaks and quenching (200) Bragg plane are interpreted as the growth of the CdS shell. Linear optical properties were investigated using Urbach analysis and Tauc formula. It was found that the density of states of QD conduction and valence bands are three dimensional. The estimated sizes of PbS QDs and PbS/CdS using exciton absorption peaks at room temperature are 1.8 and 2.7 nm, respectively, which are in good agreement with the strain–size plot analysis. The growth of the CdS shell resulted in a considerable decrease in the nonlinearity refractive index and a significant increase in the nonlinear absorption.

Methods that allow for high-throughput synthesis of magnetic nanoparticles are necessary to more feasibly fabricate materials for real-world applications. To accomplish this, in this article, we describe a versatile electrospray-based synthesis method for the synthesis of magnetic cobalt ferrite nanoparticles. This method has the potential to be readily scaled up using methods similar to those currently used in place for the large-scale electrospinning of fibers. To mitigate film formation as often seen with electrospraying ceramics onto a flat plate collector, we developed a method where the magnetic cobalt ferrite nanoparticles were electrosprayed into a silicone oil–based liquid collector. The as-sprayed particles were then crystalized by salt calcining with sodium chloride at 800 °C. The synthesized magnetic nanoparticles obtained using this method had an average particle diameter of 20.7 ± 11.5 nm. This liquid collection method for the synthesis of cobalt ferrite also presents a versatile platform for the synthesis of a wide range of functional nanomaterials and nanocomposites.

Ab initio design of polymer nanocomposite materials for high breakdown strength requires prediction of localized trap states at the polymer–filler interface. Systematic first-principles calculations of realistic interfaces can be challenging, particularly for amorphous polymers and fillers that necessitate the calculation of ensembles of large unit cells with hundreds of atoms. We present a computational approach for automatically generating reasonable structures for amorphous polymer–filler interfaces, combining classical molecular dynamics and Monte Carlo simulations. We identify trap states by analyzing the localization of electronic eigenstates calculated using density functional theory on ensembles of interface structures, clearly distinguishing shallow trap states from delocalized band-edge states. Applying this approach to silica–polyethylene interfaces as an initial example, we find under-coordination and distorted coordination structures at amorphous silica surfaces contribute a combination of deep and shallow traps at these interfaces, whereas polyethylene does not generate localized interfacial states.

A novel photocatalyst Tm3+/Yb3+–co-doped bismuth molybdate (Bi2MoO6) were synthesized via the hydrothermal method. The samples were characterized through X-ray diffraction, field emission scanning electron microscopy, transmission electron microscopy, X-ray photoelectron spectroscopy (XPS), UV-vis diffuse reflectance spectra, and photoluminescence. XPS characterization confirmed the doped rare earth elements. Analysis of the optical properties explained the up-conversion process and its effect on the photocatalytic performance. The as-synthesized samples were employed to decompose Rhodamine B to value its photocatalytic activities under visible light irradiation. The doped samples showed an enhanced photocatalytic activity compared with the bare Bi2MoO6. When the ratio of Tm3+ and Yb3+ was 0.5:5, the degradation efficiency was the highest of 96.1% within 25 min, which was higher than that (74.9%) of pure Bi2MoO6. Moreover, the photocatalytic mechanism of improving the photocatalytic properties was discussed. Besides, the sample showed a super stability in photocatalytic activity. A novel catalyst for industrial pollutant degradation was proposed.

This article reports findings when using a molybdenum–tungsten (MoW) interlayer for diamond thin film deposition on steel substrates. The main focus was on the postdeposition stress within the diamond films and its impact on the coating's tribological properties. The effect of MoW interlayer thickness and the effect of chemical vapor deposition (CVD) process temperature have been investigated. Nanocrystalline diamond films were deposited on steel substrates with MoW interlayers (thickness of 1.1, 4.5, and 8.3 μm) at two different deposition temperatures (650 and 875 °C). It was found that when depositing good quality diamond films on steel substrates, increasing interlayer thickness and decreasing CVD process temperature have to be jointly considered to obtain the optimal result. The diamond-coated steel substrates with the 8.3 μm interlayer deposited at the lower CVD processing temperature exhibited the least residual stress combined with excellent mechanical properties.

Electronic devices have revolutionized society’s trajectories within, and interactions with, the world. The skin on our bodies holds incredible functionalities, such as stretchability and degradability, which only recently are being explored for electronic systems and have the potential to revolutionize device applications and disposal. Polymeric materials are especially poised to realize stretchable and transient electronics. In this article, strategies are reviewed for synthesizing and utilizing biodegradable and elastomeric organic materials, followed by component-specific materials approaches and examples of assembled stretchable and transient systems. Stretchable and biodegradable organic electronic devices will call upon intersections of different fields, which promise to open up new frontiers for electronics in the biomedical, exploratory, sensory, and consumer electronics fields.