We here design and fabricate a new kind of copper matrix composites, where titanium carbide nanoparticles are in situ incorporated into and embedded within the copper matrix, by virtue of laser powder-bed-fusion (L-PBF) process. We made a multiscale examination on the microstructures of the additively manufactured samples, unraveling that there are many unusual microstructural features, including grain refinement, the existence of high-density dislocations, and supersaturation of titanium solute atoms in the as-printed metal matrix composites. These unique microstructural features are mainly interpreted by the intense thermal history and the rapid solidification nature of the L-PBF process. The resultant composites then integrate the most important four strengthening mechanisms in metals: grain boundary strengthening, dislocation strengthening, solid solution strengthening, and second-phase strengthening, rendering this new kind of copper matrix composites a remarkably high yield strength (~490 MPa) and large uniform elongation (~12%), surpassing many high-performance copper matrix composites and copper alloys.

In this study, uniaxial tensile loading simulations were performed on several single crystalline copper nanoporous (NP) structures with varying relative density (RD) via molecular dynamics simulations. From the results, two distinctive deformation patterns were observed: structures with a low RD went through coarsening, and structures with a high RD did not. During coarsening, dislocations are nucleated because of the high surface stress induced by the thin ligaments. These dislocations drive the merging of ligaments as well as nodes and lead to an increase in the differences between the size of nodes and ligaments. The disproportional nodes and ligaments result in a lowered strength. In addition, larger nodes provide more favorable circumstances for the formation of sessile dislocations, which hinder the movement of other propagating Shockley partials and result in strain hardening. Subsequently, lower RD structures offer anomalously high strain-hardening potential, whereas high RD structures show better strength but poor deformability. These results help us in better understanding the plastic behavior of NP structures as a function of their RD.

This work demonstrated the possibility to integrate electrochemical molecularly imprinted polymers (e-MIPs) on microelectrodes to detect organic pollutants. e-MIPs are a cross-linked polymer with specific target binding cavities with a redox tracer inside. e-MIPs were obtained by precipitation copolymerization of ferrocenylmethyl methacrylate as a functional monomer and a redox tracer with ethylene glycol dimethacrylate as a cross-linker and bisphenol A as a target molecule. FTIR and elemental analysis confirmed the presence of ferrocene inside the polymers. Nitrogen adsorption/desorption experiments and binding isotherms demonstrated the presence of binding cavities inside the e-MIP. The electrochemical properties of the e-MIP were characterized in organic/aqueous media before their patterned on microelectrode.

Localized deformation, including that by the deformation-induced shearing martensitic phase transformation, is responsible for hardening and embrittlement in irradiated face-centered cubic alloys. These localized deformation processes can have profound consequences on the mechanical integrity of common structural metals used in extreme radiation environments such as nuclear reactors. This article aims to review and understand exactly how irradiation affects the martensitic phase transformation in face-centered cubic alloys, with an emphasis on austenitic stainless steel, given its ubiquity in the archival literature. The influence of irradiation on stacking fault energy and subsequent implications on the phase transformation are discussed. Mechanisms by which irradiation-induced microstructures enhance the phase transformation are also described, including the surface energy contribution of irradiation-induced cavities (i.e., voids and bubbles) toward the critical martensite nucleation energy, and partial dislocation–cavity interactions. A deformation mechanism map illustrates how irradiation-induced cavities can modulate the martensitic transformation pathway.

Thermal barrier coating is a high-temperature protective technology widely used in industrial gas turbines. However, the failure of coating peeling because of the generation of thermally grown oxide (TGO) at the interface during service hinders its further application. In this study, Raman spectroscopy and wedge indentation are used to determine the TGO residual stress and the interface energy release rate, respectively. The effect of TGO on the interfacial fracture toughness during the growth process was discussed. Raman spectroscopy test results show that the residual stress of TGO is about 0.5 GPa. Wedge indentation test results illustrate that high-temperature heat treatment could accelerate the interface degradation of thermal barrier coatings. Stress analysis and test research demonstrate that the microcracks induced by compressive stress of TGO will propagate with increasing heating time, ending with failure of barrier coatings.

Natural systems displaying optical properties have for long been an inspiration for new classes of optical constructs. Using the same families of materials employed by Nature in combination with their directed assembly allows access to n-dimensions of control to, ultimately, generate optical systems with multiple coexisting functions. This review provides an overview of lab-made optical systems made of protein and polysaccharide-derived materials found in naturally occurring optical systems. Recent advances in optical biomimicry and bioinspired, polyfunctional optical structures are presented, addressing attributes such as sensing, edible devices, biologically activity, and resorbable optical formats.

Chitosan is one of the most versatile biopolymers available with established properties such as antimicrobial, antitumor, anti-inflammatory, mucoadhesive, and more. It has been in biomedical research for long, but still the bench-to-bedside translation is hampered because of viscosity and solubility issues. The only commercial application of chitosan has been in hemostatic dressings. Chitosan oligosaccharide (COS), on the other hand, is highly promising in a similar research area where chitosan's limitations come into the way. COS is highly soluble in water, and its viscosity is very less than that of the parent chitosan. Although COS retains properties very similar to those of chitosan, there has been minuscule volume of research on this water-soluble chitosan. COS has been successfully used as a drug delivery vehicle in various research. COS has also shown to have osteogenic ability. It has been used as a coating on experimental orthopedic implants because of its antibacterial properties. As of now, COS is not a much-explored biopolymer, although it could be an important biopolymer for its capacity in biomedical research. This article reviews various properties and reports of COS relevant for biomedical applications.

In this article, Al75Cu25 (at.%) ribbons were dealloyed by HCl, H2C2O4, H3PO4, and NaOH solutions, respectively, to prepare nanoporous copper (NPC). The dealloying behavior is varied with dealloying solutions, allowing modulating the microstructure and porosity of the NPC. Al75Cu25 ribbons are fully dealloyed in HCl, H2C2O4, and NaOH solutions, whereas they are partially dealloyed in H3PO4 solution. Except the NPC prepared in the NaOH solution, no obvious cracks are traced in other samples. The surface diffusivity (Ds) of Cu atoms along the alloy/solution interfaces is varied with solutions, producing the NPC with different microstructure. NPC with higher specific surface area can be obtained by dealloying the Al75Cu25 ribbons in the HCl solution. Compared with the dealloying in H2C2O4, H3PO4, and NaOH solutions, the dealloying in 10 wt% HCl solution for 25 min at 90 ± 1 °C facilitates the best NPC in this work.

Materials that show superior light-emitting and catalytic properties are in high demand among the scientific community owing to their applications in the areas of optoelectronics and (opto)electrocatalysis. In this work, we have synthesized sub-10-nm Pr2Sn2O7 (PSO) and Pr2Sn2O7:Bi3+ (PSOB) nanoparticles (NPs) and investigated their optical and electrochemical properties. On ultraviolet irradiation, PSO NPs display blue emission because of the presence of oxygen vacancies. Interestingly, PSOB NPs have higher blue emission intensity than undoped PSO NPs owing to the increase in oxygen vacancy defect density induced by Bi3+ doping. Moreover, PSOB NPs display higher efficiency in terms of current density than PSO NPs as a catalyst toward the oxygen evolution reaction (OER). The kinetic OER models of PSO and PSOB NPs are quite different as displayed by their different Tafel slopes. Interestingly and as another advantage, the PSOB sample is more conducting with low impedance value than the PSO counterpart. With all these advantages due to high oxygen vacancies induced by Bi3+ doping, PSOB NPs have a great potential to be used as blue phosphors, charge storage devices, and capacitors.

In this work, filament based on ɛ-polycaprolactone (PCL) and containing the bioactive ceramics nanohydroxyapatite (nHap) and Laponite® (Lap) was prepared by the extrusion process. To obtain the material, a mass ratio of 89:10:1 (PCL:nHap:Lap) was used, and structural and morphological characterization was realized. In addition, cytotoxicity (using Allium cepa bulbs) and viability tests on L929 cells also were performed. The results showed that filament (diameter of 1.79 ± 0.17 mm) presented a good dispersion of nHap and Lap into polymeric matrices. Fourier transform infrared spectroscopy identified typical bands at 1720, 1091, and 1045 cm−1 addressed to PCL and nHAp, In addition, Lap was identified through dispersive energy system and X-ray diffraction analyses. All filaments did not exhibit cytotoxic effects.

The study investigated novel wear and corrosion resistance of stainless steel and 316 stainless steel samples which were successfully prepared by laser melting deposition. Phase composition, microstructure, microhardness, wear resistance, and electrochemical corrosion resistance were studied. The experimental results showed that novel stainless steel was mainly composed of α-Fe and a few carbide phase (Cr, Fe)7C3. The microhardness of novel stainless steel was about 2.7 times greater than 316 stainless steel. Meanwhile, the specific wear rate of novel stainless steel and 316 stainless steel was 2.63 × 10−5 mm3/N m and 1.63 × 10−4 mm3/N m, respectively. The wear volume of 316 stainless steel was 6.19 times greater than novel stainless steel. The corrosion current and the corrosion potential of novel stainless steel and 316 stainless steel were 1.02 × 10−7 A/cm2 and 1.5 × 10−7 A/cm2, and −138.8 mV, −135.9 mV, respectively, in 3.5 wt% NaCl solution. Therefore, both microhardness and wear resistance of novel stainless steel were greatly improved, with high corrosion resistance.

Fluorescent quantum dots (QDs) modified with polyethylene glycol (PEG) and albumin bovine serum (BSA) have profound application in the detection and treatment of hepatocellular carcinoma (HCC) cells. In the present study, the effects and mechanism of PEG and BSA modification on the cytotoxicity of QDs have been explored. It was found that the diameter of the as-prepared QDs, PEG@QDs, BSA@QDs is 3–5 nm, 4–5 nm, and 4–6 nm, respectively. With increase of the treatment time from 0 to 24 h, the HCC cell viability treated with QDs, PEG@QDs, and BSA@QDs obviously decreases, showing a certain time-dependent manner. When the concentration of several nanomaterials is increased from 10 to 90 nM, the cell viability decreases accordingly, exhibiting a certain concentration-dependent manner. Under the same concentration change conditions, the reactive oxygen species contents of cells treated by QDs, PEG@QDs, and BSA@QDs also rise from 7.9 × 103, 6.7 × 103, and 4.7 × 103 to 13.2 × 103, 14.3 × 103, and 12.3 × 103, respectively. In these processes, superoxide dismutase does not play a major role. This study provides strong foundation and useful guidance for QD applications in the diagnosis and treatment of HCC.

The present article reports on a comprehensive atomic-scale investigation on S-series precipitates in 2024 aluminum alloy. Cs-corrected high-angle annular dark-field scanning transmission electron microscopy is applied to reveal the fine atomic-scale structure of precipitates at early ageing state. Geometrics phase analysis is used for elucidating the induced strain field from precipitates. The precipitate sequence of S-series precipitates in 2024 Al alloy is identified as follows: super saturated solid solutions (s.s.s.s.) → clusters (GPB zone) → S′ phase → S phase. The interfaces between precipitates acting as precursor of S′ phase are well characterized. One typical characteristic of S-series phase precipitates is the coexistence of clusters and subsequent metastable phases. Transformation of metastable phases is characterized. Corresponding hardness structure relationship is revealed, and S′ phase is considered as the key strengthening structure in S-series precipitates in 2024 Al alloys.

Tungsten (W) alloy is of difficulty in processing for conventional way because of its high melting point. Here, W alloy sample with the addition of 3 wt% Ta was prepared by selective laser melting. The influence of volumetric energy density (VED) on the surface morphology and the relative density was discussed, and microstructure, phase composition, and microhardness were investigated. The results show that a smooth surface and high relative density (95.79%) can be obtained under optimal VED. The W–Ta substitutional solid solution formed because of the replacement of Ta atom. There are strip and block fine grains in the W–3Ta sample with no significant texture. In addition, subgrain structure with a size of around 1 μm formed inside the strip grain, owing to the large thermal gradient and extremely fast cooling rate. Finally, the W–3Ta alloy shows higher microhardness than that obtained by traditional methods.