The immobilization of cytochrome c (cyt c) on tea polyphenol functionalized and reduced graphene oxide (TPG) was carried out by a simple adsorption process. Intriguingly, TPG with large surface area exhibited excellent adsorption behaviors and good biocompatibility. The adsorbed materials were characterized by various methods including scanning electron microscopy (SEM), atomic force microscopy (AFM), X-ray diffraction (XRD), and Fourier transform infrared spectroscopy (FTIR). And the effects of adsorption behavior of cyt c were discussed in detail. The results showed the adsorption behavior was dependent on the pH value and showed a high adsorption capacity as high as 1.414 × 104 mg/g and was friendly to normal cells (mouse fibroblast cell line, L929). In conclusion, we proposed the introduction of TPG as novel material and used the adsorption method to immobilize cyt c, which would provide a novel material and simple method for the enrichment of protein.

The formation of low-angle grain boundaries (LABs) in the rejoined platforms of a Ni-based single crystal superalloy under different directional solidification rates was investigated by the experimental investigation and the ProCAST simulation. The results showed that the growth morphology and orientation evolution of dendrites in the platforms were different under the withdrawal rates in the range of 60–100 μm/s and then resulted in different types of LABs. At lower withdrawal rates, the longitudinal LABs were common in the rejoined platforms. Both the sliver defects and the orientation deviation of original primary dendrites from two independent growth paths could cause the longitudinal LABs in the platforms. At higher withdrawal rates, the dendrite growth patterns were more complex and the secondary branches with lateral growth tended to deviate from their original orientation, eventually leading to the formation of some transverse LABs. Finally, some suggestions to prevent the formation of different LABs are provided.

The 2Cr13/316L multilayered composite plates were fabricated by hot rolling with recycle heating step. The effect of rolling reductions on microstructure and properties was investigated. The 2Cr13 layer consists of martensite and lath ferrite, but the middle layer has less ferrite than both sides. The content and grains of ferrite increase with the increase of the reduction and number of reheating, which leads to a decrease in the hardness of the 2Cr13 layer. The hardness of the 2Cr13 layer is determined by the volume ratio of martensite and ferrite. Tensile strength of the specimens with the rolling reduction of 72% and 82% reached 815.8 MPa and 763.4 MPa, while elongations were 20% and 20.8%, respectively. With the increase of the rolling reduction, the fracture mode also changed from cleavage fracture to dimple fracture. There were no cracks and delamination when the 2Cr13/316L composite plate bent to 130° and 180°, which indicated better interfacial bonding.

Two different sized As(0) nanoparticles As1 (50 ± 7 nm) and As2 (70 ± 10 nm) are prepared by reducing arsenite with NaBH4 in the pH range 7–9, at controlled temperature (10 and 40 °C). Further, galvanic replacement reaction is used exploiting the reducing nature of As(0) to prepare two different sized hollow gold nanoparticles (HGNPs) AuNP1 (55 ± 7 nm) and AuNP2 (72 ± 7 nm). These HGNPs exhibit high catalytic activity towards 4-nitrophenol reduction under various conditions following first-order kinetics. AuNP1 shows ~6.6 time higher turnover frequency compared with that of AuNP2 due to its smaller size. Both catalysts are recycle able.

Theoretical investigations on ferroelectric tunnel junctions (FTJs) with asymmetric electrodes and a composite barrier are presented. A large tunneling electroresistance effect exists for the Pt/SrTiO3/BaTiO3/SrRuO3 junction; on the other hand, exchange of the dielectric and ferroelectric layer stacking sequence can seriously degrade the performance. These correlations are rationalized by the proposed concept of an asymmetry factor, defined as the ratio between the average barrier heights of FTJs for two opposite polarization orientations. We show that a large asymmetry factor is beneficial to FTJs. This work may provide a way to enhance the performance of FTJs by structure engineering.

In the present work, the TiB2-reinforced AA6061 composites were successfully in situ synthesized by laser surface alloying using a mixture of Ti and AlB2 powders. The microstructure evolution and properties of the composites were systematically studied. The results showed that TiB2 particles displayed a homogeneous distribution in the aluminum matrix with controllable contents and morphologies. By adjusting the molar ratio of alloying powders, phase constitution of the composites was varied. Thermodynamic calculation was used to analyze the phase selection during the solidification. It was found that the morphology of TiB2 particles was converted from hexagonal plate into rod-like structure with an increase of Ti contents. Transmission electron microscopy results illustrated that the in situ synthesized TiB2 particles exhibited a well-bonded interface with the Al matrix. Properties characterization revealed a significant enhancement in microhardness and abrasion resistance compared with the aluminum substrate attributed to the presence of the TiB2 reinforcements. The strengthening and wear mechanism were also discussed.

In certain alloy systems, a liquid of a fixed composition freezes to form a mixture of two solid phases, one of which may be faceted and the other nonfaceted (i.e., a ‘degenerate’ or irregular eutectic). The role of trace metallic additions on the microstructure of the eutectic has received significant research interest over the last half-century, culminating in advances in theoretical, computational, and experimental fronts. The drastic morphological, topological, and crystallographic changes that accompany metallic additions strongly influence the mechanical properties of the as-synthesized eutectic microstructure. In this review, we survey the mechanistic origins leading to a modified eutectic microstructure and describe the current status in the field of eutectic solidification in the presence of metallic modifying agents. We will also discuss the remaining challenges and future opportunities that would help move the field forward and enable bottom–up tuning of the complex degenerate microstructures to technological demands.

SnO2 aerogels were successfully synthesized by using SnCl4, ammonium hydroxide (AH), formamide, propylene oxide, and tetraethoxysilane as tin source, reaction promoter, drying control chemical additive (DCCA), gel accelerator, and surface modifier, respectively, via the sol–gel method, combined with subsequent ambient pressure drying of sol–gel. The results of Fourier transform infrared spectroscopy proved that the CH3CH2OSi-bond was transferred to SnO2 gel. A contact angle measuring instrument was utilized for the study of hydrophicity and hydrophobicity of SnO2 aerogels, and the complete porous skeleton structure of SnO2 aerogels was confirmed by field emission scanning electron microscopy (FESEM) and nitrogen adsorption–desorption analyzer, denoting AH allowed SnO2 aerogels to shape more macropores. Based on the thermal resistance tester, it showed that the SnO2 aerogels had low thermal conductivity. The biggest specific surface area and lowest thermal conductivity of SnO2 aerogels were 447.26 m2/g and 0.0717 K/(m•K), respectively.

Because of rapid solidification involved in the laser or e-beam based additive manufacturing (AM) process, solution treatable metallic parts made by these methods usually possess a unique nonequilibrium microstructure which changes significantly during subsequent thermal treatment. Such evolution alters the size, morphology, length scale, and distribution of microstructural features and has a substantial impact on thermal properties and possibly on electrical properties as well. This study focuses on effects of microstructural evolution on thermal properties of an additively manufactured AlSi10Mg part. The changes of thermal properties such as thermal expansion, heat capacity, thermal diffusivity, and thermal conductivity as a function of thermal treatment are reported. The results show that the formation of supersaturated primary α aluminum and unique cellular structure imparted by fast solidification in the AM process are the major cause for the low thermal diffusivity and low thermal conductivity observed in this solution treatable, as-built part. A correlation between microstructural evolution and changes in thermal properties is established. Advantages and tailoring of the thermal properties of additively built parts are discussed. Implications of these results are important for other additively manufactured components based on popular solution treatable alloys.

Magnesium is a biodegradable material that has potential application in cardiovascular stent development: its excellent mechanical properties and blood compatibility make it highly useful in interventional therapy. Nevertheless, the following shortcomings restrict its further application: antihyperplasia function and promoting surface endothelialization. In this study, we immobilized a specific link peptide of endothelial cells, Arg-Glu-Asp-Val (REDV), onto polydopamine (PDA)-deposited Mg–Zn–Y–Nd alloy surface via covalent reaction to improve the growth of the endothelial cells. The PDA/REDV coating with optimized parameters maintained the good blood compatibility of the Mg–Zn–Y–Nd alloy at the biomimetic speed of the blood flow and significantly inhibited the growth of the vascular smooth muscle cells and macrophage attachment/activation, which indicated its better functions in antihyperplasia and anti-inflammation. In particular, the PDA/REDV coating not only showed consistent results in promoting the attachment of endothelial cells as reported elsewhere, but also displayed the ability of enhancing the viability of endothelial cells (or inhibiting apoptosis), suggesting its pro-endothelialized function through different pathways. In summary, this PDA/REDV coating addressed the above-mentioned shortcomings of the magnesium alloy, which may promise its wider application.

Traditional manufacturing methods restrict the expansion of thermoelectric technology. Here, we demonstrate a new manufacturing approach for thermoelectric materials. Selective laser melting, an additive manufacturing technique, is performed on loose thermoelectric powders for the first time. Layer-by-layer construction is realized with bismuth telluride, Bi2Te3, and an 88% relative density was achieved. Scanning electron microscopy results suggest good fusion between each layer although multiple pores exist within the melted region. X-ray diffraction results confirm that the Bi2Te3 crystal structure is preserved after laser melting. Temperature-dependent absolute Seebeck coefficient, electrical conductivity, specific heat, thermal diffusivity, thermal conductivity, and dimensionless thermoelectric figure of merit ZT are characterized up to 500 °C, and the bulk thermoelectric material produced by this technique has comparable thermoelectric and electrical properties to those fabricated from traditional methods. The method shown here may be applicable to other thermoelectric materials and offers a novel manufacturing approach for thermoelectric devices.

Atom probe tomography (APT) is rising in influence across many parts of materials science and engineering thanks to its unique combination of highly sensitive composition measurement and three-dimensional microstructural characterization. In this invited article, we have selected a few recent applications that showcase the unique capacity of APT to measure the local composition at structural defects. Whether we consider dislocations, stacking faults, or grain boundary, the detailed compositional measurements tend to indicate specific partitioning behaviors for the different solutes in both complex engineering and model alloys we investigated.

Thin films of insulating Ti1−xNixO2 (x = 0.00, 0.05, 0.10, and 0.15) are synthesized by the spray pyrolysis technique. All the films are seen to crystallize into polycrystalline anatase phase of TiO2. However, weak signature of the NiTiO3 phase is also observed for the films having higher Ni ion concentration. Optical absorption analysis suggests nonmonotonous band gap decrease from 3.67 to 3.59 eV with respect to added concentration of Ni ions unto ‘x’ = 0.10 in the TiO2 matrix. The presence of ferromagnetic ordering at room temperature in Ni incorporated TiO2 films is revealed by M–H measurements. Calculated values of saturation magnetization indicate that the observed ferromagnetism is not due to the presence of Ni clusters or segregation of other ferromagnetic phase. Electrically insulating nature of the films suggests that the observed FM ordering is most probably due to the ferromagnetic interaction between bound magnetic polarons which formed due to the creation of oxygen vacancies or defects.

Modeling static and dynamic contact angles is a great challenge in studying wetting and de-wetting. We propose a new slip boundary model based on the Navier–Stokes equations, and establish a realistic continuum approach to simulate the contact line dynamics in 3-D. To validate our model, a water droplet interacting with micrometer-sized patterns of a hybrid hydro-phobic/-philic surface is studied numerically and compared with experimental measurements. Good agreement has been observed with four pillar spacings in the static, receding, and advancing modes. Moreover, details of the droplet–surface interaction are revealed, i.e., penetrations, sagging, local, and global contact angles.

AgBr-modified Bi2WO6 nanosheets were successfully synthesized using a CTAB-assisted hydrothermal method followed by a facile deposition–precipitation procedure. The as-prepared photocatalysts were characterized using X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), transmission electron microscopy (TEM), UV-vis diffuse reflectance spectroscopy (DRS), Brunauer–Emmett–Teller (BET), and photoluminescence emission spectroscopy (PL). AgBr nanoparticles were found evenly distributed on the surface of the Bi2WO6 nanosheets. The AgBr/Bi2WO6 nanocomposite demonstrated enhanced pollutant decolorization efficiency in eliminating Rhodamine B (RhB), methyl orange (MO), and phenol aqueous solutions under simulated solar light irradiation. It has been noticed that the adsorption performance of both Bi2WO6 nanosheets and AgBr-modified Bi2WO6 nanosheets played a more important role in the decolorization of pollutants, such as RhB and MO, than their photocatalytic ability. The high adsorption efficiency of the photocatalysts was mainly attributed to the increased surface area and the exposed reactive facets of the materials.

We report a rapid combustion synthesis method for producing band gap tunable gallium zinc oxynitrides, a material of interest for water splitting applications. By varying the ratio of zinc and gallium, we can tune the band gap from 2.22 to 2.8 eV. Furthermore, nitrogen can be incorporated up to nearly 50% via replacement of oxygen without the need for high temperatures or an additional ammonolysis step. X-ray photoelectron spectroscopy (XPS) and EDX analysis suggests a preferential segregation of Zn to the surface of the as-synthesized particles, though the surface Ga/Zn molar ratio in the as-synthesized particles is correlated with the Ga/Zn molar ratio of the precursor materials. Photoelectrochemical measurements show that the oxynitride powders are photoactive under both AM1.5 and visible-only (λ > 435 nm) irradiation. Hydrogen and oxygen were both evolved in half-reaction experiments under simulated AM1.5 irradiation without externally applied bias, although addition of an OER catalyst did not enhance the rate of oxygen formation, suggesting that intra- and interparticle recombination are significant.

Highly ordered wrinkling morphologies of liquid crystalline polymer films are demonstrated based on simple multi-rubbing. The spontaneous pattern formation of periodic wrinkling morphology is achieved through utilizing plasma treatment on a predefined alignment layer. The multi-directional ordering on the alignment layer obtained through selectively covering the alignment layer with a protective layer, which is chemically inert and keeps alignment properties during another rubbing process. The ordering of the wrinkle pattern can be tailored through a molecular orientation of liquid crystal (LC) and a process condition, including film thickness, plasma treatment, and rubbing. The proposed methods enable the spontaneous pattern formation of well-aligned one- or two-dimensionally periodic microstructures over a large area, without an additional template or patterning steps. Since the LC polymer incorporated the optical anisotropic mesogenic groups into polymer chains, it has an optical birefringence in the film and it can be utilized for optical devices requiring a microstructure on a surface.

Electrically conducting substrates have shown much promise as neuronal scaffolds and in other biologic and biomedical applications where a smart and electrically interactive material is needed. Most materials that are inherently conducting are not suitable for biomedical applications and lack biocompatibility or biostability. On the other hand, biologically stable and compatible materials must first be manipulated, modified, and treated in order to impart the necessary electrical conductivity to the material. Here, the authors have investigated the response of PC-12 cells to two types of conducting carbon-based aerogels with different surface roughness. Results show that carbon-based aerogels support cell adhesion, proliferation, and neurite extension. The effects of surface roughness have also been investigated.

We report the synthesis and optical properties of pure ZnS and Ag doped ZnS nanostructures. ZnS(Ag) was synthesized by using the hydrothermal technique and later annealed at different temperatures under vacuum conditions. It was observed that the photoluminescence (PL) emission from the ZnS(Ag) nanostructures can be easily tuned from the blue (445 nm) to green (530 nm) region of visible light by varying the annealing temperature. This tunability has been attributed to the introduction of excess sulfur vacancy states, which is evident from the PL excitation spectra. This observed change in the PL emission wavelength can be highly beneficial in the imaging screens where ZnS is regularly used and can be easily interfaced with the silicon photodiodes showing maximum sensitivity at 550 nm.

Here we present the synthesis of porous platinum–palladium macrobeams templated from high aspect ratio Magnus’ salt needle derivatives. The combination of [PtCl4]2− and/or [PdCl4]2− with [Pt(NH3)4]2+ ions results in salt needles ranging from 15 to 300 µm in length. Electrochemical reduction of the salt templates results in porous macrobeams with a square cross-section. Porous side wall texture and elemental composition was controlled with initial platinum to palladium salt ratio. Macrobeam free-standing films exhibited a specific capacitance up to 11.73 F/g and a solvent accessible surface area of 26.6 m2/g. These salt-templated porous platinum–palladium macrobeams offer a promising material for fuel cell catalysis.