High-dielectric constant all-organic composite films consisting of polyaniline (PANI) filler and poly(butylene succinate) host were synthesized by simple blending process. The chemical structures and morphology of the composite films were characterized by Fourier transform infrared spectroscopy and scanning electron microscopy, respectively. The dielectric properties of the composite films with different filler concentrations were studied in the frequency range of 100–106 Hz. A percolation phenomenon was observed in the composite films with a percolation threshold vc = 19.7% and the dielectric constant was 10 times that of the pure host material. The enhancement in the dielectric constant can be ascribed to Maxwell–Wagner–Sillars polarization and the low-dielectric loss to good dispersion of PANI filler in the host. As the host polymer is biodegradable, it may be applied as a “green” dielectric material.

A gradient structure was synthesized on the surface of Zr55Al10Ni5Cu30 alloy with high glass-forming ability by laser surface melting (LSM). Along the laser incident direction, the surface remelted alloy exhibits gradient microstructure distributed in the sequence of amorphous structure, nanocrystal- reinforced amorphous matrix composite (transitional layer A), dendrites–amorphous phase composite (transitional layer B), and crystalline phases from the top surface to the substrate. The formation mechanism of this gradient structure is discussed based on the experimental results of the microstructure together with the finite volume simulation of the process of LSM treatment. The friction coefficient of the transitional layer A is ∼2.5 times lower than those of the other layers under the same sliding friction condition, and possible reasons for this phenomenon are discussed in connection with the rolling motion and material transfer mechanism. The transitional layer B exhibits the best wear resistance among all the structures studied here, which is related to the optimized ratio of microhardness to reduced Young’s modulus (H/Er).

The hexagonal mesoporous silica MCM-41 nanospheres with Au nanorods (AuNRs) as core have been synthesized via a modified Stöber method by a process of hydration and condensation of tetraethoxysilane in a water–ethanol mixture. The AuNR@MCM-41 nanocomposites combine the photothermal characteristic with the mesopore of MCM-41 in one body. We utilized these core–shell materials for ibuprofen encapsulation and release in the simulated body fluid (pH 7.4) for the first time. The results certificated AuNR@MCM-41 nanocomposites as novel dual-functional materials could realize the light-driven release of drug due to the photothermal effect of the AuNRs. Such novel nanomaterials offer a new way for cancer treatment which combine hyperthermia with the chemotherapeutic drugs by synergistic effect.

In small-scale testing at elevated temperatures, impurities in inert gases can pose problems so that testing in vacuum would be desirable. However, previous experiments have indicated difficulties with thermal stability and instrument noise. To investigate this, measurements of the temperature changes in a modified nanoindenter have been made and their influence on the displacement and load measurements is discussed. It is shown that controlling the temperatures of the indenter tip and the sample enabled flat punch indentations of gold, a good thermal conductor, to be carried out over several minutes at 665 °C in vacuum, as well as permitting thermal stability to be quickly re-established in site-specific microcompression experiments. This allowed compression of nickel superalloy micropillars up to sample temperatures of 630 °C with very low levels of oxidation after 48 h. Furthermore, the measured Young moduli, yield and flow stresses were consistent with literature data.

Graphene oxide nanoplatelets (GONPs) were obtained by unraveling helical-ribbon carbon nanofibers (HR-CNF) using a modified Hummers and Offeman method in conjunction with ultrasonication. In this account, we carry out a complete evaluation of the effect of different oxidative agent concentrations on the resulting platelet materials. Transmission electron microscopy, atomic force microscopy, Fourier transform infrared, x-ray diffraction, x-ray photoelectron spectroscopy, and thermogravimetric analysis were performed to carefully characterize GONPs resulting from the oxidative process. Comparative experiments using multiwall carbon nanotubes (MWCNTs) and graphite were also carried out. Our studies suggest that the oxidation treatment is more effective in HR-CNFs than in MWCNTs. Furthermore, the unraveling of HR-CNFs results in GONPs consisting of less stacked layers when compared to other starting materials such as graphite. Therefore, HR-CNFs appear to be excellent precursors to produce few-layered GONPs.

The properties of widely used Ni–Ti-based shape memory alloys (SMAs) are highly sensitive to the underlying microstructure. Hence, controlling the evolution of microstructure during high-temperature deformation becomes important. In this article, the “processing maps” approach is utilized to identify the combination of temperature and strain rate for thermomechanical processing of a Ni42Ti50Cu8 SMA. Uniaxial compression experiments were conducted in the temperature range of 800–1050 °C and at strain rate range of 10−3 and 102 s−1. Two-dimensional power dissipation efficiency and instability maps have been generated and various deformation mechanisms, which operate in different temperature and strain rate regimes, were identified with the aid of the maps and complementary microstructural analysis of the deformed specimens. Results show that the safe window for industrial processing of this alloy is in the range of 800–850 °C and at 0.1 s−1, which leads to grain refinement and strain-free grains. Regions of the instability were identified, which result in strained microstructure, which in turn can affect the performance of the SMA.

Titanium oxide matrix was prepared by sol-gel adding fluoxetine [Prozac (C17H18NF3O)] during the reaction of gelation. This nanostructured material was studied by Fourier transform infrared (FTIR) spectroscopy, N2 adsorption, and x-ray diffraction to detect the interaction between the drug and the matrix. The complex nature of FTIR signals for the matrix and the drug did not allow observation of the interactions; however, using the density functional theory formalism, two stable complexes are suggested to be formed on the drug–matrix system. Both complexes are formed through H bond interactions involving the amine group in fluoxetine and the hydroxylated sites in titanium xerogel. They were found to be energetically stable and independent of the titanium model core cluster used in the calculations.

This article focuses on the use of spherical nanoindentation measurements to estimate the pressure of cavitation impacts and its statistical distribution. Indeed, nanoindentation techniques are supposed to represent an effective tool in this field due to the similarities between substrate deformation under liquid impact and indentation testing. First, nanoindentation experiments were used to extract the mechanical parameters of a Nickel–Aluminum–Bronze alloy; second, pitting tests were performed at different operating pressures, and the geometrical characteristics of the pits were measured; and finally, the spectra of impact pressure and loads responsible for material erosion were obtained by coupling the findings of indentation tests with the analysis of pitting tests. Results assessed the capability of the proposed methodology to quantify the hydrodynamic aggressiveness of the cavitating flow. This procedure, which assumes the material itself as a sensor that is able to detect the impact loads, could represent an alternative solution to pressure transducers in estimating the cavitation intensity.

This article describes cracking during microcompression of Si, InAs, MgO, and MgAl2O4 crystals and compares this with previous observations on Si and GaAs micropillars. The most common mode of cracking was through-thickness axial splitting, the crack growing downward from intersecting slip bands in pillars above a critical size. The splitting behavior observed in all of these materials was quantitatively consistent with a previous analysis, despite the differences in properties and slip geometry between the different materials. Cracking above the slip bands also occurred either in the side or in the top surface of some pillars. The driving forces for these modes of cracking are described and compared with observations. However, only through-thickness axial splitting was observed to give complete failure of the pillar; it is, therefore, considered to be the most important in determining the brittle-to-ductile transitions that have been observed.

Spherical indentation, particularly at low loads, can ensure fully reversible deformations, suitable for the study of viscoelastic properties. However, there are growing concerns about the effective indenter radius in contact at small penetrations and the effect of thermal drift. The aim of this study was to characterize spherical indentation on polymethylmethacrylate (PMMA) and fused silica (FS). Several types of indentation experiments were performed on PMMA to determine its viscoelastic behavior, and a corresponding model was applied to calculate the main mechanical properties. A series of measurements on FS were performed to determine the effective indenter radius and thermal drift of the indentation system. It was shown that at low depths the effective radius of the spherical indenter can substantially differ from the nominal one and calibration of the indenter might be necessary for certain experiments. The effect of thermal drift and its consequences on creep measurements were discussed.

Using a recently developed multidimensional nanocontact system designed for a quantitative measurement of lateral contact stiffness in the 10–106 N/m stiffness range (or 10–1000 nm contact size), we found a crystallographic-orientation-dependent lateral-stiffness reduction relative to the elastic prediction at contact sizes around 50 nm for polished Ni single crystal surface in air. The slidingless measurement is enabled by a frequency-specific, continuous stiffness measurement technique. Based on an interface microslip model and an anisotropic elastic contact analysis, the resulting friction stress is found to increase monotonically when the tested lateral direction rotates away from the closely packed direction.

ZnS:Cu,Cl,Mn,Te, which shows red AC powder electroluminescence (ACPEL) emission, was synthesized using a conventional wet synthesis and a sealed vessel method. The photoluminescence (PL) and ACPEL were characterized. After the second firing, 0.5 wt% tellurium (Te)-doped ZnS:Cu,Cl,Mn,Te phosphor shows almost red PL emission from the 4T1–6A1 transition of Mn2+ ions, which are affected by the Te. Extended x-ray absorption fine structure analysis on the Mn K edge proved that the substitution of sulfur (S) with Te changes the local crystal field of the Mn2+ ions and shifts an orange emission (∼588 nm) to a red emission (∼650 nm). A red ACPEL emission is first shown in 0.5 wt%Te-doped ZnS:Cu,Cl,Mn,Te after the third firing phosphor even though its luminance is not very high. The origin of the ACPEL emission is assumed to be not a CuxS–ZnS p–n junction but a CuxTe–ZnS p–n junction. Raman spectra were characterized to support that the red ACPEL emission is probably attributed to a CuxTe–ZnS p–n junction.

A series of red-emitting phosphors with compositions of La2(Mo1−zSiz)2O9:0.05Eu3+ (0 ≤ z ≤ 0.10) with strong near-UV absorption were prepared by solid-state method. The structure and luminescence properties were investigated by x-ray powder diffraction, UV–vis diffuse reflectivity, and photoluminescence spectra. The luminescent properties as a function of Si4+ concentrations were systematically studied. Under excitation of a wide range near-UV (250–430 nm) or blue light, Si4+-doped series phosphors exhibit characteristic red emission of Eu3+ peaked at 615 nm. The incorporation of Si4+ into La2Mo2O9:0.05Eu3+ phosphor leads to the improvement of the excitation broad band and sharp peaks, as well as the broadening of charge transfer band. Appropriate amount of Si4+ doping can enhance the red luminescence intensity. Finally, the possible reasons for the luminescence enhancement via the corporation of Si4+ were explained.

Physical aging induced by an exposure of As–Se, As–S, and Ge–Se glasses to the light of different discrete wavelengths is studied using differential scanning calorimetry technique. The value of this effect is compared to the physical aging caused by natural storage in the dark. It is shown that a choice of As or Ge atoms does not influence significantly the spectral dependence of light-assisted physical aging, whereas substitution of Se with S causes drastic changes in the magnitude of the effect. The mechanism of the observed light-induced phenomena is discussed in terms of transient and metastable displacements of network chalcogen atoms.

Calcium phosphates form a vast family of biominerals, which have attracted much attention in fields like biology, medicine, and materials science, to name a few. Solid state Nuclear Magnetic Resonance (NMR) is one of the few techniques capable of providing information about their structure at the atomic level. Here, examples of recent advances of solid state NMR techniques are given to demonstrate their suitability to characterize in detail synthetic and biological calcium phosphates. Examples of high-resolution 31P, 1H (and 17O), solid state NMR experiments of a 17O-enriched monocalcium phosphate monohydrate-monetite mixture and of a mouse tooth are presented. In both cases, the advantage of performing fast Magic Angle Spinning NMR experiments at high magnetic fields is emphasized, notably because it allows very small volumes of sample to be analyzed.

An analysis of indentation hardness data from three ceramic materials, zirconium diboride, silicon carbide, and titanium nitride, is presented to extract the fundamental deformation parameters at 295 to 623 K. The measured activation volume was of the order of 1 × b3 to 4 × b3 (b is the Burgers vector). The calculated activation energies were in the range of 0.75 to 1.61 eV and are typical of lattice-controlled dislocation glide mechanism. Using finite difference simulations, it was demonstrated that there is a significant difference between the plastic strain rate and the total strain rate for materials showing substantial elastic deformation (i.e., large hardness/elastic modulus ratio). Therefore, the measured total strain rates must be converted into plastic strain rates, which require a reduction during loading and an increase during the dwell at maximum load. Additionally, importance of quantification of instrumental thermal drift was discussed and use of either short duration indentation tests or high loads was emphasized.

Magnetoelectric (ME) effect has been studied in bi-rectangular structure made up of epoxy-bonded negative/positive magnetostrictive and piezoelectric flakes. The ME effect is affected by negative and positive magnetostrictive flakes. The ME voltage coefficient at resonance frequency shows a nearly constant plateau behavior with the bias magnetic field increased from 1 to 3.5 kOe. There is no interface between magnetostrictive and piezoelectric flakes required to achieve ME coupling, which provides a new choice to make ME devices.