In this paper, the responses in the microregion of three ferroic-type materials, such as ferroelectric single crystals (PMN-PT and BaTiO3), ferromagnetic alloy (Fe81Ga19), and ferroelastic alloy (Ni53Mn24Ga23), to local stress induced by Vickers indentations were studied using scanning electron-acoustic microscopy (SEAM), a powerful technique for nondestructive investigation of the microstructure of materials. The responses of ferroelectric domains, magnetic domains, and ferroelastic domains to local stress were successfully observed. These responses possess three major features including the plastic deformation underneath the indenter, the extension of microcracks induced by indentation, and the formation of new lamellar domains within the matrix domain structure. In addition, by using the unique ability of SEAM to image layer by layer, the distributions of residual stress at different depths were obtained. The generation mechanisms of the electron acoustic signals of ferroelectric domains, magnetic domains, and ferroelastic domains are discussed.

The electron energy structure of self-assembled In(Ga)As/GaAs nanostructures, quantum dots, and quantum rings was studied with capacitance-voltage spectroscopy and one-dimensional numerical simulation using Poisson/Schrödinger equations. The electron energy levels in the quantum dots and quantum rings with respect to the electron ground state of the wetting layer were determined directly from capacitance-voltage measurements with a linear lever arm approximation. In the regime where the linear lever arm approximation was not valid anymore (after the charging of the wetting layer), the energy difference between the electron ground state of the wetting layer and the GaAs conduction band edge was obtained indirectly from a numerical simulation of the conduction band under different gate voltages, which led to the erection of complete electron energy levels of the nanostructures in the conduction band.

We show a drastically improved gas–solid reaction between NH3 and LiH by mechanical treatment for LiH, generating a hydrogen gas even at room temperature. The results of x-ray photoelectron spectroscopy showed that the mechanical pretreatment was effective in reducing a hydroxide phase from the surface of LiH. It was also possible to successfully recycle back LiNH2, which is the byproduct of this hydrogen desorption reaction, to LiH under 0.5-MPa H2 flow at 573 K. Thus, the LiH–NH3 system provides a recyclable H2 storage system to generate H2 at room temperature with 8.1 mass% and 4.5 kg/100 L hydrogen capacity.

Using a spherical aberration (Cs)-corrected scanning transmission electron microscopy (STEM) and electron energy-loss spectroscopy (EELS), we investigated a 6° low-angle [001] tilt grain boundary in SrTiO3. The enhanced spatial resolution of the aberration corrector leads to the observation of a number of structural variations in the edge dislocations along the grain boundary that neither resemble the standard edge dislocations nor partial dislocations for SrTiO3. Although there appear to be many variants in the structure that can be interpreted as compositional effects, three main classes of core structure are found to be prominent. From EELS analysis, these classifications seem to be related to Sr deficiencies, with the final variety of the cores being consistent with an embedded TiOx rocksalt-like structure.

Individual triangular/hexagonal nanoplates, chain-like nanoplate assemblies, and nanobelts in the case of silver were selectively synthesized using N,N-dimethylformamide (DMF) in the presence of poly (vinyl pyrrolidone) (PVP). The molar ratio of AgNO3/PVP, concentration of AgNO3, temperature, and process time were crucial factors in determining the morphologies of the final products. Based on the experimental results, it was concluded that the products were favorable to form individual nanoplates because of the strong interaction between PVP and Ag+, and the outline of the nanoplates was controlled by the ratio of AgNO3 and PVP. The formation of novel chain-like nanoplate assemblies could be explained by the secondary growth of the nanocrystals. If the reaction continuously lasted for another 7 h, the chain-like assemblies could transform into nanobelts with width of 40∼100 nm and the length of several micrometers.

The uniaxial compressive deformation of core/shell-type Cu/Ag nanoparticles and naked Cu nanoparticles were simulated by molecular dynamics, revealing the role of nanophase boundaries in the mechanical deformation. The simulations show that single type of partial dislocations glide across the entire slip planes of the Cu cores, resulting in elongated Cu cores compared with circular Cu cores of naked Cu nanoparticles. The phase boundary is the nucleation source of dislocations, and the ultrahigh atomic level stress of part atoms in the phase boundary can ensure the movement of the single type of dislocations under compressed.

Significant shifts of the frequency of the Raman spectra of the tangential mode of single walled carbon nanotubes (SWNTs) and fluorinated tubes (FSWNTs) in composites of polybutadiene (PB) were observed relative to the pristine SWNTs indicative of the interaction between the polymer and the SWNTs. Proton NMR line width measurements demonstrate partial suppression of polymer segmental motion for both types of nanotube composites and spin-lattice relaxation results indicate that short time-scale localized motions are also affected by SWNT inclusion, more so for FSWNTs. Hardness measurements as a function of wt% SWNTs and FSWNTs in the polymer show larger enhancements of hardness in the composite with the fluorinated tubes.

Nanocrystalline strontium titanate (SrTiO3) particle/polymer hybrid was synthesized from metal–organics and 2-(methacryloyloxy)ethyl maleate (MMEM). SrTiO3 precursor was prepared from strontium isopropoxide and titanium isopropoxide in 2-methoxyethanol. Nanocrystalline SrTiO3 particle/poly-MMEM hybrid was formed by hydrolysis followed by reaction with MMEM. The crystallinity of SrTiO3 particles depended on the amount of water for hydrolysis. The nanocrystalline particles were identified to be strontium titanate by x-ray diffraction. Fourier transform infrared spectroscopy and x-ray photoelectron spectroscopy showed the presence of the chemical bond between SrTiO3 particles and the organic matrix. The fluid consisting of SrTiO3 particle/poly-MMEM and silicone oil revealed a yield stress dependent on various conditions, such as hydrolysis conditions and applied field. The hybridization was found to have a pronounced effect on the electrorheological properties of the nanoparticle/polymer-based system.

The electronic transport and magnetic properties of nanocomposites, in which nanoparticles of superconducting (SC) molybdenum carbides are embedded in a ferromagnetic (FM) carbon matrix to form a three-dimensional SC-FM network, are studied. The high-resolution transmission electron microscope observation shows that the carbon in the nanocomposites is in both ordered and disordered forms. The magnetic properties of the nanocomposites are ruled by the ferromagnetic carbon matrix. The temperature dependence of electrical resistivity of the nanocomposites is dominated by the carbon matrix, showing the semi-conductivity. The special I-V curves near the zero voltage bias of the nanocomposites are observed at low temperatures, due to the influence of contact barriers between molybdenum carbides and the carbon matrix.

Zirconium tungstate (ZrW2O8) is a unique ceramic material characterized by isotropic negative thermal expansion behavior over a wide temperature range. Incorporation of ZrW2O8 is expected to improve the dimensional stability of polymers by reducing the overall coefficient of thermal expansion (CTE). In this work, the thermal and dynamic mechanical properties of a bisphenol E cyanate ester reinforced with various loadings of ZrW2O8 are examined. Thermomechanical analysis indicates that the incorporation of ZrW2O8 results in a decrease in CTE at temperatures above and below the glass transition temperature (Tg) of the neat resin. The dynamic storage moduli of the composites reinforced with ZrW2O8 are found to increase with increasing filler loading. Furthermore, the various phase behaviors exhibited by ZrW2O8 are also examined by differential scanning calorimetry measurements.

In this study, the dense films of well-crystallized ZnO nanocrystals were successfully prepared by direct spin-coating of the colloidal solution of ZnO nanoparticles derived from the microemulsion method. The average grain sizes in the films were reasonably controlled in the range from 6.5 to 34.3 nm by simply changing the annealing temperatures. The increase in band gap energies was found in the size region less than 13.3 nm, finally resulting in 3.47 eV for the average size of 6.5 nm. The photoluminescence spectra at room temperature showed intense ultraviolet (UV) emission with faint green luminescence. The Stokes shifts of the films were estimated to be one or two orders of magnitude smaller than those of the conventional ZnO nanocrystalline films, suggesting the well crystallization and slight amounts of lattice defects in the ZnO nanoparticles. These excellent features may be favorable to make high-performance optical application such as UV emitting devices.

AlN codoped ZnO films were deposited on sapphire substrates at low temperature using a cosputter system under various N2/(N2 + Ar) flow ratios. To investigate the nitrogen function, the ratio of nitrogen ambient was varied during cosputtering. AlN codoped ZnO films with various crystallographic structures and bonding configurations were measured. With an adequate nitrogen atmosphere deposition condition and postannealing temperature at 450 °C, the p-type conductive behaviors of AlN codoped ZnO films were achieved due to the formation of Zn–N bonds. According to the low-temperature photoluminescence spectra, the binding energy (EA) of 0.16 eV for N acceptors can be calculated. Using time-resolved photoluminescence measurement, the carrier lifetime in AlN codoped ZnO films increases due to the reduction of oxygen vacancies caused by the occupation of adequate nitrogen atoms.

Photoluminescence (PL) properties of SiOx thin films deposited by pulsed laser ablation of Si in a reactive oxygen ambient and annealed in a nitrogen atmosphere were studied at room temperature. Raman spectroscopy, Fourier transform infrared spectroscopy, and optical transmission measurements were used to characterize the deposited films before and after annealing and complement the PL studies. Strong PL due to quantum confinement was observed at room temperature from Si nanocrystals with an average diameter of approximately 5 nm at 325-nm light excitation. An apparent dependence of PL on the oxygen pressure for film deposition was observed. A detailed analysis of the effects of the annealing temperature revealed a significant PL evolution in luminescence intensity, spectrum profile, peak position, and spectrum range with the annealing temperature ranging from 300 to 1200 °C. Structural variations induced by thermal annealing of the films deposited at different oxygen pressures were also discussed on the basis of their correlation with the PL evolution.

Various α-GaOOH nanorods were synthesized through a microwave-assisted method at 80 °C. In the synthesis, Ga(NO3)3 was used as the gallium source, and urea, L-cysteine, and EDTA disodium salt were used as the additives. The thermal decomposition of the as-prepared α-GaOOH nanorods could selectively produce α-, β-, and ε-Ga2O3 nanorods. X-ray diffraction, scanning electron microscopy, transmission electron microscopy, high-resolution transmission electron microscopy, and cathodoluminescence were used to characterize the resulting samples. On the basis of characterization results, the possible growth mechanisms of these various GaOOH nanorods were proposed. This study provides a controllable method to prepare various gallium oxyhydroxide and gallium oxide nanorods.

This study reports the synthesis of monosized Pr nanoparticles with a controllable size ranging from 5 to 20 nm. Pr agglomerates generated by a spark generator first size-selected by a differential mobility analyzer and subsequently sintered in-flight at different temperatures result in spherical and monocrystalline Pr nanoparticles. The dependence of size and size distribution of Pr nanoparticles has been studied as a function of deposition parameters related to spark generator, differential mobility analyzer, and sintering. Transmission electron microscopy, energy-dispersive x-ray analysis, glancing angle x-ray diffraction, and x-ray photoelectron spectroscopy studies confirm that initial Pr agglomerates and the resulting nanoparticles are metallic with d-hexagonal structure and remain stable in air during post-deposition exposure. Incomplete or partially sintered nanoparticles were found to be oxidized, resulting in the formation of amorphous oxide phase due to enhanced oxidation at grain boundaries.

Dense networks of amorphous GaSb nanofibers were fabricated by ion irradiation of bulk GaSb, and following formation, they were thermally annealed at a low temperature. Contrary to expectations, annealing of the GaSb fibers at just 50% of their melting temperature resulted in complete chemical decomposition of the nanofibers into core-shell structures consisting of crystalline Sb cores surrounded by amorphous shells. In this study, we investigate the transition of the single-phase nanofibers to their core-shell configuration, and we analyze the unique, temperature-dependent phase decomposition process. Thermodynamic considerations are discussed, and a model is presented to explain the thermally induced decomposition of the GaSb semiconductor fibers into core-shell structures, based upon the singular interaction of several size-dependent material properties.

In this study, p-type CuInSe2 (CIS) films were prepared by selenization of one-step electrodeposited Cu-In-2Se (atomic ratio) precursors. To obtain high-quality, dense, and homogeneous CIS films for solar cell application, the effects of substrate temperatures during selenization and precursor compositions on the final microstructures were systematically investigated. The precursor layers evolved in very different ways under different selenization conditions. The final microstructures and phases of the films depended critically on the precursor compositions, selenization temperature, and the selenization thermal process history. Low melting temperature CuxSe phase, which tended to segregate at the film surface, can efficiently assist the CIS grain growth. Large hexagonal CuSe platelets were formed at a temperature as low as 170 °C in Cu-rich precursor, which acted as an element-transport flux agent at higher temperature under high Se vapor and reacted with In-Se selenide to form CIS at temperatures above 500 °C. Good crystalline quality chalcopyrite CIS film was obtained at a selenization temperature of 550 °C.

In this study, the mechanical properties of human dental structures have been investigated by using instrumented nanoindentation. Immersion in solutions containing Streptococcus mutans, which is the principal cause of dental caries, was applied to tooth specimens to clarify its effect on the microstructure and mechanical properties of the dental structures. With an extended time of up to 16 h, the pH value of the S. mutans solutions dropped from 7.3 to 5.8. Therefore, after immersion in the S. mutans solutions for 16 h, slight erosions of the dental structures began; after 64 h, severe tooth decay occurred with obviously etched dental features. After 128 h, the elastic modulus of enamel and dentine dropped to 85 and 67%, respectively, of the original values of untreated specimens, and the hardness dropped to 88 and 55%, respectively.

The stable superparamagnetic colloidal suspension of chitosan-poly(acrylic acid) (CS-PAA)/Fe3O4 nanoparticles was synthesized by graft copolymerization AA on the surface of CS stabilized Fe3O4 nanoparticles. The size, size distribution, structure, and magnetic properties of the resultant CS-PAA/Fe3O4 nanoparticles were characterized by field-emission scanning electron microscopy (FE-SEM), transmission electron microscope (TEM), dynamic light scattering, Fourier transform infrared spectroscopy, x-ray diffraction, and vibrating sample magnetometry (VSM). FE-SEM and TEM showed the spherelike morphology of CS-PAA/Fe3O4 nanoparticles with their diameter ranging from 15 to 60 nm. VSM measurements indicated that CS-PAA/Fe3O4 nanoparticles preserved the superparamagnetism. CS-PAA complex was proved to be a good stabilizer to prepare the well-dispersed suspension of superparamagnetic Fe3O4 nanoparticles. The stabilizing mechanisms were attributed to the electrostatic repulsion and steric hindrance. The controlled release of entrapped camptothecin from these magnetic nanoparticles was studied and the release mechanism was analyzed.

Inorganic potassium dihydrogen phosphate (KDP) is widely known for its value as a nonlinear optical material. In this study, pure and l-arginine–doped KDP single crystals were grown by the slow solvent evaporation technique and further subjected to infrared absorption and Raman studies for the confirmation of chemical group functionalization and possible bonding between the organic and inorganic materials. The appearance in the infrared absorption spectra of additional vibrational lines, which mostly originate from disturbed N–H, C–H, and C–N bonds of the l-arginine–doped salt, confirm the interaction between KDP and the organic material. This affirmation is supported by more evidence from Raman measurements, where the disappearance of NH vibrations of the amino group is observed. We are thus led to the possibility of hydrogen bonding primarily between the nucleophilic O− of the phosphate unit of KDP and the amino group of the l-arginine.