The unique structure and mechanical properties of platelet-reinforced biological materials such as bone and seashells have motivated the development of artificial composites exhibiting new, unusual mechanical behavior. On the basis of designing principles found in these biological structures, we combined high-performance artificial building blocks to fabricate platelet-reinforced polymer matrix composites that exhibit simultaneously high tensile strength and ductility. The mechanical properties are correlated with the underlying microstructure of the composites before and after mechanical loading using transmission electron microscopy. The critical role of the strength of the platelet–polymer interface and its dependence on the platelet surface chemistry and the type of matrix polymer are studied. Thin multilayered films with highly oriented platelets were produced through the bottom-up layer-by-layer assembly of submicrometer-thin alumina platelets and either polyimide or chitosan as polymer matrix. The tensile strength and strain at rupture of the prepared composites exceeded that of nacre, whereas the elastic modulus reached values similar to that of lamellar bones. In contrast to the brittle failure of clay-reinforced composites of similar or higher strength and stiffness, our composites exhibit plastic deformation in the range of 2–90% before failure. In addition to the high reinforcing efficiency and ductility achieved, several toughening mechanisms were identified in fractured composites, namely friction, debonding, and formation of microcracks at the platelet–polymer interface, as well as plastic deformation and void formation within the continuous polymeric phase. The combination of high strength, ductility, and toughness was achieved by selecting platelets that exhibit an aspect ratio high enough to carry significant load but small enough to allow for fracture under the platelet pull-out mode. At high concentrations of platelets, the ductility gets lost because of out-of-plane misalignment of the platelets and incorporation of voids in the microstructure during processing. The designing principles applied in this study can potentially be extended to other types of platelets and polymers to obtain new, hybrid materials with tunable mechanical properties.

Poly(vinyl alcohol) (PVA) and poly(tetrafluoroethylene) (PTFE) emulsion were blended with different mass concentrations and the blended spinning solutions were electrospun into composite nanofibers. The influence of the blend ratio of PVA to PTFE and electrospinning technical parameters on the morphology and diameter of the composite nanofibers were investigated. According to the result of thermogravimetric analyzer analysis, the composite membrane was sintered at 390 °C. The membranes were then characterized by differential scanning calorimetry, attenuated total reflection-Fourier transform infrared (ATR-FTIR), and scanning electron microscopy, respectively. The mechanical properties of the membranes before and after sintering were analyzed through tensile testing. The results show that the PTFE porous membranes could be electrospun effectively, thus demonstrating their potential application as filter media.

The effects of ruthenium (Ru)-oxidation states were investigated on Ru dissolution from PtRu thin-film electrodes, with the 200 cycles between 0.4 and 1.05 V (versus normal hydrogen electrode). The Ru-oxidation states of the PtRu thin films were systematically modified by an anodic (oxidation) treatment. The anodic-treated PtRu electrodes, whose methanol-oxidation activity was similar to untreated electrodes before the 200 cycles, showed a remarkable decrease in methanol oxidation after the cycles, because of the Ru dissolution from the PtRu surface. The results suggest that the Ru-oxide species are the origin of Ru dissolution in the PtRu alloy.

The role of high current stressing during growth of the P-rich phase at the electroless Ni/Sn interface was examined by transmission electron microscopy. Prior to current stressing, two layers of Ni12P5, columnar Ni12P5 and noncolumnar Ni12P5, were formed after soldering. Upon electric stressing, the two layers of P-rich phase showed opposite growth patterns at the two opposing electrode interfaces. At the cathode, columnar growth of the P-rich phase was greatly enhanced while growth of the noncolumnar layer was inhibited. By contrast, the opposite was found at the anode where the current stressing promoted the noncolumnar growth but suppressed the growth of the columnar layer. Such a strong polarity effect resulted from directional electromigration of the key reaction species, nickel, to and from the interfacial reaction fronts. As a result of the difference in reaction mechanism, overall growth of the P-rich phase was much faster at the cathode during current stressing.

In situ observation of tin whisker growth in NdSn3 compound was carried out by using an optical microscope (OM) and scanning electron microscopy (SEM). The growth rate of Sn-whisker from NdSn3 is shown to be rapid (approximately 8-15Å/s) during exposure to room ambience, and it is accompanied by formation of a new compound, Nd(OH)3, as was confirmed by x-ray diffraction. This reaction between the Sn-RE compound and trace water in room ambience has significant influence on whisker growth. There is an electron irradiation effect on whisker growth; that is, whiskers stopped growing after being observed in SEM. Therefore, it is suggested that OM be used rather than SEM to observe the continuous whisker growth. In discussion, the driving force per Sn atom for whisker growth is estimated as 1 × 1014 N in accordance with the whisker growth rate, and its apparent force originates from a chemical potential gradient between the released Sn atoms and the whisker.

Molecular organization of self-assembled n-dimethyl-n-octadecyl-3-aminopropyltrimethoxysilychloride (DMOAP) layers on indium tin oxide (ITO) coated glass substrates was thoroughly investigated. The layer thickness for each deposition was determined by variable angle spectroscopic ellipsometry (VASE), while from static contact-angle measurements we deduced valuable information regarding the ordering of the molecular structures at the solid-air interface. In particular, the DMOAP thin film formation was studied for two different drying temperatures (85 °C and 120 °C). While at Tdrying = 85 °C we observed the formation of a molecular monolayer characterized by a close packed structure, at the higher temperature the DMOAP molecules “bend” at the substrate as they stack in relatively disordered clusters. A qualitative interpretation of this phenomenon is given, in good agreement both with the obtained experimental data and experimental investigation reported in the scientific literature. The observations regarding the DMOAP molecular level organization as a function of substrate temperature could bring essential information to the self assembly research community and also explain some important physical phenomena occurring at interfaces.

The effects of ultraviolet (UV) radiation on ultra-low-k dielectric (ULK) thin film fracture toughness were studied. This work discusses both critical and subcritical crack growth behavior under different environments. The critical fracture toughness was measured as a function of applied phase angle by using the four-point bend flexure and mixed-mode double cantilever beam techniques. Results of critical fracture toughness obtained under different loading configurations and phase angles were found to increase with the UV treatment time. In contrast, mode I subcritical fracture toughness thresholds and the crack propagation velocity appeared to be insensitive to UV curing processes. This study revealed that subcritical fracture toughness values reduced with the moisture concentration in the environment.

The growth mechanism for the out-of-plane orientation of Nd–Fe–B films has been interpreted by the adparticle mobility during film growth, from the point view of the extended structure zone model. The growth mode changes sequentially from zone II to zone Ic, with the lowered thermally induced adparticle mobility on the surface as the film grows. As such, the whole Nd–Fe–B film evolves from [00l] out-of-plane orientation to more randomly out-of-plane alignment. With the growth of the out-of-plane–oriented Nd–Fe–B film, the correlation between the magnetic properties and the alignment evolution has been studied. The coercivity variation with the film growth is understood by analyzing the nucleation-dominant reversal processes for the out-of-plane–oriented Nd–Fe–B films.

Successful growth of vertically aligned carbon nanotube (CNT) arrays on copper substrate by thermal chemical vapor deposition is reported in this paper. The effects of Ti, Ni, and Ni–Cr intermediate layers have been studied to eliminate cracking of the copper surface during the synthesis of CNTs. It was found that these intermediate layers play a critical role in achieving vertical alignment of CNTs on copper substrates. The effects of other reaction parameters such as flow rate of ethylene, concentration of water vapor, and deposition temperature have also been studied. Scanning electron microscopy, transmission electron microscopy, and micro-Raman spectroscopy were used to evaluate the quality and nature of the CNT formed.

Large-scale, well-aligned, and oriented ZnS nanorod arrays were fabricated by a novel and original template-free hydrothermal method. The ZnS nanorods were grown on the pulse-plating Zn nanocrystallines along a certain Zn crystalline direction. It was found that reaction factors such as hydrothermal reaction time, zinc source, and sulfide source concentration in the precursor solution, the acid–base property of the precursor solution, and the substrate where ZnS nanorod arrays were grown greatly influence the morphology of the final products. The growth mechanism of ZnS nanorod arrays was also studied. Pulse-plating Zn nanocrystallines were found to be essential for the growth of ZnS nanorod arrays. These ZnS nanorod arrays could be theoretically fabricated on almost any raw base plate as long as Zn nanocrystallines could be pulse-plated on it. Therefore, the as-synthesized ZnS nanorod array might be one of the promising candidates for field-emission or sensitive nanomaterials in the future.

An environmentally friendly route to prepare stable concentrated aqueous dispersions of silver nanoparticles is described. It was found that Arabic gum, a well known stabilizing agent, can also rapidly and completely reduce Ag2O to metallic silver in alkaline solutions (pH > 12.0) and elevated temperature (65 °C). The average size of the silver nanoparticles could be tailored from 10 to 30 nm by varying the experimental conditions. By hydrolyzing either enzymatically or chemically the polysaccharide, it was possible to isolate dispersed silver nanoparticles suitable for both biological and printable electronics applications. For the latter purpose, concentrated dispersions of silver particles were prepared and used for depositing thin uniform layers, which could be sintered into conductive films at low temperatures.

Polycrystalline HoGaMnO5, ErGaMnO5, and TmGaMnO5 oxides have been first prepared by soft chemistry procedures followed by high oxygen pressure treatments, to stabilize Mn4+ cations. Their crystal structures and magnetic behavior have been studied at room temperature and 5 K by neutron powder diffraction (NPD) data in complement with magnetization measurements. RGaMnO5 are orthorhombic, Pbam space group, and their crystal structures contain infinite chains of edge-sharing Mn4+O6 octahedra, interconnected by pyramidal Ga3+O5 and RO8 units. For R = Ho, a = 7.2810(4), b = 8.4526(4), and c = 5.6668(3) Å; for R = Er, a = 7.2575(3), b = 8.4357(3), and c = 5.6613(2) Å; and for R = Tm, a = 7.2438(3), b = 8.4124(3), and c = 5.6509(2) Å, at room temperature. Above 300 K the reciprocal magnetic susceptibility follows a Curie-Weiss law. In the paramagnetic region, a positive Weiss constant suggests the presence of ferromagnetic interactions, which have been investigated by low-temperature NPD for R = Er, Tm. The 5 K patterns show a detectable long-range magnetic ordering over the Mn and R positions, ferromagnetically aligned along the x-direction.

Effect of H2O2 on synthesis and powder properties such as surface area and agglomerate size of nanocrystalline Ce0.8M0.2O1.90 (M: Sm, Gd) was explored by treating cerium nitrate and rare-earth nitrate with NaOH in the presence/absence of H2O2. The resultant products were characterized by x-ray diffraction, Raman spectroscopy, thermo-gravimetry–differential thermal analysis, dynamic light scattering, surface area analysis, high-resolution transmission electron microscopy, and x-ray photoelectron spectroscopy. The presence of H2O2 was found to have a profound effect on powder properties such as surface area and particle size of these doped ceria samples and results in smaller crystallite size, softer agglomerates, and larger surface area. A mechanism is proposed to explain the observed better powder properties of the samples. It was also shown that the samples prepared in the presence of H2O2 can lower the conversion temperature of CO to CO2, proving these to be better catalysts. Interestingly, temperature-programmed reduction studies on Sm3+-doped samples showed that the doping in conjunction with the use of H2O2 leads to enhanced reduction properties of the samples over multiple cycles.

Three solid solutions of pyrochlores in the series Nd2-yearsGdyZr2O7 (y = 0.8, 1.0, 1.2) were synthesized by the gel combustion method using citric acid as fuel. This results in a soft agglomerate powder as verified by dynamic light scattering. The single-phase nature of the products has been confirmed by x-ray diffraction. The increase in full width at half-maxima in the Raman spectra with an increase in Gd3+ content indicates that disorder increases with Gd3+ content. The morphology and particle size of the products were investigated by transmission electron microscopy. Scanning electron microscopy study reveals that the sintered pellets have a density higher than 92% of theoretical densities. The total ionic conductivity measurements in the temperature range 375–800 °C show that with the increase of disorder (Gd3+ content) in the system the activation energy of conduction increases from 0.98 to 1.06 eV and the preexponential factor, which is proportional to the number of mobile species, also follow the same trend of increase. The total conductivity measured in reducing atmosphere shows no change in electrical conductivity, which verifies a negligible contribution of electronic contribution in this system.

By optimizing the heating rate during spark-plasma-sintering (SPS) processing, a high-strength transparent spinel (MgAl2O4) can be successfully fabricated for only a 20-min soak at 1300 °C. For the heating rates of ≤10 °C/min, the spinel exhibits an excellent combination of in-line transmission (50–70%), four-point-bending strength (>400 MPa), and hardness (>15 GPa). The excellent optical and mechanical properties can be ascribed to the superimposed effects of the sub-micrograin size, fine-pore size, and low porosity, which are related closely to the heating rate during the SPS processing. The present study demonstrates that to attain a high-strength transparent spinel at low temperatures and short sintering times, the low-heating-rate SPS processing is more efficient compared with the high-heating-rate SPS processing.

The thermoelectric LaFe3CoSb12 nanopowders were synthesized by the hydro/solvo thermal method. The effects of different solvents were investigated by using only the potassium antimony tartrate as Sb source. Also, the effects of the different Sb sources were investigated by using only water as solvent on the morphologies of the resulting nanopowders. The results show that a mixture of nanoparticles and nanorods can be obtained in aqueous solution of cetyltrimethylammonium bromide or ethylenediamine-tetra-acetic disodium salt. In ethylenediamine only nanorods can be obtained, and in ethylene glycol only nanoparticles can be obtained. The other morphologies of the LaFe3CoSb12, such as particle-like, nest-shaped, branch-shaped, or feather-like crystalline, can be synthesized in water by selecting a suitable Sb source.

Mg-Li-Al alloy was prepared by ingot casting and then underwent subsequent reactive ball milling. A Mg-Li-Al-H complex hydride was obtained under a 0.4 MPa hydrogen atmosphere at room temperature, and as high as 10.7 wt% hydrogen storage capacity was achieved, with the peak desorption temperature of the initial step at approximately 65 °C. The evolution of the reaction during milling, as well as the effect of Li/Al ratio in the raw materials on the desorption properties of the hydrides formed, were studied by x-ray diffraction and simultaneous thermogravimetry and differential scanning calorimetry techniques. The results showed that mechanical milling increases the solubility of Li in Mg, leading to the transformation of bcc β(Li) solid solution to hcp α(Mg) solid solution, the latter continues to incorporate Li and Al, which stimulates the formation of Mg-Li-Al-H hydride. A lower Li/Al ratio resulted in faster hydrogen desorption rate and a greater amount of hydrogen released at a low temperature range, but sacrificing total hydrogen storage capacity.

The structural characteristics of TiMn1.5Vx (x = 0.1–0.5) alloys and the hysteresis phenomenon in the TiMn1.5Vx-H2 system have been studied. The TiMn1.5Vx alloy consists mainly of the C14 Laves phase plus some of the BCC solid solution phase, depending on x. The lattice parameters of the C14 Laves phase increase slightly as x increases from 0.1 to 0.2 but are invariant with a further increase in x up to 0.3–0.5. The pressure-composition isotherms clearly show a pressure hysteresis in the TiMn1.5Vx-H2 system which decreases with an increase in the x value mainly due to the equilibrium pressure change for hydride formation. The free energy loss during hydride formation is related to not only the volume expansion, but also the elastic strain in the TiMn1.5Vx alloy itself, that is, prior to hydrogen absorption.

Novel ultrafine eutectic composites containing structural and spatial heterogeneities have been systematically developed in an Mg–Cu–Zn ternary system. Microstructural investigations of the ultrafine eutectic composites revealed that the bimodal eutectic structure consists of a mixture of cellular-type fine (α-Mg + MgZn2) and anomalous-type coarse (α-Mg + MgZn2 + MgCuZn) eutectic structures. An Mg72Cu5Zn23 alloy composed of the bimodal eutectic structure without micron-scale α-Mg dendrites presents a strong improvement of yield strength up to 455 MPa with a decent plastic strain of 5%. The rotation of the bimodal eutectic colony along the interfaces is considered to be an effective way to dissipate the stress localization thus enhancing the macroscopic plasticity.

The effect of prestrain on microstructure and mechanical behavior of aged Ti–10V–2Fe–3Al alloy was investigated. The results showed that prestrain caused the tensile strength to decrease by 5%, but the elongation to fracture significantly improved by about 200%, in comparison with the unstrained samples, using a much shorter aging time. Transmission electron microscopy investigations showed that nano-sized alpha (α) particles homogeneously precipitated in the beta (β) matrix, and continuous α films formed along grain boundaries in the unstrained and aged samples. However, in the prestrained samples, the coarse stress induced martensite laths decomposed into α- and β-phases in the form of alternately arranged plates, which suppressed formation of the continuous grain boundary α films during aging. The hardness of the prestrained samples was lower than that of the unstrained samples after the same aging treatments. The enhancement of ductility can be mainly attributed to the suppression of grain boundary α films and the reduced hardness in prestrained samples.