The constraint factor, C (given by the hardness-yield strength ratio H/Y in the fully plastic regime of indentation), in metallic glasses, is greater than three, a reflection of the sensitivity of their plastic flow to pressure. Furthermore, C increases with increasing temperature. In this work, we examine if this is true in amorphous polymers as well, through experiments on amorphous poly(methyl methacrylate) (PMMA). Uniaxial compression as well as spherical indentation tests were conducted in the 248–348 K range to construct H/Y versus indentation strain plots at each temperature and obtain the C-values. Results show that C increases with temperature in PMMA as well. Good correlation between the loss factors, measured using a dynamic mechanical analyzer, and C, suggest that the enhanced sensitivity to pressure is possibly due to β-relaxation. We offer possible mechanistic reasons for the observed trends in amorphous materials in terms of relaxation processes.

To evaluate mechanical properties by means of nanoindentation, information on the contact area is crucial. However, the contact area is not directly accessible in experiments and is usually calculated according to the Oliver and Pharr procedure, which turned out to be unsatisfying when applied to viscoelastic materials like polymers. In this study, complementary in situ indentation testing and finite element analysis (FEA) were performed on silicone elastomers. Through this combination of techniques, several individual error sources in the conventional contact area determination have been identified and quantified. For shallow penetrations, contact areas after Oliver and Pharr were up to 40% smaller than the in situ testing results; for larger penetrations, the contact size was overestimated by approximately 6%. The deviations of the resulting mechanical properties were approximately 10%. Viscoelastic effects could be captured if dynamic indentation testing was performed.

An analytical solution was derived for the indentation of a cell using atomic force microscopy. It was found that the contribution of the cell membrane to the overall indentation stiffness is dependent on the size of the indenter. When a small indenter [for example, an atomic force microscopy (AFM) tip] is used to probe the mechanical properties of cells, the cell membrane and its prestress were important in interpreting indentation data. The solution allows the partition of contributions from the membrane and the interior soft phase. The apparent elastic modulus of the cell and the prestress of the cell membrane can be extracted. In addition, the modulus of the cell membrane could be estimated from the extracted apparent modulus if the interior soft phase of the cell was known and vice versa. However, when a large indenter is used (for example, a microbead attached to the cantilever beam of the AFM), the contribution of the cell membrane is negligible.

In this work, the effects of conical indentation variables on the load–depth indentation curves were analyzed using finite element modeling and dimensional analysis. A factorial design 26 was used with the aim of quantifying the effects of the mechanical properties of the indented material and of the indenter geometry. Analysis was based on the input variables Y/E, R/hmax, n, θ, E, and hmax. The dimensional variables E and hmax were used such that each value of dimensionless Y/E was obtained with two different values of E and each value of dimensionless R/hmax was obtained with two different hmax values. A set of dimensionless functions was defined to analyze the effect of the input variables: Π1 = Pl/Eh2, Π2 = hc/h, Π3 = H/Y, Π4= S/Ehmax, Π6 = hmax/hf, and Π7 = Wp/WT. These six functions were found to depend only on the dimensionless variables studied (Y/E, R/hmax, n, θ). Another dimensionless function, Π5 = β, was not well defined for most of the dimensionless variables and the only variable that provided a significant effect on β was θ. However, β showed a strong dependence on the fraction of the data selected to fit the unloading curve, which means that β is especially susceptible to the error in the calculation of the initial unloading slope.

The influence of prior cold deformation on precipitating of alpha phase as well as the variation of hardness during aging has been investigated in solution-treated Ti-10Mo-8V-1Fe-3.5Al alloys. The results show that alpha phase precipitation could be obviously accelerated by the prior cold deformation. In the predeformed samples, a network pattern structure was observed with an optical microscope after aging treatment. It could be attributed to the phenomenon that the plate-shape alpha precipitates prefer to nucleate and grow in the regions with a high density of dislocations, especially inside slip bands. The hardness of both the predeformed and undeformed TB3 specimens after different aging times was measured and further predicted by a proposed strengthening model based on the grain refinement mechanism of the beta phase. The predicted results are consistent with the experimental results, especially in the later aging stages.

Cr3+/Ni2+ co-doped optically transparent magnesium aluminosilicate glass-ceramics containing MgAl2O4 nanocrystals have been prepared by heat-treatment. Greatly enhanced broadband near-infrared emission centered at 1216 nm in Cr3+/Ni2+ co-doped glass ceramics is observed when compared with the Ni2+ single-doped glass ceramics under 532 nm excitation. The observed enhancement of infrared emission is attributed to the energy transfer from Cr3+ to Ni2+ ions in the nanocrystalline phase, which leads to the emission due to 3T2(3F) → 3A2(3F) transition of octahedral Ni2+ ions.

The structural evolution with temperature of some V2O5 gels and thin films is presented, and the role of the hydrolysis conditions is investigated. Several techniques, i.e., x-ray diffraction, differential thermal analysis, infrared, and temperature-dependent Raman spectroscopy, have been used to follow the thermal behavior of the samples. When the bulk xerogels begin to change from a nanocrystalline phase to the orthorhombic α-V2O5, in the temperature range 280 to 300 °C, a growth of vanadium oxide nanotubes also occurs, while at higher temperatures the crystallization into the α phase prevails. A slightly different evolution is observed for heat treated thin films, which show a structure containing polyvanadate chains near room temperature. They also present a growth of nanotubes for intermediate temperatures and a complete crystallization into the α phase when the temperature is further increased.

MAX-phase carbides (M is an early transition metal, A is an A-group element) exhibit an interesting bonding characteristic of alternative stacking of strong M–C bonds and relatively weak M–A bonds in one direction. In the present first-principles total energy calculations, we establish the relationship between mechanical properties and electronic structure for ternary M2AC (M = Ti, V, Cr, A = Al, Si, P, S) carbides. By systematically tuning elements on the M and A sites, pronounced enhancements of bulk modulus, elastic stiffness, and ideal shear strength are achieved in V-containing V2AC (A = Al, Si, P, and S) carbides. It is suggested that tailoring on the A site is more efficient than on the M site in strengthening the mechanical properties of studied serial carbides. The results highlight a general trend for tailor-made mechanical properties of ternary M2AC carbides by control of chemical bonding.

We have fabricated La0.6Ca0.4MnO3 periodic arrays exhibiting tunable optical properties and magnetic properties using nontoxic and environmentally friendly electron beam resist made from La0.6Ca0.4MnO3 sol-gel precursor. We studied their unique optical properties by using the spectral microreflectometer and their magnetic properties using the superconducting quantum interference device and magnetic force microscopy. Additionally, the resist has the ability to demonstrate both positive and negative resist behaviors depending on the electron beam dosage. With these special characteristics, we can fabricate periodic structure on a thin film possessing controlled optical reflectance properties with one fixed design electron beam pattern without changing the structural parameters but changing the electron beam dosage only. Our approach provides an uncomplicated route for the fabrication of nanometer scale magnetic patterns, which serve as the building blocks in the search for novel properties of periodic magnetic arrays.

We developed a new Cu–Zn wetting layer for Pb-free solders. By adding Zn to the Cu wetting layer, intermetallic growth in the Sn–Ag–Cu (SAC) solder interfaces was delayed. Cu3Sn intermetallic compounds and microvoids were not observed in the SAC/Cu–Zn interfaces after aging. The drop reliability of the SAC solder/Cu–Zn joints was excellent.

The thermal coarsening of nanoporous Au was examined and compared with the thermal instability of Au nanoparticles. The nanoporous Au was coarsened at temperatures far below the melting temperature of Au nanoparticles, which possess sizes similar to the nanoligaments. Differential scanning calorimetry characterization of nanoporous Au exhibited an exothermal peak around 470 K. These results suggest that solid-state process like recrystallization, rather than melting, is responsible for the thermal coarsening of nanoporous Au.

We report our observations on the homoepitaxial diamond growth by microwave plasma chemical vapor deposition (MPCVD) experiments on Type Ib diamond substrates conducted by varying three independent variables. In a feed gas mixture of H2, N2, O2, and 13CH4, the amount of nitrogen was varied in the range of 0 to 4000 ppm, the amount of methane was varied from 2% CH4/H2 to 6% CH4/H2, and the substrate temperature was varied in the range of 850 to 1200 °C. We used isotopically enriched carbon-13 methane gas as the source of carbon in the plasma to clearly distinguish the grown diamond layer from the underlying substrate using Raman spectroscopy. The x-ray rocking curve measurements confirmed the homoepitaxial nature of the deposited layers with a slight increase in the full width at half-maximum for sample grown with the highest nitrogen content in the plasma. Optical and atomic force microscopy revealed dramatic changes in surface morphology with variation in each parameter. The nitrogen incorporation in carbon-13 diamond layers was monitored through photoluminescence spectroscopy of nitrogen–vacancy complexes. A twentyfold increase in diamond growth rate was clearly achieved in this multivariable study.

Lamellar liquid crystal (Lα) was formed by room temperature ionic liquid [Bmim]PF6, nonionic surfactant Tween 85, and H2O. The microstructure of this lamellar liquid crystal was investigated by small angle x-ray diffraction (SAXD) and 2H NMR (nuclear magnetic resonance). Ag nanoparticles with relatively uniform dispersion were prepared successfully in this Lα phase. The rheological and lubrication properties of the Lα phase and the Lα/Ag nanoparticle mixed system were also investigated. The results showed that the structure strength, anti-wear capacity, and lubrication properties of the Lα phase were enhanced with an increasing amount of Tween 85, but were impaired with an increasing amount of H2O. Increasing the amount of [Bmim] PF6 could also make the structural strength weaker, but the lubrication properties of the system were improved because of the inherent lubrication properties of ionic liquid. The presence of the Ag nanoparticles in the lamellar phase could also enhance the structural strength, anti-wear capacity, and lubrication properties.

This paper reports on the preparation and characterization of nickel ferrite (NiFe1.98O4) ceramics doped with Bi2O3 as sintering aid. Focus has been on the effects of concentration of Bi2O3 and sintering temperature on the densification, grain growth, dielectric, and magnetic properties of the NiFe1.98O4 ceramics, with an aim at developing magnetodielectric properties, with almost equal real permeability and permittivity, as well as sufficiently low magnetic and dielectric loss tangents, over 3 to 30 MHz (high frequency or HF band). X-ray diffraction results indicated that there is no obvious reaction between NiFe1.98O4 and Bi2O3, at Bi2O3 levels of up to 7 wt% and temperatures up to 1150 °C. The addition of Bi2O3 facilitated a liquid phase sintering mechanism for the densification of NiFe1.98O4 ceramics. The addition of Bi2O3 not only improved the densification but also promoted the grain growth of NiFe1.98O4 ceramics. To achieve sufficiently low dielectric loss tangent, the concentration of Bi2O3 should not be less than 5 wt%. The low dielectric loss tangents of the samples doped with high concentrations of Bi2O3 can be attributed to the full densification of the ceramics. Magnetic properties of the NiFe1.98O4 ceramics, as a function of sintering temperature and Bi2O3 concentration, can be qualitatively explained by the Globus model. Promising magnetodielectric properties have been obtained in the sample doped with 5% Bi2O3 and sintered at 1050 °C for 2 h. The sample has almost equal values of permeability and permittivity of ∼12, together with low dielectric and magnetic loss tangents, over 3 to 30 MHz. This material might be useful for the miniaturization of HF (3 to 30 MHz) antennas.

In this article, we report on enhanced broadband near-infrared emission in Yb–Bi codoped phosphate glasses. The emission intensity of Yb–Bi codoped glass was ˜32 times larger than that of Bi-doped glass when excited with 980-nm laser diode. The highest 1/e fluorescent lifetime of Yb–Bi codoped glass reached 1650 μs. The dependence of emission intensity and fluorescent lifetime on Yb2O3 concentration was investigated. The enhancement of the near-infrared emission is due to energy transfer from Yb3+ (2F5/2–2F7/2) transition to Bi ions, and the highest energy transfer efficiency reached 50%. Yb–Bi codoped phosphate glass should be a promising candidate for broadband optical amplification.