Four kinds of extruded Mg–X at.% Zn binary alloys (X = 1.9, 2.4, 3.0, and 3.4) were used to examine the effect of precipitate volume fraction on fracture toughness. All the alloys had fine grain sizes of 1–3 μm and fine sphere-shaped precipitates of 50–60 nm. The volume fraction of precipitates increased with additional zinc content. The results of mechanical property tests showed that the extruded Mg–2.4 at.% Zn alloy exhibited the best balance of strength and fracture toughness. One of the reasons was the different volume fraction of precipitates at the grain boundaries, which was the source of void formation. According to the fracture surface observations and ductile fracture model analysis, the volume fraction of precipitates of 2%–4% was shown to be enough to improve the fracture toughness for the fine-grained magnesium alloys; i.e., higher contents of zinc atoms were not needed to enhance the mechanical properties.

The environmental sustainability of materials used in construction applications is driving a requirement for the quanti-fcation of performance attributes of such materials. For example, the European Union (EU) Energy Performance in Buildings Directive will give commercial buildings an energy rating when rented or sold. The Code for Sustainable Homes launched by the U.K. Government's Department for Communities and Local Government (CLG) in January 2007 sets out the requirement for all new homes to be carbonneutral by 2016. In addition, homes in the United Kingdom will need to signifcantly reduce water consumption from today's average 160 liters (1) per person per day to less than 801 per person per day. Similarly stringent targets are required for waste, materials, and other factors. Such environmental and energy standards are complementing characteristics such as strength, stiffness, durability, impact, cost, and expected life with factors such as “environmental profle,” “ecopoints” (a single unit measurement of environmental impact arising from a product throughout its lifecycle that is used in the United Kingdom), “carbon footprint” (amount of CO2 produced for the lifecycle of the item), “recycled content,” and “chain of custody” (a legal term that refers to the ability to guarantee the identity and integrity of a specimen from collection through to reporting of test results).

Instead of conventional grain-refinement treatments for improving the ductility of fully lamellar TiAl alloys, multiorientational, lamellar, subcolony refinement with good ductility has been achieved simply by using an electric-current pulse treatment. The microstructural refinement mechanism is attributed to the transformation on heating of γ laths in the prior large-grain lamellar structure to Widmanstätten α in several orientations, which on subsequent cooling forms lamellar structure colonies in multiple orientations. This kind of refined multiple-colony lamellar structure was found to enhance the ductility of the TiAl alloy.

Crystallographic ordering and defects in WSe2 thin films with ultralow thermal conductivity are characterized by electron imaging and diffraction in cross-sectional geometry. The results show that the film consists of oriented, coherent crystallites that are a few nanometers in diameter. Two films of different thickness with different thermal conductivity are compared. We show that the film with a lower thermal conductivity is characterized by less coherent crystallites with a greater degree of misorientation.

Reducing CO2 emissions from the use of fossil fuel is the primary purpose of carbon dioxide capture and storage (CCS). Two basic approaches to CCS are available.1,2 In one approach, CO2 is captured directly from the industrial source, concentrated into a nearly pure form, and then pumped deep underground for long-term storage (see Figure 1). As an alternative to storage in underground geological formations, it has also been suggested that CO2 could be stored in the ocean. This could be done either by dissolving it in the mid-depth ocean (1–3 km) or by forming pools of CO2 on the sea bottom where the ocean is deeper than 3 km and, consequently, CO2 is denser than seawater. The second approach to CCS captures CO2directly from the atmosphere by enhancing natural biological processes that sequester CO2 in plants, soils, and marine sediments. All of these options for CCS have been investigated over the past decade, their potential to mitigate CO2 emissions has been evaluated,1 and several summaries are available.1,3,4

Self-assembled core-shelled hierarchical structures consisting of single-crystalline pyramid Zn microtip as a core, converted ZnO coating as the shell, and the grown ZnO nanowires as branches, have been prepared. Such ZnO hierarchical structures fabricated by a simple aqueous chemical growth method on Zn foil substrate are expected to be easily integrated into nanodevices. These self-organized structures are superior to both the random nanoarchitecture arrays formed in vapor system and the precipitated nanostructures suspended in the solution. Because of the easier transportation of electrons from the metallic core to ZnO branches, the self-assembled core-shelled hierarchical structures exhibit better field-emission characteristics.

The present study investigated the micro-impact fracture behavior of various lead-free solder joints, including Sn–1Ag–0.1Cu–0.02Ni–0.05In, Sn–1.2Ag–0.5Cu–0.05Ni, and Sn–1Ag–0.5Cu. The fracture that occurs within the solder joint corresponds to a higher impact fracture energy (1.35 mJ), while the fracture at the interface between the solder joint and intermetallic compound acquires a smaller impact energy (0.82 mJ). Two types of fracture mechanisms were proposed based on observations of the fracture morphology and the impact curve for the solder ball joints. The longer deflection distance, referring to better elongation, exists for the mechanism corresponding to the higher fracture energy.

It was recently revealed that some processes of hydrating tricalcium silicate are altered by the addition of dicalcium silicate. Previous neutron scattering results revealed two critical tri/dicalcium silicate compositions. At one composition, changes in the early time hydration kinetics were observed that result in the formation of more products (reflected in increased 28 day strength), despite dicalcium silicate being essentially unreactive at early times. At the other composition, changes in the early-time hydration kinetics were observed that correspond to reduced strength. The current work uses scanning electron microscope analysis with backscattered electron imaging of 50 day hydrated tri- and dicalcium silicate mortars to reveal that at the former critical composition increased hydration of the tricalcium silicate phase occurs, and at the latter critical composition, the amount of dicalcium silicate reacted is decreased.

Compositionally graded (Ba1−xSrx)TiO3 (BST) thin films (with 0.0 ⩽ x ⩽ 0.25) were grown by pulsed laser deposition on the (100)MgO single-crystal substrates covered with a conductive La0.5Sr0.5CoO3 (LSCO) layer as a bottom electrode. Their epitaxial growth, dielectric response, and microstructure were characterized. The epitaxial relationships between the BST, LSCO, and MgO can be determined as [001]BST//[001]LSCO//[001]MgO and (100)BST//(100)LSCO//(100)MgO, from the x-ray diffraction (rocking curve, ϕ scans) and electron-diffraction patterns. Dielectric data showed that the room temperature values of the dielectric constant and dielectric loss of the graded BST films were 630 and 0.017 at 100 kHz, respectively. Cross-sectional transmission electron microscopy (TEM) images reveal that both the BST films and the LSCO bottom electrode grow with a columnar structure, and they have flat interfaces and overall uniform thickness across the entire specimen. Cross-sectional high-resolution TEM images reveal that at the LSCO/MgO(100) interface, an interfacial reaction is not seen, whereas edge-type interfacial dislocations with their extra half-planes residing in the LSCO side are observed with an average interval of 2.20 nm, close to the theoretical value of 2.15 nm. At/near the LSCO/BST interface, the graded BST films grow perfectly and coherently on the LSCO lattice because they have the same type of crystal structure and almost same lattice constants, and no interfacial dislocations are observed. Planar TEM images show that the graded films exhibit granular and/or polyhedral morphologies with an average grain size of 50 nm, and the aligned rectangular-shaped voids were also observed. High-resolution TEM images show that the length sizes of voids vary from 8 to 15 nm, and with width of 5 to 10 nm along the 〈001〉 direction in the (100) plane.

A multiscale modeling approach applied to the stiffness prediction of polymers with high cross-link density is discussed. The material of focus in this work is the ionic polymer Nafion®. The approach applies rotational isomeric state theory in combination with a Monte Carlo methodology to develop a simulation model for polymer chain conformation. From this a large number of end-to-end chain lengths between cross links are generated; the probability density function of these lengths is estimated with the most appropriate Johnson family method. This estimation is used in a Boltzmann statistical thermodynamics approach to the multiscale prediction of stiffness. This work addresses the importance of the simulated polymer chain length in the generation of stable predictions. The multiscale prediction is found to be physically reasonable; the approach has the potential of serving as a first-order prediction tool for properties that are experimentally difficult or impossible to measure.

Nanocrystalline lead zirconate titanate (PZT) and lead lanthanum zirconate titanate (PLZT) have been synthesized in powder form by a single-step auto-ignition of metal–polymer gel precursor. The nanocrystalline powders were characterized using analytical transmission electron microscopy (TEM) equipped with an energy-dispersive x-ray spectrometer (EDXS) for composition analysis. For both PZT and PLZT, nanoparticles of sizes as low as 1–5 nm along with larger nanoparticles of sizes up to 30 nm are observed in the TEM. The selected-area diffraction (SAD) patterns from the nanoparticles revealed a face-centered cubic (fcc) crystal structure for both PZT and PLZT with a lattice parameter of ∼0.51 nm. The formation of PZT and PLZT nanoparticles of sizes below 5 nm with metastable fcc crystal structure has been observed for the first time. It is concluded that, as the crystal size decreases, the system assumes crystal structures of higher symmetry initially through small changes in lattice parameters and, in extreme cases, through chemical disorder for ultrafine nanoparticles.

Rapid thermal annealing (RTA) processing under N2 and O2 ambient is suggested and characterized in this work for improvement of SiCOH ultra-low-k (k = 2.4) film properties. Low-k film was deposited by plasma-enhanced chemical vapor deposition (PECVD) with decamethylcyclopentasiloxane and cyclohexane precursors. The PECVD films were treated by RTA processing in N2 and O2 environments at 550 °C for 5 min, and k values of 1.85 and 2.15 were achieved in N2 and O2 environments, respectively. Changes in the k value were correlated with the chemical composition of C–Hx and Si–O related groups determined from the Fourier transform infrared (FTIR) analysis. As the treatment temperature was increased from 300 to 550 °C, the signal intensities of both the CHx and Si–CH3 peaks were markedly decreased. The hardness and modulus of the film processed by RTA have been determined as 0.44 and 3.95 GPa, respectively. Hardness and modulus of RTA-treated films were correlated with D-group [O2Si–(CH3)2] and T-group [O3Si–(CH3)] fractions determined from the FTIR Si–CH3 bending peak. The hardness and modulus improvement in this work is attributed to the increase of oxygen content in (O)x–Si–(CH3)y by rearrangement.

Artificial molecular machines capable of converting chemical, electrochemical, and photochemical energy into mechanical motion represent a high-impact, fast-growing field of interdisciplinary research. These molecular-scale systems utilize a “bottom-up” technology centered upon the design and manipulation of molecular assemblies and are potentially capable of delivering efficient actuation at length scales dramatically smaller than traditional microscale actuators. As actuation materials, molecular machines have many advantages, such as high strain (40%–60%), high force and energy densities, and the capability to maintain their actuation properties from the level of a single molecule to the macroscale. These advantages have inspired researchers to develop molecular-machine–based active nanomaterials and nanosystems, including electroactive and photoactive polymers. This article will discuss the structures and properties of artificial molecular machines, as well as review recent progress on efforts to move molecular machines from solution to surfaces to devices.

The microstructure and residual stress of sputter-deposited yttria-stabilized zirconia (YSZ) films are presented as a function of thickness (5–1000 nm), deposition pressure (5–100 mTorr), and post-deposition temperature. The as-deposited residual stress of YSZ ranges from −1.4 GPa to 100 MPa with variations in sputtering conditions. Transitions from compressive to tensile stress are identified with variations in working pressure and film thickness. The origins and variations in as-deposited stress are determined to be from tensile stress due to grain coalescence/growth, and compressive stresses are due to forward sputtering/“atomic peening” of target atoms. The evolution of residual stress with post-deposition annealing shows a tensile stress hysteresis of up to 1 GPa for films deposited at low working pressures. This hysteresis is believed to be due to crystallization and the diffusive relief of compressive stresses initially generated by atomic peening during deposition. Discussion and evaluation of other common residual stress mechanisms are presented throughout.

Polymers are highly attractive for their inherent properties of mechanical flexibility, light weight, and easy processing. In addition, some polymers exhibit large property changes in response to electrical stimulation, much beyond what is achievable by inorganic materials. This adds significant benefit to their potential applications.

The focus of this issue of MRS Bulletin is on polymers that are electromechanically responsive, which are also known as electroactive polymers (EAPs). These polymers respond to electric field or current with strain and stress, and some of them also exhibit the reverse effect of converting mechanical motion to an electrical signal.

There are many types of known polymers that respond electromechanically, and they can be divided according to their activation mechanism into field-activated and ionic EAPs. The articles in this issue cover the key material types used in these two groups, review the mechanisms that drive them, and provide examples of applications and current challenges. Recent advances in the development of these materials have led to improvement in the induced strain and force and the further application of EAPs as actuators for mimicking biologic systems and sensors. As described in this issue, the use of these actuators is enabling exciting applications that would be considered impossible otherwise.

Porous magnesium with directional cylindrical pores (or “lotus-type” porous magnesium) was fabricated through the use of hydrogen decomposed from MgH2 powders during unidirectional solidification. Liquid magnesium was cast into a mold in which MgH2 powders were placed and was unidirectionally solidified, which achieved growth of pores elongated along the direction of solidification. The effect of the amount of the MgH2 powders on the pore structure (porosity, diameter, and number density of pores) and the change in the pore structure along the pore growth direction were clarified. The porosity and number density of pores increase with increasing amount of MgH2 powder, and the average diameter of pores decreases with increasing amount of MgH2 powder. The pore structure changes with the growth of pores along the solidification direction.