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The integration of materials and architectural features at multiple length scales into structural mechanics has shifted the paradigm of structural design toward optimally engineered structures, which resulted in, for example, the Eiffel Tower. This structural revolution paved the way for the development of computational design approaches used in modern-day construction. Similar principles are now being applied to the design and manufacture of architected materials with a suite of properties determined a priori and attained through multiscale approaches. These new material classes potentially offer breakthrough advances in almost every branch of technology: from ultra-lightweight and damage-tolerant structural materials to safe and efficient energy storage, biomedical devices, biochemical, and micromechanical sensors and actuators, nanophotonic devices, and textiles. When reduced to the microscale, such materials embody the characteristics of both the constituent material, which brings the effects of its microstructure and ensuing properties at the relevant characteristic length scales, as well as the structure, which is driven by architected design. This issue gives an overview of the current state of the art of this new class of materials.
We present a survey of modeling techniques used to describe and predict architected cellular metamaterials, and to optimize their topology and geometry toward tailoring their mechanical properties such as stiffness, strength, fracture toughness, and energy absorption. Architectures of interest include truss-, plate-, and shell-based networks with and without periodicity, whose effective mechanical behavior is simulated by tools such as classical finite elements, further scale-bridging techniques such as homogenization and concurrent scale-coupling, and effective continuum descriptions of the underlying discrete networks. In addition to summarizing advances in applying the latter techniques to improve the properties of metamaterials and featuring prominent examples of structure–property relations achieved this way, we also present recently introduced techniques to improve the optimization process toward a full exploitation of the available design space, accounting for both linear and nonlinear material behavior.
A material’s properties are derived from its constituent material composition and its structural hierarchy across length scales down to the nanometer level. At submicron length scales, materials exhibit unique size-affected mechanical properties such as enhanced strength, ductility, and flaw tolerance, but these are generally lost in bulk materials. Emerging fabrication methods have enabled the creation of materials with controllable architectures down to the nanoscale. These micro- and nanoarchitected materials utilize both resilient architectures and size-affected constituent materials to achieve unprecedented mechanical properties such as ultrahigh strength at low density, recoverability after large applied strains in intrinsically brittle materials, and metamaterial properties such as chirality and negative static compressibility. In this article, we describe the governing principles behind these materials and outline recent progress in the field. We unravel the details of the deformation and failure processes to facilitate a fundamental understanding of effective materials properties and provide a guideline for the design of the next generation of nanoarchitected materials.
Architected materials play an essential role in achieving next-generation electrochemical systems with unprecedented power and energy capabilities. The geometry and chemistry of architected materials can be engineered to address key areas of performance, including electrochemical kinetics and mechanics. Electrochemical kinetics impact key metrics such as power density, efficiency, and lifetime in batteries, fuel cells, and sensors. Additionally, electrochemical reactions can dramatically change material composition, which may result in large strains (in the hundreds of percent) that cause mechanical failure. In this article, we summarize advances in energy storage offered by architected materials and highlight fabrication methods used to realize these advances. We also discuss electrochemistry as an enabling tool for architected materials with functionality beyond energy storage and sensing.
Porphyrinic compounds are of increasing interest to the materials science community, yet little attention has been paid to crystallographically controlled voids and channels in these materials. We have conducted an initial survey of the voids and channels in a random subset of 1000 porphyrinic compounds with known crystal structures. From calculations using a rolling-probe subroutine, we have found that about 5% of these compounds have line-of-sight channels, which differ in their topology depending on the crystallography. A small but significant number of porphyrinic compounds have calculated void contents of >25 volume %. We discuss in detail the void and channel characteristics, including pore-size distribution, of four representative compounds, with technological implications.
Macro-mesoporous zirconium titanate monoliths have been successfully prepared via a sol–gel process accompanied by phase separation, with poly(ethylene oxide) (PEO) as a phase separation inducer and N-methylformamide (NFA) as a gelation accelerator. The size and morphology of macropores are controlled by the PEO and NFA amount. By choosing appropriate starting composition, the co-continuous structure could be obtained. The as-dried gel is amorphous, the pore size is in the range of 0.05–0.5 μm, the porosity is 46%, and the surface area is 111 m2/g. After heat treatment at 500 °C, the gel transforms into the phase ZrTiO4, the macropore diameter decreases slightly, the porosity increases to 63%, and the surface area decreases to 40 m2/g. Moreover, the macroporous structure is well maintained, and the skeleton becomes dense and smooth. The samples have macropores, mesopores, and micropores before and after heat treatment.
In the recent years, there has been high interest in renewable energy and highly efficient devices, promoted by the need to stop changing weather patterns. One of the most interesting methods for this is using thermoelectric materials, which are low cost and highly durable. However, the need for higher efficiency values and a higher resistance to oxidation leads to a technological problem in the field of coating. Due to its diverse properties, glass coating has been proposed as a solution to both sublimation of the thermoelectric materials and oxidation. Lead silicate glasses with 30% PbO were doped with 0–5% of Na2O and B2O3 to produce glasses with different properties. Differential scanning calorimetry and dilatometry measurements showed that the glass temperature can vary between 428 and 505 °C. The softening temperature is varied between 493 and 560 °C. Below Tg, the coefficient of thermal expansion is varied between 5.9 and 9 ppm/K and above Tg it varied between 17 and 58 ppm/K. This allows the tuning of the glass composition for each thermoelectric material, such as 0.5% B and 1% Na doped PbO -SiO2 glass for skutterudites and 1% doped B and 1% Na doped for Mg2Si, PbTe, and GeTe.
To examine the influence of ultrasonic irradiation on electrochemical migration (ECM), the morphology of micro/nanodeposits and current change were studied. The morphology of deposits synthesized by ECM varied with the types of ultrasonic irradiation: continuous or pulsed irradiation generates only particles or deposits composed of wires, dendrites, and particles. The measured ECM current change over time concludes that both mechanical and sonochemical effects contributed to the morphological change of deposits. Shock waves by cavitation mechanically formed the fragmented deposits and the sonochemical effect decreases the ionic concentration corresponding to decreasing current, inhibiting the formation of wires and dendritic deposits.
Two rapidly solidified (RS) Mg ribbons with the compositions of Mg97Zn2Gd1 and Mg90Zn5Gd5 (at.%) were first prepared by the planar flow casting method. These RS ribbons were subsequently consolidated by spark plasma sintering (SPS). The use of SPS on the RS ribbons was demonstrated to be an effective processing route to control W-phase precipitation process while keeping fine grains. The size of W-phase particles was less than 200 nm in Mg97Zn2Gd1 alloy and smaller than 500 nm in Mg90Zn5Gd5 alloy. The content of W phase was approximately 34 vol% and 41 vol% in the two SPS bulks, respectively. The compressive properties showed that the yield compressive stress (YCS) and ultimate compressive stress of the Mg97Zn2Gd1 alloy reached 200 MPa and 390 MPa, respectively, and an elongation of 0.24. The corresponding values for the Mg90Zn5Gd5 alloy were 313 MPa, 504 MPa, and 0.14, respectively. Based on the results of the quantitative analysis, W-phase nanoparticles with size less than 100 nm exhibited obviously strengthening effect in the Mg alloys. It highlighted that the W-phase nanoparticles contributed a large proportion of the YCS in the Mg97Zn2Gd1 alloy and a relatively small proportion for that of the Mg90Zn5Gd5 alloy.
A piezoelectric biomedical microelectromechanical system (bioMEMS) cantilever device was designed and fabricated to act as either a sensing element for muscle tissue contraction or as an actuator to apply mechanical force to cells. The sensing ability of the piezoelectric cantilevers was shown by monitoring the electrical signal generated from the piezoelectric aluminum nitride in response to the contraction of iPSC-derived cardiomyocytes cultured on the piezoelectric cantilevers. Actuation was demonstrated by applying electrical pulses to the piezoelectric cantilever and observing bending via an optical detection method. This piezoelectric cantilever device was designed to be incorporated into body-on-a-chip systems.