Abstract:The mechanical properties of ordinary materials degrade substantially with reduced density, due to the bending of their structural elements under applied load. We report a class of micro-architected materials that maintain a nearly constant stiffness per unit mass density, even at ultra-low density. This performance derives from a network of nearly isotropic microscale unit cells with high structural connectivity and nanoscale features, whose structural members are designed to carry loads in tension or compression. Production of these microlattices, with constituent materials ranging from polymers to metals and ceramics, is made possible by using projection microstereolithography, an additive micromanufacturing technique, combined with nanoscale coating and postprocessing. We found that these materials exhibit ultra-stiff properties across more than three orders of magnitude in density, regardless of the constituent material. One Sentence Summary:We report a class of micro-architected materials that change their stiffness linearly with reduced density.Main Text: Nature has found a way to achieve mechanically efficient materials by evolving cellular structures. Natural cellular materials, including honeycomb (1) (wood, cork) and foamlike structures, such as trabecular bone (2), plant parenchyma (3), and sponge (4), combine low weight with superior mechanical properties. For example, lightweight balsa has a stiffness-toweight ratio comparable to that of steel along the axial loading direction (5). Inspired by these naturally occurring cellular structures, manmade lightweight cellular materials fabricated from a wide array of solid constituents are desirable for a broad range of applications including structural components (6, 7), energy absorption (8, 9), heat exchange (10, 11), catalyst supports (12), filtration (13,14), and biomaterials (15,16). However, the degradation in mechanical properties can be drastic as density decreases (17,18). A number of examples among recently reported low-density materials include graphene elastomers (19), metallic micro-lattices (20), carbon nanotube foams (21), and silica aerogels (22,23). For instance, the Young's modulus of low-density silica aerogels (22, 23) decreases to 10 kPa (10 -5 % of bulk ) at a density of less than 10 mg/cm 3 (< 0.5% of bulk). This loss of mechanical performance is because most natural and engineered cellular solids with random porosity, particularly at relative densities less than 0.1%, exhibit a quadratic or stronger scaling relationship between Young's modulus and density as well as between strength and density. Namely, E/E s ~ (/ s ) n and y ys ~ (/ s ) n , where E is Young's modulus, is density, y is yield strength, and s denotes the respective bulk value of the solid constituent material property. The power n of the scaling relationship between relative material density and the relative mechanical property depends on the material's microarchitecture. Conventional cellular foam materials with stochastic porosity are known to...
The presence of large amounts of nondiamond carbon in detonation-synthesized nanodiamond (ND) severely limits applications of this exciting nanomaterial. We report on a simple and environmentally friendly route involving oxidation in air to selectively remove sp(2)-bonded carbon from ND. Thermogravimetric analysis and in situ Raman spectroscopy shows that sp(2) and sp(3) carbon species oxidize with different rates at 375-450 degrees C and reveals a narrow temperature range of 400-430 degrees C in which the oxidation of sp(2)-bonded carbon occurs with no or minimal loss of diamond. X-ray absorption near-edge structure spectroscopy detects an increase of up to 2 orders of magnitude in the sp(3)/sp(2) ratio after oxidation. The content of up to 96% of sp(3)-bonded carbon in the oxidized samples is comparable to that found in microcrystalline diamond and is unprecedented for ND powders. Transmission electron microscopy and Fourier transform infrared spectroscopy studies show high purity 5-nm ND particles covered by oxygen-containing surface functional groups. The surface functionalization can be controlled by subsequent treatments (e.g., hydrogenization). In contrast to current purification techniques, the air oxidation process does not require the use of toxic or aggressive chemicals, catalysts, or inhibitors and opens avenues for numerous new applications of nanodiamond.
High surface area nanoporous carbon has been prepared by thermo-chemical etching of titanium carbide TiC in chlorine in the temperature range 200-1200 °C. Structural analysis showed that this carbide-derived carbon (CDC) was highly disordered at all synthesis temperatures. Higher temperature resulted in increasing ordering and formation of bent graphene sheets or thin graphitic ribbons. Soft X-ray absorption near-edge structure spectroscopy demonstrated that CDC consisted mostly of sp 2 bonded carbon. Small-angle X-ray scattering and argon sorption measurements showed that the uniform carbon-carbon distance in cubic TiC resulted in the formation of small pores with a narrow size distribution at low synthesis temperatures; synthesis temperatures above 800 °C resulted in larger pores. CDC produced at 600-800 °C show great potential for energy-related applications. Hydrogen sorption experiments at −195.8 °C and atmospheric pressure showed a maximum gravimetric capacity of ∼ 330 cm 3 /g (3.0 wt.%). Methane sorption at 25 °C demonstrated a maximum capacity above 46 cm 3 /g (45 vol/vol or 3.1 wt.%) at atmospheric pressure. When tested as electrodes for supercapacitors with an organic electrolyte, the hydrogen-treated CDC showed specific capacitance up to 130 F/g with no degradation after 10 000 cycles.
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