Poisson’s ratio (ν) defines a material’s propensity to laterally expand upon compression, or laterally shrink upon tension for non-auxetic materials. This fundamental metric has traditionally, in some fields, been assumed to be a material-independent constant, but it is clear that it varies with composition across glasses, ceramics, metals, and polymers. The intrinsically elastic metric has also been suggested to control a range of properties, even beyond the linear-elastic regime. Notably, metallic glasses show a striking brittle-to-ductile (BTD) transition for ν-values above ~0.32. The BTD transition has also been suggested to be valid for oxide glasses, but, unfortunately, direct prediction of Poisson’s ratio from chemical composition remains challenging. With the long-term goal to discover such high-ν oxide glasses, we here revisit whether previously proposed relationships between Poisson’s ratio and liquid fragility (m) and atomic packing density (Cg) hold for oxide glasses, since this would enable m and Cg to be used as surrogates for ν. To do so, we have performed an extensive literature review and synthesized new oxide glasses within the zinc borate and aluminoborate families that are found to exhibit high Poisson’s ratio values up to ~0.34. We are not able to unequivocally confirm the universality of the Novikov-Sokolov correlation between ν and m and that between ν and Cg for oxide glass-formers, nor for the organic, ionic, chalcogenide, halogenide, or metallic glasses. Despite significant scatter, we do, however, observe an overall increase in ν with increasing m and Cg, but it is clear that additional structural details besides m or Cg are needed to predict and understand the composition dependence of Poisson’s ratio. Finally, we also infer from literature data that, in addition to high ν, high Young’s modulus is also needed to obtain glasses with high fracture toughness.
more »
« less
Fracture toughness of a metal–organic framework glass
Metal-organic framework glasses feature unique thermal, structural, and chemical properties compared to traditional metallic, organic, and oxide glasses. So far, there is a lack of knowledge of their mechanical properties, especially toughness and strength, owing to the challenge in preparing large bulk glass samples for mechanical testing. However, a recently developed melting method enables fabrication of large bulk glass samples (>25 mm3) from zeolitic imidazolate frameworks. Here, fracture toughness (
- Award ID(s):
- 1762292
- PAR ID:
- 10155624
- Publisher / Repository:
- Nature Publishing Group
- Date Published:
- Journal Name:
- Nature Communications
- Volume:
- 11
- Issue:
- 1
- ISSN:
- 2041-1723
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
More Like this
-
-
more » « less
Abstract The understanding of the mechanical properties in glass nanofibers remains a challenge. As the fiber diameter decreases, surface-to-volume atom fraction increases, making the impact of surface defects more significant. To elucidate these effects, we employed classical molecular dynamics (MD) simulations to investigate how fiber dimensions and the surface layer influence the mechanical properties of silica glass nanofibers. Our simulation methodology included fibers of varying diameters, generated using two different production methods (i.e. “cutting” and “casting” methods) that produce different degrees of surface atomic defects, and compared with bulk samples without surface atoms. The defect-rich surface layer of these fibers was carefully analyzed. Then, MD tensile simulations were performed to analyze the effect of the fiber surface on the mechanical properties and to explain the onset of the brittle-to-ductile transition experimentally observed at a few tens of nanometers. The results revealed that the surface layer maintains a fixed thickness independent of the fiber diameter, resulting in a pronounced increase of the fiber defects in thin fibers. Also, the tensile test simulations show that surface defects significantly reduce tensile strength, without appreciably increasing ductility compared to bulk samples. In turn, we show that the brittle-to-ductile transition is not caused by the surface defects, but related to a balance between fracture energy and elastic energy, which varies with fiber length. Using experimental values of different glass properties, our theory predicted a threshold length of around 200 nm, below which ductile fracture dominates, in reasonable agreement with experimental results.
Graphic abstract -
more » « less
During the course of exploring crystallization conditions in generating metal–organic frameworks (MOFs) for use in the crystalline sponge method, two discrete metal–organic complexes, namely, aqua[2,4,6-tris(pyridin-4-yl)-1,3,5-triazine]zinc(II) bromide, [Zn(C18H12N6)(H2O)]Br2, and aqua[2,4,6-tris(pyridin-4-yl)-1,3,5-triazine]zinc(II) chloride, [Zn(C18H12N6)(H2O)]Cl2, were encountered. Structures in the orthorhombic space group
Pnma (No. 62) for the bromide congener at 299 K and the chloride congener at 100 K were obtained. A phase transition for the bromide congener occurred upon cooling from 299 to 100 K, yielding a crystal polymorph with four domains that exhibits monoclinicP 21/m space-group symmetry (No. 11), which arises from conformational changes. The main intramolecular contacts that contribute to the crystal packing in all observed structures are H...H, Halide...H/H...Halide, C...H/H...C, and N...H/H...N. Intramolecular hydrogen bonding between the Zn-bound water and non-Zn-bound pyridyl N atoms is a prominent feature within the three-dimensional networks. Aromatic π-stacking between the non-Zn-bound pyridine rings and contacts involving the halide ligands further stabilize the crystal packing. -
more » « less
Abstract Oxide glasses are one of the most important engineering and functional material families owing to their unique features, such as tailorable physical properties. However, at the same time intrinsic brittleness has been their main drawback, which severely restricts many applications. Despite much progress, a breakthrough in developing ultra‐damage‐resistant and ductile oxide glasses still needs to be made. Here, a critical advancement toward such oxide glasses is presented. In detail, a bulk oxide glass with a record‐high crack resistance is obtained by subjecting a caesium aluminoborate glass to surface aging under humid conditions, enabling it to sustain sharp contact deformations under loads of ≈500 N without forming any strength‐limiting cracks. This ultra‐high crack resistance exceeds that of the annealed oxide glasses by more than one order of magnitude, making this glass micro‐ductile. In addition, a remarkable indentation behavior, i.e., a time‐dependent shrinkage of the indent cavity, is demonstrated. Based on structural analyses, a molecular‐scale deformation model to account for both the ultra‐high crack resistance and the time‐dependent shrinkage in the studied glass is proposed.
-
more » « less
Abstract Muddy marine sediments are elastic materials in which bubbles grow and worms extend their burrows by fracture. Bubble growth and burrowing behavior are dependent on the stiffness and fracture toughness (
K Ic) of these muds. This article describes a custom laboratory apparatus to measure the fracture toughness of muddy, cohesive sediments using a bubble injection method. The system induces fracture in sediment samples by incrementally injecting air through a needle inserted into the sediment. The increasing pneumatic pressure is monitored until it drops abruptly, indicating bubble formation. Fracture toughness is then calculated from the peak pressure at which fracture occurred, following cavitation rheology methods developed for soft gels. The system has produced measurements that compare well to previous data but with better spatial resolution, allowing for characterization of spatial heterogeneity on small scales.
