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Crack nucleation and growth during dynamic indentation of chemically-strengthened glass
Dynamic point impact loading is a primary cause of fracture of glass screens on mobile devices. An improved understanding of crack initiation and evolution under high-speed indentation could contribute to the development of materials with better performance, but experimental observations are challenging due to the short timescales and limited depth-of-field of optical microscopy. To address this need, we have observed fracture of a chemically-strengthened glass during dynamic indentation using in situ x-ray phase-contrast imaging (XPCI). Median cracks initiate below the surface of the glass, at a depth approximately corresponding to the depth at which the surface residual compressive stress diminishes to zero. These cracks initially propagate at ~10ms –1 , rapidly accelerating to > 100ms –1 . We also observe some evidence for rate-dependent behavior, in that indentation at the lowest rates studied here (below about ~0.15ms –1 ) fails to initiate cracks regardless of the depth of the indentation (up to 18μm), while indentation at higher rates produces median cracks that either arrest or cause complete fracture, depending on the depth of indentation.
Far-field triggering of foreshocks near the nucleation zone of the 5 September 2012 (MW 7.6) Nicoya Peninsula, Costa Rica earthquake
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A framework for nucleation in electrochemical systems and the effect of surface energy on dendrite growth
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Interface dislocation patterns and dislocation nucleation in face-centered-cubic and body-centered-cubic bicrystal interfaces
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Local micro-mechanical stress conditions leading to pore nucleation during dynamic loading
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Stress-induced transition from vacancy annihilation to void nucleation near microcracks
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Influence of sub-zero temperature on nucleation and growth of copper nanoparticles in electrochemical reactions
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Nucleation and growth of γ-Fe precipitate in Cu-2%Fe alloy aged under high magnetic field
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Unseeded, spontaneous nucleation of spherulitic magnesium calcite
Most of the sedimentary carbonates deposited in the marine environments are composed of calcium carbonate minerals with varying amounts of incorporated Mg 2+ . However, understanding how interactions of impurities with carbonate and their incorporation affect sediments behavior remains a challenge. Here, a new insight is obtained by monitoring solution composition, morphology, and electrokinetic potential of carbonate particles formed in a spontaneous unseeded batch precipitation experiment using electrochemical and scanning electron microscopy methods. The solid composition and growth rate are extracted from changes in the bulk composition and fitted to chemical affinity rate law, revealing that the precipitation pathway consists of second-order dissolution and first-order precipitation. The molecular dynamics simulations show that the lattice strain induced by randomly substituting Ca 2+ by Mg 2+ stabilizes spherical nanoparticles and reduces their surface area and volume. Combining kinetics and thermodynamics insight, we conclude that variation in the carbonate bulk and interfacial energies, along with the solution supersaturation, lead to the dissolution-precipitation transformation pathway from Mg-rich to Mg-poor carbonate phase that preserves spherulitic morphology. Furthermore, our findings are relevant for long-standing questions of how impurities influence diagenesis of carbonate sediments and spherulitic carbonate particles' origin.
Ground-state exciton emission of InAs quantum dots produced by focused-ion-beam-directed nucleation
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Crystallography and elastic anisotropy in fatigue crack nucleation at nickel alloy twin boundaries
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A case for local icosahedral order in undercooled metallic liquids and the influence on the nucleation barrier
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The Role of Chemical Free Energy and Elastic Strain in the Nucleation of Zirconium Hydride
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