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      Random critical point separates brittle and ductile yielding transitions in amorphous materials

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          Abstract

          <p id="d4318525e253">Understanding how amorphous solids yield in response to external deformations is crucial both for practical applications and for theoretical reasons. Here we show that despite large differences in the materials’ microscopic interactions, a degree of universality emerges as there are only two ways in which amorphous solids respond to a deformation: One, typical of well-annealed materials, is characterized by an abrupt failure with a macroscopic stress drop and the sudden emergence of sharp shear bands; the other, typical of poorly annealed materials, shows merely a smooth crossover. By varying the preparation protocol, one can change the response of a given material from one to the other, and this change is controlled by a random critical point. </p><p class="first" id="d4318525e256">We combine an analytically solvable mean-field elasto-plastic model with molecular dynamics simulations of a generic glass former to demonstrate that, depending on their preparation protocol, amorphous materials can yield in two qualitatively distinct ways. We show that well-annealed systems yield in a discontinuous brittle way, as metallic and molecular glasses do. Yielding corresponds in this case to a first-order nonequilibrium phase transition. As the degree of annealing decreases, the first-order character becomes weaker and the transition terminates in a second-order critical point in the universality class of an Ising model in a random field. For even more poorly annealed systems, yielding becomes a smooth crossover, representative of the ductile rheological behavior generically observed in foams, emulsions, and colloidal glasses. Our results show that the variety of yielding behaviors found in amorphous materials does not necessarily result from the diversity of particle interactions or microscopic dynamics but is instead unified by carefully considering the role of the initial stability of the system. </p>

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          Mechanical behavior of amorphous alloys

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            Is Open Access

            Dynamics of Viscoplastic Deformation in Amorphous Solids

            We propose a dynamical theory of low-temperature shear deformation in amorphous solids. Our analysis is based on molecular-dynamics simulations of a two-dimensional, two-component noncrystalline system. These numerical simulations reveal behavior typical of metallic glasses and other viscoplastic materials, specifically, reversible elastic deformation at small applied stresses, irreversible plastic deformation at larger stresses, a stress threshold above which unbounded plastic flow occurs, and a strong dependence of the state of the system on the history of past deformations. Microscopic observations suggest that a dynamically complete description of the macroscopic state of this deforming body requires specifying, in addition to stress and strain, certain average features of a population of two-state shear transformation zones. Our introduction of these new state variables into the constitutive equations for this system is an extension of earlier models of creep in metallic glasses. In the treatment presented here, we specialize to temperatures far below the glass transition, and postulate that irreversible motions are governed by local entropic fluctuations in the volumes of the transformation zones. In most respects, our theory is in good quantitative agreement with the rich variety of phenomena seen in the simulations.
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              Ductile versus brittle behaviour of crystals

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                Author and article information

                Journal
                Proceedings of the National Academy of Sciences
                Proc Natl Acad Sci USA
                Proceedings of the National Academy of Sciences
                0027-8424
                1091-6490
                June 26 2018
                June 26 2018
                June 26 2018
                June 11 2018
                : 115
                : 26
                : 6656-6661
                Article
                10.1073/pnas.1806156115
                6042060
                29891678
                7d65994e-7aa4-42d9-8c4d-8ec05eb753e2
                © 2018
                History

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