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A disordered material that cannot relax to equilibrium, such as an amorphous or glassy solid, responds to deformation in a way that depends on its past. In experiments we train a 2D athermal amorphous solid with oscillatory shear, and show that a suitable readout protocol reveals the shearing amplitude. When shearing alternates between two amplitudes, signatures of both values are retained only if the smaller one is applied last. We show that these behaviors arise because individual clusters of rearrangements are hysteretic and dissipative, and because different clusters respond differently to shear. These roles for hysteresis and disorder are reminiscent of the return-point memory seen in ferromagnets and many other systems. Accordingly, we show how a simple model of a ferromagnet can reproduce key results of our experiments and of previous simulations. Unlike ferromagnets, amorphous solids disorder is unquenched; they require training to develop this behavior.
We demonstrate that irreversible structural reorganization is not necessary for the observation of yield behaviour in an amorphous solid. While the majority of solids strained to their yield point do indeed undergo an irreversible reorganization, we
Athermal systems across a large range of length scales, ranging from foams and granular bead packings to crumpled metallic sheets, exhibit slow stress relaxation when compressed. Experimentally they show a non-monotonic stress response when decompres
We present the results of simulation studies of a model binary metal-metalloid alloy in which we characterize and explain the local coordination structure, the intermediate structure associated with the packing of these coordination polyhedra and the
First systematic spin probe ESR study of water freezing has been conducted using TEMPOL and TEMPO as the probes. The spin probe signature of the water freezing has been described in terms of the collapse of narrow triplet spectrum into a single broad
Structural colors are produced by wavelength-dependent scattering of light from nanostructures. While living organisms often exploit phase separation to directly assemble structurally colored materials from macromolecules, synthetic structural colors