Robert Ivancic

When deformed beyond their elastic limits, crystalline solids flow plastically via particle rearrangements localized around structural defects. Disordered solids also flow, but without obvious structural defects. We link structure to plasticity in disordered solids via a microscopic structural quantity, "softness," designed by machine learning to be maximally predictive of rearrangements. Experimental results and computations enabled us to measure the spatial correlations and strain response of softness, as well as two measures of plasticity: the size of rearrangements and the yield strain. All four quantities maintained remarkable commonality in their values for disordered packings of objects ranging from atoms to grains, spanning seven orders of magnitude in diameter and 13 orders of magnitude in elastic modulus. These commonalities link the spatial correlations and strain response of softness to rearrangement size and yield strain, respectively.

We experimentally characterize heterogeneous nonexponential relaxation in bidisperse supercooled colloidal liquids utilizing a recent concept called "softness" [Phys. Rev. Lett. 114, 108001 (2015)PRLTAO0031-900710.1103/PhysRevLett.114.108001]. Particle trajectory and structure data enable classification of particles into subgroups with different local environments and propensities to hop. We determine residence times t_{R} between particle hops and show that t_{R} derived from particles in the same softness subgroup are exponentially distributed. Using the mean residence time t[over ¯]_{R} for each softness subgroup, and a Kramers' reaction rate model, we estimate the activation energy barriers E_{b} for particle hops, and show that both t[over ¯]_{R} and E_{b} are monotonic functions of softness. Finally, we derive information about the combinations of large and small particle neighbors that determine particle softness, and we explicitly show that multiple exponential relaxation channels in the supercooled liquid give rise to its nonexponential behavior.

Amorphous solids are critical in the design and production of nanoscale devices, but under strong confinement these materials exhibit changes in their mechanical properties which are not well understood. Phenomenological models explain these properties by postulating an underlying defect structure in these materials but do not detail the microscopic properties of these defects. Using machine learning methods, we identify mesoscale defects that lead to shear banding in model polymer nanopillars well below the glass transition temperature as a function of pillar diameter. Our results show that the primary structural features responsible for shear banding on this scale are fluctuations in the diameter of the pillar. Surprisingly, these fluctuations are quite small compared to the diameter of the pillar, less than half of a particle diameter in size. At intermediate pillar diameters, we find that these fluctuations tend to concentrate along the minor axis of shear band planes. We also see the importance of mean "softness" as a classifier of shear banding grow as a function of pillar diameter. Softness is a new field that characterizes local structure and is highly correlated with particle-level dynamics such that softer particles are more likely to rearrange. This demonstrates that softness, a quantity that relates particle-level structure to dynamics on short time and length scales, can predict large time and length scale phenomena related to material failure.

Polymer blends can yield superior materials by merging the unique properties of their components. However, these mixtures often phase separate, leading to brittleness. While compatibilizers can toughen these blends, their vast design space makes optimization difficult. Here, we develop a model to predict the toughness of compatibilized glassy polymer mixtures. This theory reveals that compatibilizers increase blend toughness by creating molecular bridges that stitch the interface together. We validate this theory by directly comparing its predictions to extensive molecular dynamics simulations in which we vary polymer incompatibility, chain stiffness, compatibilizer areal density, and blockiness of copolymer compatibilizers. We then parameterize the model using self-consistent field theory and confirm its ability to make predictions for practical applications through comparison with simulations and experiments. These results suggest that the theory can optimize compatibilizer design for industrial glassy polymer blends in silico while providing microscopic insight, allowing for the development of next-generation mixtures.

Elastoplastic lattice models for the response of solids to large-scale deformation typically incorporate structure only implicitly via a local yield strain that is assigned to each site. However, the local yield strain can change in response to a nearby or even distant plastic event in the system. This interplay is key to understanding phenomena such as avalanches in which one plastic event can trigger another, leading to a cascade of events, but is typically neglected in elastoplastic models. To include the interplay one could calculate the local yield strain for a given particulate system and follow its evolution, but this is expensive and requires knowledge of particle interactions that aren't necessarily pairwise additive or possible to extract from experiments. Instead, we use a structural quantity, ``softness,'' obtained using machine learning to correlate with imminent plastic rearrangements. We show that softness correlates with local yield strain and use it to construct a ``structuro-elasto-plasticity'' model that reproduces particle simulation results reasonably well for several observable quantities, confirming that we capture the influence of the interplay of local structure, plasticity, and elasticity on material response.