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Robert M. McMeeking

Publications and source records attributed to Robert M. McMeeking.

4 recordsLinked to original sources

On the chemo-thermo-mechanics of constrained reactive mixtures of solids

Building upon the classical chemo-mechanical theory of Larch{é} and Cahn for equilibrium, numerous studies have investigated the transport of species in solids, with or without trapping phenomena. In most applications -- such as the swelling of hydrogels, hydrogen embrittlement in metals, and the transport of lithium or sodium in battery electrodes -- the formation of a new phase or compound can be directly associated with the concentration of the diffusing species. In the present work, we focus on the formation of solid mixtures made of multiple compounds, each characterized by its own volumetric expansion coefficient. Such a scenario arises, for instance, during the sodiation of tin anodes, among other systems. The classical chemo-mechanical framework is naturally recovered as a particular case of the proposed formulation. The theoretical framework developed herein elucidates and differentiates the concepts of phases and flowing species, while establishing rigorous connections between them. The present note is restricted to the general formulation of the governing equations, whereas application-specific developments will be addressed in forthcoming publications.

cond-mat.soft↗

Ferroelastic toughening: can it solve the mechanics challenges of solid electrolytes?

The most promising solid electrolytes for all-solid-state Li batteries are oxide and sulfide ceramics. Current ceramic solid electrolytes are brittle and lack the toughness to withstand the mechanical stresses of repeated charge and discharge cycles. Solid electrolytes are susceptible to crack propagation due to dendrite growth from Li metal anodes and to debonding processes at the cathode/electrolyte interface due to cyclic variations in the cathode lattice parameters. In this perspective, we argue that solutions to the mechanics challenges of all-solid-state batteries can be borrowed from the aerospace industry, which successfully overcame similar hurdles in the development of thermal barrier coatings of superalloy turbine blades. Their solution was to exploit ferroelastic and transformation toughening mechanisms to develop ceramics that can withstand cyclic stresses due to large variations in temperature. This perspective describes fundamental materials design principles with which to search for solid electrolytes that are ferroelastically toughened.

cond-mat.mtrl-sci↗

Contraction of polymer gels created by the activity of molecular motors

We propose a theory based on non-equilibrium thermodynamics to describe the mechanical behavior of an active polymer gel created by the inclusion of molecular motors in its solvent. When activated, these motors attach to the chains of the polymer network and shorten them creating a global contraction of the gel, which mimics the active behavior of a cytoskeleton. The power generated by these motors is obtained by ATP hydrolysis reaction, which transduces chemical energy into mechanical work. The latter is described by an increment of strain energy in the gel due to an increased stiffness. This effect is described with an increment of the cross-link density in the polymer network, which reduces its entropy. The theory then considers polymer network swelling and species diffusion to describe the transient passive behavior of the gel. We finally formulate the problem of uniaxial contraction of a slab of gel and compare the results with experiments, showing good agreement.

cond-mat.soft↗

Poroelastic toughening in polymer gels: A theoretical and numerical study

We explore the Mode I fracture toughness of a polymer gel containing a semi-infinite, growing crack. First, an expression is derived for the energy release rate within the linearized, small-strain setting. This expression reveals a crack tip velocity-independent toughening that stems from the poroelastic nature of polymer gels. Then, we establish a poroelastic cohesive zone model that allows us to describe the micromechanics of fracture in gels by identifying the role of solvent pressure in promoting poroelastic toughening. We evaluate the enhancement in the effective fracture toughness through asymptotic analysis. We confirm our theoretical findings by means of numerical simulations concerning the case of a steadily propagating crack. In broad terms, our results explain the role of poroelasticity and of the processes occurring in the fracturing region in promoting toughening of polymer gels.

cond-mat.soft↗