Diffusion in Solids and Phase Transitions

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Motivation

Many technologically important materials — hydrogen-storage alloys, lithium-ion electrode materials, gels, shape-memory alloys — undergo coupled deformation and species diffusion. The diffusion drives compositional changes that modify the elastic modulus and natural shape of the solid; conversely, stress alters the chemical potential and thus the kinetics of diffusion. At low temperatures or high concentrations, these systems also exhibit phase separation, described by Cahn–Hilliard-type free energies with double-well structure. Understanding the interplay between mechanics, diffusion, and phase transitions at the PDE level is both mathematically rich and practically important.

This research thread started from thermomechanical models for shape-memory alloys and expanded to cover hydrogen storage, doubly nonlinear Cahn–Hilliard systems, and large-strain poromechanics, through a long-running collaboration with T. Roubíček (Prague) and E. Bonetti, P. Colli, and L. Scarpa.


Details

Shape-memory alloys under electromagnetic loading (2009–2013)

Shape-memory alloys (SMAs) are intermetallics that undergo a reversible martensitic phase transformation. When the alloy is also ferromagnetic (as in Ni–Mn–Ga), the transformation can be triggered or guided by a magnetic field. The thermomechanical analysis of such systems requires coupling elastoplasticity, magnetism, heat conduction, and electric conduction.

Hydrogen storage: stress effects and hysteresis (2014–2016)

Metal hydrides are attractive materials for solid-state hydrogen storage because of their high volumetric capacity. However, their practical use is hampered by two effects: (i) the large volumetric expansion during hydrogen absorption induces stresses that alter the absorption thermodynamics; (ii) the absorption/desorption cycle exhibits hysteresis, with different equilibrium pressures on the way in and out. Modeling both effects requires coupling diffusion to mechanics and phase transitions.

Cahn–Hilliard systems with nonlinear viscosity (2017–2020)

The Cahn–Hilliard equation with a nonlinear (logarithmic or degenerate) mobility describes phase separation in fluids and solids. A particularly challenging variant — the doubly nonlinear Cahn–Hilliard system — arises when both the chemical potential and the time derivative of the concentration are related to the concentration by nonlinear operators. This is the setting for the following series of papers with Bonetti, Colli, and Scarpa:

Large-strain poromechanics and continuum thermodynamics (2018–2022)

Alongside the Cahn–Hilliard program, a parallel effort extended the diffusion–mechanics coupling to fully nonlinear (large-strain) poroelastic bodies:

Swelling, dehydration, and shape morphing in soft materials (2022–2026)

A parallel research direction addresses the coupled chemo-mechanical and thermal response of swollen soft materials — hydrogels and edible composites — using Flory–Rehner/Flory–Huggins swelling theory. Unlike the Cahn–Hilliard thread above, the emphasis here is on moisture-driven deformation, differential shrinkage across material domains, and buckling instabilities arising from inhomogeneous dehydration.


Summary and open questions

The thread traces a progression from SMA thermodynamics (2009–2013) → hydrogen storage with stress effects (2014–2016) → abstract Cahn–Hilliard analysis (2017–2020) → large-strain poromechanics and charged diffusion (2018–2022) → geological and thermoplastic applications (2021–2024) → thermal dehydration and shape morphing in soft materials (2026). The unifying theme is the rigorous analysis of coupled nonlinear PDE systems arising at the mechanics–chemistry interface. Open questions include the derivation of effective diffusion coefficients in heterogeneous elastic media and the analysis of phase-field fracture coupled to species diffusion.