This paper presents the current state of mathematical modelling of the electrochemical behaviour of lithium-ion batteries (LIBs) as they are charged and discharged. It reviews the models developed by Newman and co-workers, both in the cases of dilute and moderately concentrated electrolytes and indicates the modelling assumptions required for their development. Particular attention is paid to the interface conditions imposed between the electrolyte and the active electrode material; necessary conditions are derived for one of these, the Butler–Volmer relation, in order to ensure physically realistic solutions. Insight into the origin of the differences between various models found in the literature is revealed by considering formulations obtained by using different measures of the electric potential. Materials commonly used for electrodes in LIBs are considered and the various mathematical models used to describe lithium transport in them discussed. The problem of upscaling from models of behaviour at the single electrode particle scale to the cell scale is addressed using homogenisation techniques resulting in the pseudo-2D model commonly used to describe charge transport and discharge behaviour in lithium-ion cells. Numerical solution to this model is discussed and illustrative results for a common device are computed.

The self-interaction force of dislocation curves in metals depends on the local arrangement of the atoms and on the non-local interaction between dislocation curve segments. While these non-local segment–segment interactions can be accurately described by linear elasticity when the segments are further apart than the atomic scale of size $\varepsilon$ , this model breaks down and blows up when the segments are $O(\varepsilon)$ apart. To separate the non-local interactions from the local contribution, various models depending on $\varepsilon$ have been constructed to account for the non-local term. However, there are no quantitative comparisons available between these models. This paper makes such comparisons possible by expanding the self-interaction force in these models in $\varepsilon$ beyond the O(1)-term. Our derivation of these expansions relies on asymptotic analysis. The practical use of these expansions is demonstrated by developing numerical schemes for them, and by – for the first time – bounding the corresponding discretisation error.

The aim of the paper is to explore non-local reverse-space matrix non-linear Schrödinger equations and their inverse scattering transforms. Riemann–Hilbert problems are formulated to analyse the inverse scattering problems, and the Sokhotski–Plemelj formula is used to determine Gelfand–Levitan–Marchenko-type integral equations for generalised matrix Jost solutions. Soliton solutions are constructed through the reflectionless transforms associated with poles of the Riemann–Hilbert problems.

The dynamics of the fragmentation equation with size diffusion is investigated when the size ranges in $(0,\infty)$ . The associated linear operator involves three terms and can be seen as a nonlocal perturbation of a Schrödinger operator. A Miyadera perturbation argument is used to prove that it is the generator of a positive, analytic semigroup on a weighted $L_1$ -space. Moreover, if the overall fragmentation rate does not vanish at infinity, then there is a unique stationary solution with given mass. Assuming further that the overall fragmentation rate diverges to infinity for large sizes implies the immediate compactness of the semigroup and that it eventually stabilizes at an exponential rate to a one-dimensional projection carrying the information of the mass of the initial value.

We consider a spherical particle levitating above a liquid bath owing to the Leidenfrost effect, where the vapour of either the bath or sphere forms an insulating film whose pressure supports the sphere’s weight. Starting from a reduced formulation based on a lubrication-type approximation, we use matched asymptotics to describe the morphology of the vapour film assuming that the sphere is small relative to the capillary length (small Bond number) and that the densities of the bath and sphere are comparable. We find that this regime is comprised of two formally infinite sequences of distinguished limits which meet at an accumulation point, the limits being defined by the smallness of an intrinsic evaporation number relative to the Bond number. These sequences of limits reveal a surprisingly intricate evolution of the film morphology with increasing sphere size. Initially, the vapour film transitions from a featureless morphology, where the thickness profile is parabolic, to a neck–bubble morphology, which consists of a uniform pressure bubble bounded by a narrow and much thinner annular neck. Gravity effects then become important in the bubble leading to sequential formation of increasingly smaller neck–bubble pairs near the symmetry axis. This process terminates when the pairs closest to the symmetry axis become indistinguishable and merge. Subsequently, the inner section of that merger transitions into a uniform-thickness film that expands radially, gradually squishing increasingly larger neck–bubble pairs into a region of localised oscillations sandwiched between the uniform film and what remains of the bubble whose radial extent is presently comparable to the uniform film; the neck–bubble pairs farther from the axis remain essentially intact. Ultimately, the uniform film gobbles up the largest outermost bubble, whereby the morphology simplifies to a uniform film bounded by localised oscillations. Overall, the asymptotic analysis describes the continuous evolution of the vapour film from a neck–bubble morphology typical of a Leidenfrost drop levitating above a flat solid substrate to a uniform-film morphology which resembles that in the case of a large liquid drop levitating above a liquid bath.

Multi-compartment models described by systems of linear ordinary differential equations are considered. Catenary models are a particular class where the compartments are arranged in a chain. A unified methodology based on the Laplace transform is utilised to solve direct and inverse problems for multi-compartment models. Explicit formulas for the parameters in a catenary model are obtained in terms of the roots of elementary symmetric polynomials. A method to estimate parameters for a general multi-compartment model is also provided. Results of numerical simulations are presented to illustrate the effectiveness of the approach.