We analyse the self-diffusiophoresis of a spherical particle animated by a non-uniform chemical reaction at its boundary. We consider two models of solute absorption, one with a specified distribution of interfacial solute flux and one where this flux is governed by first-order kinetics with a specified distribution of rate constant. We employ a macroscale model where the short-range interaction of the solute with the particle boundary is represented by an effective slip condition. The solute

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... ansport is governed by an advection–diffusion equation. We focus upon the singular limit of large Péclet numbers,$\mathit{Pe}\gg 1$. In the fixed-flux model, the excess-solute concentration is confined to a narrow boundary layer. The scaling pertinent to that limit allows the problem governing the solute concentration to be decoupled from the flow field. The resulting nonlinear boundary-layer problem is handled using a transformation to stream-function coordinates and a subsequent application of Fourier transforms, and is thereby reduced to a nonlinear integral equation governing the interfacial concentration. Its solution provides the requisite approximation for the particle velocity, which scales as$\mathit{Pe}^{-1/3}$. In the fixed-rate model, large Péclet numbers may be realized in different limit processes. We consider the case of large swimmers or strong reaction, where the Damköhler number$\mathit{Da}$is large as well, scaling as$\mathit{Pe}$. In that double limit, where no boundary layer is formed, we obtain a closed-form approximation for the particle velocity, expressed as a nonlinear functional of the rate-constant distribution; this velocity scales as$\mathit{Pe}^{-2}$. Both the fixed-flux and fixed-rate asymptotic predictions agree with the numerical values provided by computational solutions of the nonlinear transport problem.