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We theoretically study the active motion of self-diffusiophoretic Janus particles (JPs) using the Onsager-Casimir reciprocal relations. The linear and angular velocity of a single JP are shown to respectively result from a coupling of electrochemical forces to the fluid flow fields induced by a force and torque on the JP. A model calculation is provided for half-capped JPs catalysing a chemical reaction of solutes at their surface, by reducing the continuity equations of the reacting solutes to Poisson equations for the corresponding electrochemical fields. We find that an anisotropic chemical activity alone is enough to give rise to active linear motion of a JP, whereas active rotation only occurs if the JP is not axisymmetric. In the absence of specific interactions with the solutes, the active linear velocity of the JP is shown to be related to the stoichiometrically weighted sum of the friction coefficients (or hydrodynamic radii) of the reacting solutes. Our reciprocal treatment further suggests that a specific interaction with the solutes is required to observe far-field diffusiophoretic interactions between JPs, which rely on an interfacial solute excess at the JP surface. Most notably, our approach applies beyond the boundary-layer approximation and accounts for both the diffusio- and electrophoretic nature of active motion.

We present a complete reciprocal description of particle motion inside multi-component fluids that extends the conventional Onsager formulation of non-equilibrium transport to systems where the thermodynamic forces are non-uniform on the colloidal scale. Based on the dynamic length and time scale separation in suspensions, the particle flux is shown to be related to the volume-averaged coupling between the Stokes flow tensor and the thermodynamic force density acting on the fluid. The flux is then expressed in terms of thermodynamic quantities that can be computed from the interfacial properties and equation of state of the colloids. Our results correctly describe diffusion and sedimentation, and suggest that force-free phoretic motion can occur even in the absence of interfacial interactions, provided that the thermodynamic gradients are non-uniform at the colloidal surface. In particular, we derive an explicit hydrodynamic form for the phoretic force resulting from these non-uniform gradients. The form is validated by the recovery of the Henry function for electrophoresis and the Ruckenstein term for thermophoresis., Comment: The following article has been accepted by the Journal of Chemical Physics. After it is published, it will be found at https://aip.scitation.org/journal/jcp

We use a hydrodynamic reciprocal approach to phoretic motion to derive general expressions for the electrophoretic and thermophoretic mobility of weakly charged colloids in aqueous electrolyte solutions. Our approach shows that phoretic motion can be understood in terms of the interfacial transport of thermodynamic excess quantities that arises when a colloid is kept stationary inside a bulk fluid flow. The obtained expressions for the mobilities are extensions of previously known results as they can account for different hydrodynamic boundary conditions at the colloidal surface, irrespective of how the colloid-fluid interaction range compares to the colloidal radius.

We use the dynamic length and time scale separation in suspensions to formulate a general description of colloidal thermophoresis. Our approach allows an unambiguous definition of separate contributions to the colloidal flux and clarifies the physical mechanisms behind non-equilibrium motion of colloids. In particular, we derive an expression for the interfacial force density that drives single-particle thermophoresis in non-ideal fluids. The issuing relations for the transport coefficients explicitly show that interfacial thermophoresis has a hydrodynamic character that cannot be explained by a purely thermodynamic consideration. Our treatment generalises the results from other existing approaches, giving them a clear interpretation within the framework of non-equilibrium thermodynamics.

We present thermophoretic measurements in aqueous suspensions of three different polystyrene (PS) particles of varying negative charge, size and surface coating. Our measurement technique is based on the observation of the colloidal steady-state distribution using conventional bright-field microscopy, which avoids undesirable effects such as laser-induced convection or local heating. We find that the colloids with the weakest zeta potential exhibit the strongest thermophoretic effect, suggesting that surface functionality leads to a more intricate dependence of the Soret coefficient on hydrodynamic boundary conditions than predicted by existing theoretical approaches. We also study the relaxation of the colloids to steady-state and propose a model to quantify the relaxation speed, based on the time evolution of the colloidal center of mass. Our observations are well described by this model and show that the relaxation speed tends to increase with the magnitude of the thermophoretic force., Comment: 11 pages, 8 figures

We report a study of reversible adsorption of DNA-coated colloids on complementary functionalized oil droplets. We show that it is possible to control the surface coverage of oil droplets by colloidal particles, by exploiting the fact that during slow adsorption, compositional arrest takes place well before structural arrest occurs. As a consequence, we can prepare colloid-coated oil droplets with a `frozen' degree of loading, but with fully ergodic colloidal dynamics on the droplets. We illustrate the equilibrium nature of the adsorbed colloidal phase by exploring the quasi two-dimensional (2d) phase behaviour of the adsorbed colloids under the influence of depletion interactions. We present simulations of a simple model that illustrates the nature of the compositional arrest and the structural ergodicity., Comment: 9 pages, 4 figures