Diffusiophoresis, the movement of particles under a solute concentration gradient, has practical implications in a number of applications, such as particle sorting, focusing, and sensing. For diffusiophoresis in an electrolyte solution, the particle velocity is described by the electrolyte relative concentration gradient and the diffusiophoretic mobility of the particle. The electrolyte concentration, which typically varies throughout the system in space and time, can also influence the zeta potential of particles in space and time. This variation affects the diffusiophoretic behavior, especially when the zeta potential is highly dependent on the electrolyte concentration. In this work, we show that adsorbing a single bilayer (or 4 bilayers) of a polyelectrolyte pair (PDADMAC/PSS) on the surface of microparticles resulted in effectively constant zeta potential values with respect to salt concentration throughout the experimental range of salt concentrations. This allowed a constant potential model for diffusiophoretic transport to describe the experimental observations, which was not the case for uncoated particles in the same electrolyte system. This work highlights the use of simple polyelectrolyte pairs to tune the zeta potential and maintain constant values for precise control of diffusiophoretic transport.