We present a theoretical framework for unidirectional electromagnetohydrodynamic flow of dilute electrolytes under perpendicular magnetic fields. Starting from the Navier–Stokes equation coupled with the Poisson–Nernst–Planck formulation, we show that the problem admits a sequential decoupling: the Stokes equation is solved first to obtain the velocity profile, which defines a hydrodynamic potential entering the Nernst–Planck description of ions. This Lorentz-force-induced potential competes with electrostatic attraction and significantly alters ionic distributions. We analyze this mechanism in two canonical geometries. In planar Couette shear, it produces a Manning–Oosawa-like condensation transition in one dimension, a phenomenon absent in classical electrostatics. We derive an eigenvalue equation predicting a sharp threshold between counterion enrichment and depletion at the charged wall. In cylindrical Taylor–Couette flow, the same effect shifts the classical Manning criterion by a magnetic parameter, enabling tunable control of condensation. These findings extend Manning–Oosawa phenomenology to driven, non-equilibrium systems and provide a basis for magnetic manipulation of screening in electrolytes, with implications for microfluidics, electrochemical systems, and nonlinear boundary-value theory.

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