Write and take to be the reservoir density of each monovalent ion species. Equal electrochemical potentials in equilibrium give the Boltzmann ion densities in a symmetric electrolyte,Combining this with the electrostatic Poisson equation gives the planar Poisson-Boltzmann equation,The Debye length is . If the symbol instead denotes the combined density of both species, the factor two is absent; the per-species convention above makes the normalization explicit. At , the linearized planar screening solution obeys . With and ,
The positive ions are counterions and the negative ions are co-ions. At weak potential,They approach from above and below respectively, with equal first-order excess and deficit. For stronger negative potential, interpret the source's strong-potential comparison as a statement about , since itself is negative. Counterions become strongly concentrated near the wall, while co-ions are exponentially depleted and remain nonnegative. Linearization misses this asymmetry and would eventually predict unphysical negative co-ion density. Point-ion mean-field theory itself eventually needs finite-size and correlation corrections; it provides no steric cap at arbitrarily large counterion concentration.
For steady tangential electro-osmosis, with no imposed pressure gradient and negligible inertia, the Stokes equation is . Since ,The conditions and giveThe printed constant speed is the bulk velocity outside the double layer, not the velocity at the no-slip wall. With negative the positive counterion excess drives fluid along the applied field. The far-field value is the Helmholtz-Smoluchowski electro-osmotic velocity.[ref]
Induced-Charge Electro-osmosis and Electrophoresis by Martin Z. Bazant. Section1,page1: diffuse charge, slip velocity and plug-flow limit
For the finite channel, first model the added wall as an ideally uncharged insulating boundary with no normal field on its outer side: , while . The one-charged-wall electro-osmotic channel then hasIntegrating the same force balance and enforcing givesFor , the maximum occurs atIn that limit : the velocity rises rapidly from zero at the charged wall, reaches a maximum a few screening lengths away, then falls approximately linearly to zero at the neutral wall. One charged wall does not give a symmetric plug across a channel with no-slip at the other wall.
An alternative electrode condition means a wall held at reservoir potential; it is not the same as zero surface charge. Under that convention,with . Both boundary conventions have the same leading thin-double-layer profile above. An externally imposed pressure gradient would add a pressure-driven profile; none is specified here.
For dilute nonadsorbing uncharged polymers in equilibrium or sufficiently weak flow, the entropic polymer depletion near nonadsorbing walls suppresses chain configurations near each wall. A depletion layer of order the coil radius of gyration is expected at both walls, with a bulk-like central region when is much larger than the coil size. Strong confinement rounds this into a central enrichment. Neutrality removes a direct electrophoretic force, not excluded-volume entropy. Adsorption, concentration and strong-flow migration were not specified, so this is a conditional equilibrium sketch rather than a universal flowing-polymer profile.
Quasineutrality Created 2026-10-18 Updated 2026-10-20
On spatial scales much larger than the Debye length, a plasma may have nearly cancelling positive and negative electric charge densities while still carrying an electric current and having a nonzero electric field. Quasineutrality is an approximation on appropriate slow macroscopic scales, not an assertion that each fluid element has exactly zero charge or that charge separation can be ignored at every boundary.

