Abstract When a liquid contacts a charged solid surface, counterions in the liquid accumulate near the interface—a process traditionally described by models such as Helmholtz, Stern, and Debye‐Hückel. However, these frameworks overlook the complex interplay between inertia and surface charge, and they simplify ions as mere point charges. This study employs vibrating solid surfaces to decouple and investigate the effects of inertia, ion‐slipping, and electrostatic interactions at the molecular scale. This approach reveals “inertial layer” in the initial liquid strata, which plays a critical role in governing interface dynamics. Within this layer, a tunable Helmholtz zone is identified, where mechanical stiffness and electrostatic forces adjust in response to ion concentration. Beyond this lies a Debye screening region characterized by repulsive forces and electrostatic decoupling from the double‐layer capacitor model. Using phosphate‐buffered saline (PBS) as a model electrolyte, it is demonstrated that low ionic strength enhances interfacial stability, while high concentrations increase electrostatic repulsion, influencing nanoscale mechanical behavior. These insights refine the understanding of interfacial phenomena and hold significant implications for biosensing, catalysis, and energy storage technologies.
Bhalla et al. (Thu,) studied this question.