A novel ultrathin Nafion-palladium nanocomposite film is developed by incorporating positively charged Pd nanoparticles, stabilized with dimethylaminopyridine (DMAP), into Nation Langmuir-Schaefer (LS) films. The films show considerable activity for the redox-catalyzed hydrogen-evolution reaction, the rate of which scales with film thickness. The Nation film can be deposited on both insulating (glass) and electrode (indium-tin oxide) surfaces. The quantity of Pd natioparticles immobilized can be controlled simply via the thickness of the Nafion film. The morphology of the films are investigated using AFM, which allows the number density of nanoparticles to be estimated for the thinnest (10 layers; 18 nm) films. Incorporation of nanoparticles is also determined with cyclic voltammetry and UV-visible spectroscopy. The former method allows estimation of the electrochemically active surface area of Pd wired to the underlying electrode. A novel scanning electrochemical microscopy (SECM) approach is used to investigate the kinetics of the hydrogen evolution reaction (HER) catalyzed by Pd nanoparticles within the Nation film, which allows the intrinsic activity to be determined. Single nanoparticle reactivities are extracted and are comparable to the activity of native nanoparticles on glass and to bulk Pd. It is found that neither Nation encapsulation nor DMAP functionalization impair the electrocatalytic activity of these nanoparticles towards the HER. Nation encapsulation thus provides a framework for the formation of interfaces, whose activity scales with film thickness. The creation of 3D materials opens up the possibility of carrying out redox-mediated hydrogen evolution using solution species as the electron donor.