An important materials parameter of actuators is their strain-charge coupling coefficient, ψ = δε/δq V , where ε denotes the linear, uniaxial strain. For PPy, the magnitude and sign of ψ depend on the synthesis conditions, the species of transferred ions, the solvent and the mechanical boundary conditions. [4,5,11,21-23] Besides the magnitude of the straincharge coupling, the response time is an important characteristic of actuators. For PPy, the underlying charge transport kinetics include both, ionic transport and the formation of electronically conducting zones along the polymer chains. [24,25] If the potential interval is restricted so that the PPy is kept in its oxidized state with high electronic conductivity, the ion exchange is rate controlling. Similar to classical interdiffusion, the time constant for equilibration after a change in E increases with the square of the diffusion distance. [24-26] Acceptable response times thus require small actuator dimensions in at least one direction. Therefore, many studies investigate PPy as a thin film (typically not exceeding 10 µm) on an electrically conductive substrate. Examples for such actuators are bilayered bending cantilevers [27-29] which may exhibit roughened interfaces for enhanced adhesion, [30] multilayered axial strain actuators [31] or coated fibers spun to yarns. [10] Nanometer-thin PPy films allow for particularly fast reaction times. [15,32] For PPy films with a thickness of about 10 µm, the actuation response time increases to minutes. [33,34] Free-standing PPy actuators with a thickness of ≈100 µm and a cross-sectional gradient in microstructure have been investigated in the context of wireless actuation. [35,36] They exhibit similar response times. For even thicker geometries, the response will be prohibitively slow. PPy actuators with spatial dimensions of mm or above can be realized with PPy-coated nanoskeleton structures, such as multi-walled carbon nanotube networks [37] or electrospun microribbons. [38] In these architectures, a liquid electrolyte in the pore space provides a fast pathway for long-range ion transport. Metal-PPy-electrolyte hybrid materials obtained by the imbibition of PPy-coated nanoporous metals [39] represent a particularly interesting case, because their skeleton structure is load-bearing under compression. This enables actuation against an external compressive load by free-standing macroscopic bodies without a supporting device structure. Furthermore, the mechanical behavior of nanoporous metals has been intensively studied. [40-45] This provides the opportunity for a This work studies the actuation of hybrid materials made from nanoporous gold, polypyrrole, and aqueous electrolyte. The deposition protocol affords a conformal polypyrrole coating on the entire internal interface of millimetersized nanoporous metal specimens made by dealloying. The hybrid material emerges when the remaining pore space is filled with perchloric acid. The metal serves as load-bearing and electronically conductive substrate, the polypyrrole...