wileyonlinelibrary.comthe infl uence of nanoscale confi nement on conjugated polymer chain alignment were carried out on nanoimprinted conjugated polymer fi lms [ 4 ] and on conjugated polymer fi bers formed within nanoporous dielectric templates. [ 12,13 ] In these studies, induced polymer chain alignment was observed and occurred in the direction normal to the confi nement direction due to the fl ow of the polymer chains and the interaction between the polymer and the substrate/sidewall. [ 4 ] Additionally, since conjugated polymerbased thin-fi lm optoelectronics have lower device effi ciencies compared with inorganic devices, [ 14 ] various optically-active nanostructures have been employed to manipulate light in thin conjugated polymer fi lms due to the unique optical properties of nanostructures. Examples include: 1) patterned nonmetallic transparent substrates (patterned on either the outer surface [ 15 ] or inner surface [ 16 ] of the device), whereby the scattering properties of the patterned substrates were employed to improve light extraction effi ciency from the light-emitting organic active layer; 2) addition of plasmonic nanostructures to take advantage of their light scattering and optical near-fi eld properties. [ 17 ] Plasmonic nanostructures employed were either metallic nanoparticles/nanowires embedded into the devices' active layer and/or hole/electron transport layer, [ 18,19 ] or nanostructure arrays introduced onto the metallic electrodes. [ 20 ] In particular, nanohole arrays in metallic thin fi lms have been used as both back electrodes [ 21 ] as well as front electrodes, [ 22,23 ] and showed improvements in light in-coupling or out-coupling, depending on the optoelectronic application. Most of the previous studies employing nanohole arrays were carried out on periodic arrays fabricated by nanoimprint lithography, [ 22 ] e-beam lithography [ 24 ] or focused-ion beam milling, [ 25 ] since the periodicity of the nanohole array played an important role in their plasmonic properties. [ 26 ] However, random nanoporous metal has also shown promising plasmonic and photonic properties, [27][28][29][30] and can be fabricated by large-area nonlithographic methods, such as dealloying. [ 31 ] Here, we develop a nonlithographic, thermally-assisted dewetting method to fabricate nanoporous silver (NPAg) fi lms with different morphologies over areas >1 cm 2 . We study the infl uence of NPAg on both the chain morphology Disordered nanoporous silver (NPAg) thin fi lms fabricated by a thermally assisted dewetting method are employed as a platform to infl uence chain alignment, morphology, and optical properties of three well-known conjugated polymers. Grazing-incidence wide-angle X-ray scattering (GIWAXS) measurements show that the porous structure of the metal induces close Ï-Ï stacking of poly(3-hexylthiophene) (P3HT) chains and extended, planar chain conformations of poly(9,9-di-n -octylfl uorenyl-2,7-diyl) (PFO) and poly[(9,9-di-n -octylfl uorenyl-2,7-diyl)-alt -(benzo[2,1,3]thiadiazol-4,8-diyl)] (F8BT)...