We report on the synthesis and characterization of water-dispersible, mechanically stable conjugated polymer nanoparticles (CPNs) in shelled architecture with tunable emission and controllable photometric properties via cross-linking. Using a reprecipitation method, white-emitting polymer nanoparticles are prepared in different sizes by varying the concentration of polymer; the emission kinetics are tuned by controlling the shell formation. For this purpose, polyfluorene derivatives containing azide groups are selected that can be decomposed under UV light to generate very reactive species, which opportunely facilitate the inter- and intra-cross-linking of polymer chains to form shells. Nanoparticles before and after UV treatment are characterized by various techniques. Their size and morphologies are determined by using dynamic light scattering (DLS) measurements and imaging techniques including scanning electron microscopy (SEM) and atomic force microscopy (AFM). For optical characterization, UV-vis and steady-state and time-resolved fluorescent spectroscopies are performed. Solid-state behaviors of these CPNs are also investigated by forming films through drop-casting. Moreover, the photometric calculations are also performed for films and dispersions to determine the color quality. A device has been constructed to show proof-of-principle white light generation from these nanoparticles. Additionally, mechanical stability studies are performed and demonstrated that these nanoparticles are indeed mechanically stable by removing the solvent after cross-linking using a freeze-dryer and redispersing in water and THF. Optical and imaging data confirm that the redispersed particles preserve their shapes and sizes after cross-linking.