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Unparalleled temporal and spatial control of colloidal chemical processes introduces immense potential for the manufacturing, modification, and manipulation of latex particles. This review highlights major advances in photochemistry, both as stimulus and response, to generate unprecedented functionality in polymer colloids. Light-based chemical modification generates polymer particles with unique structural complexity, and the incorporation of photoactive functionalities transforms inert particles into photoactive nanodevices. Latex photo-functionality, which is reflected in both the colloidal and coalesced states, enables photochromism, photoswitchable aggregation, tunable fluorescence, photoactivated crosslinking and solidification, and photomechanical actuation. Previous literature explores the capacity of photochemistry, which complements the rheological and processing advantages of latex, to expand beyond traditional coatings applications and enable disruptive technologies in critical areas including nanomedicine, data security, and additive manufacturing. 

Abstract A series of polymer nanocomposites containing single‐walled carbon nanotubes (SWNTs) are prepared from polymerizable quaternary ammonium surfactants using photo‐polymerization and investigated by means of polarized optical microscopy, small‐angle X‐ray scattering, and rheological measurements. The surfactant monomers with various alkyl chains of nonpolar tails form lyotropic liquid crystalline (LLC) mesophases in aqueous medium with hexagonal packing of cylindrical micelles. The physical adsorption of nonpolar tails of surfactants on the surface of SWNTs results in de‐bundled nanotubes. The LLC phase diagram is investigated as functions of alkyl chain length, concentration, temperature, and SWNTs. As such, addition of SWNTs does not change the hexagonal mesophases but enhances the order–disorder transition temperatures and alters the rheological behaviors. After photo‐polymerization, the microstructures of hexagonal packing are changed while addition of SWNTs does not disrupt the resulting microstructures. The polymerized composites are consistent with both lamellar and gyroid nanostructures and a possible model is proposed to interpret the observed phenomenon. Under the shear flow, the defect‐free monodomain structures are obtained in the LLC phase and subsequently locked in the solid film after polymerization.