Multifunctional Photonic Janus Particles.

Photonic Janus particles with a sphere fused to a cone are created from the phase separation of dendronized brush block copolymers (den-BBCP) and poly(4-vinylpyridine)-r-polystyrene (P4VP-r-PS) during the solvent evaporation of oil-in-water emulsions. Rapid self-assembly of den-BBCP generates well-ordered lamellar structures stacking along the long axis of the particles, producing structural colors that are dependent on the incident light angle. The colors are tunable over the visible spectrum by varying the molecular weight of den-BBCP. The P4VP-r-PS phase can undergo further surface modifications to produce multifunctional photonic Janus particles. Specifically, real-time magnetic control of the reflected color is achieved by coating the P4VP-r-PS phase with citric acid-capped Fe3O4 nanoparticles. Charged biomolecules (i.e., antibodies) are electrostatically immobilized to the Fe3O4 coating for potential applications in biosensing. As a demonstration, a new photonic sensor for the foodborne pathogen Salmonella is developed with antibody-modified photonic Janus particles, where the angle-dependent structural color plays a key role in the sensing mechanism.

Dynamic Coloration of Complex Emulsions by Localization of Gold Rings Near the Triphase Junction.

Multiphase microscale emulsions are a material platform that can be tuned and dynamically configured by a variety of chemical and physical phenomena, rendering them inexpensive and broadly programmable optical transducers. Interface engineering underpins many of these sensing schemes but typically focuses on manipulating a single interface, while engineering of the multiphase junctions of complex emulsions remains underexplored. Herein, multiphilic triblock copolymer surfactants are synthesized and assembled at the triphase junction of a dynamically reconfigurable biphasic emulsion. Tailoring the linear structure and composition of the polymer surfactants provides affinity to each phase of the complex emulsion (hydrocarbon, fluorocarbon, and continuous water phase), yielding selective localization of polymers around the triphase junction. Conjugation of these polymers with gold nanoparticles, forming structured rings, affords a dynamic reflected isotropic structural color that tracks with emulsion morphology, demonstrating the uniquely enabling nature of a functionalized triphase interface. This color is the result of interference of light along the internal hydrocarbon/fluorocarbon interface, with the gold nanoparticles scattering and redirecting light into total internal reflection competent paths. Thus, the functionalization of the triphase junction renders complex emulsions colorimetric sensors, a powerful tool toward sensitive and simple sensing platforms.

Switchable Full-Color Reflective Photonic Ellipsoidal Particles.

Full-color reflective photonic ellipsoidal polymer particles, capable of a dynamic color change, are created from dendronized brush block copolymers (den-BBCPs) self-assembled by solvent-evaporation from an emulsion. Surfactants composed of dendritic monomer units allow for the precise modulation of the interfacial properties of den-BBCP particles to transition in shape from spheres to striped ellipsoids. Strong steric repulsions between wedge-type monomers promote rapid self-assembly of polymers into large domains (i.e., 153 nm ≤ D ≤ 298 nm). Of note, highly ordered axially stacked lamellae (i.e., number of layers >100) within an ellipsoid give rise to a near-perfect photonic multilayer. The reflecting color is readily tunable across the entire visible spectrum by alteration of the molecular weight from 477 to 1144 kDa. Finally, the photonic ellipsoids are functionalized with magnetic nanoparticles organized into bands on the particle surface to produce real-time on/off coloration by magnetic field-assisted activation. In total, the reported photonic ellipsoidal particles represent a new class of switchable photonic materials.

Effect of Chemical Microenvironment in Spirothiopyran Monolayer Direct-Write Photoresists.

We study the effect of the microenvironment on writing chemical patterns into spirothiopyran monolayers over large areas in a single step with light. Surfaces functionalized with photoresponsive spirothiopyran are fabricated by chemically modifying amine-terminated monolayers. The merocyanine isomer selectively participates in a thiol-Michael addition reaction with maleimide-functionalized molecules, rendering these surfaces ideal for fast, mask-less direct writing. The local microenvironment of spirothiopyran is found to strongly influence the kinetics of photoswitching. The quantum yield of ring opening is found to be 17 times faster for spirothiopyran surrounded by a locally charged environment rich in guanidinium diluent molecules as compared to a closed-packed monolayer without diluents. Hydrophilic environments are also found to improve the kinetics of ring closing. Optimization of the diluent concentration leads to dramatic improvements in both contrast and yield of direct writing. This enables the monolayer to be used for maskless two-color photopatterning in which spatial control over patterning is obtained by varying the relative intensity of incident UV and green light. These experiments demonstrate the capacity of spirothiopyran monolayers to serve as a versatile toolbox for rapid, large-area surface functionalization.

Coupled Electromagnetic and Reaction Kinetics Simulation of Super-Resolution Interference Lithography.

Inspired by the ability of super-resolved fluorescence microscopy to circumvent the diffraction barrier, two-color super-resolution interference lithography exploits nonequilibrium kinetics in materials to achieve large-area nanopatterning while using visible light. Periodic patterns with super-resolved features down to tens of nanometers have been demonstrated in thin films and monolayers. Extending these advances to the bulk nanopatterning of thick films requires a quantitative understanding of the time-dependent interactions of optical dynamics, including absorption, diffraction, and intensity modulation at two wavelengths, with the photoactivated and inhibited reaction kinetics. Here, we develop an efficient electromagnetic (EM) perturbation theory approach that facilitates for the first time fully coupled simulations of EM and chemical kinetics in two-color interference lithography. Applied to a spirothiopyran-functionalized photoresist system, these simulations show that diffraction and absorption effects are negligible (<0.1%) for depths up to 10 µm, and that tuning exposure time and intensities can lead to concentration contrast up to 80%. We investigate multiple exposure strategies to reduce the pitch of the line pattern including sequential exposures with different times to achieve uniform lines and multiplexed exposures with equal periods. This capability to rapidly and accurately predict the coupled optical and chemical dynamics facilitates the computational design of high-precision patterns in two-color interference lithography.

Super-resolution interference lithography enabled by non-equilibrium kinetics of photochromic monolayers.

Highly parallelized optical super-resolution lithography techniques are key for realizing bulk volume nanopatterning in materials. The majority of demonstrated STED-inspired lithography schemes are serial writing techniques. Here we use a recently developed model spirothiopyran monolayer photoresist to study the non-equilibrium kinetics of STED-inspired lithography systems to achieve large area interference lithography with super-resolved feature dimensions. The linewidth is predicted to increase with exposure time and the contrast is predicted to go through a maximum, resulting in a narrow window of optimum exposure. Experimental results are found to match with high quantitative accuracy. The low photoinhibition saturation threshold of the spirothiopyran renders it especially conducive for parallelized large area nanopatterning. Lines with 56 and 92 nm FWHM were obtained using serial and parallel patterning, respectively. Functionalization of surfaces with heterobifunctional PEGs enables diverse patterning of any desired chemical functionality on these monolayers. These results provide important insight prior to realizing a highly parallelized volume nanofabrication technique.