Transparent Polymer Opal Thin Films with Intense UV Structural Color

We report on shear-ordered polymer photonic crystals demonstrating intense structural color with a photonic bandgap at 270 nm. Our work examines this UV structural color, originating from a low refractive index contrast polymer composite system as a function of the viewing angle. We report extensive characterization of the angle-dependent nature of this color in the form of ‘scattering cones’, which showed strong reflectivity in the 275–315 nm range. The viewing range of the scattering was fully quantified for a number of planes and angles, and we additionally discuss the unique spectral anisotropy observed in these structures. Such films could serve as low-cost UV reflection coatings with applications in photovoltaics due to the fact of their non-photobleaching and robust mechanical behavior in addition to their favorable optical properties

Transparent Polymer Opal Thin Films with Intense UV Structural Color

We report on shear-ordered polymer photonic crystals demonstrating intense structural color with a photonic bandgap at 270 nm. Our work examines this UV structural color, originating from a low refractive index contrast polymer composite system as a function of the viewing angle. We report extensive characterization of the angle-dependent nature of this color in the form of ‘scattering cones’, which showed strong reflectivity in the 275–315 nm range. The viewing range of the scattering was fully quantified for a number of planes and angles, and we additionally discuss the unique spectral anisotropy observed in these structures. Such films could serve as low-cost UV reflection coatings with applications in photovoltaics due to the fact of their non-photobleaching and robust mechanical behavior in addition to their favorable optical properties

Thermo-Responsive Ultrafiltration Block Copolymer Membranes Based on Polystyrene-block-poly(diethyl acrylamide)

Within the present work, a thermo-responsive ultrafiltration membrane is manufactured based on a polystyrene-block-poly(diethyl acrylamide) block copolymer (BCP). The poly(diethyl acrylamide) block segment features a lower critical solution temperature (LCST) in water, similar to the well-known poly(N-isopropylacrylamide), but having increased biocompatibility and without exhibiting a hysteresis of the thermally induced switching behavior. The BCP is synthesized via sequential “living” anionic polymerization protocols and analyzed by 1H-NMR spectroscopy, size exclusion chromatography, and differential scanning calorimetry. The resulting morphology in the bulk state is investigated by transmission electron microscopy (TEM) and small-angle X-ray scattering (SAXS) revealing the intended hexagonal cylindrical morphology. The BCPs form micelles in a binary mixture of tetrahydrofuran and dimethylformamide, where BCP composition and solvent affinities are discussed in light of the expected structure of these micelles and the resulting BCP membrane formation. The membranes are manufactured using the non-solvent induced phase separation (NIPS) process and are characterized via scanning electron microscopy (SEM) and water permeation measurements. The latter are carried out at room temperature and at 50 °C revealing up to a 23-fold increase of the permeance, when crossing the LCST of the poly(diethyl acrylamide) block segment in water

Thermo-Responsive Ultrafiltration Block Copolymer Membranes Based on Polystyrene-block-poly(diethyl acrylamide)

Within the present work, a thermo-responsive ultrafiltration membrane ismanufactured based on a polystyrene-block-poly(diethyl acrylamide) blockcopolymer (BCP). The poly(diethyl acrylamide) block segment features a lowercritical solution temperature (LCST) in water, similar to the well-knownpoly(N-isopropylacrylamide), but having increased biocompatibility andwithout exhibiting a hysteresis of the thermally induced switching behavior.The BCP is synthesized via sequential “living” anionic polymerizationprotocols and analyzed by1H-NMR spectroscopy, size exclusionchromatography, and differential scanning calorimetry. The resultingmorphology in the bulk state is investigated by transmission electronmicroscopy (TEM) and small-angle X-ray scattering (SAXS) revealing theintended hexagonal cylindrical morphology. The BCPs form micelles in abinary mixture of tetrahydrofuran and dimethylformamide, where BCPcomposition and solvent affinities are discussed in light of the expectedstructure of these micelles and the resulting BCP membrane formation. Themembranes are manufactured using the non-solvent induced phaseseparation (NIPS) process and are characterized via scanning electronmicroscopy (SEM) and water permeation measurements. The latter arecarried out at room temperature and at 50°C revealing up to a 23-foldincrease of the permeance, when crossing the LCST of the poly(diethylacrylamide) block segment in water