Polarization-Dependent Thin Films with Biaxial Anisotropic Absorption Constructed by a Single Coating and Subsequent Topochemical Polymerization of Chromophores.

For the construction of hierarchical superstructures with biaxial anisotropic absorption, a newly synthesized diacetylene-functionalized bipyridinium is self-assembled to use an electron-accepting host for capturing and arranging guests. The formation of the donor-acceptor complex triggers an intermolecular charge transfer, leading to chromophore activation. Polarization-dependent multichroic thin films are prepared through a sequential process of single-coating, self-assembly, and topochemical polymerization of host-guest chromophores. Molecular packing structures constructed in the single-layer optical thin film possess orthogonal absorption axes for two different wavelengths. By tuning the linear polarization angle, the color of the optical thin film can be intentionally controlled. This single-layered multichroic film provides a new pathway for the development of anticounterfeiting and multiplexing encryptions.

Synthesis of Deuterated and Sulfurated Polymers by Inverse Vulcanization: Engineering Infrared Transparency via Deuteration.

The synthesis of deuterated, sulfurated, proton-free, glassy polymers offers a route to optical polymers for infrared (IR) optics, specifically for midwave IR (MWIR) photonic devices. Deuterated polymers have been utilized to enhance neutron cross-sectional contrast with proteo polymers for morphological neutron scattering measurements but have found limited utility for other applications. We report the synthesis of perdeuterated d14-(1,3-diisopropenylbenzene) with over 99% levels of deuteration and the preparation of proton-free, perdeuterated poly(sulfur-random-d14-(1,3-diisopropenylbenzene)) (poly(S-r-d14-DIB)) via inverse vulcanization with elemental sulfur. Detailed structural analysis and quantum computational calculations of these reactions demonstrate significant kinetic isotope effects, which alter mechanistic pathways to form different copolymer microstructures for deutero vs proteo poly(S-r-DIB). This design also allows for molecular engineering of MWIR transparency by shifting C-H bond vibrations around 3.3 µm/3000 cm-1 observed in proteo poly(S-r-DIB) to 4.2 µm/2200 cm-1. Furthermore, the fabrication of thin-film MWIR optical gratings made from molding of deuterated-sulfurated, proton-free poly(S-r-d14-DIB) is demonstrated; operation of these gratings at 3.39 µm is achieved successfully, while the proteo poly(S-r-DIB) gratings are opaque at these wavelengths, highlighting the promise of MWIR sensors and compact spectrometers from these materials.

Photo-Crosslinkable Inorganic/Organic Sulfur Polymers.

Inverse vulcanization techniques are used to fabricate thermodynamically stable, sulfur polymers. Sulfur-based polymers exhibit higher refractive indices and improved transparency in the mid-wave infrared region compared with most organic polymers. Herein, the postsynthetic modification of sulfur polymers created via inverse vulcanization to generate novel, inorganic/organic photoresists is discussed. Amine-containing sulfur resins are postfunctionalized with cross-linkable alkynes. The sulfur-based materials undergo rapid photo-crosslinking to generate patternable films within 10 min under UV irradiation (365 nm). The development of these resins enables sulfur polymers to be utilized in processes where spatial and hierarchical control is necessary. The generation of this class of materials also expands on sulfur-based organic polymer systems with optical applications.

Electro-optic characteristics of stabilized cholesteric liquid crystals with non-liquid crystalline polymer networks.

Extensive prior research has explored the stabilization of the CLC phase with polymer networks. These prior efforts have demonstrated both tunable and switchable electro-optic reconfiguration of the selective reflection of the CLC phase. Recently, we and other groups have detailed that polymer stabilization of the CLC phase with liquid crystalline monomers retains "structural" chirality (e.g., the chiral phase templates the morphology of the achiral polymer network). Here, we demonstrate that structural chirality can be retained in aliphatic, non-liquid crystalline monomers. PSCLCs prepared by photoinitiated polymerization of aliphatic polymer networks exhibit reversible electro-optic responses. Facilitated by the retention of structural chirality in aliphatic stabilizing polymer networks, we explore the role of surface affinity and crosslink density in the transfer of structural chirality to the liquid crystal media.

Correlation of Structure with Crystalline to Amorphous Phase Transitions of 1,3,6-Substituted Fulvene-Derived Molecular Glasses.

An investigation into the crystalline to amorphous phase transitions of prepared 1,3,6-substituted pentafulvenes showed the expected reversible heated melt and cooling recrystallization in only a few examples. Systematic incorporation of bulky substituents at the 6-position of the fulvene ring led to the nonreversible thermal behavior, rendering phases that were locked into glassy, vitrified states. These molecular glasses produced physically translucent and amorphous features with glass transition temperatures in the range of 61-77 °C, comparable with high-strength plastics such as polyethylene terephthalate. Additionally, the melting point transitions and the resulting heat of fusion values were found to be directly influenced by the nature of the 6-position substituent. Single crystal X-ray crystallography showed that in some cases, fulvenes possessing fused aromatics exhibited a high degree of intermolecular π-π stacking. These results point to a class of molecular glass formers as host materials possessing tunable bulk properties for potentially new optical applications.

Improved Performance of Glucose Bioanodes Using Composites of (7,6) Single-Walled Carbon Nanotubes and a Ferrocene-LPEI Redox Polymer.

The effect of incorporating different types of carbon nanotubes into composite films of a redox polymer (FcMe2-C3-LPEI) and glucose oxidase (GOX) was investigated. The composite films were constructed by first forming a high-surface area network film of either single-walled carbon nanotubes (SWNTs) or multiwalled carbon nanotubes (MWNTs) on a glassy carbon electrode (GCE) by solution casting of a suspension of Triton-X-100 dispersed SWNTs. Next a glucose responsive redox hydrogel was formed on top of the nanotube-modified electrode by cross-linking FcMe2-C3-LPEI with glucose oxidase via ethylene glycol diglycidyl ether (EGDGE). Electrochemical and enzymatic measurements showed that composite films made with (7,6) SWNTs produced a higher response (3.3 mA/cm2) to glucose than films made with (6,5) SWNTs (1.8 mA/cm2) or MWNTs (1.2 mA/cm2) or films made without SWNTs (0.7 mA/cm2). We also show that the response of the composite films could be systematically varied by fabricating SWNT films with different weight ratios of (7,6) and (6,5) SWNTs. Optimization of the (7,6) SWNTs loading and the redox polymer-enzyme film produced a glucose response of 11.2 mA/cm2. Combining the optimized glucose films with a platinum oxygen breathing cathode into a biofuel cell produced a maximum power density output of 343 µW/cm2.

Blue-shifting tuning of the selective reflection of polymer stabilized cholesteric liquid crystals.

We report on electrically-induced, large magnitude (>300 nm), and reversible tuning of the selective reflection in polymer stabilized cholesteric liquid crystals (PSCLCs) prepared from negative dielectric anisotropy nematic liquid crystal hosts. The electrically-induced blue shift in the selective reflection of the PSCLCs is distinguished from our prior reports of bandwidth broadening and red-shifting tuning of the selective reflection in PSCLCs. The dominant factor in delineating the electro-optic response of the PSCLCs detailed here are the preparation conditions. Specifically, long exposure to UV intensity exceeding 250 mW cm-2. Other factors are shown to contribute to the response, including the type and concentration of photoinitiator.

Electrochemical Characterization of Layer-By-Layer Assembled Ferrocene-Modified Linear Poly(ethylenimine)/Enzyme Bioanodes for Glucose Sensor and Biofuel Cell Applications.

Ferrocenylhexyl- and ferrocenylpropyl-modified linear poly(ethylenimine) (Fc-C6-LPEI, Fc-C3-LPEI) were used with periodate-modified glucose oxidase (p-GOX) in the layer-by-layer assembly of enzymatic bioanodes on gold. Fc-C6-LPEI/p-GOX and Fc-C3-LPEI/p-GOX films of 16 bilayers were capable of generating up to 381 ± 3 and 1417 ± 63 µA cm(-2), respectively, in response to glucose. These responses are greater than those of analogous bioanodes fabricated using conventional cross-linking techniques and are extremely high for planar, low surface area, single-enzyme electrodes. (Fc-C3-LPEI/p-GOX)8 films generated 86 ± 3 µW cm(-2) at pH 7.0 and 149 ± 7 µW cm(-2) at pH 5.0, when poised against an air-breathing platinum cathode in a compartment-less biofuel cell. An increase in power output with decreasing pH was shown to be a result of increases in the platinum cathode performance, indicating it is the rate-limiting electrode in the biofuel cells. The effect of fabrication wash time on the buildup of material at the electrode's surface was probed using cyclic voltammetry (CV) and constant potential amperometry. The use of electrochemical techniques as a diagnostic tool for studying the material deposition process is discussed. CV peak separation (ΔE), surface coverage of the electroactive ferrocene (ΓFc), and amperometric sensitivity of the enzyme to glucose (Jmax), studied as a function of numbers of bilayers, showed that physisorption of materials onto the surface results from initial patchy deposition, rather than in distinctly uniform layers.

Synthesis, Electrochemical Characterization, and Linear Free Energy Relationship of 1,3-Diphenyl-6-alkyl/arylfulvenes.

A series of 1,3-diphenyl-6-alkyl/arylfulvenes was prepared, and the electrochemical properties were investigated. The addition of phenyl groups about the fulvene raised the reduction potential and helped to stabilize the electrochemically generated radical anion. The addition of various functional groups onto the phenyl ring at the 6-position of 1,3,6-triphenylfulvene results in a linear free energy relationship between reduction potential and the Hammett substituent constant, σ. Further extending the conjugation at the 6-position of 1,3-diphenyl-6-arylfulvenes increases the reversibility of the redox reactions, but does not appear to further stabilize the generated radical anion. This in-depth investigation provides evidence that the compounds studied may have utility in light-harvesting applications.

The Role of Dithiocarbamate Catalysts in the Diversification of Sulfur Speciation Towards Anionic Sulfur.

Recently, there has been growing interest in the implementation of various "catalysts" to further diversify the substrate scope for inverse vulcanization reactions. While there have been several proposals on the mechanism of how these catalysts work, the speciation of sulfur in these mixtures has remained elusive. As a key component to understanding when and if these catalysts are appropriate, we sought to elucidate the role of dithiocarbamate species in inverse vulcanization reactions by attempting to characterize the speciation of sulfur. The reaction efficacy for various substrates containing different functional groups with sulfur, either with or without a metal dithiocarbamate, potassium diethyldithiocarbamate (K-DTC), suggests the formation of a rapidly fluctuating sulfur speciation and, most importantly, the presence of anionic sulfur. The work concludes with some suggestions on best practices for the utilization of dithiocarbamate catalysts based on our results.

Switchable Optical Properties of Dyes and Nanoparticles in Electrowetting Devices.

The optical properties of light-absorbing materials in optical shutter devices are critical to the use of such platforms for optical applications. We demonstrate switchable optical properties of dyes and nanoparticles in liquid-based electrowetting-on-dielectric (EWOD) devices. Our work uses narrow-band-absorbing dyes and nanoparticles, which are appealing for spectral-filtering applications targeting specific wavelengths while maintaining device transparency at other wavelengths. Low-voltage actuation of boron dipyromethene (BODIPY) dyes and nanoparticles (Ag and CdSe) was demonstrated without degradation of the light-absorbing materials. Three BODIPY dyes were used, namely Abs 503 nm, 535 nm and 560 nm for dye 1 (BODIPY-core), 2 (I2BODIPY) and 3 (BODIPY-TMS), respectively. Reversible and low-voltage (≤20 V) switching of dye optical properties was observed as a function of device pixel dimensions (300 × 900, 200 × 600 and 150 × 450 µm). Low-voltage and reversible switching was also demonstrated for plasmonic and semiconductor nanoparticles, such as CdSe nanotetrapods (abs 508 nm), CdSe nanoplatelets (Abs 461 and 432 nm) and Ag nanoparticles (Abs 430 nm). Nanoparticle-based devices showed minimal hysteresis as well as faster relaxation times. The study presented can thus be extended to a variety of nanomaterials and dyes having the desired optical properties.

Tuning of optical properties and phase behavior of Nanomaterial-stabilized blue phase liquid crystals.

HYPOTHESIS: Nanoparticles of various shapes and sizes can affect the optical properties and blue phase (BP) stabilization of BP liquid crystals (BPLCs). This is because nanoparticles, which are more compatible with the LC host, can be dispersed in both the double twist cylinder (DTC) and disclination defects in BPLCs. EXPERIMENTS: This study presents the first systematic study of the use of CdSe nanoparticles having various sizes and shapes (spheres, tetrapods and nanoplatelets) to stabilize BPLCs. Unlike previous studies using commercial nanoparticles (NPs), we custom-synthesized NPs with the same core and nearly identical long chain hydrocarbon ligand materials. Two LC hosts were used to investigate the NP effect on BPLCs. FINDINGS: The size and shape of nanomaterials greatly influence the interaction with LCs, and the dispersion of NPs in the LC medium affects the position of the BP reflection band and the stabilization of BPs. Spherical NPs were found to be more compatible with the LC medium than tetrapod shape and platelet shape NPs, resulting in a wider temperature range of BP and a redshift of the reflection band of BP. In addition, the inclusion of spherical NPs tuned the optical properties of BPLCs to a significant extent, whereas BPLCs with nanoplatelets displayed a limited influence on the optical properties and temperature window of BPs due to poor compatibility with LC hosts. The tunable optical behavior of BPLC as a function of the type and concentration of NPs has not been reported.

Recent Advances in Electro-Optic Response of Polymer-Stabilized Cholesteric Liquid Crystals.

Cholesteric liquid crystals (CLC) are molecules that can self-assemble into helicoidal superstructures exhibiting circularly polarized reflection. The facile self-assembly and resulting optical properties makes CLCs a promising technology for an array of industrial applications, including reflective displays, tunable mirror-less lasers, optical storage, tunable color filters, and smart windows. The helicoidal structure of CLC can be stabilized via in situ photopolymerization of liquid crystal monomers in a CLC mixture, resulting in polymer-stabilized CLCs (PSCLCs). PSCLCs exhibit a dynamic optical response that can be induced by external stimuli, including electric fields, heat, and light. In this review, we discuss the electro-optic response and potential mechanism of PSCLCs reported over the past decade. Multiple electro-optic responses in PSCLCs with negative or positive dielectric anisotropy have been identified, including bandwidth broadening, red and blue tuning, and switching the reflection notch when an electric field is applied. The reconfigurable optical response of PSCLCs with positive dielectric anisotropy is also discussed. That is, red tuning (or broadening) by applying a DC field and switching by applying an AC field were both observed for the first time in a PSCLC sample. Finally, we discuss the potential mechanism for the dynamic response in PSCLCs.

White light thermoplasmonic activated gold nanorod arrays enable the photo-thermal disinfection of medical tools from bacterial contamination.

The outspread of bacterial pathogens causing severe infections and spreading rapidly, especially among hospitalized patients, is worrying and represents a global public health issue. Current disinfection techniques are becoming insufficient to counteract the spread of these pathogens because they carry multiple antibiotic-resistance genes. For this reason, a constant need exists for new technological solutions that rely on physical methods rather than chemicals. Nanotechnology support provides novel and unexplored opportunities to boost groundbreaking, next-gen solutions. With the help of plasmonic-assisted nanomaterials, we present and discuss our findings in innovative bacterial disinfection techniques. Gold nanorods (AuNRs) immobilized on rigid substrates are utilized as efficient white light-to-heat transducers (thermoplasmonic effect) for photo-thermal (PT) disinfection. The resulting AuNRs array shows a high sensitivity change in refractive index and an extraordinary capability in converting white light to heat, producing a temperature change greater than 50 °C in a few minute interval illumination time. Results were validated using a theoretical approach based on a diffusive heat transfer model. Experiments performed with a strain of Escherichia coli as a model microorganism confirm the excellent capability of the AuNRs array to reduce the bacteria viability upon white light illumination. Conversely, the E. coli cells remain viable without white light illumination, which also confirms the lack of intrinsic toxicity of the AuNRs array. The PT transduction capability of the AuNRs array is utilized to produce white light heating of medical tools used during surgical treatments, generating a temperature increase that can be controlled and is suitable for disinfection. Our findings are pioneering a new opportunity for healthcare facilities since the reported methodology allows non-hazardous disinfection of medical devices by simply employing a conventional white light lamp.

When Chirophotonic Film Meets Wrinkles: Viewing Angle Independent Corrugated Photonic Crystal Paper.

Light manipulation strategies of nature have fascinated humans for centuries. In particular, structural colors are of considerable interest due to their ability to control the interaction between light and matter. Here, wrinkled photonic crystal papers (PCPs) are fabricated to demonstrate the consistent reflection of colors regardless of viewing angles. The nanoscale molecular self-assembly of a cholesteric liquid crystal (CLC) with a microscale corrugated surface is combined. Fully polymerizable CLC paints are uniaxially coated onto a wrinkled interpenetrating polymer network (IPN) substrate. Photopolymerization of the helicoidal nanostructures results in a flexible and free-standing PCP. The facile method of fabricating the wrinkled PCPs provides a scalable route for the development of novel chirophotonic materials with precisely controlled helical pitch and curvature dimensions. The reflection notch position of the flat PCP shifts to a lower wavelength when the viewing angle increased, while the selective reflection wavelength of wrinkled PCP is remained consistent regardless of viewing angles. The optical reflection of the 1D stripe-wrinkled PCP is dependent on the wrinkle direction. PCPs with different corrugated directions can be patterned to reduce the angular-dependent optical reflection of wrinkles. Furthermore, 2D wavy-wrinkled PCP is successfully developed that exhibit directionally independent reflection of color.

Remote-controllable and encryptable smart glasses: a photoresponsive azobenzene molecular commander determines the molecular alignments of liquid crystal soldiers.

For the development of optically encryptable smart glass that can control the molecular alignment of liquid crystals (LCs), an azobenzene-based reactive molecule (ARM) capable of trans-cis photoisomerization is newly designed and synthesized. Photo-triggered LC-commandable smart glasses are successfully constructed by the surface functionalization technique using 3-aminopropyltriethoxysilane (APTMS) coupling agent and an ARM. The surface functionalization with the ARM is verified by spectroscopic analysis and various observations including changes in the wettability and surface morphology. Using the ARM-treated substrate, the LC command cell which can effectively switch the molecular orientation of nematic LC (E7) by the irradiation of UV and visible light is demonstrated. The results of optical investigation demonstrate the directional correlation between light and photoisomerization, revealing the tilt mechanism of azobenzene units. The capability to control the molecular orientation of LCs remotely and selectively allows the development of remote-controllable and encryptable smart glasses.

Tuning the electrowetting behavior of quantum dot nanofluids.

HYPOTHESIS: The electrowetting behavior of droplets can be altered by the inclusion of salts, surfactants, or nanoparticles. We propose that varying the properties of cadmium selenide/zinc sulfide quantum dots will affect the electrowetting behavior of fluorescent nanofluids. Information gathered will allow for greater control of fluid properties when designing a colloidal system in an electrowetting environment. EXPERIMENTS: Aqueous-based quantum dots were functionalized with mercaptocarboxylic acid ligands of various chain length and binding motifs by a room temperature phase transfer method. The size and concentration of the quantum dot were varied, and droplets of the resulting nanofluids were exposed to increasing amounts of voltage. The change in contact angle was evaluated and correlated to the surface chemistry, size, and concentration of the quantum dots. FINDINGS: Quantum dot nanofluids with longer alkyl chains have the most pronounced change in contact angle and were the most stable under applied voltage. The size of the nanoparticles does not significantly impact the electrowetting behavior at low concentration (3 µM), but nanofluids containing smaller diameter quantum dots show enhanced electrowetting behavior at higher concentration (27 µM). The fluorescent properties of the QD nanofluids studied were not affected after repeated electrowetting cycles.

Effect of Amorphous Crosslinker on Phase Behavior and Electro-Optic Response of Polymer-Stabilized Blue Phase Liquid Crystals.

Blue phase liquid crystals (BPLCs) composed of double-twisted cholesteric helices are promising materials for use in next-generation displays, optical components, and photonics applications. However, BPLCs are only observed in a narrow temperature range of 0.5-3 °C and must be stabilized with a polymer network. Here, we report on controlling the phase behavior of BPLCs by varying the concentration of an amorphous crosslinker (pentaerythritol triacrylate (PETA)). LC mixtures without amorphous crosslinker display narrow phase transition temperatures from isotropic to the blue phase-II (BP-II), blue phase-I (BP-I), and cholesteric phases, but the addition of PETA stabilizes the BP-I phase. A PETA content above 3 wt% prevents the formation of the simple cubic BP-II phase and induces a direct transition from the isotropic to the BP-I phase. PETA widens the temperature window of BP-I from ~6.8 °C for BPLC without PETA to ~15 °C for BPLC with 4 wt% PETA. The BPLCs with 3 and 4 wt% PETA are stabilized using polymer networks via in situ photopolymerization. Polymer-stabilized BPLC with 3 wt% PETA showed switching between reflective to transparent states with response times of 400-500 µs when an AC field was applied, whereas the application of a DC field induced a large color change from green to red.

Electrowetting Behavior and Digital Microfluidic Applications of Fluorescent, Polymer-Encapsulated Quantum Dot Nanofluids.

Digital microfluidics is a liquid-handling technology capable of rapidly and autonomously controlling multiple discrete droplets across an array of electrodes and has seen continual growth in the fields of chemistry, biology, and optics. This technology is enabled by rapidly switching the wettability of a surface through the application of an electric field: a phenomenon known as electrowetting-on-dielectric. The results reported here elucidate the wetting behavior of fluorescent quantum dot nanofluids by varying the aqueous-solubilizing polymers, changing the size of the nanocrystals, and the addition of surfactants. Nanofluid droplets were demonstrated to have very large changes in contact angle (>100°) by employing alternating current voltage to aqueous droplets within a dodecane medium. The stability of quantum dot nanofluids is also evaluated within a digital microfluidics platform, and the optical properties are not perturbed even under high voltages (250 V). Multiple fluorescent droplets with varying emission can be simultaneously actuated and rapidly mixed (<10 s) to generate a new nanofluid with optical properties different from the parent solutions.

Pixelated Polymers: Directed Self Assembly of Liquid Crystalline Polymer Networks.

Polymeric materials are pervasive in modern society, in part attributable to the diverse range of properties that are accessible in these materials. Polymers can be stiff or soft, dissipative or elastic, adhesive or nonstick. Localizing the properties of polymeric materials can be achieved by a number of methods, including self-assembly, lithography, or 3-d printing. Here, we detail recent advances in the preparation of "pixelated" polymers prepared by the directed self-assembly of liquid crystalline monomers to yield cross-linked polymer networks (liquid crystalline polymer networks, LCN, or liquid crystalline elastomers, LCE). Through the local and arbitrary control of the orientation of the liquid crystalline units, monolithic elements can be realized with spatial variation in mechanical, thermal, electrical, optical, or acoustic properties. Stimuli-induced variation of these properties may enable paradigm-shifting end uses in a diverse set of applications.