Monolithic Chiral Nematic Organization of Cellulose Nanocrystals under Capillary Confinement.

We demonstrate bioenabled crack-free chiral nematic films prepared via a unidirectional flow of cellulose nanocrystals (CNCs) in the capillary confinement. To facilitate the uniform long-range nanocrystal organization during drying, we utilized tunicate-inspired hydrogen-bonding-rich 3,4,5-trihydroxyphenethylamine hydrochloride (TOPA) for physical cross-linking of nanocrystals with enhanced hydrogen bonding and polyethylene glycol (PEG) as a relaxer of internal stresses in the vicinity of the capillary surface. The CNC/TOPA/PEG film is organized as a left-handed chiral structure parallel to flat walls, and the inner volume of the films displayed transitional herringbone organization across the interfacial region. The resulting thin films also exhibit high mechanical performance compared to brittle films with multiple cracks commonly observed for capillary-formed pure CNC films. The chiral nematic ordering of modified TOPA-PEG-CNC material propagates through the entire thickness of robust monolithic films and across centimeter-sized surface areas, facilitating consistent, vivid iridescence, and enhanced circular polarization. The best performance that prevents the cracks was achieved for a CNC/TOPA/PEG film with a minimal, 3% amount of TOPA. Overall, we suggest that intercalation of small highly adhesive molecules to cellulose nanocrystal-polymer matrices can facilitate uniform flow of liquid crystal phase and drying inside the capillary, resulting in improvement of the ultimate tensile strength and toughness (77% and 100% increase, respectively) with controlled uniform optical reflection and enhanced circular polarization unachievable during regular drying conditions.

Switchable Photonic Bio-Adhesive Materials.

A soft photonic bio-adhesive material is designed with real-time colorimetrical monitoring of switchable adhesion by integrating a responsive bio-photonic matrix with mobile hydrogen-binding networking. Synergetic materials sequencing creates a unique iridescent appearance directly coupled with both adhesive ability and shearing strength, in a highly reversible manner. The responsive photonic materials, having a physically hydrogen-bonded chiral nematic organization, vary their adhesion strength due to a transition in cohesive and interfacial failure mechanism in humid surroundings. The bright color appearance shifts from blue to red to transparent and back due to a change in pitch length of the chiral helicoidal organization that also triggers coupled changes in both mechanical strength and interfacial adhesion. Such reversible strength-adhesion-iridescence triple-coupling phenomenon is further explored for design of super-strong switchable bio-adhesives for synthetic/biological surfaces with quick remotely triggered sticky-to-nonsticky transitions, removable conformal soft stickers, and wound dressings with visual monitoring of the healing process, to colorimetric stickers for contaminated respiratory masks.

Marine Structural Protein Stability Induced by Hofmeister Salt Annealing and Enzymatic Cross-Linking.

The Humboldt squid is one of the fiercest marine predators thanks in part to its sucker ring teeth that are biopolymer blends of a protein isoform family called suckerin with compression strength that rivals silkworm silk. Here, we focus on the popular suckerin-12 isoform to understand what makes the secondary structure of this biopolymer different in water and the potential role of diverse physical and chemical cross-linkings. By choosing a salt post-treatment, in accordance with the Hofmeister series, we achieved film stability with salt annealing that is comparable to chemical cross-links. By correlating the film morphology with the protein secondary structure changes, suckerin-12 films were shown to contract upon treatment with kosmotropic salts and exhibited increased stability in water. These changes are related to the rearrangement of suckerin-12 secondary structure from random coils and helices to ß-sheets. Overall, understanding secondary structure changes caused by aqueous and ionic environments can be instructive for the tuning of the suckerin film sclerotization, its conversion to a tough biological material, and to ultimately produce the natural squid sucker ring teeth.

Large and Emissive Crystals from Carbon Quantum Dots onto Interfacial Organized Templates.

Here, we report template-assisted assembly of emissive carbon quantum dot (CQD) microcrystals on organized cellulose nanocrystals templates at the liquid-air interface. This large-scale assembly is facilitated by the complementary amphiphilic character of CQDs and cellulose nanocrystals in the organized nematic phase. The resulting large microcrystals up to 200 µm across show unusually high emission that is not observed for limited CQDs aggregates. The dense crystal packing of CQDs in the layered fashion suppresses local molecular rotations and vibrations, thus restricting the intermolecular energy transfer and corresponding quenching phenomena. The as-prepared crystals are mechanically stable and can be exploited for recyclable catalysis, enabling applications beyond the individual nanoparticles or disordered aggregates. The ligand-templated assembly can be used to diversify CQD crystal architectures to guide formation of fibers, microplates, and micro-flowers.

Self-regenerating giant hyaluronan polymer brushes.

Tailoring interfaces with polymer brushes is a commonly used strategy to create functional materials for numerous applications. Existing methods are limited in brush thickness, the ability to generate high-density brushes of biopolymers, and the potential for regeneration. Here we introduce a scheme to synthesize ultra-thick regenerating hyaluronan polymer brushes using hyaluronan synthase. The platform provides a dynamic interface with tunable brush heights that extend up to 20 microns - two orders of magnitude thicker than standard brushes. The brushes are easily sculpted into micropatterned landscapes by photo-deactivation of the enzyme. Further, they provide a continuous source of megadalton hyaluronan or they can be covalently-stabilized to the surface. Stabilized brushes exhibit superb resistance to biofilms, yet are locally digested by fibroblasts. This brush technology provides opportunities in a range of arenas including regenerating tailorable biointerfaces for implants, wound healing or lubrication as well as fundamental studies of the glycocalyx and polymer physics.

Self-Assembly of Emissive Nanocellulose/Quantum Dot Nanostructures for Chiral Fluorescent Materials.

Chiral fluorescent materials with fluorescent nanoparticles assembled into a chiral structure represent a grand challenge. Here, we report self-assembled emissive needle-like nanostructures through decorating cellulose nanocrystals (CNCs) with carbon quantum dots (CQDs). This assembly is facilitated by the heterogeneous amphiphilic interactions between natural and synthetic components. These emissive nanostructures can self-organize into chiral nematic solid-state materials with enhanced mechanical performance. The chiral CQD/CNC films demonstrate an intense iridescent appearance superimposed with enhanced luminescence that is significantly higher than that for CQD films and other reported CQD/CNC films. A characteristic fluorescent fingerprint signature is observed in the CQD/CNC film, proving the well-defined chiral organization of fluorescent nanostructures. The chiral organization of CQDs enables the solid CQD/CNC film to form a right-hand chiral fluorescence with an asymmetric factor of -0.2. Additionally, we developed chemical 2D printing and soft lithography patterning techniques to fabricate the freestanding chiral fluorescent patterns that combines mechanical intergrity and chiral nematic structure with light diffraction and emission.

High Thermoelectric Power Factor Organic Thin Films through Combination of Nanotube Multilayer Assembly and Electrochemical Polymerization.

In an effort to produce effective thermoelectric nanocomposites with multiwalled carbon nanotubes (MWCNT), layer-by-layer assembly was combined with electrochemical polymerization to create synergy that would produce a high power factor. Nanolayers of MWCNT stabilized with poly(diallyldimethylammonium chloride) or sodium deoxycholate were alternately deposited from water. Poly(3,4-ethylene dioxythiophene) [PEDOT] was then synthesized electrochemically by using this MWCNT-based multilayer thin film as the working electrode. Microscopic images show a homogeneous distribution of PEDOT around the MWCNT. The electrical resistance, conductivity (σ) and Seebeck coefficient (S) were measured before and after the PEDOT polymerization. A 30 bilayer MWCNT film (<1 µm thick) infused with PEDOT is shown to achieve a power factor (PF = S2σ) of 155 µW/m K2, which is the highest value ever reported for a completely organic MWCNT-based material and competitive with lead telluride at room temperature. The ability of this MWCNT-PEDOT film to generate power was demonstrated with a cylindrical thermoelectric generator that produced 5.5 µW with a 30 K temperature differential. This unique nanocomposite, prepared from water with relatively inexpensive ingredients, should open up new opportunities to recycle waste heat in portable/wearable electronics and other applications where low weight and mechanical flexibility are needed.

Ultrastrong, Chemically Resistant Reduced Graphene Oxide-based Multilayer Thin Films with Damage Detection Capability.

Multilayer thin films of graphene oxide (GO) and poly(vinylamine) (PVAm) were deposited via layer-by-layer assembly. Poly(vinylamine) pH was used to tailor film thickness and GO layer spacing. Graphene oxide concentration in the films was controlled through simple pH adjustment. Thermal reduction of the PVAm/GO multilayer thin films rendered them electrically conductive, which could be further tailored with PVAm pH. These reduced films also exhibited exceptionally high elastic modulus of 30 GPa and hardness of 1.8 GPa, which are among the highest of any graphene-filled polymer composite values ever reported. Cross-linking of these films with glutaraldehyde improved their chemical resistance, allowing them to survive strongly acidic or salty solutions. Additionally, scratches in the films can be instantaneously detected by a simple electrical resistance measurement. These films are promising for a variety of packaging and electronic applications.

Thick growing multilayer nanobrick wall thin films: super gas barrier with very few layers.

Recent work with multilayer nanocoatings composed of polyelectrolytes and clay has demonstrated the ability to prepare super gas barrier layers from water that rival inorganic CVD-based films (e.g., SiOx). In an effort to reduce the number of layers required to achieve a very low oxygen transmission rate (OTR (<0.01 cc/m(2)·day·atm)) in these nanocoatings, buffered cationic chitosan (CH) and vermiculite clay (VMT) were deposited using layer-by-layer (LbL) assembly. Buffering the chitosan solution and its rinse with 50 mM Trizma base increased the thickness of these films by an order of magnitude. The OTR of a 1.6-µm-thick, six-bilayer film was 0.009 cc/m(2)·day·atm, making this the best gas barrier reported for such a small number of layers. This simple modification to the LbL process could likely be applied more universally to produce films with the desired properties much more quickly.