RESUMEN
Magnetic fields have been used to uniformly align the lyotropic chiral nematic (cholesteric) liquid crystalline (LC) phase of biopolymers to a global orientation and optical appearance. Here, we demonstrate that, in contrast, weak and patterned magnetic field gradients can create a complex optical appearance with the variable spatial local organization of needle-like magnetically decorated cellulose nanocrystals. The formation of optically patterned thin films with left- and right-handed chiral and achiral regions is observed and related to local magnetic gradient-driven vortices during LC suspension flow. We trace the localized flow directions of the magnetically decorated nanocrystals during evaporation-induced assembly, demonstrating how competing evaporation and field-induced localized flow affect the twisted organization within magnetically induced vortices. The simulations suggested that localized twisting inversion originates from the interplay between the direction and strength of the local-depth-related magnetic gradients and the receding front through peripheral magnetic gaps. We propose that this finding will lead to magnetically patterned photonic films.
RESUMEN
Chiral metal-organic frameworks (MOFs) have gained rising attention as ordered nanoporous materials for enantiomer separations, chiral catalysis, and sensing. Among those, chiral MOFs are generally obtained through complex synthetic routes by using a limited choice of reactive chiral organic precursors as the primary linkers or auxiliary ligands. Here, we report a template-controlled synthesis of chiral MOFs from achiral precursors grown on chiral nematic cellulose-derived nanostructured bio-templates. We demonstrate that chiral MOFs, specifically, zeolitic imidazolate framework (ZIF), unc-[Zn(2-MeIm)2 , 2-MeIm=2-methylimidazole], can be grown from regular precursors within nanoporous organized chiral nematic nanocelluloses via directed assembly on twisted bundles of cellulose nanocrystals. The template-grown chiral ZIF possesses tetragonal crystal structure with chiral space group of P41 , which is different from traditional cubic crystal structure of I-43â m for freely grown conventional ZIF-8. The uniaxially compressed dimensions of the unit cell of templated ZIF and crystalline dimensions are signatures of this structure. We observe that the templated chiral ZIF can facilitate the enantiotropic sensing. It shows enantioselective recognition and chiral sensing abilities with a low limit of detection of 39â µM and the corresponding limit of chiral detection of 300â µM for representative chiral amino acid, D- and L- alanine.
RESUMEN
Flexible and mechanically robust gel-like electrolytes offer enhanced energy storage capabilities, versatility, and safety in batteries and supercapacitors. However, the trade-off between ion conduction and mechanical robustness remains a challenge for these materials. Here, we suggest that the introduction of ionic hyperbranched polymers in structured sustained ionogels will lead to both enhanced ion conduction and mechanical performance because of the hyperbranched polymers' ionically conductive groups and the complementary interfacial interactions with ionic liquids. More specifically, we investigate the effect of hyperbranched polymers with carboxylate terminal groups and imidazolium counterions with various ionic group densities on the properties of ionogels composed of coassembled cellulose nanofibers (CNFs) and cellulose nanocrystals (CNCs) as sustainable open pore frame for ionic liquid immersion. The addition of hyperbranched polymers leads to the formation of highly interconnected openly porous, lightweight, and shape-persistent materials by harnessing hydrogen bonding between the polymers and the CNFs/CNCs "frame". Notably, these materials possess a 2-fold improvement in ionic conductivity combined with many-fold increase in Young's modulus, tensile strength, and toughness, making them comparable to common reinforced nanocomposite materials. Furthermore, the corresponding thin-film gel supercapacitors possess enhanced electrochemical cycling stability upon repeated bending with an 85% capacitance retention after 10â¯000 cycles, promising new insight in the development of simultaneously conductive and flexible gel electrolytes with sustained performance.
RESUMEN
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.
