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Yu, Huaizhe

Publications and source records attributed to Yu, Huaizhe.

8 records
All sourcesNASA NTRSDOE OSTI
DOE OSTI2024

Actuating Liquid Crystals Rapidly and Reversibly by Using Chemical Catalysis

Abstract Microtubules and catalytic motor proteins underlie the microscale actuation of living materials, and they have been used in reconstituted systems to harness chemical energy to drive new states of organization of soft matter (e.g., liquid crystals (LCs)). Such materials, however, are fragile and challenging to translate to technological contexts. Rapid (sub‐second) and reversible changes in the orientations of LCs at room temperature using reactions between gaseous hydrogen and oxygen that are catalyzed by Pd/Au surfaces are reported. Surface chemical analysis and computational chemistry studies confirm that dissociative adsorption of H 2 on the Pd/Au films reduces preadsorbed O and generates 1 ML of adsorbed H, driving nitrile‐containing LCs from a perpendicular to a planar orientation. Subsequent exposure to O 2 leads to oxidation of the adsorbed H, reformation of adsorbed O on the Pd/Au surface, and a return of the LC to its initial orientation. The roles of surface composition and reaction kinetics in determining the LC dynamics are described along with a proof‐of‐concept demonstration of microactuation of beads. These results provide fresh ideas for utilizing chemical energy and catalysis to reversibly actuate functional LCs on the microscale.

Chemistry↗
DOE OSTI2021

Methods, systems, and media for detecting the presence of an analyte

In accordance with some embodiments, methods, systems, and media for detecting the presence of are provided. In some embodiments, a method of detecting an analyte is provided, the method comprising: capturing an image of liquid crystals; determining one or more features based on the brightness of the pixels in the image; providing the one or more features to a trained support vector machine, wherein the support vector machine was trained using images captured of other liquid crystals when exposed to a first analyte and the other liquid crystals exposed to a second analyte; and receiving an indication from the support vector machine indicating whether the liquid crystals have been exposed to the first analyte.

Abbott, Nicholas L.↗
DOE OSTI2018

Redox-Triggered Orientational Responses of Liquid Crystals to Chlorine Gas

Surface-supported liquid crystals (LCs) that exhibit orientational and thus optical responses upon exposure to ppb concentrations of Cl 2 gas are reported. Computations identified Mn cations as candidate surface binding sites that undergo redox-triggered changes in the strength of binding to nitrogen-based LCs upon exposure to Cl 2 gas. Guided by these predictions, μm-thick films of nitrile- or pyridine-containing LCs were prepared on surfaces decorated with Mn 2+ binding sites as perchlorate salts. Following exposure to Cl 2 , formation of Mn 4+ (in the form of MnO 2 microparticles) was confirmed and an accompanying change in the orientation and optical appearance of the supported LC films was measured. In unoptimized systems, the LC orientational transitions provided the sensitivity and response times needed for monitoring human exposure to Cl 2 gas. Finally, the response was also selective to Cl 2 over other oxidizing agents such as air or NO 2 and other chemical targets such as organophosphonates.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗
DOE OSTI2018

Computational Chemistry-Guided Design of Selective Chemoresponsive Liquid Crystals Using Pyridine and Pyrimidine Functional Groups

Computational chemistry-guided designs of chemoresponsive liquid crystals (LCs) with pyridine or pyrimidine groups that bind to metal-cation-functionalized surfaces to provide improved selective responses to targeted vapor species (dimethylmethylphosphonate (DMMP)) over nontargeted species (water) are reported. The LC designs against experiments are tested by synthesizing 4-(4-pentyl-phenyl)-pyridine and 5-(4-pentyl-phenyl)-pyrimidine and quantifying LC responses to DMMP and water. Consistent with the computations, pyridine-containing LCs bind to metal-cation-functionalized surfaces too strongly to permit a response to either DMMP or water whereas pyrimidine-containing LCs undergo a surface-driven orientational transition in response to DMMP without interference from water. The computation predictions are not strongly dependent on assumptions regarding the degree of coordination of the metal ions but are limited in their ability to predict LC responses when using cations with mostly empty d orbitals. Overall, this work identifies a promising new class of chemoresponsive LCs based on pyrimidine that exhibits enhanced tolerance to water, a result that is important because water is a ubiquitous and particularly challenging chemical interferent in chemical sensing strategies based on LCs. The work also provides further evidence of the transformative utility of computational chemistry methods to design LC materials that exhibit selective orientational responses in specific chemical environments.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗
DOE OSTI2018

The role of anions in adsorbate-induced anchoring transitions of liquid crystals on surfaces with discrete cation binding sites

We report a combined theoretical and experimental effort to elucidate systematically for the first time the influence of anions of transition metal salt-decorated surfaces on the orientations of supported films of nematic liquid crystals (LCs) and adsorbate-induced orientational transitions of these LC films. Guided by computational chemistry predictions, we find that nitrate anions weaken the binding of 4'-n-pentyl-4-biphenylcarbonitrile (5CB) to transition metal cations, as compared to perchlorate salts, although binding is still sufficiently strong to induce homeotropic (perpendicular) orientations of 5CB. In addition, we find the orientations of the LC to be correlated across all metal cations investigated by a molecular anchoring energy density that is calculated as the product of the single-site binding energy and metal cation binding site density on the surface. The weaker single-site binding energy caused by nitrate also facilitates competitive binding of adsorbates to the metal cations, leading to more facile orientational transitions induced by adsorbates. Finally, our analysis suggests that nitrate anions recruit water via hydrogen bonding to the metal binding sites, modulating further the relative net binding energies of 5CB and adsorbates to surfaces decorated with metal nitrates. After accounting for the presence of water, we find a universal exponential relationship between the calculated displacement free energies and measured dynamic response of LCs to adsorbates for all metal salts studied, independent of the metal salt anion.

Szilvási, Tibor↗