Search Results (667)

Cutin, a natural polyester, has attracted attention as a precursor for bio-based materials mimicking plant cuticles, particularly in food packaging. Most studies focus on polycondensation of hydrolyzed cutin fractions or combining cutin hydrolysates with other components; however, cutin precipitation, conditions affecting it, and cutin isolate film properties, without addition of other filmogenic material, remain insufficiently understood. Owing to the pH-dependent solubility of cutin, which progressively decreases as pH is lowered from strongly alkaline to acidic conditions, this study investigates the influence of pH on cutin dispersion formation and characteristics, and evaluates the impact of these dispersion properties on the formation and performance of self-assembled cutin isolate films, with a view to developing films with improved water-barrier and moisture-resistance properties. The influence of three plasticizers, glycerol, propylene glycol, and polyethylene glycol 400, at two concentrations was also evaluated. Results demonstrated that pH is the primary factor influencing cutin isolate dispersion characteristics and film performance, with decreasing pH promoting cutin precipitation and particle aggregation, thereby inducing changes in film structure. The strongest effects were observed for swelling, solubility, and tensile strength, followed by water vapor permeability, elongation at break, and thickness. Plasticizer type mainly affected moisture content and significantly influenced permeability and thickness, while concentration of plasticizer primarily impacted permeability. Interactions between pH and plasticizer significantly influenced most properties. Films prepared from cutin dispersions at pH 6.5 and pH 5 with polyethylene glycol (10%) showed the best balance of mechanical and barrier properties. Additionally, films prepared from the cutin solutions at pH 12 with glycerol (20%) exhibited good mechanical performance and high solubility, suitable for specific applications. Full article

This paper develops, implements, and uses a novel methodology that integrates global and local geometric modeling of ellipsoids and transforms curvatures and shape descriptors into energy metrics that provide curvature-driven mechanistic insight into self-assembly driving force pathways associated with fiber and film formation. Global parameterization, based on eccentricities, and local parameterization, based on mean and Gaussian curvatures, are mapped into shape and curvedness parameterizations that clearly distinguish critical shape effects from curvedness effects in contrast to classical mean and Gaussian curvature methodologies. Finally, the mechanistic insights are illustrated using a liquid membranology model, transforming the geometric descriptors into bending energy densities that point the way to fiber and film assembly pathways. Full article

The explosive demand for flexible wearable and portable devices imposes stringent requirements on the mechanical, energy storage, and sensing properties of functional materials. Although two-dimensional (2D) transition metal carbides and nitrides (MXene) possess high conductivity and pseudocapacitance, their severe self-restacking and intrinsic brittleness restrict their practical applications. Herein, a facile vacuum filtration and hot-pressing densification strategy is proposed to fabricate nacre-inspired MXene-based films. By incorporating one-dimensional (1D) high-aspect-ratio TEMPO-oxidized cellulose nanofibrils (TOCNFs), the self-restacking of MXene is effectively suppressed. The optimal M20F5 composite film exhibits a coordinated electromechanical balance, maintaining an electrical conductivity of 1.07 × 10⁶ S m⁻¹ while enduring 2124 folding cycles. For energy storage, the assembled symmetric supercapacitor delivers a specific capacitance of 828.92 F g⁻¹ at 0.5 mA cm⁻² and maintains an energy density of 13.75 Wh kg⁻¹ at a power density of 9500 W kg⁻¹. Furthermore, acting as a piezoresistive sensor, the film achieves reliable detection, spanning from bimodal gait recognition to subtle physiological pulses. This work establishes a viable material design strategy for next-generation supercapacitors and intelligent wearable systems. Full article

Localized surface plasmon resonance (LSPR) is an optical phenomenon that occurs when light interacts with free electrons on the surface of metallic thin films, producing intensified electromagnetic fields at specific sites, often called “hot spots”. LSPR-based sensing technologies respond to chemical and associated optical interfacial changes. Inherent advantages include enhanced sensitivity, compact size, low production cost, and strong potential for integration into portable, point-of-care diagnostic systems. This study focuses on a detailed investigation into the surface functionalization of localized surface plasmon resonance (LSPR)-based nanohole array (NHA) sensors for biomedical applications. Gold-coated NHA surfaces were functionalized using polyethylene glycol (PEG) self-assembled monolayers (SAMs), enabling specific attachment of biomolecular species. As a proof-of-concept, bovine serum albumin (BSA) and SARS-CoV-2 nanobody proteins were successfully immobilized on the PEGylated surfaces. Individual steps of surface modification including PEGylation, protein immobilization and nanobody immobilization were validated through a dual-method approach which combined measurement of LSPR optical spectral shifts and x-ray photoelectron spectroscopy (XPS) chemical analyses. Reproducibility was assessed across multiple sensors and repeated trials, confirming the repeatability of each functionalization and binding process. The sensor system, consisting of NHA-based plasmonic platform, microfluidics, and a portable optical spectrometer, exhibits the capability for reliable and sensitive, label-free detection of biomolecular targets, including viral antigens, in liquid-phase environments. Full article

Growing environmental concerns associated with non-renewable and persistent materials have intensified the search for sustainable alternatives, with cellulosic fibers and nanocellulose emerging as promising candidates. This review examines diverse product opportunities where interdigitation plays a critical role, including nanopaper and barrier films, wet wipe technologies, spun cellulose-based yarns, hydrogels, and composite materials. Particular emphasis is placed on the interplay between colloidal stability, fibrillar alignment, hydrogen bonding, and time-dependent network evolution in governing material performance. Additionally, emerging strategies such as hydroentanglement, ice-templating, in situ crosslinking, and post-formation modification are discussed as means to optimize interdigitated structures. The article further explores how conventional papermaking processes may be reimagined to better exploit interdigitation through innovations in fiber dispersion, alignment, and controlled crosslinking. Interdigitation is presented not as a discrete processing tool but as a unifying framework for understanding and engineering hierarchical cellulose networks. By leveraging the inherent fibrillar nature of cellulose and the dynamics of self-assembly, this paradigm offers new pathways towards the development of next-generation, high-performance, bio-based products that contribute to a circular economy. Full article

A study was conducted on the construction of sulfonated poly(aryl ether ketone) nanomicelles and their dispersion–displacement synergistic behavior in deep oil recovery. Unlike conventional surfactant systems, inorganic nanoparticle-based EOR materials, and polymeric nanofluids that mainly rely on interfacial tension reduction, wettability alteration, or viscosity regulation, this study constructs self-assembled sulfonated poly(aryl ether ketone) nanomicelles that integrate a rigid aromatic backbone, ionizable sulfonic acid groups, nanoscale dispersion, and interfacial regulation within one polymeric architecture. Sulfonated poly(aryl ether ketone) nanomicelles were prepared by combining polymer sulfonation with solvent-induced self-assembly, and their structural features, dispersion stability, interfacial behavior, porous-media transport, and displacement performance were systematically evaluated. Spectroscopic characterization confirmed the successful introduction of sulfonic acid groups into the polymer backbone. The resulting nanomicelles exhibited an average hydrodynamic diameter of 117.8 nm, a polydispersity index of 0.186, and a zeta potential of −38.6 mV in deionized water, while a value of −27.4 mV was still maintained at a salinity of 150,000 mg/L, indicating good electrostatic stability under highly mineralized conditions. Further evaluation showed that the 0.30 wt% system retained a transmittance of 97.4% after 15 d of static standing, and its particle size remained at 151.7 nm even under 120 °C and 150,000 mg/L, demonstrating favorable thermal–salinity tolerance. At the same concentration, the oil–water interfacial tension decreased to 6.9 mN/m at 1800 s, while the contact angle of oil-aged quartz was reduced from 118.4° to 58.7°, indicating effective regulation of both the oil–water interface and the solid surface wettability. During microscopic displacement, the residual oil area fraction decreased from 32.8% after water flooding to 14.6%, and cluster-like oil, corner oil, and film-like oil were reduced from 14.6%, 9.8%, and 8.4% to 5.9%, 4.2%, and 4.5%, respectively. In core flooding, the incremental oil recovery reached 13.2%, the final water cut decreased to 81.2%, and the injection pressure increased only from 0.42 MPa to 0.68 MPa. These results indicate that sulfonated poly(aryl ether ketone) nanomicelles promote deep residual-oil mobilization through the combined effects of stable dispersion, interfacial regulation, and effective transport, with 0.30 wt% identified as the preferred concentration range. The main scientific contribution of this work is to establish a structure–dispersion–interface–transport–displacement relationship for SPAEK nanomicelles under deep-reservoir conditions, providing a polymeric nanomicelle-based strategy distinct from conventional surfactant, sulfonated polymer, and nanoparticle flooding systems. Full article

In oil and gas development, the oil displacement efficiency of single surfactants is inherently constrained. While synergistic interactions between salt ions and surfactants can enhance displacement performance by modulating interfacial properties and wettability, the underlying mechanisms remain insufficiently understood. This study systematically investigated the synergistic effects of two monovalent salts (NaCl, KCl) and four surfactants through macroscopic characterization of interfacial property and microfluidic displacement experiments using microfluidic device with dead-end structures. The results show that salt type and concentration significantly influence interfacial dynamics. The four selected surfactants exhibit gel-like behavior through molecular self-assembly in aqueous solutions, and their synergistic interaction with salt ions enhances oil displacement efficiency by modulating interfacial characteristics. High-salinity solutions reduce interfacial tension, with CTAB exhibiting a concentration-dependent decrease, while NP-10 behavior is governed by both surfactant and salt concentrations. The presence of Na⁺ generally resulted in lower IFT, improved interfacial viscoelasticity, and more favorable wettability alteration compared to K⁺. One-way analysis of variance confirmed that salt type is the main factor affecting recovery rate (p < 0.05). Notably, 0.2% CTAB+50,000 mg/L NaCl combination achieved the highest recovery rate owing to an optimal balance between interfacial adsorption, film viscoelasticity, and wettability alteration. This investigation elucidates the mechanisms driving surfactant–salt synergism and proposes an optimized surfactant and salt formulation to enhance oil recovery through tailored interfacial properties. Full article

Reduced graphene oxide (rGO) wrapped with poly(styrenesulfonate) (PSS) forms a stable hybrid material (rGO/PSS) capable of producing ultrathin films with promising barrier properties for Direct Methanol Fuel Cell (DMFC) applications. These films aim to mitigate methanol crossover, one of the major limitations of DMFC technology. In this work, we investigate the mechanisms underlying the methanol barrier effect of rGO/PSS, while maintaining water permeability. Classical Molecular Dynamics simulations were employed to explore the structural and dynamic properties of rGO/PSS at different polymer ionization fractions in a solvent mixture of water, methanol, and hydronium. The influence of the sulfonation fraction on film self-assembly was analyzed, including its impact on PSS conformation, rGO sheet distribution, and PSS–rGO interactions. Finally, the effect of the rGO/PSS structure on solvent diffusion was investigated, and the mechanisms responsible for the selective transport of methanol were elucidated. Full article

As a green energy technology, triboelectric nanogenerators (TENGs) convert mechanical energy into electricity and have gained significant attention in response to growing global environmental concerns. However, the widespread use of petroleum-based polymers as triboelectric materials in high-performance TENGs raises concerns over plastic pollution. In this work, we report a high-performance biodegradable TENG utilizing chitosan/laser-induced graphene (LIG) composite films as triboelectric layers. Modified chitosan substrates were first converted into LIGs via a convenient one-step CO₂ laser engraving, subsequently incorporated into chitosan matrices to form homogeneous composite films. A TENG device was designed by pairing the LIG/chitosan composite film with the fluorinated ethylene propylene (FEP) film, and copper electrodes. The introduction of LIG effectively strengthens charge storage and dielectric properties of the chitosan matrix, thereby significantly boosting the triboelectric output performance. Experimental results demonstrate that the as-assembled TENG with an LIG concentration of 1 wt.% achieves a peak open-circuit voltage of 196 V and short-circuit current of 2.1 μA, with a maximum power density of 295 mW/m². It can drive LED lights and small low-power electronic devices. Furthermore, the designed TENG device exhibits good biodegradability, flexibility, and stability, serving as a self-powered sensor for monitoring human joint movements. This work provides a simple and scalable strategy for integrating laser-induced graphene with biomass-based polymers, offering new insights into the design of high-performance, biobased triboelectric materials. Full article

The emergence of membrane boundaries represents a decisive transition in the origin of life, yet the molecular nature of the earliest abiotic membranes remains uncertain. Existing models based on simple fatty acids, while experimentally tractable, often lack the environmental robustness required under fluctuating prebiotic conditions. Furthermore, the absence of clear pathways linking primitive amphiphiles to later phospholipid systems highlights the need for chemically continuous intermediate frameworks. Here, we explore borate-bridged amphiphile–carbohydrate conjugates as plausible intermediates between simple prebiotic surfactants and modern lipid bilayers. These conjugates arise from low-molecular-weight polyols—including glycerol, butane-1,2,3,4-tetraol, pentane-1,2,3,4,5-pentaol, and hexane-1,2,3,4,5,6-hexitol—reacting with long-chain alkyl ethers and borate species under alkaline conditions, enabling reversible coupling to ribose and other vicinal diol-containing sugars. This chemistry integrates three essential properties for early compartmentalization: hydrolytically robust ether-linked hydrophobic domains, multivalent and highly hydrated headgroups, and environmentally responsive borate coordination. Comparative physicochemical analysis suggests that single-tail alkylglycerol derivatives preferentially form micelles and interfacial films, while di- and tri-tail tetritol and pentitol conjugates favor lamellar assemblies and vesicle formation across realistic prebiotic pH and salinity ranges. Hexitol-based systems, particularly those bearing three hydrophobic chains, may act as membrane-stabilizing components that enhance rigidity and reduce permeability under extreme conditions. We propose that heterogeneous mixtures dominated by two-tail polyol diethers, supplemented by tri-tail stabilizers and surface-active alkylglycerols, could provide mechanically robust, pH-tunable, and sugar-decorated abiotic membranes. Such borate-mediated amphiphiles offer a chemically coherent framework linking carbohydrate stabilization, ether lipid persistence, and dynamic self-assembly, potentially representing a transitional stage in the evolutionary pathway from primitive amphiphilic films to biologically encoded membranes. Full article

By combining hanging-drop self-assembly with melt infiltration and selective inversion, we fabricate millimetric and free-standing curved photonic heterostructures that integrate infiltrated-opal, inverse-opal, embossed, and white-scattering 2.5D metasurface domains within a single continuous body. These architectures enable configurations inaccessible to planar fabrication, including naturally formed concavities within convex inverse-opal films and alternating ordered/single-layer regions that preserve local coherence while introducing disorder at larger scales. Across these heterogeneous curved landscapes, we observe optical phenomena absent in flat photonic structures—spectrally selected lateral collimation, geometry-shifted ghost images, and transmission-derived valleys shaped by curvature-mediated Bragg extraction. Their origin lies in the geometric constraints inherent to curved assemblies, where spatially varying normals, non-parallel lattice orientations, and topologically required defects couple order and disorder into a distributed-coherence regime. This coupling expands the accessible photonic state space, establishing curvature as an active functional degree of freedom rather than a geometric constraint, positioning the self-assembled photonic heterostructures as a scalable route toward multifunctional 3D metasurfaces and new regimes of light–matter interaction. Full article

Bioadhesive materials capable of operating under aqueous conditions are of considerable interest for biomedical and materials science applications. Peptide-based systems represent an attractive platform for such materials due to their structural tunability, inherent biocompatibility, and ability to form supramolecular networks through noncovalent interactions. In this work, a focused library of tyrosine-containing dehydropeptides was designed and synthesized to investigate how molecular architectures influence self-assembly, hydrogel formation and adhesive properties. The peptides were synthesized using a solution-phase Boc strategy and systematically varied with respect to N-terminal protection and C-terminal functionality. The N-protected dehydropeptides formed supramolecular hydrogels through multiple gelation triggers, including pH reduction and heating–cooling cycles. Rheological characterization confirmed the formation of viscoelastic networks with tunable mechanical properties, with storage moduli reaching tens of kilopascals depending on peptide structure. Scanning electron microscopy revealed dense fibrous nanostructures consistent with supramolecular hydrogel formation. The N,C-deprotected dehydropeptides displayed reduced gelation propensity but formed cohesive films with measurable adhesive performance toward hydrophilic substrates. Lap-shear tests demonstrated high shear strengths for the hydrophilic films, highlighting their structural robustness under stress. Overall, this study provides insights into the structure–property relationships governing tyrosine-containing dehydropeptide assemblies and demonstrates their potential as minimalistic building blocks for supramolecular adhesive materials. Full article

In this study, we investigate the impact of processing strategies on the nanoscale morphology and photophysical behavior of donor–acceptor thin films composed of the polymeric donor PBDTTTPD and the n-type acceptor PNDI(2HD)2T. The blend morphology and interfacial characteristics were systematically tuned using three distinct fabrication techniques: spin-coating, convective self-assembly, and space-confined solvent vapor annealing. Atomic force microscopy and photoluminescence spectroscopy were employed to elucidate structure–property correlations relevant to all-polymer optoelectronic systems. Films processed via convective self-assembly exhibited nanoscale features with extensive donor–acceptor intermixing, leading to the most efficient photoluminescence quenching of nearly 85%, indicative of enhanced exciton dissociation and charge transfer. In contrast, as-cast films displayed moderately mixed morphologies with approximately 81% quenching, serving as a reference state. The solvent vapor annealing method induced pronounced phase segregation and the formation of larger domains, resulting in reduced photoluminescence quenching efficiency of about 52%. These findings demonstrate that the nanoscale morphology, and consequently the photophysical response, of PBDTTTPD:PNDI(2HD)2T blends can be precisely tailored through processing, providing valuable design guidelines for all-polymer optoelectronic applications such as organic photovoltaics and field-effect transistors. Full article

Amidst the high global reliance on petroleum, this study addresses energy inefficiency in beam-pumping units used for oil extraction. We developed a tubular solid–liquid triboelectric nanogenerator (TENG) based on fluorinated polydimethylsiloxane (PDMS) films. Self-assembled surface modification with fluorosilane molecular chains enhanced charge transfer, achieving a 2.7-fold increase with 13F-PDMS. The enclosed tubular design utilizes periodic liquid-electrode contact to generate a volumetric effect. Experiments investigated the influence of liquid composition and device configuration on performance. Using a 1.69 mol/L FeCl₃ solution with four series-connected units, the TENG reached 29 V and 263 nA, powering 150 LEDs. This demonstrates its potential for harvesting reciprocating mechanical energy from pumping units to reduce operational energy consumption. Full article

The two-dimensional chiral self-assembly and chiral separation of achiral Ext-TEB molecules on a Bi(111) surface were investigated using low-temperature scanning tunneling microscopy (LT-STM). At low coverage, the molecules self-assembled into chiral clusters. As the coverage increased, a monolayer film with a non-edge-sharing honeycomb structure was formed. This supramolecular structure exhibited organizational chirality, accompanied by chiral separation. Upon annealing, part of the non-edge-sharing honeycomb structure transformed into a close-packed structure, while retaining the organizational chirality, supramolecular chirality, and pronounced chiral separation. Furthermore, applying a higher bias was found to induce a transition in the electronic state of the non-edge-sharing honeycomb structure, converting it into an edge-sharing honeycomb configuration. This study reveals that the chirality of 1,3,5-tris(4-ethynylphenyl) benzene (Ext-TEB) arises from the rotation of the side-chain phenyl rings, which is induced by the rotation of the molecular axis relative to the substrate lattice. This work presents a strategy for the preparation of chiral nanostructures from achiral molecules due to the spontaneous chiral symmetry generation. Full article