Smart Materials Research Articles

Mechanical Properties Comparison of Isotropic vs. Anisotropic Hybrid Magnetorheological Elastomer-Fluid.

Magnetorheological (MR) materials are smart materials that can change their rheological characteristics when exposed to a magnetic field. Such rheological properties include viscosity and dynamic modulus. MR materials have emerged as one of the most efficient smart materials that can modify mechanical and viscoelastic characteristics. Depending on the medium used, MR materials can be classified into two types: magnetorheological fluids (MRFs) and magnetorheological elastomers (MREs). MREs are classified as isotropic or anisotropic based on CIP distribution inside the elastomer matrix. A unique hybrid material incorporating MRE and MRF is constructed in this work to investigate, compare, and the dynamic properties of isotropic, anisotropic, hybrid isotropic, and hybrid anisotropic MREs under various magnetic fields (0, 104, and 160.2 mT). The created samples are subjected to extensive testing, including static and dynamic evaluations. In the static tests, experiments use a compression linear displacement mode with a fixed maximum gap change of 3 mm. The temperature is maintained at a constant level of 24 °C throughout the 40 s test duration for each test, and the magnetic field is incrementally increased by varying the number of magnets, ranging from 0 to 160.2 mT for dynamic qualities using compression oscillations on a dynamic mechanical analyzer (DMA), including frequency and strain-dependent data. These experiments, carried out using sinusoidal shear movements, include an excitation frequency range of 0.1 Hz to 15 Hz while preserving, with a fixed shear strain of 2%.

From Conventional to Programmable Matter Systems: A Review of Design, Materials, and Technologies

Programmable matter represents a system of elements whose interactions can be programmed for a certain behavior to emerge (e.g., color, shape) upon suitable commands (e.g., instruction, stimuli) by altering its physical characteristics. Even though its appellation may refer to a morphable physical material, programmable matter has been represented through several approaches from different perspectives (e.g., robots, smart materials) that seek the same objective: controllable behavior such as smart shape alteration. Researchers, engineers, and artists have expressed interest in the development of smart modeling clay as a novel alternative to conventional matter and classical means of prototyping. Henceforth, users will be able to do/undo/redo forms based on computed data (CAD) or interactions (sensors), which will help them unlock more features and increase the usefulness of their products. However, with such a promising technology, many challenges need to be addressed, as programmable matter relies on energy consumption, data transmission, stimuli control, and shape formation mechanisms. Furthermore, numerous devices and technologies are created under the name of programmable matter, which may pose ambiguity to the control strategies. In this study, we determine the basic operations required to form a shape, then review different realizations using the shape shifting ability of programmable matter and their fitting classifications, and finally discuss potential challenges.

Shape Memory Polyurethane Composite With Fast Response to Near-Infrared Light Based on Tannic Acid-Iron and Dynamic Phenol-Carbamate Network.

Intelligent materials derived from green and renewable bio-based materials garner widespread attention recently. Herein, shape memory polyurethane composite (PUTA/Fe) with fast response to near-infrared (NIR) light is successfully prepared by introducing Fe3+ into the tannic acid-based polyurethane (PUTA) matrix through coordination between Fe3+ and tannic acid. The results show that the excellent NIR light response ability is due to the even distribution of Fe3+ filler with good photo-thermal conversion ability. With the increase of Fe3+ content, the NIR light response shape recovery rate of PUTA/Fe composite films is significantly improved, and the shape recovery time is reduced from over 60 s to 40s. In addition, the mechanical properties of PUTA/Fe composite film are also improved. Importantly, owing to the dynamic phenol-carbamate network within the polymer matrix, the PUTA/Fe composite film can reshape its permanent shape through topological rearrangement and show its good NIR light response shape memory performance. Therefore, PUTA/Fe composites with high content of bio-based material (TA content of 15.1-19.4%) demonstrate the shape memory characteristics of fast response to NIR light; so, it will have great potential in the application of new intelligent materials including efficient and environmentally friendly smart photothermal responder.

A Discotic Mesogenic near-infrared absorbing dye and its application in photo-responsive liquid crystal elastomers

Near-infrared (NIR) light-responsive liquid crystal elastomers (LCEs) doped with organic small-molecule photothermal agents have garnered scientific attention. However, the challenge remains in designing and synthesizing mesogenic photothermal dyes with absorption wavelengths greater than 800 nm. In this research, we design a novel discotic mesogenic NIR absorbing dye, namely the nickel bis(dithiolene) complex YHD868, and prepare NIR-responsive LCE/YHD868 composite films. The discotic mesogenic molecule YHD868 possesses a columnar hexagonal mesophase and exhibits intense NIR absorption at 868 nm, with a photothermal conversion efficiency of about 27 % and a molar extinction coefficient of approximately 30000 M−1·cm−1. Due to the strong NIR absorption of YHD868, combined with its excellent photothermal stability, the LCE/YHD868 composite films exhibit remarkable photoresponse and mechanical properties. Even at a low doping concentration of 0.2 wt%, the composite film can achieve a tensile strength of 9.8 MPa and an elongation at break of 165 %. Under 880 nm NIR irradiation (3.3 W·cm−2), the film can complete reversible photo-induced shrinking deformation in just 2 s, with a shrinkage ratio of about 64 %. This work offers a new approach for the development of photo-responsive smart soft materials.

Investigation of a 2-DOF GER fluid damper in cut mode

Dampers incorporating smart materials have attracted significant interest for their application in vibration and shock isolation. Traditionally, these dampers work through shear, flow, and squeeze modes, each unique in its strengths and limitations. However, this study introduces a working mode, termed cut mode, which integrates the strengths of these existing modes. Structurally resembling the flow mode, operationally akin to the shear mode, and behaving similarly to the squeeze mode, the cut mode promises a novel approach to damping. Consequently, extensive research has been conducted at the particle level to develop a mathematical model for the cut mode, grounded in chain formation and breaking mechanisms. Thereafter, a verification prototype damper was designed to demonstrate this concept’s practicality, with the Giant Electrorheological (GER) fluid—a rheological fluid with exceptional yield strength—being employed. This damper features a multilayer cylindrical structure tailored for the cut mode, providing 2-degree of freedom (DOF) damping capabilities. This dual-DOF design is ideal for robotic arm joint applications, as it can offer damping for both axial translation and circumferential rotation simultaneously. In addition, four orifice boards were designed, fabricated, and tested to optimize and enhance the effectiveness of the cut mode further. The results are impressive, the proposed cut mode damper exhibits superior performance characteristics, indicating its great potential for engineering applications.

PH-Controllable Redox Responsive Amphiphilic Viologens for Switchable Emulsions.

A pH and redox dual responsive amphiphilic viologen is synthesized, which can be reversibly transformed among the zwitterionic (SVa), monovalent anionic (SV+), and divalent anionic (SVH2+) forms upon pH variation, exhibiting pH-controllable redox responsive properties. Switchable Pickering emulsions with different droplet size and viscosity are prepared by the mixture of hydrophilic silica nanoparticles and the viologens (SV+ or SVH2+) at acidic conditions, while such combination yielded an oil-in-dispersion emulsion at neutral pH value. Not only can rapid reversible demulsification/stabilization of the Pickering emulsions be achieved by redox reactions, but the rate of redox-demulsification can also be controlled by pH trigger. The dual-responsive amphiphilic viologens have potential applications in developing intelligent colloid materials and molecular logic systems.

Profiling and optimized extraction of bioactive polyphenolic compounds from young, red-fleshed apple using eco-friendly deep eutectic solvents

Red-fleshed apple cultivars with an enhanced content of polyphenolic compounds have attracted increasing interest due to their promising health benefits. Here, we have analysed the polyphenolic content of young, red-fleshed apples (RFA) and optimised extraction conditions of phenolics by utilising natural deep eutectic solvents (NDES). We also compare the antioxidant, neuroprotective and antimicrobial activities of NDES- and methanol-extracted phenolics from young RFA. High-performance liquid chromatography coupled to high-resolution mass spectrometry (HPLC-HRMS) was used for phenolics identification and quantification. Besides young RFA, ripe red-fleshed, young and ripe white-fleshed apples were analysed, revealing that young RFA possess the highest phenolic content (2078.4 ± 4.0 mg gallic acid equivalent/100 g), and that ripe white-fleshed apples contain the least amount of phenolics (545.0 ± 32.0 mg gallic acid equivalent/100 g). The NDES choline chloride-glycerol containing 40 % w/w H2O gave similar yields at 40 °C as methanol. In addition, the polyphenolics profile, and bioactivities of the NDES extract from young RFA were comparable that of methanol extracts. Altogether, our data show that NDES extracts of young RFA are a promising source of bioactive polyphenolics with potential applications in diverse sectors, e.g., for functional food production, smart material engineering and natural therapies.

Growth of CQD/PPy on cotton cloth as a binder-free high-performance flexible electrode for symmetric supercapacitor

Benefited from the continuous development of nanomaterials, wearable microelectronics with flexible and miniaturized features are booming, and smart textiles are attracting more attentions because of their superior flexibility and perfect safety. The combination of conductive polymers and flexible substrates has created a new field for flexible supercapacitors. Herein, cotton cloth (CC), which is commonly used in daily life, was selected as the flexible substrate and a layer of CQDs was uniformly grown on the CC fibers, and then pyrrole was directly grown on CC by in-situ polymerization under Fe3+ initiation to realize the tight bonding between the conductive polymer and the flexible substrate. The electrochemical properties of the composite electrode could be controlled by changing the amount of CQD. The obtained CC@CQD@PPy electrode has a high specific capacitance (C) of 537.9 F/g at 0.5 A/g. The assembled symmetric CC@CQD@PPy supercapacitor exhibits an excellent energy density (E) of 18.7 Wh/kg at a power density (P) of 125.0 W/kg, and a supreme cycling stability with a capacitance retention of 77.9 % after 10,000 cycles. In addition, the CC@CQD@PPy supercapacitor has excellent flexibility, with almost unchanged electrochemical performance under different bending angles, and the assembled all-solid-state supercapacitor has good electrochemical properties.

Handedness-Inverted and Stimuli-Responsive Circularly Polarized Luminescent Nano/Micromaterials Through Pathway-Dependent Chiral Supramolecular Polymorphism.

The precise manipulation of supramolecular polymorphs has been widely applied to control the morphologies and functions of self-assemblies, but is rarely utilized for the fabrication of circularly polarized luminescence (CPL) materials with tailored properties. Here, this work reports that an amphiphilic naphthalene-histidine compound (NIHis) readily self-assembled into distinct chiral nanostructures through pathway-dependent supramolecular polymorphism, which shows opposite and multistimuli responsive CPL signals. Specifically, NIHis display assembly-induced CPL from the polymorphic keto tautomer, which become predominant during enol-keto tautomerization shifting controlled by a bulk solvent effect. Interestingly, chiral polymorphs of nanofiber and microbelt with inverted CPL signals can be prepared from the same NIHis monomer in exactly the same solvent compositions and concentrations by only changing the temperature. The tunable CPL performance of the solid microbelts is realized under multi external physical or chemical stimuli including grinding, acid fuming, and heating. In particular, an emission color and CPL on-off switch based on the microbelt polymorph by reversible heating-cooling protocol is developed. This work brings a new approach for developing smart CPL materials via supramolecular polymorphism engineering.

Layer-by-layer self-assembly of durable, breathable and enhanced performance thermoelectric fabrics for collaborative monitoring of human signal

Thermoelectric devices have received widespread attention in next-generation flexible electronics due to their excellent self-powered characteristics, multifunctionality and high integrability. However, current thermoelectric devices suffer from drawbacks such as poor durability, complex preparation processes, and terrible air permeability which is the necessary metric in wearing comfort. Here, we propose a layer-by-layer (LBL) self-assembly strategy to prepare multifunctional thermoelectric fabrics with enhanced thermoelectric performance and durability. Based on the self-assembly effect, the interfacial bonding between the thermoelectric material and the fabric substrate is effectively improved, so that the thermoelectric properties of the fabrics can still be maintained stable after 2000 bending cycles and 600 washing cycles. Moreover, this strategy increases the electrical conductivity of the fabric by a factor of 4 without affecting the fabric’s air permeability (up to 400 mm s−1 at 50 Pa) and tensile properties (strains exceeding 100 %). Due to its wearability and multifunctionality, the fabric was designed as a synergistic monitoring system that includes facial respiration monitoring and knee joint motion monitoring for continuous monitoring of the athlete’s dynamic body condition. This thermoelectric fabric shows amazing potential for advanced smart textiles, soft robotics and human–computer interaction.

Nature-inspired miniaturized magnetic soft robotic swimmers

State-of-the-art biomedical applications such as targeted drug delivery and laparoscopic surgery are extremely challenging because of the small length scales, the requirements of wireless manipulation, operational accuracy, and precise localization. In this regard, miniaturized magnetic soft robotic swimmers (MSRS) are attractive candidates since they offer a contactless mode of operation for precise path maneuvering. Inspired by nature, researchers have designed these small-scale intelligent machines to demonstrate enhanced swimming performance through viscous fluidic media using different modes of propulsion. In this review paper, we identify and classify nature-inspired basic swimming modes that have been optimized over large evolutionary timescales. For example, ciliary swimmers like Paramecium and Coleps are covered with tiny hairlike filaments (cilia) that beat rhythmically using coordinated wave movements for propulsion and to gather food. Undulatory swimmers such as spermatozoa and midge larvae use traveling body waves to push the surrounding fluid for effective propulsion through highly viscous environments. Helical swimmers like bacteria rotate their slender whiskers (flagella) for locomotion through stagnant viscid fluids. Essentially, all the three modes of swimming employ nonreciprocal motion to achieve spatial asymmetry. We provide a mechanistic understanding of magnetic-field-induced spatiotemporal symmetry-breaking principles adopted by MSRS for the effective propulsion at such small length scales. Furthermore, theoretical and computational tools that can precisely predict the magnetically driven large deformation fluid–structure interaction of these MSRS are discussed. Here, we present a holistic descriptive review of the recent developments in these smart material systems covering the wide spectrum of their fabrication techniques, nature-inspired design, biomedical applications, swimming strategies, magnetic actuation, and modeling approaches. Finally, we present the future prospects of these promising material systems. Specifically, synchronous tracking and noninvasive imaging of these external agents during in vivo clinical applications still remains a daunting task. Furthermore, their experimental demonstrations have mostly been limited to in vitro and ex vivo phantom models where the dynamics of the testing conditions are quite different compared the in vivo conditions. Additionally, multi-shape morphing and multi-stimuli-responsive modalities of these active structures demand further advancements in 4D printing avenues. Their multi-state configuration as an active solid-fluid continuum would require the development of multi-scale models. Eventually, adding multiple levels of intelligence would enhance their adaptivity, functionalities, and reliability during critical biomedical applications.

Experimental and numerical analysis of bending performance for a glass-epoxy composite with integrated sheet-shaped shape memory alloy actuator elements

Shape memory alloys (SMA) belong to the group of smart materials and show particularly a promising potential for an active functionalization of lightweight composite structures with respect to enabling smart structures. In this work, various manufacturing concepts for the integration of thin sheet-shaped SMA actuator elements in a thin glass-epoxy composite beam are experimentally and numerically studied with regard to its bending deformation performance realized by thermal induced shape memory effect of the SMA actuator element. For numerical modeling, the shape memory effect of the SMA on structural level, a three-dimensional thermomechanical constitutive material model is applied. In the experiments, the same deformation pattern of the composite beam was observed for all integration concepts investigated, with the degree of deformation showing strong differences both when the shape memory effect is activated and deactivated. The complex material behavior of the SMA actuator under bending deformation is modeled via the finite element method with sufficient accuracy including existing tension and compression loads.

Gold(I)-Thiolate Coordination Polymers as Multifunctional Materials: The Case of Au(I)-p-Fluorothiophenolate.

Gold-sulfur interaction has vital importance in nanotechnologies and material chemistry to design functional nanoparticles, self-assembled monolayers, or molecular complexes. In this paper, a mixture of only two basic precursors, such as the chloroauric acid (HAu(III)Cl4) and a thiol molecule (p-fluorothiophenol (p-HSPhF)), are used for the synthesis of gold(I)-thiolate coordination polymers. Under different conditions of synthesis and external stimuli, five different functional materials with different states of [Au(I)(p-SPhF)]n can be afforded. These gold-thiolate compounds are (i) red emissive, flexible, and crystalline fibers; (ii) composite materials made of these red emissive fibers and gold nanoparticles; (iii) amorphous phase; (iv) transparent glass; and (v) amorphous-to-crystalline phase-change material associated with an ON/OFF switch of luminescence. The different functionalities of these materials highlight the great versatility of the gold(I) thiolate coordination polymers with easy synthesis and diverse shaping that may have great potential as sustainable phosphors, smart textiles, sensors, and phase change memories.

Multistimuli-responsive tetraphenylethene molecular switches displaying acid-sensing, photochromism, and metal ion detection properties

Aggregation-induced emission (AIE) smart materials with multiple stimulus responses have a wide range of applications. Here, a series of tetraphenylethylene (TPE) derivatives, TPEN1S3, TPEN2S2, TPEN3S1 were synthesized. The sensitivity of molecules to pH, UV light, and metal ions could be effectively tuned by modulating the ratio of amino to sulfonic acid groups. These TPE derivatives exhibited yellow emissions in aggregated state due to the AIE characteristics. Acidification conversion of the NH2 groups to NH3+ for three molecules induced the suppression of intramolecular charge transfer (ICT), which resulted in a 72–102 nm blue shift in the fluorescence emission. Solid powders of these compounds exhibited reversible protonation-deprotonation process induced by HCl/NH3·H2O vapor. TPEN1S3, TPEN2S2 and TPEN3S1 in solution could be photoactivated and emit blue fluorescence (ca. 482 nm, 475 nm, and 480 nm). Photocyclo-dehydrogenation reactions of compounds were triggered by the UV irradiation and the maximum cyclization ratios could reach 12%, 66%, and 50%, respectively. Protonation of NH2 group significantly enhanced the rate of the photocyclo-dehydrogenation reaction. Furthermore, the solid powders of protonated compounds displayed pronounced reversible photochromic properties due to the generation of cyclization intermediate. In addition, TPEN1S3, TPEN2S2, and TPEN3S1 exhibited responsiveness to a diverse range of metal ions. Specifically, the TPEN2S2 molecule functioned as a photo sensor for Li + ions with a blue shift in fluorescence emission. The limit of detection (LOD) value was 0.679 μM. These multiple stimuli-responsive AIE molecules hold significant potential for use in advanced photo-controlled patterning, encryption applications, and the detection of metal ions.

Enhancing fire safety, electromagnetic interference shielding, and photothermal conversion performances of wearable polyamide fabrics through eco-friendly coatings

The demand for smart textiles in wearable technology has significantly increased in the last decade. However, the inherent flammability of most textiles poses a big challenge, especially when exposed to elevated surface temperatures induced by electrical or optical stimuli, increasing the risk of fire. The process of synthesizing flame retardants involves the use of organic solvents, which is not in line with the requirements of sustainable development. This research focuses on establishing an eco-friendly and stable coating for polyamide 6 (PA6) fabric through a solvent-free synthesis and innovative alternating deposition method. It has been demonstrated that the treated PA6 fabric exhibits rapid self-extinguishing properties, eliminating melt dripping and achieving a remarkable limiting oxygen index of 25.5%. Furthermore, the peak heat release rate and total heat release rate of the treated PA6 fabric decrease by 32.9% and 22.7%, respectively, compared to that of the control PA6. Under simulated sunlight exposure at an intensity of 150 mW·cm−2, the treated PA6 fabric rapidly reaches a surface temperature of 78.6 °C within 300 s. Additionally, the treated PA6 fabric demonstrates an electromagnetic interference (EMI) shielding efficiency of 24.0 dB in the X-band, highlighting the efficacy of the innovative coating. This result is attributed to the conductive network formed by the alternating deposition of MXene and polyphosphamide. This work not only improves the fire safety in wearable textiles but also presents a promising and green strategy for developing multifunctional wearable textiles with enhanced safety features.

Introduction of photochromic properties to UiO-66-NH2 via “click”-modification by spiropyran molecule

We present a study on incorporating spiropyran photoactive molecules into the UiO-66-NH2 scaffold. Initially, we modified spiropyran molecules by introducing functional groups to facilitate covalent bonding with the MOF structure. Spiropyran molecules with carboxylic groups demonstrated the ability to coordinate zirconium in defect pores of the MOF. Alternatively, the aldehyde group showed potential for forming C–N bonds with amino groups of BDC-NH2 linkers. To validate the formation of C–N bonds within the MOF scaffold, we synthesized a complex salt of spiropyran and individual BDC-NH2 linkers. DFT calculations support our conclusions. We observed that upon introducing the photoactive moiety, the UiO-66-NH2 framework exhibited photoresponse, as demonstrated by FTIR experiments. Based on experimental data and computational results, we hypothesize that both incorporation mechanisms are viable in the functionalization process. However, steric hindrances may impede the incorporation of spiropyran into the pores, leading to surface modification instead. The elucidated mechanisms hold promise for the development of photoresponsive MOF-based smart materials.

Uncovering the Recent Progress of CNC-Derived Chirality Nanomaterials: Structure and Functions.

Cellulose nanocrystal (CNC), as a renewable resource, with excellent mechanical performance, low thermal expansion coefficient, and unique optical performance, is becoming a novel candidate for the development of smart material. Herein, the recent progress of CNC-based chirality nanomaterials is uncovered, mainly covering structure regulations and function design. Undergoing a simple evaporation process, the cellulose nanorods can spontaneously assemble into chiral nematic films, accompanied by a vivid structural color. Various film structure-controlling strategies, including assembly means, physical modulation, additive engineering, surface modification, geometric structure regulation, and external field optimization, are summarized in this work. The intrinsic correlation between structure and performance is emphasized. Next, the applications of CNC-based nanomaterials is systematically reviewed. Layer-by-layer stacking structure and unique optical activity endow the nanomaterials with wide applications in the mineralization, bone regeneration, and synthesis of mesoporous materials. Besides, the vivid structural color broadens the functions in anti-counterfeiting engineering, synthesis of the shape-memory and self-healing materials. Finally, the challenges for the CNC-based nanomaterials are proposed.

Advances in smart materials soft actuators on mechanisms, fabrication, materials, and multifaceted applications: A review

The soft actuators of smart materials have attracted significant attention in recent years due to their unique functions and distinctive characteristics. The actuators are composed of smart materials that can demonstrate substantial alterations in their dimensions, shape, or mechanical characteristics when subjected to external stimuli, including but not limited to temperature, light, electricity, or magnetic fields. These aforementioned characteristics render them highly advantageous for various applications, including tissue engineering, prosthetics, surgical robots, drug delivery, and soft robotics. A deeper understanding of the principles of the actuators is crucial for their development and application expansion. This article provides a comprehensive analysis of soft actuators made from smart materials, explaining their underlying concepts, operational mechanisms, material composition, production techniques, and the diverse range of applications across various fields, including tissue engineering, prosthetics, surgical robotics, drug delivery systems, and the emerging field of soft robotics. This review further highlights the current challenges and prospects to address these problems to enable their ability to revolutionize into a variety of different technical fields.

Synthetic oil gels with organoclays in the formulation of magnetorheological fluids

Magnetorheological fluids (MRF) are smart composite materials that, under an external magnetic field, show a reversible solid-liquid transition in less than 10 ms. This study aimed to evaluate which organoclays would jellify a synthetic oil for the formulation of MRF. Three dispersant additives for carbonyl iron powder were evaluated. Fifteen different gelling additives from four clay families, bentonites, hectorites, montmorillonites, and mixed mineral thixotropes (MMT), were dispersed in oil only, keeping the same concentration, without iron particles. The gels were then tested through amplitude and frequency sweeps in oscillatory rheometry to evaluate their viscoelastic behavior. The thixotropy of the gels was measured through the “three-interval” test in a rheometer. After selecting the best gelling additive to prepare the MRF, three dispersing additives had their rheology evaluated to determine the best magnetorheological effect and redispersibility after 1 year of sample preparation. In the linear viscoelastic region, all MMT clays resulted in a weak viscoelastic gel (G′∼100 to 300 Pa and G″∼30 to 50 Pa). Some of the bentonite clays jellified, and others did not. The best organoclays were montmorillonites and hectorites, which formed consistent viscoelastic gels (G′∼1 to 5 kPa and G″∼70 to 250 Pa). The best organoclay presented a yield stress σ0 = (42 ± 3) Pa, a storage modulus G′ = (2690 ± 201) Pa, and a cohesive energy density (CED) = 98 mJ/m3, and it was selected to explore the rheology of MRF with three dispersant additives: octan-1-ol, octan-1-amine, and L-α-Phosphatidylcholine. All the MRFs were prepared using carbonyl iron powder HS (BASF SE) in oil gels and with the same organoclay. All three dispersant additives showed a thixotropic recovery above 100% in the three-interval test. Regarding the redispersibility after 1 year, the MRF formulations with octan-1-amine and lecithin were reproved, as they reached normal force peaks of 19 and 24 N, while the work was 28 and 415 mJ, respectively. The best MRF was formulated with octan-1-ol, and resulted in a normal force of 0.33 N and 3.4 mJ at 35 mm of vane penetration. Therefore, we conclude that the MRF with octan-1-ol and montmorillonite #6 showed a better balance between thixotropy, MR effect, and, above all, good redispersibility.

Dual-Responsive MXene-Functionalized Wool Yarn Artificial Muscles.

Fiber-based artificial muscles are promising for smart textiles capable of sensing, interacting, and adapting to environmental stimuli. However, the application of current artificial muscle-based textiles in wearable and engineering fields has largely remained a constraint due to the limited deformation, restrictive stimulation, and uncomfortable. Here, dual-responsive yarn muscles with high contractile actuation force are fabricated by incorporating a very small fraction (<1wt.%) of Ti3C2Tx MXene/cellulose nanofibers (CNF) composites into self-plied and twisted wool yarns. They can lift and lower a load exceeding 3400 times their own weight when stimulated by moisture and photothermal. Furthermore, the yarn muscles are coiled homochirally or heterochirally to produce spring-like muscles, which generated over 550% elongation or 83% contraction under the photothermal stimulation. The actuation mechanism, involving photothermal/moisture-mechanical energy conversion, is clarified by a combination of experiments and finite element simulations. Specifically, MXene/CNF composites serve as both photothermal and hygroscopic agents to accelerate water evaporation under near-infrared (NIR) light and moisture absorption from ambient air. Due to their low-cost facile fabrication, large scalable dimensions, and robust strength coupled with dual responsiveness, these soft actuators are attractive for intelligent textiles and devices such as self-adaptive textiles, soft robotics, and wearable information encryption.