Search Results (82)

Visual impairments pose a significant global health challenge, and visual electrophysiological (EP) acquisition plays a pivotal role in diagnosing ophthalmic diseases. However, traditional electrodes still encounter limitations such as inadequate mechanical adaptability and reusability. This study proposes a stretchable and transparent electrode (STE) consisting of a conductive paste/indium tin oxide layer on a polymethyl methacrylate substrate. Leveraging an island–bridge design, the STE renders reliable performance even after being subjected to 1000 cycles of 25% lateral strain and 18% diagonal strain, exhibiting exceptional mechanical flexibility and realizing seamless attachment to soft tissue. Furthermore, optimized conductive paste layer thickness yields a signal-to-noise ratio comparable to commercial electrodes, achieving equivalent performance to Ag/AgCl electrodes in electroretinogram (ERG), electrooculography (EOG), and visual evoked potential (VEP) acquisition. The STE’s mechanical suitability and inconspicuous features hold significant potential for widespread clinical adoption in ophthalmic diagnostics and personalized eye healthcare, offering improved comfort, reusability, and diagnostic precision. Full article

With the rapid development of flexible electronic skin materials, the demand for ion-conductive hydrogels is constantly growing. Specifically, these ion-conductive hydrogels are required to simultaneously exhibit excellent mechanical properties, high conductivity, and multifunctionality. Moreover, this performance requirement needs to be met in complex environments. However, the rapid production of hydrogels that combine high conductivity and photochromic properties remains a major challenge. In this study, a simple one-pot method was employed to successfully prepare multifunctional photochromic hydrogels by incorporating ammonium molybdate (Mo₇) and lithium chloride (LiCl) into a dual-network hydrogel composed of polyacrylamide (PAAm) and sodium alginate (SA). PAAm/SA/Mo₇/LiCl (PSML) hydrogels exhibit excellent comprehensive performance, including superior conductivity (average value of 164 S/cm), rapid UV response time (<20 s), good color-changing reversibility, outstanding high stretchability (peak value of 2800%), and high transparency (>70%). The design ingeniously combines two types of synergistic effects: the synergistic effect of the dual-network structure and that of the multifunctional component functional additives (Mo₇, LiCl). Specifically, the PSML hydrogel integrates photochromic properties, excellent mechanical properties, good anti-freezing properties, and 3D printability through this design. Due to these outstanding properties, the PSML hydrogel shows broad application prospects in fields such as flexible strain sensors, information storage, and encryption devices. Full article

Development of biodegradable packaging materials and valorization of agri-food waste are necessary to produce more sustainable materials while reducing the environmental impact. Starch-based biocomposite films reinforced with beer bagasse fractions with different purification degrees were developed and characterized in structural, mechanical, thermal and optical properties. To this aim, 5% and 10% (w/w) of either beer bagasse (BB) or its lignocellulosic-rich fibers (LF), obtained by subcritical water extraction at temperatures between 110 and 170 °C, were incorporated into starch matrices. Elastic modulus and tensile strength values increased by up to eight-fold and 2.5-fold, respectively, compared to the control film. The incorporation of BB or LF significantly enhanced the mechanical resistance of the films. In general, the increment in the filler:polymer ratio significantly increased the EM values (p < 0.05), while decreasing the stretchability of the films around 80–85%, regardless of the type of filler. This effect suggests a good interfacial adhesion between the fillers and the polymeric matrix, as observed by FESEM. The biocomposite films exhibited a dark reddish appearance, reduced transparency, light blocking barrier capacity and remarkable antioxidant activity due to the presence of phenolic compounds in the fibers. The water vapor and oxygen barrier properties were better preserved when using the more purified LF obtained at 170 °C. Overall, starch films reinforced with beer bagasse fractions showed strong potential for the development of biodegradable food packaging materials. Full article

In recent decades, flexible electronics have witnessed remarkable advancements in multiple fields, encompassing wearable electronics, human–machine interfaces (HMI), clinical diagnosis, and treatment, etc. Nevertheless, conventional rigid electronic devices are fundamentally constrained by their inherent non-stretchability and poor conformability, limitations that substantially impede their practical applications. In contrast, conductive hydrogels (CHs) for electronic skin (E-skin) and healthcare monitoring have attracted substantial interest owing to outstanding features, including adjustable mechanical properties, intrinsic flexibility, stretchability, transparency, and diverse functional and structural designs. Considerable efforts focus on developing CHs incorporating various conductive materials to enable multifunctional wearable sensors and flexible electrodes, such as metals, carbon, ionic liquids (ILs), MXene, etc. This review presents a comprehensive summary of the recent advancements in CHs, focusing on their classifications and practical applications. Firstly, CHs are categorized into five groups based on the nature of the conductive materials employed. These categories include polymer-based, carbon-based, metal-based, MXene-based, and ionic CHs. Secondly, the promising applications of CHs for electrophysiological signals and healthcare monitoring are discussed in detail, including electroencephalogram (EEG), electrocardiogram (ECG), electromyogram (EMG), respiratory monitoring, and motion monitoring. Finally, this review concludes with a comprehensive summary of current research progress and prospects regarding CHs in the fields of electronic skin and health monitoring applications. Full article

Transparent conductive electrodes (TCEs) are essential components in modern optoelectronic devices, including organic light-emitting diodes and solar cells, sensors, and flexible displays. Indium tin oxide has been the dominant material for TCEs due to its high transparency and conductivity. However, its brittleness, high cost, and increasingly limited availability pose significant challenges for electronics. Crack-template (CT)-assisted fabrication has emerged as a promising technique to develop metal mesh-based TCEs with superior mechanical flexibility, high conductivity, and excellent optical transmittance. This technique leverages the spontaneous formation of random and continuous microcrack networks in sacrificial templates, followed by metal deposition (e.g., Cu, Ag, Al, etc.), to produce highly conductive, scalable, and low-cost electrodes. Various crack formation strategies, including controlled drying of polymer suspensions, mechanical strain engineering, and thermal processing, have been explored to tailor electrode properties. Recent studies have demonstrated that crack-templated TCEs can achieve transmittance values exceeding 85% and sheet resistances below 10 Ω/sq, with mesh line widths as low as ~40 nm. Moreover, these electrodes exhibit enhanced stretchability and robustness under mechanical deformation, outperforming ITO in bend and fatigue tests. This review aims to explore recent advancements in CT engineering, highlighting key fabrication methods, performance metrics across different metals and substrates, and presenting examples of its applications in optoelectronic devices. Additionally, it will examine current challenges and future prospects for the widespread adoption of this emerging technology. Full article

Recent advancements in wearable electronics have significantly enhanced human–device interaction, enabling applications such as continuous health monitoring, advanced diagnostics, and augmented reality. While progress in material science has improved the flexibility, softness, and elasticity of these devices for better skin conformity, their optical properties, particularly transparency, remain relatively unexplored. Transparent wearable electronics offer distinct advantages: they allow for non-invasive health monitoring by enabling a clear view of biological systems and improve aesthetics by minimizing the visual presence of electronics on the skin, thereby increasing user acceptance. Hydrogels have emerged as a key material for transparent wearable electronics due to their high water content, excellent biocompatibility, and tunable mechanical and optical properties. Their inherent softness and stretchability allow intimate, stable contact with dynamic biological surfaces. Furthermore, their ability to support ion-based conductivity is advantageous for bioelectronic interfaces and physiological sensors. Current research is focused on advancing hydrogel design to improve transparency, mechanical resilience, conductivity, and adhesion. The core components of transparent wearable systems include physiological sensors, energy storage devices, actuators, and real-time displays. These must collectively balance efficiency, functionality, and long-term durability. Practical applications span continuous health tracking and medical imaging to next-generation interactive displays. Despite progress, challenges such as material durability, scalable manufacturing, and prolonged usability remain. Addressing these limitations will be crucial for the future development of transparent, functional, and user-friendly wearable electronics. Full article

As conductive materials, ionogels have attracted significant attention for their potential applications in flexible wearable electronics. However, preparing an ionogel with mechanical properties akin to human skin while also achieving transparency, adhesion, and low hysteresis through simple processes remains challenging. Here, we introduce a multifunctional ionogel synthesized via a one-step photopolymerization method. By leveraging the good compatibility between the ionic liquid and the polymer network, as well as the hydrogen bonding and chemical crosslinking within the gel network, we achieved an ionogel with high transparency (>98%), stretchability (fracture strain of 19), low hysteresis (<5.83%), strong adhesion, robust mechanical stability, excellent electrical properties, a wide operating temperature range, and a tunable modulus (1–103 kPa) that matches human skin. When used as a conductor in soft actuators, the ionogel enabled a large area strain of 36% and a fast electromechanical conversion time of less than 1 s. The actuator demonstrated good actuation performance with voltage and frequency dependence, electrochemical stability, and outstanding durability over millions of cycles. This study provides a simple and effective method to produce multifunctional ionogels with tailored mechanical properties that match those of human skin, paving the way for their application in flexible wearable electronics. Full article

This work introduces an ultraviolet (UV)-curable elastomer through the co-polymerization of aliphatic polyurethane acrylate and hydroxypropyl acrylate via UV irradiation. The UV-curable elastomer presents superior mechanical properties (elongation at a break of 2992%) and high transparency (94.8% at 550 nm in the visible light region). A robust hydrogel–elastomer stretchable sensor is fabricated by coating an ionic hydrogel on the surface of an elastomer, which enables real-time monitoring of human motion. In addition, the UV-curable elastomer can be used for 3D printing, as demonstrated by complex lattice structures using a digital light processing 3D printer. Full article

Nowadays, conductive hydrogels show significant prospects as strain sensors due to their good stretchability and signal transduction abilities. However, traditional hydrogels possess poor anti-freezing performance at low temperatures owing to the large number of water molecules, which limits their application scope. To date, constructing a hydrogel-based sensor with balanced stretchability, conductivity, transparency, and anti-freezing properties via simple methods has proven challenging. Here, a fully physically crosslinked poly(hydroxyethyl acrylamide)–glycerol–sodium chloride (PHEAA–Gl–NaCl) hydrogel was obtained by polymerizing hydroxyethyl acrylamide in deionized water and then soaking it in a saturated NaCl solution of glycerol and water. The PHEAA–Gl–NaCl hydrogel had good transparency (~93%), stretchability (~1300%), and fracture stress (~287 kPa). Owing to the presence of glycerol and sodium chloride, the PHEAA–Gl–NaCl hydrogel had good anti-freezing properties and conductivity. Furthermore, the PHEAA–Gl–NaCl hydrogel-based strain sensor possessed good sensitivity and cyclic stability, enabling the detection of different human motions stably and in a wide temperature range. Based on the above characteristics, the PHEAA–Gl–NaCl hydrogel has broad application prospects in flexible electronic materials. Full article

Recently, eutectogels have emerged as ideal candidates for flexible wearable strain sensors. However, the development of eutectogels with robust mechanical strength, high stretchability, excellent transparency, and desirable conductivity remains a challenge. Herein, a covalently cross-linked eutectogel was prepared by exploiting the high solubility of oligoethylene glycol in a polymerizable deep eutectic solvent (DES) form of acrylic acid (AA) and choline chloride (ChCl). The resulting eutectogel exhibited high transparency (90%), robust mechanical strength (up to 1.5 MPa), high stretchability (up to 962%), and desirable ionic conductivity (up to 1.22 mS cm⁻¹). The resistive strain sensor fabricated from the eutectogel exhibits desirable linear sensitivity (GF: 1.66), wide response range (1–200%), and reliable stability (over 1000 cycles), enabling accurate monitoring of human motions (fingers, wrists, and footsteps). We believe that our DES-based eutectogel has great potential for applications in wearable strain sensors with high sensitivity and reliability. Full article

The potential applications of stretchable strain sensors in wearable electronics have garnered significant attention. However, developing susceptible stretchable strain sensors for practical applications still poses a considerable challenge. The present study introduces a stretchable strain sensor that utilizes silver nanowires (AgNWs) embedded into a polydimethylsiloxane (PDMS) substrate. The AgNWs have high flexibility and electrical conductivity. A stretchable AgNW/Pat-PDMS conductive film was prepared by arranging nanowires on the surface of PDMS using a simple rod coating method. Depending on the orientation angle, the overlap area between nanowires varies, resulting in different levels of separation under a given strain. Due to the separation of the nanowire and the change in current path geometry, the variation in strain resistance of the sensor can be primarily attributed to these factors. Therefore, precision in strain regulation can be adjusted by altering the angle θ (0°, 60°, or 90°) of the nanowire. At the same time, the stability of the AgNW/Pattern-PDMS (AgNW/Pat-PDMS) conductive film application was verified by preparing a sandwich structure PDMS/AgNW/Pat-PDMS stretchable strain sensor. The sensor exhibited high sensitivity within the operating sensing range (gauge factor (GF) of 15 within ~120% strain), superior durability (20,000 bending cycles and 5000 stretching cycles), and excellent response toward bending. Full article

With the swift advancement of wearable electronics and artificial intelligence, the integration of electronic devices with the human body has advanced significantly, leading to enhanced real-time health monitoring and remote disease diagnosis. Despite progress in developing stretchable materials with skin-like mechanical properties, there remains a need for materials that also exhibit high optical transparency. Supercapacitors, as promising energy storage devices, offer advantages such as portability, long cycle life, and rapid charge/discharge rates, but achieving high capacity, stretchability, and transparency simultaneously remains challenging. This study combines the stretchable, transparent polymer PEDOT:PSS with MnO₂ nanoparticles to develop high-performance, stretchable, and transparent supercapacitors. PEDOT:PSS films were deposited on a PDMS substrate using a spin-coating method, followed by electrochemical deposition of MnO₂ nanoparticles. This method ensured that the nanosized MnO₂ particles were uniformly distributed, maintaining the transparency and stretchability of PEDOT:PSS. The resulting PEDOT:PSS/MnO₂ nanoparticle electrodes were gathered into a symmetric device using a LiCl/PVA gel electrolyte, achieving an areal capacitance of 1.14 mF cm⁻² at 71.2% transparency and maintaining 89.92% capacitance after 5000 cycles of 20% strain. This work presents a scalable and economical technique to manufacturing supercapacitors that combine high capacity, transparency, and mechanical stretchability, suggesting potential applications in wearable electronics. Full article

In the evolving landscape of portable electronics, there is a critical demand for components that meld stretchability with optical transparency, especially in supercapacitors. Traditional materials fall short in harmonizing conductivity, stretchability, transparency, and capacity. Although poly(3,4-ethylenedioxythiophene):poly(styrene sulfonate) (PEDOT:PSS) stands out as an exemplary candidate, further performance enhancements are necessary to meet the demands of practical applications. This study presents an innovative and effective method for enhancing electrochemical properties by homogeneously incorporating Ru(III) into PEDOT:PSS. These Ru(III) PEDOT:PSS complexes are readily synthesized by dipping PEDOT:PSS films in RuCl₃ solution for no longer than one minute, leveraging the high specific capacitance of Ru(III) while minimizing interference with transmittance. The supercapacitor made with this Ru(III) PEDOT:PSS complex demonstrated an areal capacitance of 1.62 mF cm⁻² at a transmittance of 73.5%, which was 155% higher than that of the supercapacitor made with PEDOT:PSS under comparable transparency. Notably, the supercapacitor retained 87.8% of its initial capacitance even under 20% tensile strain across 20,000 cycles. This work presents a blueprint for developing stretchable and transparent supercapacitors, marking a significant stride toward next-generation wearable electronics. Full article

Stretchable ionogels, as soft ion-conducting materials, have generated significant interest. However, the integration of multiple functions into a single ionogel, including temperature tolerance, self-adhesiveness, and stability in diverse environments, remains a challenge. In this study, a new class of fluorine-containing ionogels was synthesized through photo-initiated copolymerization of fluorinated hexafluorobutyl methacrylate and butyl acrylate in a fluorinated ionic liquid 1-butyl-3-methyl imidazolium bis (trifluoromethylsulfonyl) imide. The resulting ionogels demonstrate good stretchability with a fracture strain of ~1300%. Owing to the advantages of the fluorinated network and the ionic liquid, the ionogels show excellent stability in air and vacuum, as well as in various solvent media such as water, sodium chloride solution, and hexane. Additionally, the ionogels display impressive wide temperature tolerance, functioning effectively within a wide temperature range from −60 to 350 °C. Moreover, due to their adhesive properties, the ionogels can be easily attached to various substrates, including plastic, rubber, steel, and glass. Sensors made of these ionogels reliably respond to repetitive tensile-release motion and finger bending in both air and underwater. These findings suggest that the developed ionogels hold great promise for application in wearable devices. Full article

In order to prepare polyimide (PI) films with a low dielectric constant and excellent comprehensive performance, a two-step method was employed in this study to integrate β-cyclodextrin into a semi-aromatic fluorine-containing polyimide ternary system. By introducing trifluoromethyl groups to reduce the dielectric constant, the dielectric constant was further reduced to 2.55 at 10 MHz. Simultaneously, the film exhibited noteworthy thermal stability (a glass transition temperature exceeding 300 °C) and a high coefficient of thermal expansion. The material also demonstrated outstanding mechanical properties, boasting a strength of 122 MPa and a modulus of 2.2 GPa, along with high optical transparency (transmittance reaching up to 89% at 450 nm). Moreover, the inherent high transparency of colorless polyimide (CPI) combined with good stretchability contributed to the attainment of a low dielectric constant. This strategic approach not only opens up new opportunities for novel electroactive polymers but also holds potential applications in flexible displays, circuit printing, and chip packaging. Full article