Applications In Flexible Electronics Research Articles

Liquid-free, tough and transparent ionic conductive elastomers based on nanocellulose for multi-functional sensors and triboelectric nanogenerators

Stretchable and transparent ionic conductors have attracted great interest due to their promising applications in flexible wearable electronics. The obvious drawbacks of gel-based ionic conductors such as hydrogels (e.g., evaporation or freezing of water) have driven the demand for liquid-free ionic conductors. This paper reports a new strategy for fabricating transparent, liquid-free ionic conductive elastomers based on renewable nanocellulose. A three-dimensional cellulose skeleton was constructed through ionic cross-linking, and the physically and chemically cross-linked dual network structure was prepared by in situ polymerization of the polymerizable deep eutectic solvent (PDES) therein. The homogeneous three-dimensional cross-linked network provides a site for energy dissipation and ionic migration. Results show that the elastomers retain good transparency and achieve significantly improved mechanical strength, toughness and ionic conductivity. Therefore, they can be applied as multi-functional sensors and triboelectric nanogenerators (TENG). For the optimized TENG, output voltage, current and charge reach 115 V, 6 μA, and 40 nC, respectively. A maximum output power density of 0.35 W/m2 is achieved, and the collected mechanical energy can light up LEDs and power an electronic clock. In addition, the elastomers maintain reliable performance even at low/high temperatures, enabling use in harsh environments. In conclusion, this study developed a promising strategy for the construction of sustainable liquid-free ionic conductors utilizing natural polysaccharides.

Mimosa plant leaf-inspired 180° foldable lithium-ion batteries with enhanced electrochemical-mechanical behaviors

Developing high-performance batteries with flexibility is crucial for flexible electronic applications. Although various types of flexible battery designs have been proposed in recent years to improve cycling performance and flexibilities, their application is limited in the most widely used flexible device, namely foldable screen smartphones, due to their inability of 180° folding. Here, inspired by the unique dynamic property of the mimosa plant leaf, we design a bio-inspired flexible lithium-ion battery (FLIB) containing thick energy-storage modules, analogous to the leaflets, and electrical contact part, analogous to the leaf stalk. This design resulted in a FLIB with high flexibility (180° folding and bending), cycling stability, and scalability. Notably, our FLIB demonstrated an improved cycling performance, even under harsh dynamic deformations (10,000-times dynamic 180° folding and 7500-times dynamic bending). The potential mechanisms of mechanical protection for the FLIB were investigated through finite element analysis, further proving its remarkable mechanical endurance. Therefore, our flexible battery design meets the demand of flexible devices for stable power supply under various deformation states. This work sheds new light on the structural innovations and practicality of flexible batteries for future applications.

Highly compressible porous polyethyleneimine/chitosan composite aerogel with excellent mechanical properties as wide detection range sensors for human motion monitoring

AbstractBiomass three‐dimensional composite aerogels have garnered significant attention in the realm of wearable electronic skin owing to their favorable properties, including excellent human compatibility, environmentally benign degradability, and continuous porous architecture. However, conventional biomass aerogels suffer from inadequate mechanical flexibility, susceptibility to irreversible deformation under high compressive stress, and limited reusability, thereby constraining their applicability in sensing technologies. To address these limitations, this study presents the development of porous CCS/KH560/PEI/CNT‐COOH (CKPC) composite aerogels through a freeze–drying process. Chemical crosslinking was achieved using silane coupling agent (KH560) with carboxymethyl chitosan (CCS) and polyethyleneimine (PEI), while carboxylated carbon nanotubes (CNT‐COOH) were incorporated as conductive fillers. This approach successfully overcame the issues of poor mechanical properties, low elasticity, and unbalanced sensitivity‐sensing range trade‐off in chitosan‐based aerogel sensors. The results revealed that the porous CKPC aerogels exhibited a remarkable mechanical compressive strain of 86.3% while maintaining structural integrity post‐unloading. The CKPC composite aerogel‐based sensor demonstrated a high sensitivity of 42.9 within a wide strain range of 60%–76.3%, accompanied by a stable and repeatable electrical signal response across varying strains. The porous structure of the CKPC conductive aerogel sensor holds promising applications in human motion monitoring and flexible electronics.

Optimizing optoelectronic properties and energy harvesting potential of Co-doped LaFeO3: A DFT-based investigation

In response to the growing demand for advanced optoelectronic materials, this comprehensive investigation explores the effects of Co substitution on LaFeO3 using density functional theory. The study provides novel insights into the mechanical and optical properties of the doped structures. Structural stability is assessed through structural optimization, elastic stability tests, and enthalpy of formation calculations. The doped compounds exhibit significant improvements in electronic and optical properties, including enhanced thermal conductivity and reflectivity. Band structure analysis reveals metallic attributes and the Moss-Burstein effect, while magnetic property assessments indicate a decrease in magnetic moment due to Fe-Co degeneracy resulting from higher Co content. Mechanical analysis of elastic moduli B, G, and Y demonstrates enhanced durability and strength with metal-like conductivity, attributed to reduced anharmonicity. The study also highlights increased bond flexibility, suggesting potential applications in flexible electronics and UV light reflectors for effective shielding against photon radiation.

High‐Performance Zn2+‐Crosslinked MXene Fibers for Versatile Flexible Electronics

AbstractThe advent of flexible electronics has prompted the development of functional fibers with superior mechanical and electrical properties. MXenes, a novel family of 2D functional materials, have a variety of potential applications in flexible electronics. Herein, wet‐spinning is employed to continuously assemble Ti3C2Tx MXene liquid crystals into macroscopic fibers. Meanwhile, Zn2+ is introduced into the fiber to eliminate the electrostatic repulsion between the MXene nanosheets and enhance interlayer interactions and sheet alignment. The as‐obtained MXene fibers have strong mechanical strength (150.7 MPa), high electrical conductivity (3637.9 S cm−1), and good flexibility that facilitates weaving and knotting, making them suitable for fabric‐like flexible devices. The sound pressure sensors are woven from MXene fibers, which feature quick response time (286 ms) and recovery time (642 ms), ultra‐high sensitivity (280.2 kPa−1), and a low detection limit (0.1 Pa). Sound detection and recording are achieved using this sensor. MXene fibers as wearable thermal management devices are also demonstrated, exhibiting fast Joule thermal responses and good cycling stability.

Conductive Inks with Chemically Sintered Silver Nanoparticles at Room Temperature for Printable, Flexible Electronic Applications

Conductive inks composed of chemically sintered silver (Ag) nanoparticles were prepared. The enlargement of particle size was accompanied by the increase in conductivity of the Ag nanoparticle ink. The resistance of the as-prepared and sintered Ag nanoparticles printed on different substrates was measured, and results showed that the formulated conductive ink works best on glossy paper. This is due to the compatibility of the conductive ink with the porosity and surface roughness of the glossy paper. The conductive ink formulation was also used as printer ink, and results showed a decrease in resistance as the printing pass was increased.

Temperature-Tolerant Versatile Conductive Zwitterionic Nanocomposite Organohydrogel toward Multisensory Applications.

Conductive hydrogels (CHs) are emerging materials for next generation sensing systems in flexible electronics. However, the fabrication of competent CHs with excellent stretchability, adhesion, self-healing, photothermal conversion, multisensing, and environmental stability remains a huge challenge. Herein, a nanocomposite organohydrogel with the above features is constructed by in situ copolymerization of zwitterionic monomer and acrylamide in the existence of carboxylic cellulose nanofiber-carrying reduced graphene oxide (rGO) plus a solvent displacement strategy. The synergy of abundant dipole-dipole interactions and intermolecular hydrogen bonds enables the organohydrogel to exhibit high stretchability, strong adhesion, and good self-healing. The presence of glycerol weakens the formation of hydrogen bonds between water molecules, endowing the organohydrogel with excellent environmental stability (-40 to 60 °C) to adapt to different application scenarios. Importantly, the multimodal organohydrogel presents excellent sensing behavior, including a high gauge factor of 16.3 at strains of 400-1440% and a reliable thermal coefficient of resistance (-4.2 °C-1) over a wide temperature widow (-40 to 60 °C). Moreover, the organohydrogel displays a highly efficient and reliable photothermal conversion ability due to the favorable optical absorbing behavior of rGO. Notably, the organohydrogel can detect accurate human activities at ambient temperature, demonstrating potential applications in flexible intelligent electronics.

Structural design and simulation of PDMS/SiC functionally graded substrates for applications in flexible hybrid electronics

Structural design and simulation of PDMS/SiC functionally graded substrates for applications in flexible hybrid electronics

Ultrahigh Energy Storage Performance of BiFeO3-BaTiO3 Flexible Film Capacitor with High-Temperature Stability via Defect Design.

Nanoengineering polar oxide films have attracted great attention in energy storage due to their high energy density. However, most of them are deposited on thick and rigid substrates, which is not conducive to the integration of capacitors and applications in flexible electronics. Here, an alternative strategy using van der Waals epitaxial oxide dielectrics on ultra-thin flexible mica substrates is developed and increased the disorder within the system through high laser flux. The introduction of defects can efficiently weaken or destroy the long-range ferroelectric ordering, ultimately leading to the emergence of a large numbers of weak-coupling regions. Such polarization configuration ensures fast polarization response and significantly improves energy storage characteristics. A flexible BiFeO3-BaTiO3 (BF-BT) capacitor exhibits a total energy density of 43.5 J cm-3 and an efficiency of 66.7% and maintains good energy storage performance over a wide temperature range (20-200 °C) and under large bending deformation (bending radii ≈ 2mm). This study provides a feasible approach to improve the energy storage characteristics of dielectric oxide films and paves the way for their practical application in high-energy density capacitors.

Freeze–Thaw-Induced, Metal Ion Cross-Linked, Mechanically Robust, and Highly Stretchable Composite Poly(vinyl alcohol) Hydrogels for Flexible Electronic Applications

Freeze–Thaw-Induced, Metal Ion Cross-Linked, Mechanically Robust, and Highly Stretchable Composite Poly(vinyl alcohol) Hydrogels for Flexible Electronic Applications

Electronic, Transport, and Optical Properties of Potential Transparent Conductive Material Rb2Pb2O3

To better verify the potential of Rb2Pb2O3 as p‐type transparent conductive oxides (TCOs), the structural, electronic, mechanical, transport, and optical properties of Rb2Pb2O3 are calculated in detail under the framework of density functional theory. Significantly, Rb2Pb2O3 is a p‐type semiconductor with an indirect 2.82 eV bandgap. Herein, the Pb‐6p and O‐2p orbits hybridized to form ionic PbO bonds, which determines the degree of localization of electrons in valence band maximum. Interestingly, the RbO bond is extremely weak, and the Rb atom is rarely involved in bonding interactions. This contributes to isotropy, ductility, and good mobility of Rb2Pb2O3, making it soft and suitable for application in flexible electronics. More importantly, as a transparent conductive material, Rb2Pb2O3 not only shows good transparency in the visible region but also has good electrical conductivity. Therefore, Rb2Pb2O3 as an intrinsic p‐TCO with good performance is preliminarily identified. The theoretical finding provides a new candidate for p‐TCOs and paves the way for further performance improvement of Rb2Pb2O3.

Enhanced Thermoelectric Properties of Exfoliated BN Nanosheets/Single-Walled Carbon Nanotube Composite Films for Applications in Flexible Electronics

Enhanced Thermoelectric Properties of Exfoliated BN Nanosheets/Single-Walled Carbon Nanotube Composite Films for Applications in Flexible Electronics

3D printed auxetic metamaterials with tunable mechanical properties and morphological fitting abilities

Research on creating special structures with a negative Poisson’s ratio, known as auxetic metamaterials, is widely conducted for potential applications in flexible electronics, aerospace, biomedicine, and other fields. Auxiticity is the phenomenon of transverse expansion that occurs when stretched longitudinally. However, conventional metamaterial tunable properties have certain limitations, mainly in the form of limited Poisson’s ratio tuning range and transverse deformation. In this work, a series of symmetric antichiral auxetic structures with significant auxetic effect and low Poisson’s ratio of −5 are designed and fabricated by 3D printing. Based on the manipulating of unit parameters and the use of shape memory polymers, the auxetic metamaterials exhibit tunable mechanical properties and programmable shape memory behaviors. Owing to these features, the auxetic metamaterials are demonstrated to achieve excellent shape-fitting and size-fitting capabilities, which are followed by expanding in a full range to contact any objects (due to auxiticity) and then contract to conform their shapes (due to shape memory). By integrating flexible electromyography(EMG) electrodes, the shape memory auxetic metamaterials can be used as self-adaptive wearable devices to fit with human limbs, which can ensure the good attachment, high signal to Noise Ratio (SNR), and breathability when collect EMG signals.

MXene-based all-solid flexible electrochromic microsupercapacitor

With the increasing demand for multifunctional optoelectronic devices, flexible electrochromic energy storage devices are being widely recognized as promising platforms for diverse applications. However, simultaneously achieving high capacitance, fast color switching and large optical modulation range is very challenging. In this study, the MXene-based flexible in-plane microsupercapacitor was fabricated via a mask-assisted spray coating approach. By adding electrochromic ethyl viologen dibromide (EVB) into the electrolyte, the device showed a reversible color change during the charge/discharge process. Due to the high electronic conductivity of the MXene flakes and the fast response kinetics of EVB, the device exhibited a fast coloration/bleaching time of 2.6 s/2.5 s, a large optical contrast of 60%, and exceptional coloration efficiency. In addition, EVB acted as a redox additive to reinforce the energy storage performance; as a result, the working voltage window of the Ti3C2-based symmetric aqueous microsupercapacitor was extended to 1 V. Moreover, the device had a high areal capacitance of 12.5 mF cm−2 with superior flexibility and mechanical stability and showed almost 100% capacitance retention after 100 bending cycles. The as-prepared device has significant potential for a wide range of applications in flexible and wearable electronics, particularly in the fields of camouflage, anticounterfeiting, and displays.

Wide-humidity, anti-freezing and stretchable multifunctional conductive carboxymethyl cellulose-based hydrogels for flexible wearable strain sensors and arrays

Hydrogels play an important role in the design and fabrication of wearable sensors with outstanding flexibility, high sensitivity and versatility. Since hydrogels lose and absorb water during changes in humidity and temperature, it is critical and challenging to obtain hydrogels that function properly under different environmental conditions. Herein, a dual network hydrogel based on tannic acid (TA) reinforced polyacrylamide (PAM) and sodium carboxymethylcellulose (CMC) was constructed, while the introduction of the green solvents Solketal and LiCl endowed the hydrogel with greater possibilities for further modification to improve the water content and consistency of the mechanical properties over 30–90 % RH. This composite hydrogel (PTSL) has long-term stability, excellent mechanical strength, and freezing resistance. As strain sensors, they are linear over the entire strain range (R2 = 0.994) and have a high sensitivity (GF = 2.52 over 0–680 % strain range). Furthermore, the hydrogel's exceptional electrical conductivity and freezing resistance are a result of the synergistic effect of Solketal and LiCl, which intensifies the contact between the water molecules and the colloidal phase. This research could address the suitability of hydrogels over a wide range of humidity and temperature, suggesting great applications for smart flexible wearable electronics in harsh environmental conditions.

Highly conductive, rapid self-healing, and anti-freezing poly(3,4-ethylenedioxythiophene)/lignosulfonate-cationic guar gum ionogels for multifunctional sensors

Soft ionic conductors exhibit immense potential for applications in soft ionotronics, including ionic skin, human–machine interface, and soft luminescent device. Nevertheless, the majority of ionogel-based soft ionic conductors are plagued by issues such as freezing, evaporation, liquid leakage, and inadequate self-healing capabilities, thereby constraining their usability in complex environments. In this study, we present a novel strategy for fabricating conductive ionogels through the proportionally mixing cationic guar gum (CGG), water, 1-butyl-3-methylimidazolium chloride (BmimCl)/glycerol eutectic-based ionic liquid, and poly(3,4-ethylenedioxythiophene)/lignosulfonate (PEDOT/LS). The resultant benefits from strong hydrogen bonding and electrostatic interactions among its constituents, endowing it with an ultrafast self-healing capability (merely 30 s) while sustaining high electrical conductivity (~16.5 mS cm−1). Moreover, it demonstrates exceptional water retention (62 % over 10 days), wide temperature tolerance (−20 to 60 °C), and injectability. A wearable sensor fabricated from this ionogel displayed remarkable sensitivity (gauge factor = 17.75) and a rapid response to variations in strain, pressure, and temperature, coupled with both long-term stability and wide working temperature range. These attributes underscore its potential for applications in healthcare devices and flexible electronics.

Enhanced n-Type Thermoelectric Properties and Structure Evolution of Carbonized Metal-Coordination Polydopamine.

Carbonized polydopamine (cPDA) exhibits a nitrogenous graphite-like structure with n-type semiconductor property. However, the low electrical conductivity and Seebeck coefficient of cPDA cannot meet the needs of flexible thermoelectric devices. In this study, a series of metal ions were coordinated with cPDA to enhance n-type thermoelectric properties. At 300 K, all metal-coordination cPDA (metal-cPDA) samples obtain lower thermal conductivity compared to cPDA. Mn-cPDA exhibits the greatest Seebeck coefficient of -25.94 μV K-1, which is almost six times higher than cPDA. Fe-cPDA shows the best electrical conductivity of 2.45 × 105 S m-1. An optimal power factor (PF) value of 11.93 μW m-1 K-2 is achieved in Ca-cPDA with the enhanced electrical conductivity of 9.5 × 104 S m-1 and Seebeck coefficient of -11.24 μV K-1. Using Fourier transform infrared spectroscopy (FTIR), energy dispersive X-ray spectroscopy (EDX), X-ray photoelectron spectroscopy (XPS), Raman spectroscopy, X-ray diffraction (XRD), and transmission electron microscopy (TEM), we revealed the structural characterization of metal-cPDA. Our results indictate that the different metal ions (Mn2+, Zn2+, Mg2+, Al3+, Ca2+, and Fe3+) exert varying influences on the growth of graphite-like structure within metal-cPDA, which lead to the evolution of electrical conductivity. We observe that the carrier density and carrier mobility depend on both the degree of graphitization and the metal-ion coordination, which work together on electrical conductivity and Seebeck coefficient. These findings and understanding of the thermoelectric properties of PDA-based materials will help to realize high-performance n-type thermoelectric materials for flexible electronic device applications.

Multifunctional Conductive Hydrogel Interface for Bioelectronic Recording and Stimulation.

The past few decades have witnessed the rapid advancement and broad applications of flexible bioelectronics, in wearable and implantable electronics, brain-computer interfaces, neural science and technology, clinical diagnosis, treatment, etc. It is noteworthy that soft and elastic conductive hydrogels, owing to their multiple similarities with biological tissues in terms of mechanics, electronics, water-rich, and biological functions, have successfully bridged the gap between rigid electronics and soft biology. Multifunctional hydrogel bioelectronics, emerging as a new generation of promising material candidates, have authentically established highly compatible and reliable, high-quality bioelectronic interfaces, particularly in bioelectronic recording and stimulation. This review summarizes the material basis and design principles involved in constructing hydrogel bioelectronic interfaces, and systematically discusses the fundamental mechanism and unique advantages in bioelectrical interfacing with the biological surface. Furthermore, an overview of the state-of-the-art manufacturing strategies for hydrogel bioelectronic interfaces with enhanced biocompatibility and integration with the biological system is presented. This review finally exemplifies the unprecedented advancement and impetus toward bioelectronic recording and stimulation, especially in implantable and integrated hydrogel bioelectronic systems, and concludes with a perspective expectation for hydrogel bioelectronics in clinical and biomedical applications.

Mechanically robust and electrically conductive nanofiber composites with enhanced interfacial interaction for strain sensing

Electrically conductive fiberfibre/fabric composites (ECFCs) are competitive candidates for use in wearable electronics. Therefore, it is essential to develop mechanically robust ECFC strain sensors with sensing performance. In this study, MXene assembly and hot-pressing were combined to prepare strong yet breathable ECFCs for strain and temperature sensing. Hydrogen bonding between MXene and polyurethane (PU) and ultrasonication-induced interfacial sintering were responsible for MXene nanosheets assembly on the PU nanofibers. MXene decoration made PU nanofibers electrically conductive, resulting in a conductive network. Hot-pressing improved interface adhesion among the conductive nanofibers. Thus, the mechanical properties of the nanofiber composites, including tensile strength, toughness and fracture energy, were enhanced. The nanofiber composites exhibited surface stability and durability. When the nanofiber composites were used as strain sensors, they showed breathability with a linear resistance response ranging from 1 % to 100 % and cycling stability. In addition, they produced stable sensing signals over 1000 cycles when a notch was present. They could also monitor temperature variations with a negative temperature coefficient (−0.146 %/°C). This study provides an interfacial regulation method for the preparation of multi-functional nanofiber composites with potential applications in flexible and wearable electronics.

Self-healing and reprocessable biobased non-isocyanate polyurethane elastomer with dual dynamic covalent adaptive network for flexible strain sensor

Owing to the nontoxicity of monomers, non-isocyanate polyurethane elastomers have attracted considerable attention, yet the synthesis and functionalization are still challenging. Herein, self-healing and reprocessable biobased non-isocyanate polyurethane (NIPU) elastomers with dual dynamic covalent adaptive network (DDCAN) by disulfide bonds and dynamic imine bonds were synthesized as substrate for the construction of flexible strain sensor with MXene as conductive substance. The tensile strength and elongation at break of the NIPU elastomer were 3.22 MPa and 234 %, respectively. Thanks to the formation of DDCAN, the NIPU elastomer showed high healing efficiency of 97.5 % after healing at room temperature for 24 h. Interestingly, the NIPU elastomer possessed superior reprocessing capability and the tensile strength after three reprocessing cycles reached 136.1 % of the original one, which was attributed to the increase of crosslinking points caused by topological rearrangement. In addition, the NIPU elastomer-based flexible strain sensor exhibited fast response (response time = 60 ms) and excellent repeatability (1000 bending-releasing cycles) and was successfully applied for human motion detection and speech recognition. The findings in this work conceivably stand out as a new methodology for the preparation of biobased and functional elastomers, which will greatly promote the sustainable development and application of flexible electronics.