Conductive Network Research Articles

In Situ Synthesis of CoMoO4 Microsphere@rGO as a Matrix for High-Performance Li-S Batteries at Room and Low Temperatures

Lithium–sulfur batteries (Li-S batteries) have attracted wide attention due to their high theoretical energy density and the low cost of sulfur cathode material. However, the poor conductivity of the sulfur cathode, the polysulfide shuttle effect, and the slow redox kinetics severely affect their cycling performance and Coulombic efficiencies, especially under low-temperature conditions, where these effects are more exacerbated. To address these issues, this study designs and synthesizes a microspherical cobalt molybdate@reduced graphene oxide (CoMoO4@rGO) composite material as the cathode material for Li-S batteries. By growing CoMoO4 nanoparticles on the rGO surface, the composite material not only provides a good conductive network but also significantly enhances the adsorption capacity to polysulfides, effectively suppressing the shuttle effect. After 100 cycles at room temperature with a current density of 1 C, the reversible specific capacity of the battery stabilizes at 805 mAh g−1. Notably, at −20 °C, the S/CoMoO4@rGO composite achieves a reversible specific capacity of 840 mAh g−1. This study demonstrates that the CoMoO4@rGO composite has significant advantages in suppressing polysulfide diffusion and expanding the working temperature range of Li-S batteries, showing great potential for applications in next-generation high-performance Li-S batteries.

Multilayer Bionic Tunable Strain Sensor with Mutually Non‐Interfering Conductive Networks for Machine Learning‐Assisted Gesture Recognition

AbstractFlexible strain sensors capable of acquiring tiny mechanical signals and attaching to various irregular surfaces are becoming prevalent in physiological measurement, soft robotics, and human‐machine interaction. However, the advancement of flexible strain sensors is substantially impeded by the intrinsic compromise between sensitivity and the range of detectable signals. Inspired by the multilayer structure of nacre in nature, a carbon nanotubes (CNTs)/graphene (GR)/graphene (GR)/thermoplastic polyurethane (TPU) mat (CGGTM) is prepared by electrospinning and high‐pressure spraying technology. By designing a multilayer structure with mutually non‐interfering conductive networks, the resulting CGGTM possesses a low detection limit (0.05% strain), high sensitivity (gauge factor, GF > 152537), large detection range (up to 364% strain), fast response/recovery time (80 ms/100 ms), and excellent cyclic durability (up to 1000 cycles). Furthermore, the CGGTM also exhibits satisfactory triboelectric performances when assembled into a triboelectric nanogenerator (TENG, 3 × 3 cm2), including high triboelectric output (open‐circuit voltage Voc = 135.4 V, short‐circuit current Isc = 1.25 µA) and power density (88 mW m−2), enabling reliable power supply, self‐powered sensing, and pulse monitoring capability. Finally, CGGTM is successfully applied to the collection of biological signals and multi‐gesture motion recognition assisted by machine learning algorithms, which holds promise for intelligent interaction with gestures in the future.

Long‐Life All‐Solid‐State Batteries Enabled by Cold‐Pressed Garnet Composite Electrolytes with Enhanced Li+ Conduction

AbstractGarnet Li7La3Zr2O12 (LLZO)‐based solid‐state electrolytes (SSEs) hold promise for realizing next‐generation lithium metal batteries with high energy density. However, the high stiffness of high‐temperature sintered LLZO makes it brittle and susceptible to strain during the fabrication of solid‐state batteries. Cold‐pressed LLZO exhibits improved ductility but suffers from insufficient Li+ conductivity. Here, we report cold‐pressed Ta‐doped LLZO (Ta−LZ) particles integrated with ductile Li6PS5Cl (LPSC) via a Li+ conductive Li‐containing Ta−Cl structure. This configuration creates a continuous Li+ conduction network by enhancing the Li+ exchange at the Ta−LZ/LPSC interface. The resulting Ta−LZ/LPSC SSE exhibits Li+ conductivity of 4.42×10−4 S cm−1 and a low activation energy of 0.31 eV. Li symmetric cells with Ta−LZ/LPSC SSE demonstrate excellent Li dendrite suppression ability, with an improved critical current density of 5.0 mA cm−2 and a prolonged cycle life exceeding 600 h at 1 mA cm−2. Our finding provides valuable insights into developing cold‐pressed ceramic powder electrolytes for high‐performance all‐solid‐state batteries.

Advanced Flexible Wearable Electronics from Hybrid Nanocomposites Based on Cellulose Nanofibers, PEDOT:PSS and Reduced Graphene Oxide

The need for responsible electronics is leading to great interest in the development of new bio-based devices that are environmentally friendly. This work presents a simple and efficient process for the creation of conductive nanocomposites using renewable materials such as cellulose nanofibers (CNF) from enzymatic pretreatment, poly(3,4-ethylenedioxythiophene)-poly(styrenesulfonate) (PEDOT:PSS), and/or reduced graphene oxide (rGO). Different combinations of CNF, rGo, and PEDOT:PSS were considered to generate homogeneous binary and ternary nanocomposite formulations. These formulations were characterized through SEM, Raman spectroscopy, mechanical, electrical, and electrochemical analysis. The binary formulation containing 40 wt% of PEDOT:PSS resulted in nanocomposite formulations with tensile strength, Young’s modulus, and a conductivity of 70.39 MPa, 3.87 GPa, and 0.35 S/cm, respectively. The binary formulation with 15 wt% of rGO reached 86.19 MPa, 4.41 GPa, and 13.88 S/cm of the same respective properties. A synergy effect was observed for the ternary formulations between both conductive elements; these nanocomposite formulations reached 42.11 S/cm of conductivity and kept their strength as nanocomposites. The 3D design strategy provided a highly conductive network maintaining the structural integrity of CNF, which generated homogenous nanocomposites with rGO and PEDOT:PSS. These formulations can be considered as greatly promising for the next generation of low-cost, eco-friendly, and energy storage devices, such as batteries or electrochemical capacitors.

3D printer fabrication of boron doped Cu-MWCNT/PLA electrodes: Investigation of its efficiency in electrocatalytic hydrogen production

In this study, three-dimensional (3D) electrodes based on MWCNT-Cu/PLA with high electrocatalytic efficiency, large surface area and different amounts of nano‑boron doped MWCNT-Cu/PLA were fabricated using Fused Granular Fabrication (FGF) method with a 3D printer. When FE-SEM images are examined, MWCNT fibers and copper particles are seen more clearly on the surface due to the formation of more dense conductive networks between the conductive carbon fibers trapped in the PLA structure due to the increasing amount of boron. When XRD results are examined, it is observed that the characteristic peaks belonging to the face-centered cubic structure of Cu are dominant and the crystal size increases as MWCNT addition and boron doping increase. When Raman spectra were analyzed to investigate the internal structural changes of MWCNTs, three characteristic bands corresponding to the D band (defect), G band (graphite band) and G' band (D overtone) of MWCNTs were determined and it was observed that the ID/IG ratio decreased with increasing boron doping compared to MWCNT-Cu/PLA electrode. The B1s spectrum of the 3D 0.8B@MWCNT-Cu/PLA electrode confirmed the presence of boron with the peak corresponding to B@C bonds at 191.2 eV. The obtained 3D electrocatalysts were used as cathodes in an electrolysis cell in aqueous solution containing 1 M KOH and their catalytic efficiency in hydrogen evolution reaction (HER) was tested. In order to increase the activity of the 3D electrodes, unlike the literature, they were activated by electrochemical activation process without using organic solvent and HER measurements of the activated electrodes were performed. Before activation, the charge transfer resistance (Rct) value of the Cu/PLA electrode, which was 6219.00 Ω cm−2, decreased to 681.90 Ω cm−2 after 5 % MWCNT doping. It is seen that with boron doping, a greater decrease in Rct value is realized, reaching values of 66.50–74.56 Ω cm−2. The cathodic Tafel slopes show that the Volmer reaction is the rate-determining step for HER and the rate-determining step is the electrochemical adsorption of hydrogen on the metal surface. In addition, energy efficiency tests of the 3D electrodes in HER were also performed and electrochemically active surface areas were determined. Thus, this study has taken an important step toward using 3D electrocatalysts, which are produced with more cost and more flexible designs, unlike previous production techniques, for hydrogen energy production.

Novel Structures for PV Solar Cells: Fabrication of Cu/Cu2S-MWCNTs 1D-Hybrid Nanocomposite

The production of cost-effective novel materials for PV solar cells with long-term stability, high energy conversion efficiency, enhanced photon absorption, and easy electron transport has stimulated great interest in the research community over the last decades. In the presented work, Cu/Cu2S-MWCNTs nanocomposites were produced and analyzed in the framework of potential applications for PV solar cells. Firstly, the surface of the produced one-dimensional Cu was covered by Cu2S nanoflake. XRD data prove the formation of both Cu and Cu2S structures. The length and diameter of the one-dimensional Cu wire were 5–15 µm and 80–200 nm, respectively. The thickness of the Cu2S nanoflake layer on the surface of the Cu was up to 100 nm. In addition, the Cu/Cu2S system was enriched with MWCNTs. MWCNs with a diameter of 50 nm interact by forming a conductive network around the Cu/Cu2S system and facilitate quick electron transport. Raman spectra also prove good interfacial coupling between the Cu/Cu2S system and MWCNTs, which is crucial for charge separation and electron transfer in PV solar cells. Furthermore, UV studies show that Cu/Cu2S-MWCNTs nanocomposites have a wide absorption band. Thus, MWCNTs, Cu, and Cu2S exhibit an intense absorption spectrum at 260 nm, 590 nm, and 972 nm, respectively. With a broad absorption band spanning the visible–infrared spectrum, the Cu/Cu2S-MWCNTs combination can significantly boost PV solar cells’ power conversion efficiency. Furthermore, UV research demonstrates that the plasmonic character of the material is altered fundamentally when CuS covers the Cu surface. Additionally, MWCN-Cu/Cu2S nanocomposite exhibits hybrid plasmonic phenomena. The bandgap of Cu/Cu2S NWs was found to be approximately 1.3 eV. Regarding electron transfer and electromagnetic radiation absorption, the collective oscillations in plasmonic metal-p-type semiconductor–conductor MWCNT contacts can thus greatly increase energy conversion efficiency. The Cu/Cu2S-MWCNTs nanocomposite is therefore a promising new material for PV solar cell application.

Stretchable conducting polymer PEDOT:PSS treated with hard‐cation‐soft‐anion ionic liquid designed from molecular modeling

AbstractPEDOT:PSS, an ionic polymer mixture of positively‐charged poly‐3,4‐ethylenedioxythiophene (PEDOT+) and negatively‐charged poly‐styrenesulfonate (PSS−), is a water‐processable and environmentally‐benign organic semiconductor and electrochemical transistor, which plays a key role in organic (bio)electronic devices. However, pristine PEDOT:PSS films form 10‐to‐30‐nm granular domains, where conducting‐but‐hydrophobic PEDOT‐rich cores are surrounded by hydrophilic‐but‐insulating PSS‐rich shells. Such morphology makes PEDOT:PSS water‐soluble and thermally stable but very poor in conductivity. A tremendous amount of effort has been made to enhance the conductivity of PEDOT:PSS by restoring the extended conduction network of PEDOT. Recently, remarkable ~5000‐fold improvements of conductivity have been achieved by mixing PEDOT:PSS with proper ionic liquids (ILs). In a series of free energy estimations using density functional theory calculation and molecular dynamics simulation, we have demonstrated that the classic hard‐soft acid–base (or cation‐anion) principle of chemistry plays an important role in such improvements. Ion exchange between PEDOT+:PSS− and A+:X− ILs helps PEDOT+ to decouple from PSS− and to grow into large‐scale conducting domains of π‐stacked PEDOT+ decorated by IL anions X−. Thus, the most spontaneous decoupling between soft (hydrophobic) PEDOT+ and hard (hydrophilic) PSS− would be induced by strong interaction with soft anions X− and hard cations A+, respectively. Such hard‐cation‐soft‐anion principles have led us to design ILs containing extremely hydrophilic (i.e., protic) cations and hydrophobic anions. Not only they indeed improve the conductivity of PEDOT:PSS but also enhance its stretchability as well. In summary, our modeling offered molecular‐level insights on the morphological, electrical, and mechanical properties of PEDOT:PSS and a molecular‐interaction‐based enhancement strategy for intrinsically stretchable conductive polymers.

Spatial‐Dependent Coupling of Electrochemistry, Mass Transport, and Stress in Silicon‐Graphite Composite Electrodes for Lithium‐Ion Batteries

AbstractThe commercialization of high‐capacity silicon materials in lithium‐ion batteries is hindered by significant volume changes. Composite anodes made from silicon and graphite, which increase battery capacity and maintain electrode structural stability, are receiving considerable attention. However, the spatial configuration of the active particles in the electrode is few investigated due to the complexity of experiments at the microscopic scale. Herein, this work focuses on electrochemical, mass transport, and stress coupling mechanisms by considering different spatial configurations of silicon and graphite. In situ electrochemical and stress measurements are first conducted to demonstrate the impact of the active material arrangement. Then, a 2D electrochemical‐mechanical model is developed considering the heterogeneity of electrochemical processes at the particle‐electrolyte interface. The results show that placing silicon in the upper active layer significantly reduces the ion transport resistance, while the graphite layer near the current collector provides a good conductive network for electron transport in the silicon layer, enhancing the performance of the composite electrode structure. By combining electrochemical and mechanical field models with experimental verification, this study deepens the understanding of composite electrode structure design, offering practical guidance for optimizing the spatial configuration of electrode materials to significantly improve battery performance.

Spherical NiS2/Ni17S18–C accelerates ion transport and enhances kinetics for lithium-sulfur battery host material

Transition metal sulfides exhibit notable catalytic activity and possess a high theoretical specific capacity as host materials in lithium-sulfur batteries. However, their restricted conductivity and sluggish Li+ transport hinder their broader application. In this research, we developed a Ni-based metal-organic framework (Ni-MOF) using nitrogen-containing benzimidazole and coupled it with a highly conductive carbon nanotube (CNT) to form NixSy (NiS2–Ni17S18)–C/CNT. The N-doped carbon skeleton derived from the MOF enhances the adsorption and chemical anchoring of polysulfides, while the even distribution of NiS2 and Ni17S18 enhances the redox reaction kinetics. Additionally, the conductive CNT networks aid in rapid electron transport, resulting in improved sulfur utilization. Consequently, the NixSy-C/CNT@S electrode demonstrates an impressive initial specific capacity of 1468 mAh g−1 at 0.2C and maintains 904.4 mAh g−1 after 200 cycles. Moreover, NixSy-C/CNT@S displays exceptional cycle stability, with a capacity retention of 76.20 % and a decay rate of only 0.05 % per cycle after 500 cycles at 0.5C. This study paves the way for the development and synthesis of cathode materials with outstanding electrochemical performance in LSBs.

Continuous Phase Separation Induced Tough Hydrogel Fibers with Ultrahigh Conductivity for Multidimensional Soft Electronics

AbstractConductive hydrogel fibers exhibit great potential in soft robots, bioelectronics, and human–machine interfaces due to the unique combination of electrical conductivity, high water content, tissue‐like mechanical properties, and 1D structure. Despite significant advances in hydrogel technologies, the typical conductive hydrogel fibers show low conductivity (<10 S cm−1), weak mechanical properties, and water stability, which makes it challenging to satisfy the requirements of practical applications. Here, a facile strategy is proposed to construct hydrogel fibers with ultrahigh conductivity and toughness by exploiting the synergistic effects of freezing‐thawing, salting‐out, and drying‐annealing. The continuous phase separation induced by the combined processes results in hierarchical structures, promoting the formation of interconnected conductive networks and increasing the fiber's crystallinity and crystal domain size. The prepared conductive hydrogel fibers exhibited ultrahigh conductivity (≈958 S cm−1), excellent mechanical properties (strength (≈6.2 MPa), stretchability (>300%), and toughness (≈10 MJ m−2)), high water content (≈75%), outstanding water stability, and fatigue resistance properties. In addition, the processibility of conductive hydrogel yarns and fabrics are demonstrated and their potential application in bioelectronics. Overall, this work presents a preparation strategy for conductive hydrogel fibers, which will facilitate the advancement of soft electronics and may inspire structural construction in other polymers.

Highly sensitive and stretchable CB/GNPs-TPU strain sensor with porous microstructure for multifunctional strain sensing

Multifunctional flexible strain sensors have garnered significant attention in recent years, particularly in the fields of smart wearable devices and human health monitoring. However, the trade-off between high sensitivity and a wide strain range limits their practical applications. This study presents a porous TPU/CB framework prepared using a water vapor-induced phase separation method, which can deform like a spring when stretched, thereby providing the sensor with a greater strain range. The graphene nanoplatelets (GNPs) were subsequently incorporated into the pores of the porous framework through ultrasonic treatment, which enhanced the sensor's sensitivity while preventing increased brittleness caused by the aggregation of conductive fillers. This structure establishes a stable conductive network, enabling the sensor to achieve high sensitivity (GF = 5902.4) across a wide strain range (327 %) while also demonstrating excellent stability and durability (over 7000 stretching/releasing cycles). The sensor can detect not only simple limb movements, such as bending of the arms and knees but also subtle muscle activities, including facial expressions and throat vocalization, thus bringing excellent human-computer interaction experience. These remarkable features position the sensor for promising applications in smart wearables and human health monitoring.

Strain Sensing Enhancement of 3D-printed Polyurethane through Surface Deposition of Carbon Black

Strain sensors for wearable electronics function by identifying mechanical deformations and translating into electrical signals. For optimal performance, electrical conductivity, electrical sensitivity, and flexibility are major properties of strain sensors. Polyurethane (PU) shows promise for custom strain sensors due to its high flexibility. Additionally, using digital light processing (DLP) 3D printing to shape PU is suitable for detecting body movements. Therefore, the aim of this study is developing 3D-printed PU to strain sensing devices, utilizing the surface coating method on 3D-printed PU with carbon black (CB) and polydimethylsiloxane (PDMS) to fabricate the (PDMS+CB)/CB/PU strain sensor. The conductive network of CB enhances sensitivity, while PDMS is incorporated to act as an adhesive for the durability of CB on the PU surface. The results of the experiment reveal a gauge factor of 6.04 with range from 1 to 10% elongation. The strain sensor of this study has high potential to use for strain sensing technology and is capable of detecting small body movements.

Vacuum Filtration-Coated Silver Electrodes Coupled with Stacked Conductive Multi-Walled Carbon Nanotubes/Mulberry Paper Sensing Layers for a Highly Sensitive and Wide-Range Flexible Pressure Sensor

Flexible pressure sensors based on paper have attracted considerable attention owing to their good performance, low cost, and environmental friendliness. However, effectively expanding the detection range of paper-based sensors with high sensitivities is still a challenge. Herein, we present a paper-based resistive pressure sensor with a sandwich structure consisting of two electrodes and three sensing layers. The silver nanowires were dispersed deposited on a filter paper substrate using the vacuum filtration coating method to prepare the electrode. And the sensing layer was fabricated by coating carbon nanotubes onto a mulberry paper substrate. Waterborne polyurethane was introduced in the process of preparing the sensing layers to enhance the strength of the interface between the carbon nanotubes and the mulberry paper substrate. Therefore, the designed sensor exhibits a good sensing performance by virtue of the rational structure design and proper material selection. Specifically, the rough surfaces of the sensing layers, porous conductive network of silver nanowires on the electrodes, and the multilayer stacked structure of the sensor collaboratively increase the change in the surface contact area under a pressure load, which improves the sensitivity and extends the sensing range simultaneously. Consequently, the designed sensor exhibits a high sensitivity (up to 6.26 kPa−1), wide measurement range (1000 kPa), low detection limit (~1 Pa), and excellent stability (1000 cycles). All these advantages guarantee that the sensor has potential for applications in smart wearable devices and the Internet of Things.

Using multi‐component carbon composite as current collector in ultra‐battery

AbstractThis study introduces a multi‐component composite as a substitute for lead grids in ultra‐battery structures. The presented composite decreases the weight and simultaneously extends the cycle life of the traditional lead‐acid battery. Overall, UBZCP (the sample containing metal oxides and polyaniline), as the best sample, increases the cyclic stability by 3.3 and 1.4 times under high rate partial state of charge (HRPSoC) mode, compared to Native and UB450 samples. Metal oxides predominantly enhance the electrical conductivity of carbon‐based composites due to catalytic effects in the reduction of graphene oxide during heat treatment. Poly aniline shows considerably positive effect of electrochemical performance due to the high pseudo‐capacitive properties, high interaction of lead ions and the nitrogen in the polymer chains and accordingly hydrogen evolution reaction (HER) inhibition. The synergistic effect of polyaniline and metal oxides makes the best performance in the UBZCP sample achieve. Also, the UBZCP sample represented an enhancement of about 1.21 and 1.39 times in battery life and specific capacity under deep discharge mode compared to the Native sample. As a result, the introduced multi‐component composite making a 3D conductive network, facilitates Pb/PbSO4 reaction reversibility, and reduces the lead sulfate crystal size.

A Facile Method in Fabricating Flexible Conductive Composites with Large-Size Segregated Structures for Electromagnetic Interference Shielding.

To resist the plastic deformation of polymer particles during hot press molding, high molecular weights, and moduli are required for composites with segregated structures, thus the prepared composites exhibit poor flexibility. Also, larger particle sizes can bring lower percolation thresholds while the ensuing greater deformation destroys the conductive network. Moreover, segregated composites still face preparation complexities. Herein, a facile method for developing flexible composites with large-size segregated structures is proposed. First, silver-coated polydopamine-modified reduced graphene oxide (Ag@PrGO), as conductive fillers, is prepared by electroless plating. Next, polydimethylsiloxane (PDMS)-coated polyolefin elastomer (POE) beads are put into a bag containing the fillers. After a simple shaking, the fillers are adhered to the POE surface as the cohesive property of cured PDMS. Finally, flexible composites with large-size segregated structures are obtained via hot pressing. Benefiting from the 2D structure of the Ag@PrGO and the ability to slip, the conductive networks possess adaptable deformability. The prepared composites exhibit excellent electrical conductivity (203.55 Scm-1) at filler volume fractions of 3.4 vol%. The EMI shielding effectiveness can reach 70dB in the X-band at a thickness of 1.9mm and remains stable after bending and rubbing damage. This work paves the way for constructing large-size segregated structures.

Hierarchical structure Fe@CNFs@Co/C elastic aerogels with intelligent electromagnetic wave absorption

AbstractDeveloping intelligent electromagnetic wave (EMW) absorption materials with real‐time response‐ability is of great significance in complex application environments. Herein, highly compressible Fe@CNFs@Co/C elastic aerogels were assembled through the electrospinning method, achieving EMW absorption through pressure changes. By varying the pressure, the effective absorption bandwidth (EAB) of Fe@CNFs@Co/C elastic aerogels shows continuous changes from low frequency to high frequency. The EAB of Fe@CNFs@Co/C elastic aerogels is 14.4 GHz (3.36–17.76 GHz), which covers 90% of the range of S/C/X/Ku bands. The theoretical simulation indicates that the external pressure prompts a reduction in the spacing between the fiber layers in the aerogels and facilitates the formation of a 3D conductive network with enhanced attenuation ability of EMW. The uniform distribution of metal particles and appropriate layer spacing can effectively optimize the impedance matching to achieve the best EMW absorption performance. This work state clearly that the hierarchically assembled elastic aerogels composed of metal–organic frameworks (MOFs) derivatives and carbon fibers are ideal dynamic EMW absorption materials for intelligent EMW response.image

Triple‐structured polyvinylidene fluoride‐based composite films with high conductivity and EM shielding properties

AbstractFunctionalized thin films with excellent flexibility and conductivity can meet the current requirements for electromagnetic(EM) shielding materials. In this paper, 2D transitions metal carbide and nitride nanomaterials Ti3C2Tx MXene were prepared by chemical exfoliation, and PVDF/MWCNTs/3 wt%/RGO@Fe3O4@ AgNWs‐10 based on PVDF/MWCNTs‐3 wt%/RGO@Fe3O4@AgNWs‐10, The samples were prepared through a simple solution mixing process followed by vacuum‐assisted filtration (VAF), and PVDF/MWCNTs/MXene/RGO@Fe3O4@AgNWs three‐layer PVDF‐based composite films, which were analyzed for electrical conductivity and EM shielding properties, which increased and then decreased with the rise in the Ti3C2Tx MXene content, in which the highest electrical conductivity of the three‐layer composite films of M3/MX‐10/R@F@Ag was obtained when the Ti3C2Tx MXene addition amount reached 10 mL as 3.9 × 103 S/m, the EMI SET is 54.9 dB, the EMI SEA is 44.8 dB, the absorption loss is 81.6%, and the SSEt of the M3/MX‐10/R@F@Ag three‐layer composite film is the highest 1672.5 dB/(cm−2·g). And the SEA/SER ratios of the M3/MX‐X/R@F@Ag three‐layer composite films are all greater than 1. The result shows that the EM attenuation mechanism of the M3/MX‐X/R@F@Ag three‐layer composite films is primarily driven by absorption loss and that the incorporation of Ti3C2Tx Mxene improves the EM shielding performance of the composite films. The relatively novel exploration of the performance study and structural design of the M3/MX‐X/R@F@Ag three‐layer EM shielding composite film provides structural design and research ideas for the application of the new MXenes material in EM shielding composites.Highlights The addition of Ti3C2Tx MXene will generate more conductive network nodules A complete 3D conductive network is constructed in the membrane This paper discusses the influence of Ti3C2Tx MXene on EM shielding Multiple internal reflections of EMW between Ti3C2Tx MXene 2D nanosheets The EM shielding mechanism of the film is discussed from the angle of 3D

Biodegradable, Self‐Adhesive, Stretchable, Transparent, and Versatile Electronic Skins Based on Intrinsically Hydrophilic Poly(Caproactone‐Urethane) Elastomer

In biomedical sciences, there is a demand for electronic skins with highly sensitive tactile sensors that have applications in patient monitoring, human–machine interfaces, and on‐body sensors. Sensor fabrication requires high‐performance conductive surfaces that are transparent, breathable, flexible, and easy to fabricate. It is also preferable if the electrodes are easily processable as wastes, for example, are degradable. In this work, the design and fabrication of hydrophilic silanol/amine‐terminated poly(caprolactone‐urethane) (SA‐PCLU) elastomer‐based breathable, stretchable, and biodegradable electrodes are reported. Ag nanowires dispersed in water are sprayed onto the intrinsically hydrophilic electrospun SA‐PCLU that became embedded into the scaffold and formed conformal hydrophilic polyurethane‐based conductive networks (HPCN). The electrodes are used to fabricate capacitive, curvature, and strain sensors, all having monomaterial composition. In addition to displaying particularly good transparencies at low sheet resistances, stretchability, hydrophilicity, and tight and conformal bonding with the target surface, the electrodes also allow the evaporation of perspiration, making them suitable for epidermal sensors for long‐time use. The application of the HPCN electrodes in flexible electronics and bionic skin applications is demonstrated through gesture monitoring experiments and swelling sensors.

A Flexible Smart Healthcare Platform Conjugated with Artificial Epidermis Assembled by Three-Dimensionally Conductive MOF Network for Gas and Pressure Sensing

The rising flexible and intelligent electronics greatly facilitate the noninvasive and timely tracking of physiological information in telemedicine healthcare. Meticulously building bionic-sensitive moieties is vital for designing efficient electronic skin with advanced cognitive functionalities to pluralistically capture external stimuli. However, realistic mimesis, both in the skin’s three-dimensional interlocked hierarchical structures and synchronous encoding multistimuli information capacities, remains a challenging yet vital need for simplifying the design of flexible logic circuits. Herein, we construct an artificial epidermal device by in situ growing Cu3(HHTP)2 particles onto the hollow spherical Ti3C2Tx surface, aiming to concurrently emulate the spinous and granular layers of the skin’s epidermis. The bionic Ti3C2Tx@Cu3(HHTP)2 exhibits independent NO2 and pressure response, as well as novel functionalities such as acoustic signature perception and Morse code-encrypted message communication. Ultimately, a wearable alarming system with a mobile application terminal is self-developed by integrating the bimodular senor into flexible printed circuits. This system can assess risk factors related with asthmatic, such as stimulation of external NO2 gas, abnormal expiratory behavior and exertion degrees of fingers, achieving a recognition accuracy of 97.6% as assisted by a machine learning algorithm. Our work provides a feasible routine to develop intelligent multifunctional healthcare equipment for burgeoning transformative telemedicine diagnosis.

Multifunctional ANF/ CNT/FCIP aerogels with superior sound and electromagnetic wave absorption and mechanical properties

Aerogels exhibit bright prospect for multifunctional applications in noise reduction, radar stealth, load bearing, etc. Existing aerogels however suffer from poor sound absorption at low frequencies, narrow-band electromagnetic wave absorption and low structural strength. Here, we propose a novel lightweight aerogel composed of aromatic polyamide nanofiber (ANF)/ carbon nanotubes (CNT)/ flake carbonyl iron powder (FCIP) to boost acoustic/electromagnetic absorption and mechanical performance simultaneously. The FCIP additives create surface roughness and enlarge the pore size of the aerogel. As a result of the enhanced viscous energy dissipation by surface roughness and better impedance match achieved due to the enlarged pores, sound absorption at low frequency is significantly improved. Besides, the electrically and magnetically conductive network generated by embedded FCIP brings about effective electromagnetic absorption covering the whole X-band. Moreover, the aerogels undergo an increase in skeleton thickness and pore size by FCIP, resulting in maximum compressive stress increment. Our study provides clear guidance for the performance enhancement of aerogels that advances the development of aerogels for multifunctional applications.