Conductive Network Research Articles

Eco-Friendly Production of Boron Nitride Nanosheets via Deep Eutectic Solvents and Their Application in Enhancing Thermal Conductivity of PVDF Composites.

Boron nitride nanosheets (BNNS) are expected to be ideal fillers because of their high thermal conductivity and excellent electrical insulation. However, it is still an open challenge to produce BNNS on a large scale using ecofriendly solvents. Here, first, we demonstrate an effective liquid exfoliation method for producing BNNS via utilizing deep eutectic solvents (DES) composed of D,L-menthol and various acids with the assistance of ultrasonication. The results show that the BNNSs with sizes of 1-2 μm in width and 6-8 nm in thickness were successfully exfoliated with a DES formulation of D,L-menthol and decanoic acid. Second, the obtained BNNSs were used for fabricating 1,6-hexanediol diacrylate@polydopamine functionalized BNNS (HDDA@BNNSs-PDA) core-shell microspheres via a Pickering emulsion method. Furthermore, these microspheres were incorporated into a polyvinylidene fluoride (PVDF) matrix to construct 3D thermally conductive networks, leading to a substantial enhancement in the thermal conductivity of the resulting composites. Impressively, the composites with only 25 wt % of BNNS loading reach a high thermal conductivity of 3.20 W/m K, which is a 1500% increase over the pure polymer matrix. This work not only provides a significant way for producing BNNSs ecofriendly but also demonstrates a tactic for constructing 3D thermally conductive networks.

Highly conductive triple network hydrogel thermoelectrochemical cells with low-grade heat harvesting

Quasi-solid thermoelectrochemical cells (TECs) are promising candidates for wearable energy harvesting devices as they enable the continuous conversion of low-grade heat into electricity. However, the TEC performance remains limited by inadequate ionic conductivity. Herein, a triple-network hydrogel consisting of polyacrylamide/poly(vinyl alcohol)/cellulose nanofiber (PAAM/PVA/CNF) is synthesized via a freeze-thaw method, and soaked in the thermogalvanic redox couple Fe(CN)63−/4– as the electrolyte. By optimizing the polymer composition and soaking time, a superior ionic conductivity of 168 mS cm−1 is achieved while maintaining a thermopower of ∼1.69 mV K−1. The high ionic conductivity is provided by the fractal microstructure of the hydrogel, as revealed by small-angle X-ray scattering (SAXS). Moreover, the as-fabricated thermoelectric generator array exhibits an exceptional power output of 28.7 μW at a temperature difference of 11.9 K. This work provides insights on the development of wearable thermoelectric materials for practical and reliable energy harvesting applications.

Boosting the zinc storage performance of vanadium dioxide by integrated morphology engineering and carbon nanotube conductive networks

Boosting the zinc storage performance of vanadium dioxide by integrated morphology engineering and carbon nanotube conductive networks

Self-Adaptive Graphdiyne/Sn Interface for High-Performance Sodium Storage.

Efficiently reconciling the substantial volume strain with maintaining the stabilities of both interfacial protection and three-dimensional (3D) conductive networks is a scientific and technical challenge in developing tin-based anodes for sodium ion storage. To address this issue, a proof-of-concept self-adaptive protection for the Sn anode is designed, taking advantage of the arbitrary substrate growth of graphdiyne. This protective layer, employing a flexible chain doping strategy, combines the benefits of 2D graphdiyne and linear chain structures to achieve 2D mechanical stability, electronic and ion conductions, ion selectivity, adequate elongation, and flexibility. It establishes close contact with the Sn particles and can adapt to dynamic size changes while effectively facilitating both electronic and ion transports. It successfully mitigates the detrimental effects of particle pulverization and coarsening induced by large-volume changes. The as-obtained Sn electrodes demonstrate exceptional stability, enduring 1800 cycles at a high current density of 2.5 A g-1. This strategy promises to address the general issues associated with large-strain electrodes in next-generation of high-energy-density batteries.

Enhancing the electrochemical properties of TiNb2O7 anodes with SP-CNT binary conductive agents for both liquid and solid state lithium ion batteries.

A high performance oxide composite electrode is obtained with a two-step solid state calcined titanium niobium oxide TiNb2O7 (TNO) anode and super P-carbon nanotube (SP-CNT) binary conductive agents. The solid state synthesized TNO-0.2C (the proportion of CNTs in the binary conductive agent is 20% wt) anode exhibits a high reversible discharge capacity of 278.6 mA h g-1 at 0.5C, a competitive rate capability with reported works that employed wet chemical methods at moderate rates (178.1 mA h g-1 at 10C), and an excellent capacity retention of 92.2% after 200 cycles at 1.5C/1.5C. The enhancement in electrochemical properties of the TNO-0.2C anode is mainly attributed to the combination of the short range and long range conductive agents in the SP-CNT binary conductive system, which guarantees an efficient electronic conductive network. The Li|Li1.3Al0.3Ti1.7(PO4)3 composite polymer electrolyte (LATPCPEs)|TNO-0.2C solid state batteries are also assembled, which deliver a high initial reversible discharge capacity of 241.3 mA h g-1 at 1C and a good capacity retention rate of 93% after 50 cycles. This work provides an efficient way to improve the electrochemical properties of TNO anodes in lithium ion batteries, especially for solid state batteries.

Stabilizing the Bulk-Phase and Solid Electrolyte Interphase of Silicon Microparticle Anode by Constructing Gradient-Hierarchically Ordered Conductive Networks.

The poor bulk-phase and interphase stability, attributable to adverse internal stress, impede the cycling performance of silicon microparticles (µSi) anodes and the commercial application for high-energy-density lithium-ion batteries. In this work, a groundbreaking gradient-hierarchically ordered conductive (GHOC) network structure, ingeniously engineered to enhance the stability of both bulk-phase and the solid electrolyte interphase (SEI) configurations of µSi, is proposed. Within the GHOC network architecture, two-dimensional (2D) transition metal carbides (Ti3C2Tx) act as a conductive "brick", establishing a highly conductive inner layer on µSi, while the porous outer layer, composed of one-dimensional (1D) Tempo-oxidized cellulose nanofibers (TCNF) and polyacrylic acid (PAA) macromolecule, functions akin to structural "rebar" and "concrete", effectively preserves the tightly interconnected conductive framework through multiple bonding mechanisms, including covalent and hydrogen bonds. Additionally, Ti3C2Tx enhances the development of a LiF-enriched SEI. Consequently, the µSi-MTCNF-PAA anode presents a high discharge capacity of 1413.7 mAh g-1 even after 500 cycles at 1.0 C. Moreover, a full cell, integrating LiNi0.8Mn0.1Co0.1O2 with µSi-MTCNF-PAA, exhibits a capacity retention rate of 92.0% following 50 cycles. This GHOC network structure can offer an efficacious pathway for stabilizing both the bulk-phase and interphase structure of anode materials with high volumetric strain.

Strain‐Tolerant Nanocomposite Conductors with Engineered Bicontinuous Phase System by Additive Liquid/Solid Assembly

AbstractIntrinsically stretchable conductors are vital components in next‐generation flexible electronics. However, solid conductive networks are generally vulnerable to external deformations due to their incompatible mechanical properties with the highly elastic substrates or matrixes. It is still challenging to achieve precisely controlled conductive structure with stable electromechanical performances. Herein, a nanocomposite conductor with 3D engineered bicontinuous phase system is developed, which is constructed by alternately arranged robust solid‐phase and conductive liquid‐phase via additive liquid/solid assembly. The proper rheological properties and extraordinary structural compatibility of the liquid‐phase prompt the formation of bridged structure within the 3D periodic solid‐phase main skeleton, giving rise to stable and even strain‐enhanced electrical and electromagnetic interference (EMI) shielding properties under external deformation. A negative resistance change of −37% along with unabated EMI shielding effectiveness and mechanical properties are obtained at 100% strain, showing negligible performance degradation even after 10,000 cycles of rigorous stretching and releasing. A strain‐tolerant pressure‐sensing device is further demonstrated using the liquid/solid nanocomposite structure, delivering a unique function of precisely recognizing the local pressure at large tensile loading interference. This work provides a new paradigm for the manufacturing of nanocomposites with desired functionalities using the adequate nanofiller reserve toward practical strain‐tolerant applications.

Mesoporous silica@polypyrrole and its epoxy composites with ultra-broadband electromagnetic wave absorption properties

Composite of powders with exceptional electromagnetic wave absorption (EMA) properties with resins is an important tactic for preparing electromagnetic wave (EMW) stealth composites. However, high expenditure, low yield and the complex synthesis of these powders constrain their utilization in composite materials. Moreover, composite materials need greater thickness to fulfill EMA requirements. This work reported a facilely producible absorber, mesoporous Silica@Polypyrrole (MSU-J@PPy), which exhibits enhanced EMA performance. The polymerization of PPy in the connected three-dimensional pores as well as on the surface of MSU-J led to the creation of conductive network thereby enhancing the conductive loss. MSU-J contributes to the lightweighting and impedance matching and promotes the formation of a non-homogeneous interface. By varying the ratio of PPy to MSU-J, precise control of EMA was realized. When the proportion of PPy to MSU-J by weight is 1.5:1, the reflection loss (RL) of MSU-J@PPy reaches an impressive −46.44 dB at 1.9 mm. The effective absorption bandwidth (EAB) is 6.08 GHz (11.92–18 GHz) at 2.1 mm thickness of the sample. Further, MSU-J@PPy and carboxylated multi-walled carbon nanotubes (cMWCNTs) was composited with epoxy resin (EP) to develop a wave-absorbing composites MSU-J@PPy/cMWCNTs/EP with ultra-broadband absorption properties and outstanding mechanical characteristics. At a thickness of 1.7 mm, the composite can effectively absorb EMW in the entire Ku band, and effective absorption across the 5.4–18 GHz range can be attained through changing the matching thickness. This work offers a novel approach for developing cost-effective, easily synthesized, and high-yield EMW absorbers, as well as their application in absorber composite materials.

High-performance and frost-resistance MXene co-ionic liquid conductive hydrogel printed by electrohydrodynamic for flexible strain sensor

Conductive hydrogels with high performance and frost resistance are essential for flexible electronics, electronic skin, and soft robots. Nonetheless, the preparation of hydrogel-based flexible strain sensors with rapid response, wide strain detection range, and high sensitivity remains a considerable challenge. Furthermore, the inevitable freezing and evaporation of water in sub-zero temperatures and dry environments lead to the loss of flexibility and conductivity in hydrogels, which seriously limits their practical application. In this work, ionic liquids (ILs) and MXene are introduced into gelatin/polyacrylamide (PAM) precursor solution, and a PAM/gelatin/ILs/MXene/glycerol (PGIMG) hydrogel-based flexible strain sensor with MXene co-ILs ion–electron composite conductive network is prepared by combining the electrohydrodynamic (EHD) printing method and in-situ photopolymerization. The introduction of ILs provides an ionic conductive channel for the hydrogel. The introduction of MXene nanosheets forms an interpenetrating network with gelatin and PAM, which not only provides a conductive channel, but also improves the mechanical and sensing properties of the hydrogel-based flexible strain sensor. The prepared PGIMG hydrogel with the MXene co-ILs ion–electron composite conductive network demonstrates a tensile strength of 0.21 MPa at 602.82 % strain, the conductivity of 1.636 × 10−3 S/cm, high sensitivity (Gauge Factor, GF = 4.17), a wide strain detection range (1–600 %), and the response/recovery times (73 ms and 74 ms). In addition, glycerol endows the hydrogel with excellent freezing (−60 °C) and water retention properties. The application of the hydrogel-based flexible strain sensor in the field of human motion detection and information transmission shows the great potential of wearable devices, electronic skin, and information encryption transmission.

Comparison of piezoresistive sensitivity based on the size of silica as secondary filler on hybrid CNT composites

Recent research has increasingly focused on the potential applications of carbon nanotube (CNT) hybrid composites in wearable sensor technologies. Piezoresistivity, which is characterized by the ability to detect alterations in electrical resistance in response to external forces, is a pivotal attribute of resistive sensors. Numerous studies have attempted to improve this performance by incorporating secondary fillers. Despite extensive efforts to comprehend the influence of the dimensions of secondary fillers on electrical conductivity under static and dynamic conditions, notable confusion persists in the literature regarding the comparative analysis of the effects of nano- and microscale secondary fillers. In this study, two distinct sizes of silica particles were introduced as secondary fillers in CNT/polymer composites, followed by a rigorous comparative analysis of their mechanical and electrical properties under static conditions. Furthermore, this study assessed the influence of the silica particle size on the electrical resistance under dynamic tensile conditions, elucidating its impact on the conductive network.

Layer-by-layer assembling redox wood electrodes for efficient energy storage

The exploration of redox-active organic materials and low tortuous thick-electrodes is attractive for energy storage. The in-situ valorized lignin on raw wood surface accompanied by layer-by-layer deposition of electro-active materials endow such spatially distributed wood electrodes with high specific capacitance. Here, we report a layer-by-layer assembled ca.1.5 mm-thick redox wood hybrid electrode with 20 mg cm-2 electro-active mass loading for efficient energy storage. The in-situ modified surface lignin in treated wood (TrW) holds promise as redox-active material with enriched nanoporosity, carbonyl functionalities, and multi-phase ionic transport structure. The carbon nanotubes (CNTs) networking with in-situ polymerized polypyrrole (PPy) nanorods three-dimensionally in the lumen of TrW afford a wool-like, highly porous nanostructure. Such a hierarchical structured PPy@CNTs@TrW electrode offers a high areal capacitance of 1.46 F cm-2 with an extraordinary energy density of 0.983 mWh cm-3 (3.68 Wh kg-1) and power density of 5.4 mW cm-3 (20.25 W kg-1). Here, the valorized surface lignin contributes contributes to electrochemical energy storage accompanied by spatially distributed PPy@CNTs in low tortuous electrodes. The electrode offers extremely low electrochemical impedance of 0.61 Ω electrode resistance and 1.57 Ω electrolyte resistance. The hybrid wood electrode showcases even higher conductivity and energy/power density than thin carbonized wood and other state-of-the-art thin electrodes made of highly conductive three-dimensional networks. This work highlights the potential of in-situ valorized lignin in developing high-performance eco-friendly thick-electrodes for electrochemical energy storage applications.

Boron Nitride/Carbon Fiber High-Oriented Thermal Conductivity Material with Leaves–Branches Structure

In the realm of thermal interface materials (TIMs), high thermal conductivity and low density are key for effective thermal management and are particularly vital due to the growing compactness and lightweight nature of electronic devices. Efficient directional arrangement is a key control strategy to significantly improve thermal conductivity and comprehensive properties of thermal interface materials. In the present work, drawing inspiration from natural leaf and branch structures, a simple-to-implement approach for fabricating oriented thermal conductivity composites is introduced. Utilizing carbon fibers (CFs), known for their ultra-high thermal conductivity, as branches, this design ensures robust thermal conduction channels. Concurrently, boron nitride (BN) platelets, characterized by their substantial in-plane thermal conductivity, act as leaves. These components not only support the branches but also serve as junctions in the thermal conduction network. Remarkably, the composite achieves a thermal conductivity of 11.08 W/(m·K) with just an 11.1 wt% CF content and a 1.86 g/cm3 density. This study expands the methodologies for achieving highly oriented configurations of fibrous and flake materials, which provides a new design idea for preparing high-thermal conductivity and low-density thermal interface materials.

Using Sandwiched Silicon/Reduced Graphene Oxide Composites with Dual Hybridization for Their Stable Lithium Storage Properties

Using silicon/reduced graphene oxide (Si/rGO) composites as lithium-ion battery (LIB) anodes can effectively buffer the volumetric expansion and shrinkage of Si. Herein, we designed and prepared Si/rGO-b with a sandwiched structure, formed by a duple combination of ammonia-modified silicon (m-Si) nanoparticles (NP) with graphene oxide (GO). In the first composite process of m-Si and GO, a core–shell structure of primal Si/rGO-b (p-Si/rGO-b) was formed. The amino groups on the m-Si surface can not only hybridize with the GO surface to fix the Si particles, but also form covalent chemical bonds with the remaining carboxyl groups of rGO to enhance the stability of the composite. During the electrochemical reaction, the oxygen on the m-Si surface reacts with lithium ions (Li+) to form Li2O, which is a component of the solid–electrolyte interphase (SEI) and is beneficial to buffering the volume expansion of Si. Then, the p-Si/rGO-b recombines with GO again to finally form a sandwiched structure of Si/rGO-b. Covalent chemical bonds are formed between the rGO layers to tightly fix the p-Si/rGO-b, and the conductive network formed by the reintroduced rGO improves the conductivity of the Si/rGO-b composite. When used as an electrode, the Si/rGO-b composite exhibits excellent cycling performance (operated stably for more than 800 cycles at a high-capacity retention rate of 82.4%) and a superior rate capability (300 mA h/g at 5 A/g). After cycling, tiny cracks formed in some areas of the electrode surface, with an expansion rate of only 27.4%. The duple combination of rGO and the unique sandwiched structure presented here demonstrate great effectiveness in improving the electrochemical performance of alloy-type anodes.

Dual‐Cooling Textile Enables Vertical Heat Dissipation and Sweat Evaporation For Thermal and Moisture Regulation

AbstractPersonal thermal management textiles have garnered a lot of attention because they can efficiently preserve the body's thermal and moisture comfort while saving energy consumption. Nonetheless, conduction cooling‐based textile research is scarce and frequently encounters obstacles like overlooking through‐plane heat conduction, moisture management, and durability assurance. Here, a dual‐cooling textile (DCT) that combines high‐efficiency heat dissipation and sweat evaporation with a 3D thermal conductive network and Janus wetting structure is demonstrated. The DCT achieves notable in‐plane and through‐plane thermal conductivity (8.57 and 0.70 W m−1 K−1), along with practical mechanical qualities (tensile fracture strength of 65 MPa), under the influence of the 3D multistage thermal conduction network. Additionally, the DCT benefits from its Janus wetting structure, exhibiting unidirectional moisture‐wicking capability (transport index of 1081%) and fast water evaporation performance (0.34 g h−1). Rapid heat dissipation and sweat evaporation are advantageous features for the cooling of the human body in both static and dynamic situations. Compared to cotton fabric, DCT can lower the temperature by up to 3.7 °C. This strategy provides a fresh perspective on the development of advanced functional textiles for personalized cooling and energy savings in buildings.

Preparation and thermal conductivity of bimodal diamond particles reinforced phenolic resin composites

AbstractThermal conductive polymer composites have broad application prospects in the field of thermal management. However, due to intrinsically low thermal conductivity of polymers, even if fillers with high mass fraction are filled, the thermal conductivity of polymer composites cannot be significantly improved. In this paper, bimodal diamond particles (70 wt.% 150 μm and 22 wt.% 25 μm) were incorporated into phenolic resin to construct continuous heat transfer pathways by close packing, thereby enhancing its thermal conductivity. The results indicated that diamond particles with smaller particle size can effectively bridge the gaps between larger ones, forming a continuous for heat conduction. As a result, a maximum thermal conductivity value of 12.45 W/(m·K) can be achieved, which is 65.5 times, 9.8 times and 8.4 times higher than pure phenolic resin, 25 μm diamond particles reinforced phenolic resin composite and 150 μm diamond particles reinforced phenolic resin composite, respectively. Furthermore, heat dissipation and water cooling experiments also confirm the superior heat dissipation performance of phenolic resin composites reinforced with bimodal diamond particles. When the heating voltage is 10 V and the water cooling rate is 30 mL/min, the upper surface temperature of bimodal diamond composites is 129.2°C lower than that of pure phenolic resin. This investigation provides a new type of polymer composite with high thermal conductivity, which has promising prospects for application in thermal management. It also provides new insights for preparing polymer composites with high thermal conductivity by close packing of bimodal particles.Highlights Surface modification of the filler enhances its combination with resin. The interfacial bonding will be enhanced by D–OH bond on diamond surface. Bimodal diamond particles lead to the formation of a closely packed structure. This special structure can form a three‐dimensional heat conduction network. The highest TC of the DD/PR composite is 12.45 W/(m·K).

Bioinspired Robust Gas-Permeable On-Skin Electronics: Armor-Designed Nanoporous Flash Graphene Assembly Enhancing Mechanical Resilience.

Soft on-skin electrodes play an important role in wearable technologies, requiring attributes such as wearing comfort, high conductivity, and gas permeability. However, conventional fabrication methods often compromise simplicity, cost-effectiveness, or mechanical resilience. In this study, a mechanically robust and gas-permeable on-skin electrode is presented that incorporates Flash Graphene (FG) integrated with a bioinspired armor design. FG, synthesized through Flash Joule Heating process, offers a small-sized and turbostratic arrangement that is ideal for the assembly of a conductive network with nanopore structures. Screen-printing is used to embed the FG assembly into the framework of polypropylene melt-blown nonwoven fabrics (PPMF), forming a soft on-skin electrode with low sheet resistance (125.2 ± 4.7 Ω/□) and high gas permeability (≈10.08mg cm⁻2 h⁻¹). The "armor" framework ensures enduring mechanical stability through adhesion, washability, and 10,000 cycles of mechanical contact friction tests. Demonstrating capabilities in electrocardiogram (ECG) and electromyogram (EMG) monitoring, along with serving as a self-powered triboelectric sensor, the FG/PPMF electrode holds promise for scalable, high-performance flexible sensing applications, thereby enriching the landscape of integrated wearable technologies.

Interlayer Structure Manipulation of FeOCl/MXene with Soft/Hard Interface Design for Safe Water Production Using Dechlorination Battery Deionization

Suffering from the susceptibility to decomposition, the potential electrochemical application of FeOCl has greatly been hindered. The rational design of the soft‐hard material interface can effectively address the challenge of stress concentration and thus decomposition that may occur in the electrodes during charging and discharging. Herein, interlayer structure manipulation of FeOCl/MXene using soft‐hard interface design method were conducted for electrochemical dechlorination. FeOCl was encapsulated in Ti3C2Tx MXene nanosheets by electrostatic self‐assembly layer by layer to form a soft‐hard mechanical hierarchical structure, in which Ti3C2Tx was used as flexible buffer layers to relieve the huge volume change of FeOCl during Cl‐ intercalation/deintercalation and constructed a conductive network for fast charge transfer. The CDI dechlorination system of FeOCl/Ti3C2Tx delivered outstanding Cl‐ adsorption capacity (158.47 ± 6.98 mg g‐1), rate (6.07 ± 0.35 mg g‐1 min‐1), and stability (over 94.49% in 30 cycles), and achieved considerable energy recovery (21.14 ± 0.25%). The superior dechlorination performance was proved to originate from the Fe2+/Fe3+ topochemical transformation and the deformation constraint effect of Ti3C2Tx on FeOCl. Our interfacial design strategy enables a hard‐to‐soft integration capacity, which can serve as a universal technology for solving the translational problem of electrode volume expansion.

Interlayer Structure Manipulation of FeOCl/MXene with Soft/Hard Interface Design for Safe Water Production Using Dechlorination Battery Deionization.

Suffering from the susceptibility to decomposition, the potential electrochemical application of FeOCl has greatly been hindered. The rational design of the soft-hard material interface can effectively address the challenge of stress concentration and thus decomposition that may occur in the electrodes during charging and discharging. Herein, interlayer structure manipulation of FeOCl/MXene using soft-hard interface design method were conducted for electrochemical dechlorination. FeOCl was encapsulated in Ti3C2Tx MXene nanosheets by electrostatic self-assembly layer by layer to form a soft-hard mechanical hierarchical structure, in which Ti3C2Tx was used as flexible buffer layers to relieve the huge volume change of FeOCl during Cl- intercalation/deintercalation and constructed a conductive network for fast charge transfer. The CDI dechlorination system of FeOCl/Ti3C2Tx delivered outstanding Cl- adsorption capacity (158.47 ± 6.98 mg g-1), rate (6.07 ± 0.35 mg g-1 min-1), and stability (over 94.49% in 30 cycles), and achieved considerable energy recovery (21.14 ± 0.25%). The superior dechlorination performance was proved to originate from the Fe2+/Fe3+ topochemical transformation and the deformation constraint effect of Ti3C2Tx on FeOCl. Our interfacial design strategy enables a hard-to-soft integration capacity, which can serve as a universal technology for solving the translational problem of electrode volume expansion.

Highly sensitive methyl parathion electrochemical sensor designed from expired mung bean-derived porous carbon embellished with cerium oxide nanoparticles

Methyl parathion (MP) is one kind of highly toxic, efficient, and broad-spectrum organic phosphorus insecticides, which may prevent and control various pests on crops. However, the unscientific usage of MP has caused serious harm to humans and ecological environment. It is very necessary to design a sensitive and selective MP analysis method to ensure the food safety and life health. In this work, we reported a low-cost and environmental-friendly strategy to prepare the expired mung bean derived porous carbon (EMBPC) with interconnected carbon conductive network and large specific surface area, which was further decorated by cerium oxide (CeO2) nanoparticles. EMBPC possessed good conductivity property and electrochemical active area, which effectively boosted the charge transfer efficiency. CeO2 nanoparticles with good biocompatibility and high catalytic capacity promoted the efficient adsorption of MP on the surface of sensing electrode due to the affinity of CeO2 nanoparticles towards the phosphate groups of MP. Furthermore, EMBPC with porous carbon conductive structure could effectively make up for the inherent disadvantage of CeO2 nanoparticles in the term of electrical conductivity. The fabricated EMBPC@CeO2/GCE sensor showed highly sensitive MP detection property with low limit of detection (LOD) of 9.028 nM. The satisfactory repeatability, reproducibility, and anti-interference ability could be achieved at the fabricated MP electrochemical sensor. For the detection of MP in food samples, the EMBPC@CeO2/GCE sensor showed satisfactory recovery rates of 95.25–112.31 % and low RSD of 1.76–4.05 %, which suggested the good application prospect of the EMBPC@CeO2/GCE sensor.

Novel Polyurethane Based, Fully Flexible, High-Performance Piezoresistive Sensor for Real-Time Pressure Monitoring.

Flexible piezoresistive pressure sensors are garnering substantial attention, in line with advancements in biointegrated and wearable electronics. However, a significant portion of piezoresistive pressure sensors suffer from the trade-off between sensitivity and pressure range. Moreover, the current piezoresistive sensors generally rely on a rigid metallic electrode, severely deteriorating their long-term durability. Herein, a fully flexible piezoresistive sensor coupling polyurethane (PU) based electrode and active sensing element is proposed to circumvent the aforementioned problems. By rationally regulating the double-permeable conductive networks within the PU matrix, an elastomeric electrode and sensing element are implemented, respectively. The assembled heterostructured configurations enable impressive sensitivity up to 7.023 kPa-1, broad pressure detection (up to 420 kPa), an ultralow pressure sensing limit (0.1 Pa), and extraordinary operation stability over 80000 cyclic pressings along with fast response/relaxation times (60 ms/80 ms). Additionally, the fully flexible sensor is capable of both real-time detection of physiological signals and mimicking keyboards, implying its viability as a high-performance pressure sensor.