A High-Performance Flexible Hydroacoustic Transducer Based on 1-3 PZT-5A/Silicone Rubber Composite.

In recent years, hydroacoustic transducers made of PZT/epoxy composites have been extensively employed in underwater detection, communication, and recognition for their high energy conversion efficiency. Despite the ease with which these transducers can be formed into complex shapes, their lack of mechanical flexibility limits their versatility across various sizes of underwater vehicles. This study introduces a novel flexible piezoelectric composite hydroacoustic transducer (FPCHT) based on a 1-3 PZT-5A/silicone rubber composite and an island-bridge flexible electrode, which can break the limitations of existing hydroacoustic transducers that do not have flexibility. The finite element method is used to optimize the structural parameters of high-performance 1-3 FPC. A large-sized (187 mm × 47 mm × 5.12 mm) FPC is fabricated using an improved cutting-filling method and packaged into the FPCHT. Compared with the planar rigid PZT/epoxy composite hydroacoustic transducer (RPCHT) of the same size, the TVR (186.5 db) of the FPCHT has increased by about 7 dB, indicating that it has better acoustic radiation performance and electroacoustic conversion efficiency. Furthermore, its electroacoustic performance exhibits excellent stability under different bending states. Therefore, the FPCHT with high electroacoustic performance is an ideal substitute for the existing RPCHT and promotes the development of hydroacoustic transducers towards flexibility and portability.

Splashing-Assisted Femtosecond Laser-Activated Metal Deposition for Mold- and Mask-Free Fabrication of Robust Microstructured Electrodes for Flexible Pressure Sensors.

Flexible pressure sensors play an indispensable role in flexible electronics. Microstructures on flexible electrodes have been proven to be effective in improving the sensitivity of pressure sensors. However, it remains a challenge to develop such microstructured flexible electrodes in a convenient way. Inspired by splashed particles from laser processing, herein, a method for customizing microstructured flexible electrodes by femtosecond laser-activated metal deposition is proposed. It takes advantage of the catalyzing particles scattered during femtosecond laser ablation and is particularly suitable for moldless, maskless, and low-cost fabrication of microstructured metal layers on polydimethylsiloxane (PDMS). Robust bonding at the PDMS/Cu interface is evidenced by the scotch tape test and the duration test over 10 000 bending cycles. Benefiting from the firm interface, the developed flexible capacitive pressure sensor with microstructured electrodes presents several conspicuous features, including a sensitivity (0.22 kPa-1 ) 73 times higher than the one using flat Cu electrodes, ultralow detection limit (<1 Pa), rapid response/recovery time (4.2/5.3 ms), and excellent stability. Moreover, the proposed method, inheriting the merits of laser direct writing, is capable of fabricating a pressure sensor array in a maskless manner for spatial pressure mapping.

Construction of Bimetallic Heterojunction Based on Porous Engineering for High Performance Flexible Asymmetric Supercapacitors.

It remains a great challenge to design and manufacture battery-type supercapacitors with satisfactory flexibility, appropriate mechanical property, and high energy density under high power density. Herein, a concept of porous engineering is proposed to simply prepare two-layered bimetallic heterojunction with porous structures. This concept is successfully applied in fabrication of flexible electrode based on CuO-Co(OH)2 lamella on Cu-plated carbon cloth (named as CPCC@CuO@Co(OH)2 ). The unique structure brings the electrode a high specific capacity of 3620 mF cm-2 at 2 mA cm-2 and appropriate mechanical properties with Young's modulus of 302.0 MPa. Density functional theory calculations show that porous heterojunction provides a higher intensity of electron state density near the Fermi level (E-Ef  = 0 eV), leading to a highly conductive CPCC@CuO@Co(OH)2 electrode with both efficient charge transport and rapid ion diffusion. Notably, the supercapacitor assembled from CPCC@CuO@Co(OH)2 //CC@AC shows high energy density of 127.7 W h kg-1 at 750.0 W kg-1 , remarkable cycling performance (95.53% capacity maintaining after 10 000 cycles), and desired mechanical flexibility. The methodology and results in this work will accelerate the transformative developments of flexible energy storage devices in practical applications.

Highly Flexible K-Intercalated MnO2 /Carbon Membrane for High-Performance Aqueous Zinc-Ion Battery Cathode.

The layered MnO2 is intensively investigated as one of the most promising cathode materials for aqueous zinc-ion batteries (AZIBs), but its commercialization is severely impeded by the challenging issues of the inferior intrinsic electronic conductivity and undesirable structural stability during the charge-discharge cycles. Herein, the lab-prepared flexible carbon membrane with highly electrical conductivity is first used as the matrix to generate ultrathin δ-MnO2 with an enlarged interlayer spacing induced by the K+ -intercalation to potentially alleviate the structural damage caused by H+ /Zn2+ co-intercalation, resulting in a high reversible capacity of 190 mAh g-1 at 3 A g-1 over 1000 cycles. The in situ/ex-situ characterizations and electrochemical analysis confirm that the enlarged interlayer spacing can provide free space for the reversible deintercalation/intercalation of H+ /Zn2+ in the structure of δ-MnO2 , and H+ /Zn2+ co-intercalation mechanism contributes to the enhanced charge storage in the layered K+ -intercalated δ-MnO2 . This work provides a plausible way to construct a flexible carbon membrane-based cathode for high-performance AZIBs.

Hierarchical 3D Electrode Design with High Mass Loading Enabling High-Energy-Density Flexible Lithium-Ion Batteries.

Flexible lithium-ion batteries (LIBs) have attracted significant attention owing to their ever-increasing use in flexible and wearable electronic devices. However, the practical application of flexible LIBs in devices has been plagued by the challenge of simultaneously achieving high energy density and high flexibility. Herein, a hierarchical 3D electrode (H3DE) is introduced with high mass loading that can construct highly flexible LIBs with ultrahigh energy density. The H3DE features a bicontinuous structure and the active materials along with conductive agents are uniformly distributed on the 3D framework regardless of the active material type. The bicontinuous electrode/electrolyte integration enables a rapid ion/electron transport, thereby improving the redox kinetics and lowering the internal cell resistance. Moreover, the H3DE exhibits exceptional structural integrity and flexibility during repeated mechanical deformations. Benefiting from the remarkable physicochemical properties, pouch-type flexible LIBs using H3DE demonstrate stable cycling under various bending states, achieving a record-high energy density (438.6 Wh kg-1 and 20.4 mWh cm-2 ), and areal capacity (5.6 mAh cm-2 ), outperforming all previously reported flexible LIBs. This study provides a feasible solution for the preparation of high-energy-density flexible LIBs for various energy storage devices.

Fabrication of polydopamine decorated carbon cloth as support material to anchor CeO2 nanoparticles for electrochemical detection of ethanol.

A flexible CeO2 nanostructured polydopamine-modified carbon cloth (CeO2/PDA/CC) interface was fabricated via electrodeposition for ethanol detection. The fabrication method involved two consecutive electrochemical steps in which dopamine was firstly electrodeposited on carbon fibers, followed by the electrochemical growth of CeO2 nanoparticles. The CeO2/PDA-based electroactive interface exerts an impressive electrochemical performance on the flexible sensor due to strong synergistic effect of the PDA functionalization with more active sites. Moreover, catalytic activity of CeO2 nanostructures anchored on highly conductive CC incorporate superior electrocatalytic performance of the fabricated interface. The designed electrochemical sensor showed a wide response to ethanol in the linear range 1 to 25 mM with a detection limit of 0.22 mM. The CeO2/PDA/CC flexible sensor showed good anti-interference ability and excellent repeatability and reproducibility (RSD = 1.67%). The fabricated interface performed well in saliva samples with satisfactory recoveries, corroborating the viability of CeO2/PDA/CC integrated interface for practical implementation.

Renewable Biopolymers Combined with Ionic Liquids for the Next Generation of Supercapacitor Materials.

The search for biocompatible and renewable materials for the next generation of energy devices has led to increasing interest in using biopolymers as a matrix component for the development of electric double-layer capacitors (EDLCs). However, using biopolymers as host matrices presents limitations in performance and scalability. At the same time, ionic liquids (ILs) have shown exceptional properties as non-aqueous electrolytes. This review intends to highlight the progress in integrating ILs and biopolymers for EDLC. While ILs have been used as solvents to process biopolymers and electrolyte materials, biopolymers have been utilized to provide novel chemistries of electrolyte materials via one of the following scenarios: (1) acting as host polymeric matrices for IL-support, (2) performing as polymeric fillers, and (3) serving as backbone polymer substrates for synthetic polymer grafting. Each of these scenarios is discussed in detail and supported with several examples. The use of biopolymers as electrode materials is another topic covered in this review, where biopolymers are used as a source of carbon or as a flexible support for conductive materials. This review also highlights current challenges in materials development, including improvements in robustness and conductivity, and proper dispersion and compatibility of biopolymeric and synthetic polymeric matrices for proper interface bonding.

High Conductivity, Semiconducting, and Metallic PEDOT:PSS Electrode for All-Plastic Solar Cells.

Plastic electrodes are desirable for the rapid development of flexible organic electronics. In this article, a plastic electrode has been prepared by employing traditional conducting polymer poly(3,4-ethylenedioxythiophene):poly(styrene sulfonate) (PEDOT:PSS) and plastic substrate polyethersulfone (PES). The completed electrode (Denote as HC-PEDOT:PSS) treated by 80% concentrated sulfuric acid (H2SO4) possesses a high electrical conductivity of over 2673 S/cm and a high transmittance of over 90% at 550 nm. The high conductivity is attributed to the regular arrangement of PEDOT molecules, which has been proved by the X-ray diffraction characterization. Temperature-dependent conductivity measurement reveals that the HC-PEDOT:PSS possesses both semiconducting and metallic properties. The binding force and effects between the PEDOT and PEI are investigated in detail. All plastic solar cells with a classical device structure of PES/HC-PEDOT:PSS/PEI/P3HT:ICBA/EG-PEDOT:PSS show a PCE of 4.05%. The ITO-free device with a structure of Glass/HC-PEDOT:PSS/Al4083/PM6:Y6/PDINO/Ag delivers an open-circuit voltage (VOC) of 0.81 V, short-circuit current (JSC ) of 23.5 mA/cm2, fill factor (FF) of 0.67 and a moderate power conversion efficiency (PCE) of 12.8%. The above results demonstrate the HC-PEDOT:PSS electrode is a promising candidate for all-plastic solar cells and ITO-free organic solar cells.

Electrochemical Double-Layer Capacitor based on Carbon@ Covalent Organic Framework Aerogels.

High energy demand results in comprehensive research of novel materials for energy sources and storage applications. Covalent organic frameworks (COFs) possess appropriate features such as long-range order, permanent porosity, tunable pore size, and ion diffusion pathways to be competitive electrode materials. Herein, we present a deep electrochemical study of two COF-aerogels shaped into flexible COF-electrodes (ECOFs) by a simple compression method to fabricate an electrochemical double-layer capacitor (EDLC). This energy storage system has considerable interest owing to its high-power density and long cycle life compared with batteries. Our result confirmed the outstanding behavior of ECOFs as EDLC devices with a capacity retention of almost 100 % after 10 000 charge/discharge cycles and, to our knowledge, the highest areal capacitance (9.55 mF cm-2 ) in aqueous electrolytes at higher scan rates (1000 mV s-1 ) for COFs. More importantly, the hierarchical porosity observed in the ECOFs increases ion transport, which permits a fast interface polarization (low τ0 values). The complete sheds light on using ECOFs as novel electrode material to fabricate EDLC devices.

Concurrent and Selective Determination of Dopamine and Serotonin with Flexible WS2 /Graphene/Polyimide Electrode Using Cold Plasma.

Makers of point-of-care devices and wearable diagnostics prefer flexible electrodes over conventional electrodes. In this study, a flexible electrode platform is introduced with a WS2 /graphene heterostructure on polyimide (WGP) for the concurrent and selective determination of dopamine and serotonin. The WGP is fabricated directly via plasma-enhanced chemical vapor deposition (PECVD) at 150 °C on a flexible polyimide substrate. Owing to the limitations of existing fabrication methods from physical transfer or hydrothermal methods, many studies are not conducted despite excellent graphene-based heterostructures. The PECVD synthesis method can provide an innovative WS2 /graphene heterostructure of uniform quality and sufficient size (4 in.). This unique heterostructure affords excellent electrical conductivity in graphene and numerous electrochemically active sites in WS2 . A large number of uniform qualities of WGP electrodes show reproducible and highly sensitive electrochemical results. The synergistic effect enabled well-separated voltammetric signals for dopamine and serotonin with a potential gap of 188 mV. Moreover, the practical application of the flexible sensor is successfully evaluated by using artificial cerebrospinal fluid.

Developing Longer-Lived Single Molecule Junctions with a Functional Flexible Electrode.

Creating single-molecule junctions with a long-lived lifetime at room temperature is an open challenge. Finding simple and efficient approaches to increase the durability of single-molecule junction is also of practical value in molecular electronics. Here it is shown that a flexible gold-coated nanopipette electrode can be utilized in scanning tunneling microscope (STM) break-junction measurements to efficiently enhance the stability of molecular junctions by comparing with the measurements using conventional solid gold probes. The stabilizing effect of the flexible electrode displays anchor group dependence, which increases with the binding energy between the anchor group and gold. An empirical model is proposed and shows that the flexible electrode could promote stable binding geometries at the gold-molecule interface and slow down the junction breakage caused by the external perturbations, thereby extending the junction lifetime. Finally, it is demonstrated for the first time that the internal conduit of the flexible STM tip can be utilized for the controlled molecule delivery and molecular junction formation.

In Situ Grown CoMn2 O4 3D-Tetragons on Carbon Cloth: Flexible Electrodes for Efficient Rechargeable Zinc-Air Battery Powered Water Splitting Systems.

The integration of energy conversion and storage systems such as electrochemical water splitting (EWS) and rechargeable zinc-air battery (ZAB) is on the vision to provide a sustainable future with green energy resources. Herein, a unique strategy for decorating 3D tetragonal CoMn2 O4 on carbon cloth (CMO-U@CC) via a facile one-pot in situ hydrothermal process, is reported. The highly exposed morphology of 3D tetragons enhances the electrocatalytic activity of CMO-U@CC. This is the first demonstration of such a bifunctional activity of CMO-U@CC in an EWS system; it achieves a nominal cell voltage of 1.610 V @ 10 mA cm-2 . Similarly, the fabricated rechargeable ZAB delivers a specific capacity of 641.6 mAh gzn -1 , a power density of 135 mW cm-2 , and excellent cyclic stability (50 h @ 10 mA cm-2 ). Additionally, a series of flexible solid-state ZABs are fabricated and employed to power the assembled CMO-U@CC-based water electrolyzer. To the best of the authors' knowledge, this is the first demonstration of an in situ-grown binder-free CMO-U@CC as a flexible multifunctional electrocatalyst for a built-in integrated rechargeable ZAB-powered EWS system.

Cell viability and cytotoxicity of inkjet-printed flexible organic electrodes on parylene C.

This study reports on the fabrication of biocompatible organic devices by means of inkjet printing with a novel combination of materials. The devices were fabricated on Parylene C (PaC), a biocompatible and flexible polymer substrate. The contact tracks were inkjet-printed using a silver nanoparticle ink, while the active sites were inkjet-printed using a poly (3,4ethylenedioxythiophene)/polystyrene sulfonate (PEDOT:PSS) solution. To insulate the final device, a polyimide ink was used to print a thick film, leaving small open windows upon the active sites. Electrical characterization of the final device revealed conductivities in the order of 103 and 102 S.cm-1 for Ag and PEDOT based inks, respectively. Cell adhesion assays performed with PC-12 cells after 96 h of culture, and B16F10 cells after 24 h of culture, demonstrated that the cells adhered on top of the inks and cell differentiation occurred, which indicates Polyimide and PEDOT:PSS inks are non-toxic to these cells. The results indicate that PaC, along with its surface-treated variants, is a potentially useful material for fabricating cell-based microdevices.

A reusable wet-transfer printing technique for manufacturing of flexible silver nanowire film-based electrodes.

To explore a simple and efficient way to fabricate thin film electrodes on flexible substrates is highly desired because of its high promising application in optoelectronics. Transfer printing technique plays a key role in the fabrication of flexible electrodes from conventional substrates to flexible substrates. Unfortunately, a simple, room temperature, environmental-friendly and reusable transfer printing technique still remains challenging. Here we demonstrated a novel water-based wet-transfer printing technique that is simple, room temperature, environmental-friendly and reusable by taking advantage of the adjustment of the intermolecular hydrogen bonding between thin film and substrates. This effective and practical transfer technique may provide an effective route to develop electronic flexible devices with high performance.

Flexible Electrostatic Transducer Array with Displacement Control for Haptic Sensing and Actuation.

We developed flexible electrostatic transducers with both a single element and a 2×2 array format to actuate at a precise displacement across a range of loads with a control circuitry and algorithm. The transducer, composed of a moving buckled film with an integrated electrode and a rigid electrode, can be used to simultaneously generate and sense displacements. A circuit and computer program were designed to demonstrate displacement control and quantify the sensing precision of the transducer. Specifically, we applied a range of voltage and load conditions to the transducer and array and measured the displacement while under loading through capacitive sensing. The change in capacitance was linear with respect to the area of the electrode in contact and matched theoretical predictions when described as a function of the displacement. The transducer was loaded with weights in the range of 5-27 mN and capacitance-driving voltage graphs were obtained. An 8Hz driving frequency was used to move the transducer, while a 10.8kHz signal was used to sense the capacitance. These were used to build a predictive model to correct for sensed load to maintain a average displacement. It was found that a transducer of dimensions 10mm × 40mm was able to maintain displacement under loads of 5-27mN, while a matrix composed of 10mm × 20mm transducers was able to maintain displacement under loads of 2.5-11mN. In general, the detection thresholds of human skin can range between 5-20mN of force and 2-20um of displacement for frequencies between 1Hz and 250Hz, so these values are in line with what is needed to build a functional haptic wearable device. The present work provides a method to quantitatively measure and control a new type of flexible transducer for a variety of haptic applications.

Flexible Tactile Sensor Based on Patterned Ag-Nanofiber Electrodes through Electrospinning.

The growing demand for intelligent equipment has greatly inspired the development of flexible devices. Thus, disparate flexible multifunctional devices, including pressure sensitive flexible/stretchable displays, have drawn worldwide research attention. Electrodes maintaining conductivity and mechanical strength against deformations are indispensable components in all prospective applications. In this work, a flexible pressure mapping sensor array is developed based on patterned Ag-nanofibers (Ag-NFs) electrode through electrospinning and lithography. The metallic Ag layer is sputtered onto the electrospinning polyvinyl alcohol (PVA) NFs. A uniform and super conductive electrode layer with outstanding mechanical performance is thus formed after dissolving PVA. Followed by the traditional lithography method, a patterned electrode array (4 × 4 sensors) is obtained. Based on the newly developed triboelectric nanogenerator (TENG) technology, a flexible pressure-mapping sensor with excellent stability towards bending deformations is further demonstrated. Moreover, a letter "Z" is successfully visualized by this pressure sensor array, encouraging more human-machine interactive implementations, such as multi-functional tactile screens.

A Biodegradable and Stretchable Protein-Based Sensor as Artificial Electronic Skin for Human Motion Detection.

Due to the natural biodegradability and biocompatibility, silk fibroin (SF) is one of the ideal platforms for on-skin and implantable electronic devices. However, the development of SF-based electronics is still at a preliminary stage due to the SF film intrinsic brittleness as well as the solubility in water, which prevent the fabrication of SF-based electronics through traditional techniques. In this article, a flexible and stretchable silver nanofibers (Ag NFs)/SF based electrode is synthesized through water-free procedures, which demonstrates outstanding performance, i.e., low sheet resistance (10.5 Ω sq-1 ), high transmittance (>90%), excellent stability even after bending cycles >2200 times, and good extensibility (>60% stretching). In addition, on the basis of such advanced (Ag NFs)/SF electrode, a flexible and tactile sensor is further fabricated, which can simultaneously detect pressure and strain signals with a large monitoring window (35 Pa-700 kPa). Besides, this sensor is air-permeable and inflammation-free, so that it can be directly laminated onto human skins for long-term health monitoring. Considering the biodegradable and skin-comfortable features, this sensor may become promising to find potential applications in on-skin or implantable health-monitoring devices.

Lithium Titanate Cuboid Arrays Grown on Carbon Fiber Cloth for High-Rate Flexible Lithium-Ion Batteries.

High-rate performance flexible lithium-ion batteries are desirable for the realization of wearable electronics. The flexibility of the electrode in the battery is a key requirement for this technology. In the present work, spinel lithium titanate (Li4 Ti5 O12 , LTO) cuboid arrays are grown on flexible carbon fiber cloth (CFC) to fabricate a binder-free composite electrode (LTO@CFC) for flexible lithium-ion batteries. Experimental results show that the LTO@CFC electrode exhibits a remarkably high-rate performance with a capacity of 105.8 mAh g-1 at 50C and an excellent electrochemical stability against cycling (only 2.2% capacity loss after 1000 cycles at 10C). A flexible full cell fabricated with the LTO@CFC as the anode and LiNi0.5 Mn1.5 O4 coated on Al foil as the cathode displays a reversible capacity of 109.1 mAh g-1 at 10C, an excellent stability against cycling and a great mechanical stability against bending. The observed high-rate performance of the LTO@CFC electrode is due to its unique corn-like architecture with LTO cuboid arrays (corn kernels) grown on CFC (corn cob). This work presents a new approach to preparing LTO-based composite electrodes with an architecture favorable for ion and electron transport for flexible energy storage devices.

Flexible 3D Porous MXene Foam for High-Performance Lithium-Ion Batteries.

2D transition-metal carbides and nitrides, named MXenes, are promising materials for energy storage, but suffer from aggregation and restacking of the 2D nanosheets, which limits their electrochemical performance. In order to overcome this problem and realize the full potential of MXene nanosheets, a 3D MXene foam with developed porous structure is established via a simple sulfur-template method, which is freestanding, flexible, and highly conductive, and can be directly used as the electrode in lithium-ion batteries. The 3D porous architecture of the MXene foam offers massive active sites to enhance the lithium storage capacity. Moreover, its foam structure facilitates electrolyte infiltration for fast Li+ transfer. As a result, this flexible 3D porous MXene foam exhibits significantly enhanced capacity of 455.5 mAh g-1 at 50 mA g-1 , excellent rate performance (101 mAh g-1 at 18 A g-1 ), and superior ultralong-term cycle stability (220 mAh g-1 at 1 A g-1 after 3500 cycles). This work not only demonstrates the great superiority of the 3D porous MXene foam but also proposes the sulfur-template method for controllable constructing of the 3D foam from 2D nanosheets at a relatively low temperature.

Interlayer Hydrogen-Bonded Metal Porphyrin Frameworks/MXene Hybrid Film with High Capacitance for Flexible All-Solid-State Supercapacitors.

2D metal-porphyrin frameworks (MPFs) are attractive for advanced energy storage devices. However, the inferior conductivity and low structural stability of MPFs seriously limit their application as flexible free-standing electrodes with high performance. Here, for the first time, an interlayer hydrogen-bonded MXene/MPFs film is proposed to overcome these disadvantages by intercalation of highly conductive MXene nanosheets into MPFs nanosheets via a vacuum-assisted filtration technology. The alternant insertion of MXene and MPFs affords 3D interconnected "MPFs-to-MXene-to-MPFs" conductive networks to accelerate the ionic/electronic transport rates. Meanwhile, the interlayer hydrogen bonds (F···HO and O···HO) contribute a high chemical stability due to a favorable tolerance to volume change caused by phase separation and structural collapse during the charge/discharge process. The synergistic effect makes MXene/MPFs film deliver a capacitance of 326.1 F g-1 at 0.1 A g-1 , 1.64 F cm-2 at 1 mA cm-2 , 694.2 F cm-3 at 1 mA cm-3 and a durability of about 30 000 cycles. The flexible symmetric supercapacitor shows an areal capacitance of 408 mF cm-2 , areal energy density of 20.4 µW h cm-2 , and capacitance retention of 95.9% after 7000 cycles. This work paves an avenue for the further exploration of 2D MOFs in flexible energy storage devices.