Implantable Electronics Research Articles

Nanoengineering approach toward ultrahigh power factor Ag2Se/polyvinylpyrrolidone composite film for flexible thermoelectric generator

Flexible thermoelectric (TE) generators (F-TEGs), able to harvest heat energy from the human body, are considered to be competitive energy supply devices for wearable and implantable electronics. Herein, we fabricate Ag2Se/polyvinylpyrrolidone (PVP) films on nylon membranes via a novel nanoengineering approach: First, small amount Ag nanoparticles decorated Ag2Se nanowires (NWs) coated with a nanolayer of PVP are synthesized via a Se NW template method, and the Ag nanoparticles react with small amount Se residues at the core of the Ag2Se NWs during hot-pressing and form Ag2Se nanograins rich in defects embedded in big Ag2Se grains. The Ag2Se nanograin has a different orientation from the big Ag2Se grain; hence, the interface between the Ag2Se nanograin and the big Ag2Se grain enhances the phonon scattering but almost does not affect the transport of carriers. An optimized film exhibits a maximum power factor of 2478 ± 67 μW m−1 K−2 (corresponding ZT ∼ 1.05) at 300 K, which is one of the highest values reported for flexible Ag2Se films. The excellent TE properties of the film are attributed to its unique microstructure: highly densified, coherent/semi-coherent Ag2Se grains, embedded Ag2Se nanograins, and a very small amount of PVP located at nanopores. Besides, the film shows good flexibility: after 1500 times bending along a rod with a radius of 4.0 mm, the electrical conductivity still maintains 90.9 %. Furthermore, a 6-leg F-TEG assembled with the optimal film generates a maximum power of 4.58 μW (corresponding power density of ∼ 31.2 W m−2) at a temperature gradient of 38.7 K. This work provides an efficient strategy for the fabrication of ultrahigh-performance Ag2Se-based flexible TE films.

Ultrathin Encapsulation Strategies with Predefined Gate Dielectric Surface Area for Flexible Crystalline Silicon Nanomembrane-Based MOS Capacitors

Ultrathin encapsulation strategies show huge potential in wearable and implantable electronics. However, insightful efforts are still needed to improve the electrical and mechanical characteristics of encapsulated devices. This work introduces Al2O3/alucone nanolaminates using hybrid atomic/molecular layer deposition for ultrathin encapsulation structures employed in crystalline silicon nanomembrane (Si NM)-based metal-oxide-semiconductor capacitors (MOSCAPs). The comprehensive electrical and mechanical analysis focused on the encapsulated and bare MOSCAPs with three gate dielectric diameters (Ø) under planar and bending conditions, including concave bending radii of 110.5 mm and 85 mm as well as convex bending radii of 77.5 mm and 38.5 mm. Combined with the Ø-related mechanical analysis of the maximum strain in the critical layers and the practical investigations of electrical parameters, the encapsulated MOSCAPs with Ø 160 μm showed the most stable electro-mechanical performance partly due to the optimized position of the neutral mechanical plane. Comparison of the electrical changes in Al2O3/alucone-encapsulated MOSCAPs with Ø 160 μm, Ø 240 μm, and Ø 320 μm showed that it is beneficial to define the gate dielectric surface area of 0.02 to 0.05 mm2 for Si NM-based wearable electronics. These findings are significant for leveraging the practical applications in ultrathin encapsulation strategies for reliable operations of crystalline Si NM-based integrated circuits.

Recent Development of Implantable Chemical Sensors Utilizing Flexible and Biodegradable Materials for Biomedical Applications.

Implantable chemical sensors built with flexible and biodegradable materials exhibit immense potential for seamless integration with biological systems by matching the mechanical properties of soft tissues and eliminating device retraction procedures. Compared with conventional hospital-based blood tests, implantable chemical sensors have the capability to achieve real-time monitoring with high accuracy of important biomarkers such as metabolites, neurotransmitters, and proteins, offering valuable insights for clinical applications. These innovative sensors could provide essential information for preventive diagnosis and effective intervention. To date, despite extensive research on flexible and bioresorbable materials for implantable electronics, the development of chemical sensors has faced several challenges related to materials and device design, resulting in only a limited number of successful accomplishments. This review highlights recent advancements in implantable chemical sensors based on flexible and biodegradable materials, encompassing their sensing strategies, materials strategies, and geometric configurations. The following discussions focus on demonstrated detection of various objects including ions, small molecules, and a few examples of macromolecules using flexible and/or bioresorbable implantable chemical sensors. Finally, we will present current challenges and explore potential future directions.

Pseudocapacitance behavior enables efficient and stable electrochemical energy conversion and storage in glucose/air enzymatic biofuel cells

Constructing an integrated system with high-efficiency and stable energy conversion and storage (ECS) is of great significance but remains challenges. Herein, we report a biodevice consisting of a bioanode of tetrathiafulvalene/glucose oxidase (TTF/GOx) immobilized on asphalt-derived porous carbon (APC) for catalyzing glucose oxidation and a biocathode of 2,2’-azinobis(3-ethylbenzothiazoline-6-sulfonate)/bilirubin oxidase (ABTS/BOD) immobilized on APC for catalyzing oxygen reduction, to achieve ECS with high-efficiency and excellent stability. The redox mediators, TTF and ABTS, used at the bioanode and biocathode, respectively, simultaneously mediate electron transfer to release electric current on discharging and serve as pseudocapacitors to achieve charge storage at open-circuit conditions, enabling high power density and self-charge capability. The biodevice of the above configuration delivers a peak power output of 5.01 mW cm−2 in the pulse discharge mode with cell voltage remaining 93.7 % of its initial value after 100 pulse discharge/self-charge cycles. This work provides a highly efficient solution to address the low power density and poor stability of the conventional enzymatic biofuel cells, showing great implications for small, implantable and wearable electronics.

Validating Operating Stability and Biocompatibility Toward SaferZinc-Based Batteries.

Wearable and implantable electronics are standing at the frontiers of science and technology, driven by the increasing demands from modernized lifestyles. Zinc-based batteries (ZBs) are regarded as ideal energy suppliers for these biocompatible electronics, but the corresponding biocompatibility validation is still in the initial stage. Meanwhile, complicated working conditions and some extreme electrolyte environments raise strict challenges, leaving less choices for safe ZBs. Toward higher operating stability and biocompatibility, this work proposes a hydrogel electrolyte featuring the moisture maintaining ability and a robust interface, which could further provide a milder environment for Zn-MnO2 batteries and Zn-air batteries. The cytotoxicity and tissue injury of batteries are evaluated with human cell lines and battery implantations on the animal models, which demonstrate the high biocompatibilityof ZBs, while preliminary wearable devices implementation further verifies their operating stability. This work may provide a pathway for developing and validating biocompatible ZBs, contributing to their future practical employment in relevant fields.

PEDOT-based stretchable optoelectronic materials and devices for bioelectronic interfaces.

The rapid development of wearable and implantable electronics has enabled the real-time transmission of electrophysiological signals in situ, thus allowing the precise monitoring and regulation of biological functions. Devices based on organic materials tend to have low moduli and intrinsic stretchability, making them ideal choices for the construction of seamless bioelectronic interfaces. In this case, as an organic ionic-electronic conductor, poly(3,4-ethylenedioxythiophene):poly(styrene sulfonate) (PEDOT:PSS) has low impedance to offer a high signal-to-noise ratio for monitoring bioelectrical signals, which has become one of the most promising conductive polymers. However, the initial conductivity and stretchability of pristine PEDOT:PSS are insufficient to meet the application requirements, and there is a trade-off between their improvement. In addition, PEDOT:PSS has poor stability in aqueous environments due to the hygroscopicity of the PSS chains, which severely limits its long-term applications in water-rich bioelectronic interfaces. Considering the growing demands of multi-function integration, the high-resolution fabrication of electronic devices is urgent. It is a great challenge to maintain both electrical and mechanical performance after miniaturization, particularly at feature sizes below 100 μm. In this review, we focus on the combined improvement in the conductivity and stretchability of PEDOT:PSS, as well as the corresponding mechanisms in detail. Also, we summarize the effective strategies to improve the stability of PEDOT:PSS in aqueous environments, which plays a vital role in long-term applications. Finally, we introduce the reliable micropatterning technologies and PEDOT:PSS-based stretchable optoelectronic devices applied at bio-interfaces.

Electrochemical and Electrical Biosensors for Wearable and Implantable Electronics Based on Conducting Polymers and Carbon-Based Materials.

Bioelectronic devices are designed to translate biological information into electrical signals and vice versa, thereby bridging the gap between the living biological world and electronic systems. Among different types of bioelectronics devices, wearable and implantable biosensors are particularly important as they offer access to the physiological and biochemical activities of tissues and organs, which is significant in diagnosing and researching various medical conditions. Organic conducting and semiconducting materials, including conducting polymers (CPs) and graphene and carbon nanotubes (CNTs), are some of the most promising candidates for wearable and implantable biosensors. Their unique electrical, electrochemical, and mechanical properties bring new possibilities to bioelectronics that could not be realized by utilizing metals- or silicon-based analogues. The use of organic- and carbon-based conductors in the development of wearable and implantable biosensors has emerged as a rapidly growing research field, with remarkable progress being made in recent years. The use of such materials addresses the issue of mismatched properties between biological tissues and electronic devices, as well as the improvement in the accuracy and fidelity of the transferred information. In this review, we highlight the most recent advances in this field and provide insights into organic and carbon-based (semi)conducting materials' properties and relate these to their applications in wearable/implantable biosensors. We also provide a perspective on the promising potential and exciting future developments of wearable/implantable biosensors.

Ultrathin Flexible Encapsulation Materials Based on Al2O3/Alucone Nanolaminates for Improved Electrical Stability of Silicon Nanomembrane-Based MOS Capacitors.

Ultrathin flexible encapsulation (UFE) using multilayered films has prospects for practical applications, such as implantable and wearable electronics. However, existing investigations of the effect of mechanical bending strains on electrical properties after the encapsulation procedure provide insufficient information for improving the electrical stability of ultrathin silicon nanomembrane (Si NM)-based metal oxide semiconductor capacitors (MOSCAPs). Here, we used atomic layer deposition and molecular layer deposition to generate 3.5 dyads of alternating 11 nm Al2O3 and 3.5 nm aluminum alkoxide (alucone) nanolaminates on flexible Si NM-based MOSCAPs. Moreover, we bent the MOSCAPs inwardly to radii of 85 and 110.5 mm and outwardly to radii of 77.5 and 38.5 mm. Subsequently, we tested the unbent and bent MOSCAPs to determine the effect of strain on various electrical parameters, namely the maximum capacitance, minimum capacitance, gate leakage current density, hysteresis voltage, effective oxide charge, oxide trapped charge, interface trap density, and frequency dispersion. The comparison of encapsulated and unencapsulated MOSCAPs on these critical parameters at bending strains indicated that Al2O3/alucone nanolaminates stabilized the electrical and interfacial characteristics of the Si NM-based MOSCAPs. These results highlight that ultrathin Al2O3/alucone nanolaminates are promising encapsulation materials for prolonging the operational lifetimes of flexible Si NM-based metal oxide semiconductor field-effect transistors.

Nitrogen-doped carbon nanotubes for self-powered memristive systems

Memristive devices are one of the promising candidates for creating neuromorphic systems due to the possibility of multilevel switching, low operating voltages and high scalability. However, as with any passive element, the memristor requires an external bias voltage to operate, which requires the inclusion of a power source in the circuit. In this regard, of great interest are works on the creation of self-powered memristive systems consisting of connecting in series a memristor and a nanogenerator that converts the energy of the external environment into electrical energy [1, 2]. Such a memristive system has a high potential for applications in aerospace and implantable electronics. At the moment, the first self-powered memristive and sensor systems based on metal oxides and piezoelectric nanogenerators (PENG) have already been developed [2]. The main problems in this area are to reduce the size of the nanogenerator and to match the output parameters of the nanogenerator and the input parameters of the memristor. In the framework of this work, these problems are being resolved by creating a self-powered memristive system based on nitrogen-doped carbon nanotubes (N-CNTs). Previously, we studied the memristive properties of N-CNTs and showed that nanotubes demonstrate reproducible multilevel switching with a resistance ratio in the high- and low-resistance states (HRS/LRS) of about 4⋅105 [3, 4]. It was found that the memristive effect in N-CNTs is due to the incorporation of nitrogen atoms into the nanotube structure and the formation of an internal piezoelectric field [4]. As part of further studies, it was found that an array of vertically aligned N-CNTs is a promising material for creating PENG: the generated output voltage is hundreds of mV and the current generated by single nanotube reaches hundreds of nA [5]. The results obtained allow us to speak about the possibility of developing a self-powered memristive system by connecting in series a memristor and PENG based on N-CNTs. To optimize the output characteristics of the PENG, in particular, the amplitude of the generated voltage, and the input switching voltage of the N-CNT-based memristor, studies were carried out to increase the piezoelectric response and reduce the switching voltage of the N-CNT resistance by changing the concentration of the dopant nitrogen in the nanotube growth process. It was found that it is necessary to grow N-CNTs with a doping nitrogen concentration of up to 12% and a high aspect ratio of length to diameter (more than 60) to create PENG with an output voltage of up to 2 V. These N-CNT parameters are provided at a low growth temperature (500–550 C°) and high ratio of acetylene and ammonia flows (1:5 - 1:6). On the contrary, the N-CNTs with a small aspect ratio (less than 30) and doping nitrogen concentrations of 4–6% are required for the manufacture of memristors with a minimum switching voltage (about 2 V), These N-CNT parameters are provided by increasing the growth temperature to 615 C° and reduction in growth time. The obtained results can be used in the development of self-powered memristive and sensor systems based on nitrogen-doped carbon nanotubes.

Design of biodegradable gelatin resistive memory with remarkable performance

For electronic systems, the substrate can be treated as a cornerstone of the overall device structure. With the growth of green electronics, the development of biodegradable substrates is of great significance. Gelatin substrates demonstrate transparency, low temperature, low cost, and fully biodegradable. In particular, gelatin of porcine source (GP) possesses excellent elasticity and high amount of hydroxyproline, which significantly improves the structural stability and memory performance of the device. The device with Ag/gelatin/Ag structure on GP substrate has illustrated non-volatile memory characteristics to be reckoned with an ON/OFF ratio of over 105, uniformly distributed switching parameters (<20 %), and steady retention time (>104 s). It is striking that the resistive switching of the GP-based device maintains stability under various curvature bending stresses (ON/OFF ratio of approximately 105) and displays repeatable resistive states undergoes 1000 cycles of bending tests, not only provides excellent structural reliability and robust mechanical flexibility but also effectively suppresses leakage current in devices, which is beneficial for flexible memory applications. Furthermore, the device possesses outstanding thermal stability, and numerous resistive switching behaviors even at 70 °C are observed. The conductive mechanism may be attributed to the ionic migration in the Ag ions chelating in amine groups of gelatin on the basis of the compelling electrical evidence for Ag/gelatin/Ag/GP devices. The biomass substrate disintegrates entirely in PBS solution without toxic residues, providing a novel design guideline for biomedical applications inspired by implantable, interventional medical, and wearable electronics.

Toward tiny high-power-density thermoelectric harvesters

Thermoelectric (TE) generators (TEGs) have recently attracted significant attention for harvesting ubiquitous heat energy to power industrial sensor nodes or wearable and implantable electronics. Such applications require that a small, fitted heat sink be incorporated into a tiny harvester to ensure conformal deployment and ease of use. Since the small heat sink will exhibit very poor heat rejection performance, the optimal structural design of the TEG device and the proper selection of its constituent TE materials are extremely important to ensure that sufficient electric power is provided to the connected post-stage circuits. Regrettably, the traditional forward design strategies, i.e., material-to-device and device-to-harvester, are often disconnected from one another and fail to form a complete chain, thereby presenting a fundamental challenge in achieving ultrahigh-power-density harvesters. Here we present a zero-dimensional model for a tiny harvester to establish a set of new metrics (not limited to the figure of merit zT) that can be used to determine the optimal TE material and to directly deduce the optimal configuration of the TEG for guaranteeing the maximum output power at various load conditions, making backward design strategy possible. Two tiny harvesters are accordingly fabricated and exhibit areal power densities 52 and 94 times that of a harvester incorporating a commercial TEG, with identical amounts of TE material used for each.

Robust Piezoelectric Biomolecular Membranes from Eggshell Protein for Wearable Sensors.

Flexible and wearable devices are drawing increasing attention due to their promising applications in energy harvesting and sensing. However, the application of wearable devices still faces great challenges, such as flexibility, repeatability, and biodegradability. Biopiezoelectric materials have been regarded as favorable energy-harvesting sources due to their nontoxicity and biocompatibility. Here, a wearable and biodegradable sensor is proposed to monitor human activities. The proposed sensor is fabricated via a low-cost, facile, and scalable electrospinning technology from nanofibers composed of eggshell membranes mixed with polyethylene oxide. It is shown that the sensor exhibits excellent flexibility, outstanding degradability, and mechanical stability over 3000 cycles under periodic stimulation. The device displays multiple potential applications, including the recognition of different objects, human motion monitoring, and active voice recognition. Finally, it is shown that the composite nanofiber membrane has good degradability and breathability. With excellent sensing performance, environmental friendliness, and ease of processing, the eggshell membrane-based sensor could be a promising candidate for greener and more environmentally friendly devices for application in implantable and wearable electronics.

Electrohydrodynamic-printed ultrathin Ti3C2Tx-MXene field-effect transistor for probing aflatoxin B1

Microarray patterns fabricated using printing technology have attracted significant research interest for the production of portable, implantable, feasible, wearable, and flexible electronics. Electrohydrodynamic (EHD) printing is an emerging, simple, and rapid electrode-patterning technology for academic and industrial applications. The development of devices composed of MXenes, 2D hexagonal crystals, which demonstrate great potential for electronic and energy storage applications, is one of the main focuses of current research efforts. Herein, we report the EHD-printed Ti3C2Tx MXene-based field-effect transistors (FET) as promising biosensors for aflatoxin B1 (AFB1) detection. The printing cycles and ink concentration were considered as the optimization objectives, and the optimized FET was validated using the output and transfer characteristics of the device. The optimized EHD-printed FET exhibited good adhesion to the substrate, high electrical conductivity, and an ideal range of resistance. The biosensor was created by functionalizing the EHD-printed MXene layers with a specific antibody against AFB1. This FET biosensor could detect the AFB1 at a concentration of 0.01 ppb with a linearity range of 0.7–20 ppb in a water medium (limit of detection = 5.689 ppb). In addition, the FET biosensor successfully detected AFB1 in food samples, such as peanut butter and meju. Thus, we have successfully demonstrated a promising EHD-printed FET biosensor for AFB1. The device is a highly selective and sensitive immunoanalytical method for AFB1 that requires no complex sample preparation steps compared with high-performance liquid chromatography.

Largely Improving the Output Performance of Stretchable Triboelectric Nanogenerators via Thermo-Compressive Technology.

Stretchable triboelectric nanogenerators (TENGs) are widely applied in wearable and implantable electronics, smart medical devices, and soft robots. However, it is still a challenge to produce stretchable TENGs with both exceptional elasticity and output performance, which limits their application scope. In this work, high-performance stretchable TENGs are developed through a thermo-compression(TC) fabrication process. In particular, a poly(vinylidene fluoride) film is compactly bound to the elastic thermoplastic polyurethane substrate, which inherits excellent stretchability with a strain of up to 815%. Furthermore, owing to the large surface area, tight contact, and effective vertical transport of tribo-induced charges between the coupled fibrous tribo-layer and soft substrate, the TC composite film-based TENGs exhibit a greater output (2-4 times) than unlaminated film-based TENGs. Additionally, the broad universality of this method is proven using various tribo- and substrate materials. The proposed technology provides a novel and effective approach to conjointly boost the output and stretchability of TENGs, showing encouraging application prospects in self-powered wearable and flexible electronics.

Poly(N‐acryloyl glycinamide) eutectogels

AbstractThe ever‐growing demand for advanced implantable and wearable electronics has stimulated the development of conductive gels with desirable functions. Hydrogels suffer from poor environmental adaptability. The ionogels prepared by dissolving polymers in ionic liquids have to face the problems of high cost of synthesis and biotoxicity concerns. Recently, eutectogels consisting of various polymer networks in eco‐friendly and cost‐effective deep eutectic solvents (DESs) have emerged as attractive alternatives to overcome the limitations associated with conventional hydrogels and ionogels. In this study, a kind of eutectogels was designed and synthesized through one‐step in situ photopolymerization of N‐acryloyl glycinamide (NAGA) without crosslinkers in low‐cost and biosafe DESs composed of choline chloride and ethylene glycol. The obtained poly(N‐acryloyl glycinamide) (PNAGA) eutectogels exhibit concentration‐dependent and adjustable mechanical properties, high electrical conductivity (about 2 mS cm−1), self‐healing ability as well as good anti‐drying and anti‐freezing properties. PNAGA eutectogels were also demonstrated to serve as conductive gels to construct pressure sensors over a relatively large temperature range. Considering the simple and easy‐to‐scale preparation process and commercially available low‐cost raw materials, favorable flexibility, high ionic conductivity, and wide‐climate tolerance, the PNAGA eutectogels as soft conductive materials have great potential for use in the fabrication of flexible electronics.

Implantable anti-biofouling biosupercapacitor with high energy performance

Biofluidic open-type supercapacitors offer significant advantages over batteries in implantable electronics. However, poor energy storage in bioelectrolytes and performance degradation owing to electrode biofouling remain challenges and hamper their implementation. In this study, we present a flexible polydopamine (PDA)-infiltrated carbon nanotube (CNT) yarn (PDA/CNT) supercapacitor with high performance in biofluids, encapsulated by a hydrogel-barrier circular knit that provides anti-biofouling protection. Infiltration of the biopolymer PDA provide a hydrophilic coating to obtain a hydrophobic CNT electrode under aqueous conditions and an energy density 250-fold higher than that of the pristine CNT in the biofluid. The PDA/CNT supercapacitor exhibited remarkable energy performance in biological fluids in terms of the maximum areal capacitance (503.91 mF cm−2), energy density (274 μWh/cm2), and power density (25.52 mW cm−2). Moreover, it demonstrated negligible capacitance loss after 10,000 repeated charge/discharge cycles and bending tests. To prevent biofouling, the PDA/CNT electrode was encapsulated in an agarose-coated circular knit that allows free movement of the electrolyte. Notably, implanting an encapsulated PDA/CNT supercapacitor into the abdominal cavity of rat resulted in stable in vivo energy storage performance without biofouling for 21 d, and the charged supercapacitor was used successfully to power a light-emitting diode in vivo.

Selective Ion Sensing Organic Electrochemical Transistors Suitable for Blood Analysis

AbstractOrganic electrochemical transistors (OECTs) have gained considerable attention due to their ability to simultaneously transduce and amplify ion‐based biological signals into electronic signals in bioelectronics. In this study, functionalized OECTs capable of detecting specific ion concentrations in aqueous solution and blood serum are investigated and described. Sodium, the most concentrated cation in the human body, is chosen as the target analyte due to its critical role in maintaining normal bodily functions such as blood pressure, nerve and muscle function, and fluid balance. These sodium ion sensors work at low source‐drain voltage, Vds = 0.4 V and gate voltage, Vg = 0 V, and demonstrate a high sensitivity of 126 μA dec−1 and a high selectivity over different cations. Furthermore, the OECT biosensors are employed to determine sodium concentration in more complex environments and demonstrated a log‐linear response within the physiological range of sodium in blood serum, ranging from 100 to 160 mm. In the final part of the study, the transistor‐based sensor is fabricated in a small‐footprint neural probe configuration and its sensing capability is investigated. These characteristics open up new opportunities for applications in wearable and implantable electronics.

Minimally invasive power sources for implantable electronics

AbstractAs implantable medical electronics (IMEs) developed for healthcare monitoring and biomedical therapy are extensively explored and deployed clinically, the demand for non‐invasive implantable biomedical electronics is rapidly surging. Current rigid and bulky implantable microelectronic power sources are prone to immune rejection and incision, or cannot provide enough energy for long‐term use, which greatly limits the development of miniaturized implantable medical devices. Herein, a comprehensive review of the historical development of IMEs and the applicable miniaturized power sources along with their advantages and limitations is given. Despite recent advances in microfabrication techniques, biocompatible materials have facilitated the development of IMEs system toward non‐invasive, ultra‐flexible, bioresorbable, wireless and multifunctional, progress in the development of minimally invasive power sources in implantable systems has remained limited. Here three promising minimally invasive power sources summarized, including energy storage devices (biodegradable primary batteries, rechargeable batteries and supercapacitors), human body energy harvesters (nanogenerators and biofuel cells) and wireless power transfer (far‐field radiofrequency radiation, near‐field wireless power transfer, ultrasonic and photovoltaic power transfer). The energy storage and energy harvesting mechanism, configurational design, material selection, output power and in vivo applications are also discussed. It is expected to give a comprehensive understanding of the minimally invasive power sources driven IMEs system for painless health monitoring and biomedical therapy with long‐term stable functions.

Electromechanical and biological evaluations of 0.94Bi0.5Na0.5TiO3–0.06BaTiO3 as a lead-free piezoceramic for implantable bioelectronics

Smart implantable electronic medical devices are being developed to deliver healthcare that is more connected, personalised, and precise. Many of these implantables rely on piezoceramics for sensing, communication, energy autonomy, and biological stimulation, but the piezoceramics with the strongest piezoelectric coefficients are almost exclusively lead-based. In this article, we evaluate the electromechanical and biological characteristics of a lead-free alternative, 0.94Bi0.5Na0.5TiO3–0.06BaTiO3 (BNT-6BT), manufactured via two synthesis routes: the conventional solid-state method (PIC700) and tape casting (TC-BNT-6BT). The BNT-6BT materials exhibited soft piezoelectric properties, with d33 piezoelectric coefficients that were inferior to commonly used PZT (PIC700: 116 pC/N; TC-BNT-6BT: 121 pC/N; PZT-5A: 400 pC/N). The material may be viable as a lead-free substitute for soft PZT where moderate performance losses up to 10 dB are tolerable, such as pressure sensing and pulse-echo measurement. No short-term harmful biological effects of BNT-6BT were detected and the material was conducive to the proliferation of MC3T3-E1 murine preosteoblasts. BNT-6BT could therefore be a viable material for electroactive implants and implantable electronics without the need for hermetic sealing.

Flexible Organic Transistors for Biosensing: Devices and Applications.

Flexible and stretchable biosensors can offer seamless and conformable biological-electronic interfaces for continuously acquiring high-fidelity signals, permitting numerous emerging applications. Organic thin film transistors (OTFTs) are ideal transducers for flexible and stretchable biosensing due to their soft nature, inherent amplification function, biocompatibility, ease of functionalization, low cost, and device diversity. In consideration of the rapid advances in flexible-OTFT-based biosensors and their broad applications, herein, a timely and comprehensive review is provided. It starts with a detailed introduction to the features of various OTFTs including organic field-effect transistors and organic electrochemical transistors, and the functionalization strategies for biosensing, with a highlight on the seminal work and up-to-date achievements. Then, the applications of flexible-OTFT-based biosensors in wearable, implantable, and portable electronics, as well as neuromorphic biointerfaces are detailed. Subsequently, special attention is paid to emerging stretchable organic transistors including planar and fibrous devices. The routes to impart stretchability, including structural engineering and material engineering, are discussed, and the implementations of stretchable organic transistors in e-skin and smart textiles are included. Finally, the remaining challenges and the future opportunities in this field are summarized.