Flexible Triboelectric Nanogenerator for Promoting the Proliferation and Migration of Human Fibroblast Cells.

Chronic wound healing is often a prolonged process with the migration and proliferation of fibroblast cells playing crucial roles. Electrical stimulation (ES) has emerged as a promising physical therapy modality to promote these key events. In this study, we address this issue by employing a triboelectric nanogenerator (TENG) as an electrical stimulator for both drug release and the stimulation of fibroblast cells. The flexible TENG with a sandwich structure was fabricated using a PCL nanofibrous layer, Kapton, and silicon rubber. The TENG could be folded to any degree and twisted, and it could return to its original shape when the force was removed. Cultured cells received ES twice and three times daily for 8 days, with a 30 min interval between sessions. By applying current in a safe range and appropriate time (twice daily), fibroblasts demonstrate an accelerated proliferation and migration rate. These observations were confirmed through cell staining. Additionally, in vitro tests demonstrated the TENG's ability to simultaneously provide ES and release vitamin C from the patch. After 2 h, the amount of released drug increased 2 times in comparison to the control group. These findings provide support for the development of a TENG for the treatment of wounds, which underlines the promise of this new technique for developing portable electric stimulation devices.

Self-powered triboelectric nanogenerator sensor for detecting humidity level and monitoring ethanol variation in a simulated exhalation environment.

Respiration stands as a vital process reflecting physiological and pathological human health status. Exhaled breath analysis offers a facile, non-invasive, swift, and cost-effective approach for diagnosing and monitoring diseases by detecting concentration changes of specific biomarkers. In this study, we employed Polyethylene oxide/copper (I) oxide composite nanofibers (PCNFs), synthesized via the electrospinning method as the sensing material to measure ethanol levels (1-200 ppm) in an exhaled breath simulator environment. The integrated contact-separation triboelectric nanogenerator was utilized to power the self-powered PCNFs exhaled breath sensor. The PCNFs-based gas sensor demonstrates promising results with values of 0.9 and 3.2 for detecting 5 ppm and 200 ppm ethanol, respectively, in the presence of interfering gas at 90% relative humidity (RH). Notably, the sensor displayed remarkable ethanol selectivity, with ratios of 10:1 to methanol and 25:1 to acetone. Response and recovery times for 200 ppm ethanol at 90 RH% were rapid, at 2.7 s and 5.8 s, respectively. The PCNFs-based exhaled breath sensor demonstrated consistent and stable performance in practical conditions, showcasing its potential for integration into wearable devices. This self-powered breath sensor enabling continuous monitoring of lung cancer symptoms and facilitating compliance checks with legal alcohol consumption limits.

Enhanced proliferation and migration of fibroblast cells by skin-attachable and self-cleaning triboelectric nanogenerator.

Skin wounds are common in accidental injuries, surgical operations, and chronic diseases. The migration and proliferation of fibroblast cells are fundamental to wound healing, which can be promoted by electrical stimulation as a physical therapy modality. Therefore, the development of portable electrical stimulation devices that can be used by patients on-site is an essential need. In the present study, a self-cleaning triboelectric nanogenerator (TENG) has been fabricated for enhancing cell proliferation and migration. The polycaprolactone­titanium dioxide (PCL/TiO2) and polydimethylsiloxane (PDMS) layers were fabricated via a facile method and used as the electropositive and electronegative pair, respectively. The effect of stimulation time on proliferation and migration of fibroblast cells was investigated. The results demonstrated that when the cells were stimulated once-a-day for 40 min, the cell viability was increased, while a long daily stimulation time has an inhibitory effect. Under electrical stimulation, the cells move toward the middle of the scratch, making the scratch almost invisible. During repeated movements, the prepared TENG connected to a rat skin generated an open-circuit voltage and a short-circuit current around 4 V and 0.2 µA, respectively. The proposed self-powered device can pave the way for a promising therapeutic strategy for patients with chronic wounds.

CNT-PDMS foams as self-powered humidity sensors based on triboelectric nanogenerators driven by finger tapping.

An increasing number of frequently applied portable electronics has raised the significance of self-powered systems. In this regard, triboelectric nanogenerators (TENGs) have drawn considerable attention due to their diversity of design and high power output. As a widely used material in TENG electrodes, polydimethylsiloxane (PDMS) shows attractive characteristics, such as electron affinity, flexibility, and facile fabrication. To achieve active TENG-based humidity sensing, we proposed a straightforward method to enhance the hydrophilicity of PDMS by two parallel approaches: 1. Porosity induction, 2. Carbon nanotube (CNT) compositing. Both of the mentioned processes have been performed by water addition during the synthesis procedure, which is not only totally safe (in contrast with the similar foaming/compositing routes), but also applicable for a wide range of nanomaterials. Applying the modified electrode as a single-electrode TENG-based humidity sensor, demonstrated an impressive enhancement of sensing response from 56% up to 108%, compared to the bare electrodes. Moreover, the detecting range of ambient humidity was broadened to higher values of 80% in a linear behavior. The fabricated humidity sensor based on a CNT-PDMS foam not only provides superior sensing characteristics but also is satisfactory for portable applications, due to being lightweight and desirably self-powered.

Self-powered ultraviolet/visible photodetector based on graphene-oxide via triboelectric nanogenerators performing by finger tapping.

Self-sufficient power sources provide a promising application of abundant electronic devices utilized in detection of ambient properties. Recently, triboelectric nanogenerators (TENGs) have been widely investigated to broaden the self-powered systems by converting the ambient mechanical agitations into electrical voltage and current. Graphene oxide (GO), not only for sensing applications but also as a brilliant energy-related nanomaterial, provides a wide range of controllable bandgap energies, as well as facile synthesis route. In this study, GO-based self-powered photodetectors have been fabricated by conflating the photosensitivity and triboelectric characteristics of freestanding GO paper. In this regard, photodetection via TENGs has been investigated in two forms of active and passive circuits for ultraviolet (UV) and visible illumination. The photodetector responsivity upon UV enhanced from 0.011 mA W-1for conventional GO-photoresistors up to 13.41 mA W-1by active photodetection setup. Moreover, applying the active-TENG improved the efficiency from 0.25% (in passive TENG) to 4.21%. Our findings demonstrate that active TENGs might enable materials with insignificant optical response to represent considerably higher light-sensitivity by means of synergizing the effect of TENG output changes with opto-electronical properties of desired layers.

A computational modelling study of excitation of neuronal cells with triboelectric nanogenerators.

Neurological disorders and nerve injuries, such as spinal cord injury, stroke, and multiple sclerosis can result in the loss of muscle function. Electrical stimulation of the neuronal cells is the currently available clinical treatment in this regard. As an effective energy harvester, the triboelectric nanogenerators (TENG) can be used for self-powered neural/muscle stimulations because the output of the TENG provides stimulation pulses for nerves. In the present study, using a computational modelling approach, the effect of surface micropatterns on the electric field distribution, induced voltage and capacitance of the TENG structures have been investigated. By incorporating the effect of the TENG inside the mathematical model of neuron's electrical behavior (cable equation with Hodgkin-Huxley model), its impact on the electrical behavior of the neurons has been studied. The results show that the TENG operates differently with various surface modifications. The performance of the TENG in excitation of neurons depends on the contact and release speed of its electrodes accordingly.

Design of effective self-powered SnS2/halide perovskite photo-detection system based on triboelectric nanogenerator by regarding circuit impedance.

Self-powered detectors based on triboelectric nanogenerators (TENG) have been considered because of their capability to convert ambient mechanical energy to electrical out-put signal, instead of conventional usage of electrochemical batteries as power sources. In this regard, the self-powered photodetectors have been designed through totally two lay out called passive and active circuit. in former model, impedance matching between the TENG and the resistance of the circuit's elements is crucial, which is not investigated systematically till now. In this paper, a cost effective novel planar photodetector (PD) based on heterojunction of SnS2 sheets and Cs0.05(FA0.83 MA0.17)0.95Pb(I0.83Br0.17)3 three cationic lead iodide based perovskite (PVK) layer fabricated which powered by graphene oxide (GO) paper and Kapton based contact-separated TENG (CS-TENG). To achieve the high performance of this device, the proper range of the load resistances in the circuit regards to TENG's characterization has been studied. In the next steps, the integrated self-powered photo-detection system was designed by applying Kapton/FTO and hand/FTO TENG, separately, in the proposed impedance matching circuit. The calculated D* of integrated self-powered SnS2/PVK supplied by tapping the Kapton and hand on FTO is 2.83 × 1010 and 1.10 × 1013 Jones under the 10 mW/cm2 of white light intensity, the investigations determine that for designing significate performance of self-powered PD supplied by TENG, the existence of the load resistance with the well match amount to the utilized TENG is crucial. Our results which can be generalized to other types of passive self-powered sensors, are substantial to both academia and industry concepts.

Nanostructured versus flat compact electrode for triboelectric nanogenerators at high humidity.

The triboelectric nanogenerator (TENG) is a promising technology for mechanical energy harvesting. TENG has proven to be an excellent option for power generation but typically TENGs output power drops significantly in humid environments. In this work, the effect of electrode's material on power output, considering smooth and nanostructured porous structures with various surface hydrophobicity, is investigated under various humidity conditions. A vertical contact-separation mode TENG is experimentally and numerically studied for four surface morphologies of Ti foil, TiO2 thin film, TiO2 nanoparticulated film, and TiO2 nanotubular electrodes. The results show that the TENG electrical output in the flat structures such as Ti foil and TiO2 thin film at 50% RH is reduced to 50% of its initial state, while in the nanoporous structures such as nanoparticle and nanotube arrays, this is observed at RH above 95%. The results show that the use of porous nanostructures in TENG due to their high surface-to-volume, and that the process of water adsorption on the pore leads to better performance than the flat surface in humid environments. Based on our study, employing nanoporous layers is vital for nanogenerators either for power generation or active sensor applications at high humidity conditions.

Enhancement of self-powered humidity sensing of graphene oxide-based triboelectric nanogenerators by addition of graphene oxide nanoribbons.

A triboelectric nanogenerator (TENG) electrode sensitive to the adsorption of water molecules has been introduced to create a self-powered humidity sensor. Graphene oxide (GO) nanosheets and graphene oxide nanoribbon (GONR) possessing oxygenated functional groups, as well as high dielectric constants, have been proposed as appropriate candidates for this purpose. GO papers have been fabricated in three forms, i.e. pure  GO paper, uniform composites of GONR and GO, and double-layer structures of GONR on top of  GO. Results showed that all of the prepared paper-based TENGs revealed excellent performances by maximum output voltage above 300 V. As active humidity sensors, the maximum voltage response values of 57%, 124%, and 78% were obtained for GO, GONR+GO, and GONR/GO TENGs, respectively. Besides high sensitivity and precision of all variants, GO+GONR TENG demonstrated a rapid response/recovery behavior (0.3/0.5 s). This phenomenon can be attributed to the higher oxygenated groups and defects on the edges of GONR, which leads to facilitating the bulk diffusion of water molecules. Our results open new avenues of GONR application as an additive to enhance the performance of self-powered humidity sensors, as well as conventional hygrometers.

Room temperature and high response ethanol sensor based on two dimensional hybrid nanostructures of WS2/GONRs.

Here in this research, room temperature ethanol and humidity sensors were prepared based on two dimensional (2D) hybrid nanostructures of tungsten di-sulfide (WS2) nanosheets and graphene oxide nanoribbons (GONRs) as GOWS. The characterization results based on scanning electron microscopy (SEM), energy dispersive X-ray spectroscopy (ESD), Raman spectroscopy and X-ray diffraction (XRD) analysis confirmed the hybrid formations. Ethanol sensing of drop-casted GOWS films on SiO2 substrate indicated increasing in gas response up to 5 and 55 times higher compared to pristine GONRs and WS2 films respectively. The sensing performance of GOWS hybrid nanostructures was investigated in different concentrations of WS2, and the highest response was about 126.5 at 1 ppm of ethanol in 40% relative humidity (R.H.) for WS2/GONRs molar ratio of 10. Flexibility of GOWS was studied on Kapton substrate with bending radius of 1 cm, and the gas response decreased less than 10% after 30th bending cycles. The high response and flexibility of the sensors inspired that GOWS are promising materials for fabrication of wearable gas sensing devices.

Fabrication of flexible self-powered humidity sensor based on super-hydrophilic titanium oxide nanotube arrays.

Stable and flexible super-hydrophilic nanotubular-based titanium oxide electrode has been utilized as the active electrode of self-powered humidity sensor. TiO2 nanotubular electrodes fabricated through anodization method and utilized in combination with Kapton electrode as the triboelectric nanogenerator (TENG). Vertical contact-separation mode TENG performance has been examined in various range of frequencies and the maximum output voltage and current more than 300 V and 40 µA respectively with maximum power of 1.25 ± 0.67 mW has been achieved at 4 Hz. The fabricated TENG has been employed as the active self-powered humidity sensor. Super-hydrophilic feature of TiO2 nanotubes resulted in full absorption of water molecules, and noticeable decrease in charge transfer across two triboelectric materials upon increasing humidity. The TiO2-based TENG sensor was exposed to various relative humidity (RH) and the results showed that by increasing the humidity the output voltage and output current decreased from 162.24 ± 35.99 V and 20.4 ± 4.93 µA at RH = 20% to 37.92 ± 1.54 V at RH = 79% and 40.87 88 6.88 ± 1.7 µA at RH = 84%, respectively, Which shows the responsivity more than 300%. This method of measuring humidity has a simple and cost-effective fabrication that has various applications in many fields such as industry and medicine.

Graphene Oxide Papers in Nanogenerators for Self-Powered Humidity Sensing by Finger Tapping.

Triboelectric nanogenerators (TENGs) offer an emerging market of self-sufficient power sources, converting the mechanical energy of the environment to electricity. Recently reported high power densities for the TENGs provide new applications opportunities, such as self-powered sensors. Here in this research, a flexible graphene oxide (GO) paper was fabricated through a straightforward method and utilized as the electrode of TENGs. Outstanding power density as high as 1.3 W.m-2, an open-circuit voltage up to 870 V, and a current density of 1.4 µA.cm-2 has been extracted in vertical contact-separation mode. The all-flexible TENG has been employed as a self-powered humidity sensor to investigate the effect of raising humidity on the output voltage and current by applying mechanical agitation in two forms of using a tapping device and finger tapping. Due to the presence of superficial functional groups on the GO paper, water molecules are inclined to be adsorbed, resulting in a considerable reduction in both generated voltage (from 144 V to 14 V) and current (from 23 µA to 3.7 µA) within the range of relative humidity of 20% to 99%. These results provide a promising applicability of the first suggested sensitive self-powered GO TENG humidity sensor in portable/wearable electronics.

Sandblasting improves the performance of electrodes of miniature electrical impedance tomography via double layer capacitance.

Effect of sandblasting of the copper electrode structures before deposition of gold thin film for micro electrical impedance tomography (EIT) system has been studied experimentally. The comparison has been performed on the unmodified copper electrodes and the sandblasted electrodes before deposition of gold layer, using structural analysis while their performance in EIT system has been measured and analyzed. The results of scanning electron microscopy and atomic force microscopy show that the sandblasting of the electrodes results in the deposition of gold film with smaller grain size and uniformly, comparing to the unmodified structure. The measurement of impedance shows that the sandblasting will increase the double layer capacitance of electrode structure which improves the impedance measurement accordingly.

Carbon Nanotube Modified Microelectrode Array for Neural Interface.

Carbon nanotubes (CNTs) coatings have been shown over the past few years as a promising material for neural interface applications. In particular, in the field of nerve implants, CNTs have fundamental advantages due to their unique mechanical and electrical properties. In this study, carbon nanotubes multi-electrode arrays (CNT-modified-Au MEAs) were fabricated based on gold multi-electrode arrays (Au-MEAs). The electrochemical impedance spectra of CNT-modified-Au MEA and Au-MEA were compared employing equivalent circuit models. In comparison with Au-MEA (17 Ω), CNT-modified-Au MEA (8 Ω) lowered the overall impedance of the electrode at 1 kHz by 50%. The results showed that CNT-modified-Au MEAs have good properties such as low impedance, high stability and durability, as well as scratch resistance, which makes them appropriate for long-term application in neural interfaces.

Coupled Ionic-Electronic Equivalent Circuit to Describe Asymmetric Rise and Decay of Photovoltage Profile in Perovskite Solar Cells.

In this research, we employed transient photo-voltage rise and decay measurements to investigate the origin of slow unsymmetrical rise and decay profiles in single and triple cation perovskite solar cells. Drastic changes in photo-voltage decay profile were observed upon insertion of Br-, Cs+ and FA+ ions into perovskite structures. In order to explain our observations, the activation energy for ionic defects was measured and an equivalent circuit model was proposed containing both electrical and ionic components. The electrical branch consists of a diode, the bulk capacitance and resistances for charge transport and recombination. In parallel we introduced an ionic branch describing the ionic response by a resistance for ionic charge transport and a capacitance describing ion accumulation at the interface to the charge transport layer. To reproduce the asymmetry of photo-voltage rise and decay, a diode with a parallel resistor is introduced leading to a belayed backflow of the accumulated ions. The results revealed that the activation energy of ionic defects became larger upon insertion of either halides or cations. There is larger amount of ionic defects in the case of MAPbI3 while the de-accumulation process of ions happens in much larger time scale in triple cation perovskite. The presence of ions at the interfaces results in band bending generating a potential barrier restraining electrons and holes from recombination; so the loss of built-in potential is delayed until de-accumulation of ionic double layer happens. Our model proposes that the loss of built-in potential depends on electrostatic potential drop, suggesting coupled electronic-ionic phenomenon in perovskite solar cells.

Origin of apparent light-enhanced and negative capacitance in perovskite solar cells.

So-called negative capacitance seems to remain an obscure feature in the analysis of the frequency-dependent impedance of perovskite solar cells. It belongs to one of the puzzling peculiarities arising from the mixed ionic-electronic conductivity of this class of semiconductor. Here we show that apparently high capacitances in general (positive and negative) are not related to any capacitive feature in the sense of a corresponding charge accumulation. Instead, they are a natural consequence of slow transients mainly in forward current of the diode upon ion displacement when changing voltage. The transient current leads to a positive or negative 'capacitance' dependent on the sign of its gradient. The 'capacitance' appears so large because the associated resistance, when thinking of a resistor-capacitor element, results from another physical process, namely modified electronic charge injection and transport. Observable for a variety of devices, it is a rather universal phenomenon related to the hysteresis in the current-voltage curve.

Gold-Plated Electrode with High Scratch Strength for Electrophysiological Recordings.

Multi electrode arrays (MEA) have been exploited in different electrophysiological applications. In neurological applications, MEAs are the vital interfaces between neurons and the electronic circuits with dual role; transmitting electric signal to the neurons and converting neural activity to the electric signal. Since the performance of the electrodes has a direct effect on the quality of the recorded neuronal signal, as well as the stimulation, the true choice of electrode material for MEA is crucial. Gold is one of the best candidates for fabrication of MEAs due to its high electrical conductivity, biocompatibility and good chemical stability. However, noble metals such as gold do not adhere well to the glass substrate. Consequently while exposing to the water, gold films are damaged, which impose limitations in the exploiting of gold thin films as the electrode. In this paper, a simple and cost effective method for the fabrication of gold electrode arrays is proposed. Using various mechanical (adhesion test and scratch strength), morphological (AFM and SEM) and electrochemical methods, the fabricated electrodes are characterized. The results show that the fabricated electrode arrays have significantly high scratch strength and stability within the aqueous medium. In addition, the electrical properties of the electrodes have been improved. The proposed electrodes have the potential to be exploited in other applications including electronics, electrochemistry, and biosensors.

Influence of Perovskite Morphology on Slow and Fast Charge Transport and Hysteresis in the Perovskite Solar Cells.

We have investigated the influence of perovskite morphology on slow and fast charge transport in the perovskite solar cells. Solar cells with different perovskite cuboid sizes (50-300 nm) have been fabricated using various methylammonium iodide concentrations. Both the low-frequency capacitance and hysteresis are maximum for the cell with the largest perovskite grains (300 nm). The low-frequency capacitance is about three orders of magnitude greater than the intermediate frequency capacitance, indicating the great role of ions on the slow responses and hysteresis. The measurement of open-circuit voltage decay indicates that for the large grains of 300 nm up to 70% of Voc remains across the cell, even after passing ∼40 s. Such a long time Voc decay demonstrates the large accumulation of the ions at the perovskite interfaces with electron and hole transport layers, which conduct slow redistribution of the charges after the light is turned off.

Light harvesting and photocurrent generation by nanostructured photoelectrodes sensitized with a photosynthetic pigment: a new application for microalgae.

Here in this study, successful conversion of visible light into electricity has been achieved through utilizing microalgal pigments as a sensitizer of nanostructured photo-electrode of dye-sensitized solar cells (DSSCs). For the first time, photosynthetic pigments extracted from microalgae grown in wastewater is employed to imitate photosynthesis process in bio-molecule-sensitized solar cells. Two designs of photoanode were employed: 10 µm nanoparticular TiO2 electrode and 20 µm long self-ordered, vertically oriented nanotube arrays of titanium dioxide films. Microalgal photosynthetic pigments are loaded on nanostructured electrodes and their photovoltaic performances have been investigated. To optimize the performance of solar cell, the time course of dye loading on the nanocrystalline TiO2 films is investigated. The performance of the cells is characterized by measuring the current-voltage (I-V) curves under AM1.5 (100 mW cm(-2)) irradiation condition. The highest efficiency of around ∼ 1%, quite comparable to green plants, is found for sensitizer-loading time of 1h.

Investigation on the dynamics of electron transport and recombination in TiO2 nanotube/nanoparticle composite electrodes for dye-sensitized solar cells.

In this work, we report on fabrication and characterization of dye-sensitized solar cells based on TiO(2) nanotube/nanoparticle (NT/NP) composite electrodes. TiO(2) nanotubes were prepared by anodization of Ti foil in an organic electrolyte. The nanotubes were chemically separated from the foil, ground and added to a TiO(2) nanoparticle paste, from which composite NT/NP electrodes were fabricated. In the composite TiO(2) films the nanotubes existed in bundles with a length of a few micrometres. By optimizing the amount of NT in the paste, dye-sensitized solar cells with an efficiency of 5.6% were obtained, a 10% improvement in comparison to solar cells with pure NP electrodes. By increasing the fraction of NT in the electrode the current density increased by 20% (from 11.1 to 13.3 mA cm(-2)), but the open circuit voltage decreased from 0.78 to 0.73 V. Electron transport, lifetime and extraction studies were performed to investigate this behavior. A higher fraction of NT in the paste led to more and deeper traps in the resulting composite electrodes. Nevertheless, faster electron transport under short-circuit conditions was found with increased NT content, but the electron lifetime was not improved. The electron diffusion length calculated for short-circuit conditions was increased 3-fold in composite electrodes with an optimized NT fraction. The charge collection efficiency was more than 90% over a wide range of light intensities, leading to improved solar cell performance.