Conductive Electrodes Research Articles

Accurately prepared the large-area and efficiently 3D electrodes for overall seawater splitting

How to achieve accurately regulation of catalytic electrodes is the challenge of designing high-performance catalytic electrodes. In this work, large area, high stability and excellent conductivity electrode are prepared via one-step mild (298 K) electroplating method and precise control of electroplating parameters on nickel foam (FeNi@NF). The FeNi@NF electrode catalyst the hydrogen/oxygen evolution reaction (HER/OER) in simulate seawater (1.0 M KOH + 0.5 M NaCl), and achieves the current density of 100 mA cm−2 with only 287 mV and 323 mV overpotential. The alkaline electrolyzer drives 100 mA cm−2 for overall water splitting at a low voltage of 1.73 V. More importantly, the catalytic performance durable for more than 5 days at the industrial current density (1000 mA cm−2), and the designed large-area 25.0 cm2 catalytic electrode can achieve stable operation of industrial proton exchange membrane electrolyser. This preparation strategy provides a new idea for the current research of energy engineering and energy storage.

MRI and CT compatible asymmetric bilayer hydrogel electrodes for EEG-based brain activity monitoring

The exploration of multi-dimensional brain activity with high temporal and spatial resolution is of great significance in the diagnosis of neurological disease and the study of brain science. Although the integration of electroencephalogram (EEG) with magnetic resonance imaging (MRI) and computed tomography (CT) provides a potential solution to achieve a brain-functional image with high spatiotemporal resolution, the critical issues of interface stability and magnetic compatibility remain challenging. Therefore, in this research, we proposed a conductive hydrogel EEG electrode with an asymmetrical bilayer structure, which shows the potential to overcome the challenges. Benefiting from the bilayer structure with different moduli, the hydrogel electrode exhibits high biological and mechanical compatibility with the heterogeneous brain-electrode interface. As a result, the impedance can be reduced compared with conventional metal electrodes. In addition, the hydrogel-based ionic conductive electrodes, which are free from metal conductors, are compatible with MRI and CT. Therefore, they can obtain high spatiotemporal resolution multi-dimensional brain information in clinical settings. The research outcome provides a new approach for establishing a platform for early diagnosis of brain diseases and the study of brain science.

Core‐Shell Structured CoP@C Cubes as a Superior Anode for High‐Rate and Stable Sodium Storage

AbstractTransition metal phosphides have emerged as a class of promising anode materials of sodium‐ion batteries owing to their excellent sodium storage capacity. However, the limited electronic conductivity and significant volume expansion have impeded their further advancement. In this work, we propose a rational design of cube‐like CoP @C composites with unique core‐shell structure via in situ phosphating and subsequent carbon coating processes. The uniform carbon coating serves as a physical buffering layer that effectively mitigates volume changes during charge/discharge processes, and prevents particle agglomeration and fragmentation, thereby enhancing the structural stability of electrode. Moreover, the nitrogen‐rich carbon layer not only provides additional active sites for sodium ion adsorption but also improves the electrode conductivity and accelerates charge transport dynamics. Consequently, the as‐synthesized CoP@C exhibits a remarkable capacity retention rate of 94.8 % after 100 cycles at 0.1 A g−1 and achieves a high reversible capacity of 146.7 mAh g−1 even under a high current density of 4.0 A g−1.

Graphene wrapped porous polyaniline/manganese oxide nanocomposites with enhanced structural stability and conductivity for high‐performance symmetric supercapacitor

AbstractManganese oxides have emerged as promising electrode materials for supercapacitors. Despite extensive efforts to improve their conductivity and structural stability through various manganese oxide/conductor nanocomposites, achieving efficient and reliable energy storage electrode materials has remained challenging. In this study, we propose a meticulous “dual enhancement” strategy, where three‐dimensional (3D) nanostructured polyaniline/manganese oxide composites (PM) are synthesized via an in situ method and further integrated with graphene wrapping to form polyaniline/manganese oxide/graphene nanocomposites (PMG). Electrochemical characterization reveals that PMG exhibits a remarkable specific capacitance of up to 403 F g−1 (at 1 A g−1), with a favorable capacitance retention of 80.2% after 5000 cycles, along with a wide potential window. This enhancement is attributed to the synergistic effects of polyaniline, which provides a supportive framework and electron transport pathways, and graphene, which offers external protection and enhances conductivity pathways. Assembled symmetrical supercapacitors demonstrate outstanding energy density (32.7–23.3 Wh kg−1) and power density (720–4500 W kg−1) at a high operating voltage of 1.8 V, surpassing the performance of many reported high‐performance supercapacitors. This study provides valuable insights for advancing manganese oxide electrode materials and is expected to catalyze their widespread adoption in energy storage applications.Highlights “Dual enhancement” is implemented by PANI supporting and rGO wrapping. The conductivity and structural stability of composite electrode is greatly enhanced. Improved capacitance (403 F g−1, 1 A g−1) and cycling stability (80.2%) is achieved. The symmetrical supercapacitor has high voltage and energy density (32.7 Wh kg−1).

Analyzing switching variability of SiNx-based RRAM in terms of Joule heating dissipation

In this paper, the switching variability of SiNx-based RRAM with reactive metal electrodes in terms of Joule heating dissipation was analyzed. The electrode with high (low) thermal conductivity showed low LRS (HRS) variability in SiNx-based RRAM. By analyzing the I–V characteristics and the current conduction mechanism, we proposed that the thermal conductivity of reactive electrodes significantly affected the number of ions involved in the switching process and the vacancies distribution in the switching layer, resulting in the difference in the switching performance. This study suggested that attention should be paid to the influence of electrode thermal conductivity on variability, providing ideas for designing RRAM with low switching variability.

Electrochemical and bioelectrochemical sulphide removal: A review

AbstractThe increased demand for energy worldwide and the focus on the green shift have raised interest in renewable energy sources such as biogas. During biogas production, sulphide (H2S, HS− and S2−) is generated as a byproduct. Due to its corrosive, toxic, odorous, and inhibitory nature, sulphide is problematic in various industrial processes. Therefore, several techniques have been developed to remove sulphide from liquid and gaseous streams, including chemical absorption, chemical dosing, bioscrubbers, and biological oxidation. This review aims to elucidate electrochemical and bioelectrochemical sulphide removal methods, which are gaining increasing interest as possible supplements to existing technologies. In these systems, the sulphide oxidation rate is affected by the reactor design and operational parameters, including electrode materials, anodic potential, pH, temperature and conductivity. Anodic and bioanodic materials are highlighted here, focusing on recent material developments and surface modification techniques. Moreover, the review focuses on sulphide generation and inhibition in biogas production processes and introduces the prospect of removing sulphide and producing methane in one single bioelectrochemical reactor. This could introduce BESs for combined biogas upgrading and cleaning, thereby increasing the methane content and removing pollutants such as sulphide and ammonia in one unit.

Carbon Nanotubes and Their Composites for Flexible Electrochemical Biosensors

AbstractFlexible biosensors play a crucial role for healthcare management and disease diagnosis. Electrochemical biosensors have attracted significant attention for wearable sensing applications owing to their numerous advantages, including high sensitivity and selectivity, inherent miniaturization and rapid response times. Challenges lie in the development of highly conductive and flexible electrodes that can be integrated with biorecognition components to engineer selective biosensor interfaces. Carbon nanotubes (CNTs) hold significant promise as materials for wearable flexible sensor fabrication. This review highlights recent strategies for fabricating conductive and flexible electrodes, whether in the form of films or fibers, based on CNTs and their composites. Additionally, the review explores emerging biosensing applications, including flexible sensors for the direct electrochemical detection of biomarkers, sensors functionalized with enzymes, antibodies, or DNA, and sensors interfaced with cells to monitor transient biochemical signals.

Interpretation of dielectric spectroscopy measurements of ferroelectric nematic liquid crystals

The magnitude of the relative permittivity of the ferroelectric nematic phase (NF) has been the subject of lively scientific discussion since the phase was recently discovered. Dielectric spectroscopy measurements (DSMs) give a huge value of relative permittivity, which depends on the cell thickness, but this is argued to result from a misinterpretation of the DSM results. We have conducted DSM using a set of cells differing in thickness of the NF layer, type of electrodes, and presence/absence of nanoscale-thick surface polymer layers. To model the DSM results, cells are presented by an equivalent electric circuit that includes a capacitor due to the NF layer with frequency dependent complex relative permittivity, capacitors due to surface layers, and a resistor describing the limited conductivity of electrodes. DSM results for different cells with the same liquid crystal in the NF phase are semiquantitatively reproduced by the same set of physical parameters if a huge relative permittivity of the NF, which is even orders of magnitude larger than the measured apparent values, is assumed. We show that the capacitance of surface layers should also be considered in cells with no polymer alignment layer on the electrodes. Published by the American Physical Society 2024

Cr2O3–NiO mixed oxides thin films for p-type transparent conductive electrodes

The Cr2O3–NiO mixed oxides’ thin films were formed by means of the layer-by-layer magnetron sputtering deposition of Cr2O3, NiO, and Cr2O3 layers on c-plane sapphire substrates. These thin-film structures, subjected to subsequent annealing, constituted a combination of the monocrystalline (0001) Cr2O3 and nonordered nickel oxide phase, which was a mixture of NiO and Ni2O3. The annealing at 900 and 1000 °С in air facilitated the diffusion of Ni and Cr atoms into the layers. Varying the annealing time allowed us to control the uniformity of the Ni and Cr distribution, the microrelief of the film surface, the transmittance in the visible region, and the sheet resistance of the Cr2O3–NiO thin-film structures. Thus, the films annealed at 900 °C during 30 min were characterized by a uniform distribution, a relatively weakly developed surface, a low sheet resistance, and the highest Haacke's Figure of Merit of 1.49 × 10–9 Ω–1. The formation of mixed Cr2O3–NiO oxides by the proposed approach was found to be an effective way to improve the performances of Cr2O3 based p-type transparent conductive electrodes.

3D printed microfluidic devices with electrodes for electrochemical analysis.

A review with 93 references describing various 3D printing approaches that have been used to create microfluidic devices containing electrodes for electrochemical detection. The use of 3D printing to fabricate microfluidic devices is a rapidly growing area. One significant research area is how to detect analytes in the devices for quantitation purposes. This review article is focused on methods used to integrate electrodes into the devices for electrochemical detection. The review is organized in terms of the methodology for integrating the electrode within the device. This includes (1) external coupling of traditional electrode materials with 3D printed devices; (2) printing conductive electrode materials as part of device printing; and (3) integrating traditional electrodes into the device as part of the print process. Example applications are given and some future directions are also outlined.

The Degradation of Rhodamine B by an Electro-Fenton Reactor Constructed with Gas Diffusion Electrode and Heterogeneous CuFeO@C Particles

Compared with conventional Fenton processes, the electro-Fenton process consumes fewer chemicals and produces less sludge, as it can generate the required Fenton’s reagents in situ. In this work, an electro-Fenton reactor was constructed to treat synthetic rhodamine B (Rh B) wastewater, in which a gas diffusion electrode (GDE) was used as a cathode to produce H2O2, and heterogeneous CuFeO@C particles were used to generate Fe2+ in situ. The results indicated that the gas diffusion electrode made of elements N-S-B and r-graphene oxide (NSB-r-GO) composites produced more H2O2 than the one made from r-graphene oxide (r-GO), under the conditions of 0.1 mol ·L−1 Na2SO4 electrolyte, 10 mA·cm−2 current density, and 1.0 L·min−1 O2 flow rate, with the accumulated H2O2 production reaching 105.43 mg·L−1. Additionally, different iron morphologies, including octahedral Fe (II), octahedral Fe (III), and tetrahedral Fe (III), were found in the calcined CuFeO@C particles, approximately 1.0 mg·L−1 of iron ions dissolved in the electrolyte was detected, which worked simultaneously as conductive electrodes in a conceptual three-dimensional electrochemical reactor consisting of a gas diffusion electrode cathode, Ti/RuSn anode, and CuFeO@C particle electrodes. No external Fenton reagents were necessary.

Laminar Flow Infrared Spectroelectrochemistry.

In this work, we advance lab-on-chip electrochemistry and spectroscopy by combining these capabilities onto a single platform, thereby achieving mid-infrared spectroelectrochemistry (SEC) for the first time. The key feature of this technique is the use of deterministic laminar flow patterns to precisely transport a reacted solution from upstream electrodes to a downstream spectral detection region. Laminar flow spectroelectrochemistry (LF-SEC) is therefore a completely new approach, which derives its distinction and advantage over traditional SEC by physically separating electrode and attenuated total reflection (ATR) elements. As such, these functional elements retain optimal properties, such as inert, highly conductive electrodes and a bare ATR element for sensitive Fourier transform infrared (FTIR) spectroscopy. By combining ATR-FTIR with a scanning aperture system, LF-SEC provides the additional advantage of spectroscopically monitoring reactions at individual electrodes. The LF-SEC system design is first optimized through a series of targeted experiments using a ferricyanide/ferrocyanide redox pair to validate electrochemical functionality, undertake spectroscopic calibration, optimize experimental parameters, and finally validate the quantitative relationship between FTIR results and the reaction rate under galvanostatic control. After optimization, we demonstrate the technique by monitoring the oxidation of the therapeutic compound ascorbic acid (vitamin C) in the presence of biomolecular interference from a molecule with an overlapping oxidation potential. We find that molecular availability causes the reaction to switch between reaction pathways, which we could finely monitor using LF-SEC. This work opens the door to future developments that take advantage of the microfluidic reactor setup, with benefits ranging from portability to high-throughput studies under precise reaction conditions.

RF NEMS switches based on graphene for low pull-in voltage and excellent RF performance

This study introduces a novel graphene RF NEMS capacitive switch and conducts an extensive analysis of its RF performance using CST and COMSOL Multiphysics software. The switch’s characteristic impedance matching is accomplished through a coplanar waveguide (CPW) structure, incorporating a dielectric layer topped with conductive graphene beam electrodes. Simulation results reveal that the monolayer graphene RF NEMS switch maintains an insertion loss of 0.003 ~ 0.015 dB and an isolation greater than 40 dB across an ultra-wideband (UWB) frequency range of DC ~ 140 GHz. Moreover, the switch demonstrates a switching time of 4.03 ps at a pull-in voltage of 1 V. The performance of multilayer graphene RF NEMS switches was also evaluated. The study further investigates the operational mechanism of the graphene RF NEMS switch and performs finite element analysis on the proposed design. The graphene RF NEMS switch discussed herein offers significant advantages, including minimal size, lightweight, cost-effectiveness, low pull-in voltage, rapid response time, excellent RF performance, and reduced space consumption in circuitry. Its potential applications span a range from L to F bands, encompassing data storage, communication systems, sensors, remote sensing and military uses.

Neodymium oxide-based hybrid phase few-layer MoS2 nanocomposite as high-performance symmetric supercapacitor electrode

The two-dimensional layered materials (for example MoS2) are potential electrodes for supercapacitors with their excellent lamellar structure, high surface area, mechanical flexibility, and potential redox activity. However, due to restacking of chemical structure and low electrical conductivity of the pure MoS2 electrodes are prevented for energy storage applications. Therefore the electrodes are made up of a composite by a mixture of MoS2 and rare-earth metals significantly addressing these issues with improved electrical conductivity, large electrochemical active surface, and shorter ion-diffusion kinetics. In the present study, the MoS2 and MoS2/Nd2O3 composite were synthesized by hydrothermal method. The structural phase identification of prepared samples was accomplished by using an X-ray diffractometer (XRD) and Raman spectra. Furthermore, TEM reveals changes in the shape of nanosheets and interlayer spacing. The GCD of symmetric MoS2/Nd2O3 composite electrodes displayed remarkable charging/discharging performance, with increased stability and rate capability. The MoS2/Nd2O3 composite shows utmost Csp of 2528.18 Fg-1 at 1 Ag-1. In addition, the CV and GCD studies suggest that the electrodes exhibit pseudocapacitive behavior and excellent energy density(E) of 191 Wh kg-1 at 1474.1 W kg-1 power density(P) in 1M H2SO4. The supercapacitor device made up of MoS2/Nd2O3 composite shows greater performance in practical LED glowing applications. Therefore, the composites make advancements in energy storage devices like batteries and supercapbatteries due to their excellent energy storage, high electrochemically active surface area, and stability.

Plasma assisted single-step synthesis of carbon-coated SrFe2O4 electrodes for enhancing supercapacitor and oxygen evolution reaction

Developing highly efficient, conductive, and porous electrode materials for superior electrochemical bifunctional applications presents a formidable challenge, particularly when considering impurity-free large-scale production. This investigation focuses on synthesizing a composite material of highly conductive amorphous carbon-coated SrFe2O4 nanoparticles to enhance supercapacitor and oxygen evolution performance. The C@SrFe2O4 nanoparticles were synthesized through a thermal plasma process utilizing argon, methane, and carbon dioxide gas environments. The prepared samples' phase, crystal structure, morphology, elemental composition, and chemical state analysis were thoroughly examined. The electrochemical performance of the prepared samples, including Fe3O4, SrO, and C@SrFe2O4 electrodes, was evaluated for their suitability in electrochemical capacitor applications. Remarkably, C@SrFe2O4 nanoparticles exhibited notable electrochemical pseudocapacitive behavior, demonstrating a significantly higher specific capacitance of 588.7 F/g at a current density of 1 A/g. Moreover, at a current density of 10 A/g, the C@SrFe2O4 electrode exhibited outstanding cycling stability, maintaining 91 % of its initial capacitance over 5000 charge-discharge cycles. Furthermore, it showcased exceptional and uniform electrocatalytic activity for the OER, requiring only 186 mV in overpotentials to achieve a current density of 10 mA/ cm2. These findings underscore the potential of mesoporous C@SrFe2O4 nanoparticles as promising materials for supercapacitors and OER applications.

Curved surface coupled structural battery composites manufactured by resin transfer molding process: Microstructure and multifunctional performance

To bridge industrial production and lab-scale research, this work demonstrates a technology to manufacture curved surface structural battery composites (CSBCs) that can simultaneously achieve electrochemical energy storage and load-bearing. The curved-surface carbon fiber structural anode and cathode are fabricated by coating the active materials on carbon fiber fabric with a vacuum-bag-assisted technique. The resin transfer molding (RTM) process is conducted to manufacture the coupled CSBCs by infusing bi-continuous phase epoxy resin electrolyte and curing at high temperatures. The microstructure of structural electrodes and CSBCs is characterized by scanning electron microscopy (SEM). Due to good interfacial compatibility between high mechanical strength carbon fiber structural electrode and high ionic conductivity solid polymer electrolyte bulk for load support, the fabricated CSBCs demonstrate a high density of 294 mWh kg−1 based on the whole mass of devices, a tensile strength of 257.4 MPa with Young's modulus of 12.9 GPa and a flexural strength of 194.1 MPa with flexural modulus of 11.1 GPa. In situ electrochemical-mechanical tests further confirm the durability of CSBCs under mechanical loads with a multifunctional efficiency of 1.07, suggesting the effectiveness of the introduced manufacturing techniques for coupled structural battery composites.

Development of nano-porous Au thin film at room temperature via ion irradiation in a-Ge/Au bilayer system followed by chemical etching of Ge

The development of nano-porous gold (NPG) via room temperature ion irradiation has been presented in detail. The bilayer thin films of a-Ge/c-Au have been irradiated by 100 MeV Ni ions with the fluence of 5 × 1013 ions cm−2 at room temperature. NPG is obtained by selectively etching Ge off from the Au matrix by dipping the Ge/Au thin film into 10 % H2O2 solution. Diffusion of Ge and Au across the interface under irradiation was confirmed by TRIM simulation and RBS spectra. The SEM image and EDX spectra confirms the formation of NPG with high purity. In addition, the statistical and fractal analysis of AFM image also confirms the formation of NPG. NPG system has been observed to show very good optical properties (low reflectance and high transmittance). The high quality NPG prepared by this method can be useful in the fields like optical sensors, transparent conductive electrodes, anti-reflective coatings, and photo-detector technology.

Body-worn and self-powered flexible optoelectronic device for metronomic photodynamic therapy

Photodynamic therapy (PDT) as a clinical method relies on appropriate light delivery to activate photosensitizers, usually necessitates the utilization of cumbersome surgical instruments and high irradiation intensity, along with the requirement for hospitalization. To extend the applicability of PDT beyond hospital for better patient mobility, we design a wearable and self-powered metronomic PDT (mPDT) system for chronic wound infection treatment. A flexible alternative current electroluminescent (ACEL) device is constructed through sandwiching an emissive layer between conductive hydrogel electrodes. This ACEL device works as a therapeutic patch by loading photosensitizer (PS) in its bottom hydrogel electrode, thus aviods the intravenous administration to patients. Under the triboelectric nanogenerator generated AC pulse, the electroluminescence produced from emissive layer can be absorbed by the PS-loaded electrode to generate reactive oxygen species for mPDT. Benefited from its arbitrary tailorability, this device can be customized into on-demand shapes and sizes. Using diabetic infected wound as a model condition, this ACEL mPDT device effectively eliminates drug-resistant bacteria and accelerates wound healing. Thus, the body-worn optoelectronic device successfully avoids the utilization of extracorporeal physical light and power sources, providing a promising strategy for convenient, user-friendly, and prolonged treatment of superficial diseases.

Fully Implantable Wireless Cardiac Pacing and Sensing System Integrated with Hydrogel Electrodes.

Cardiac pacemakers play a crucial role in arrhythmia treatment. Existing devices typically rely on rigid electrode components, leading to potential issues such as heart damage and detachment during prolonged cardiac motion due to the mechanical mismatch with cardiac tissue. Additionally, traditional pacemakers, with their batteries and percutaneous leads, introduce infection risks and limit freedom of movement. A wireless, battery-free multifunctional bioelectronic device for cardiac pacing is developed. This device integrates highly conductive (160Sm-1), flexible (Young's modulus of 80kPa is similar to that of mammalian heart tissue), and stretchable (270%) soft hydrogel electrodes, providing high signal-to-noise ratio (≈28dB) electrocardiogram (ECG)recordings and effective pacing of the beating heart. The versatile device detects physiological and biochemical signals in the cardiac environment and allows for adjustable pacing in vivo studies. Remarkably, it maintained recording and pacing capabilities 31 days post-implantation in rats. Additionally, the wireless bioelectronic device can be fully implanted in rabbits for pacing. By addressing a major shortcoming of conventional pacemakers, this device paves the way for implantable flexible bioelectronics, which offers promising opportunities for advanced cardiac therapies.

Solution combustion growth of porous ZnMn2O4 on carbon cloth to enhance zinc ions storage performance

As a positive electrode material for zinc ions storage, the large-scale application of ZnMn2O4 is severely impeded by its low conductivity and inferior cyclic durability. In this study, porous ZnMn2O4 was successfully grown on carbon cloth (ZnMn2O4@CC) for the first time using a solution combustion strategy. In the proposed combustion system, zinc nitrate and manganous nitrate were used as the oxidizing agents, while glucose served as the fuel. The in-situ growth of porous ZnMn2O4 on carbon fiber resulted in a binder-free electrode, with a coaxial core-shell architecture, improving both the structure stability and the electrode's conductivity. Compared to ZnMn2O4 powder, the zinc ions storage performance of ZnMn2O4@CC was significantly enhanced. The ZnMn2O4@CC delivered a 1st discharge-specific capacity of 281.7 mAh g−1 at 100 mA g−1, with 112.2 mAh g−1 of capacity at 500 mA g−1 after 300 cycles. The fabricated ZnMn2O4, with a large specific surface and plentiful mesopores, facilitated the wetting and penetration of the electrolyte. In addition, the porous feature can buffer the stress during the charging and discharging processes, enhancing specific capacity and cycle ability. This work not only introduces a novel method for preparing binder-free electrodes but also explores the potential application of such electrodes in zinc-ion batteries.