Bipolar Electrodes Research Articles

Highly specific detection of ROR1 cancer biomarker with bipolar electrochemiluminescence.

An electrochemiluminescence (ECL) detection system is presented integrated with a bipolar electrode system for sensitive cancer diagnosis. In order to achieve the highest electrical conductivity and redox-active surface area, MXene was chosen as the material for the bipolar electrode. As part of the detection process, the anodic pole of the bipolar electrode was modified with the receptor tyrosine kinase like orphan receptor 1 (ROR1) antibody, followed by an immunoassay using the ROR1 antibody-modified Ag triangle that was identified as significantly enhancing ECL. We measured the ECL of luminol using the anode pole of BPE as an analytical signal in the presence of H2O2. Additionally, 3D-printed microchannels were used to fabricate the BPE system, to reduce the quantity of sample required. It has been shown that the present immunosensors are low-cost and sensitive in detecting types of cancer, with an extended linear range of 10 fg mL-1 to 1 µg mL-1 in the analysis of synthetic samples and achieving an accuracy of ~ 90% in diagnosing ten unknown real samples.

Electrochemical dissolution of titanium under alternating current polarization to obtain its dioxide

Abstract The titanium electrode was polarized under the influence of alternating current (AC) at 50 Hz. The current density was varied between 100 and 5,000 A m−2. Initially, the titanium electrode oxidized, and then, titanium oxides were reduced during the cathodic half-cycle of the AC. When the cathodic half-cycle changes to the anodic half-cycle, titanium is oxidized to the trivalent state: Ti − 3 e ̄ → Ti 3 + {{\rm{Ti}}-3{\rm{e}}{\rm{̄}}\to {\rm{Ti}}}^{3+} . The direction of the AC changes depending on its frequency, causing the processes occurring on the electrodes to be periodically repeated. The current efficiency of the titanium electrode dissolution depends on the sulfuric acid concentration and electrolyte concentration, reaching up to 63.4% under optimal conditions. Bipolar electrodes were used during AC electrolysis. It was found that the decrease in the mass of titanium electrodes increases almost linearly at first, from 400 to 1,600 A m−2, and then more intensively within the current densities from 1,800 to 2,500 A m−2. It was shown that when using a bipolar electrode, the total mass loss of the electrodes is 1.38 times greater than the total mass loss during polarization without a bipolar electrode. The composition of the titanium dioxide obtained as a result of electrolysis was identified using physico-chemical analysis methods.

Single organic electrode for multi-system dual-ion symmetric batteries

The large void space of organic electrodes endows themselves with the capability to store different counter ions without size concern. In this work, a small-molecule organic bipolar electrode called diquinoxalino[2,3-a:2’,3’-c]phenazine-2,6,10-tris(phenoxazine) (DQPZ-3PXZ) is designed. Based on its robust solid structure by the π conjugation of diquinoxalino[2,3-a:2’,3’-c]phenazine (DQPZ) and phenoxazine (PXZ), DQPZ-3PXZ can indiscriminately and stably host 5 counter ions with different charge and size (Li+, Na+, K+, PF6− and FSI−). In Li/Na/K-based half cells, DQPZ-3PXZ can deliver the peak discharge capacities of 257/243/253 mAh g−1cathode and peak energy densities of 609/530/572 Wh kg−1cathode, respectively. The Li/Na/K-based dual-ion symmetric batteries can be constructed, which can be activated through the 1st charge process and show the stable discharge capacities of 85/66/72 mAh g−1cathode and energy densities of 59/50/52 Wh kg−1total mass, all running for more than 15000 cycles with nearly 100% capacity retention.

Annihilation Electrochemiluminescence Triggered by Bipolar Electrochemistry

AbstractBipolar electrochemistry (BE) combined with electrochemiluminescence (ECL) has gained considerable attention as a versatile and powerful analytical technique operating in a wireless manner. However, only co‐reactant ECL has been reported so far when using a BE setup. In this work, the generation of annihilation ECL at the anodic extremity of a bipolar electrode (BPE) is demonstrated in two different spatial arrangements of the electrodes. The reported approach is based on a synergetic effect between the asymmetric electroactivity induced across the BPE, which produces different redox states of [Ru(bpy)3]2+, and the electro‐migration mechanism of the formed ionic species, allowing the localization and concentration of the ECL emission. The presented approach demonstrating annihilation ECL via BE, paves the way for the design of easy and straightforward light‐emitting platforms for multiple applications.

Optimization design of assembly sequence for the proton exchange membrane fuel cell stacks with dimensional errors

Proton exchange membrane fuel cell (PEMFC) stacks are assembled by numerous bipolar plates (BPPs) and membrane electrode assemblies (MEAs). Component manufacturing errors are inevitably caused during the production process and brought into the stack, affecting the mechanical consistency of every cell. Aiming to improve the uniformity of the assembled stack effectively, this paper establishes a novel assembly deviation model based on the asymptotic homogenization (AH) method and proposes an assembly sequence optimization approach for the stack with dimensional errors using the genetic algorithm. The results reveal that dimensional errors significantly affect the equivalent mechanical properties of the stack. Reasonable matching of components with different types of dimensional errors is an effective method to avoid the cumulative negative impacts on the mechanical behavior of the stack. Statistically, the optimization of the assembly sequence can improve contact pressure uniformity in a 10-cell stack by more than 9.00%, while reducing the maximum contact pressure by 15.55%. This methodology is also applicable to improving the assembly uniformity of other stacked structures.

Signal Acquisition and Algorithm Design for Bioimpedance-Based Heart Rate Estimation from the Wrist

Background: Heart rate (HR) is a critical biomarker that provides insights into overall health, stress levels, and the autonomic nervous system. Pulse wave signals contain valuable information about the cardiovascular system and heart status. However, signal acquisition in wearables poses challenges, particularly when using electrical sensors, due to factors like the distance from the heart, body movement, and suboptimal electrode placement. Methods: Electrical bioimpedance (EBI) measurements using bipolar and tetrapolar electrode systems were employed for pulse wave signal acquisition from the wrist in both perpendicular and distal configurations. Signal preprocessing techniques, including baseline removal via Hankel matrix methods, normalization, cross-correlation, and peak detection, were applied to improve signal quality. This study describes the combination of sensor-level signal acquisition and processing for accurate wearable HR estimation. Results: The bipolar system was shown to produce larger ΔZ(t), while the tetrapolar system demonstrated higher sensitivity. Distal placement of the electrodes yielded greater ΔZ(t) (up to 0.231 Ω) when targeting both wrist arteries. Bandpass filtering resulted in a better signal-to-noise ratio (SNR), achieving 3.6 dB for the best bipolar setup and 4.8 dB for the tetrapolar setup, compared to 2.6 and 3.3 dB SNR, respectively, with the Savitzky–Golay filter. The custom HR estimation algorithm presented in this paper demonstrated improved accuracy over a reference method, achieving an average error of 1.8 beats per minute for the best bipolar setup, with a mean absolute percentage error (MAPE) of 8%. Conclusions: The analysis supports the feasibility of using bipolar electrode setups on the wrist and highlights the importance of electrode positioning relative to the arteries. The proposed signal processing method, featuring a preprocessing pipeline and HR estimation algorithm, provides a proof-of-concept demonstration for HR estimation from EBI signals acquired at the wrist.

Enhanced bipolar electrode electrochemiluminescence biosensor for ultrasensitive monitoring of alkaline phosphatase activity during osteoblast differentiation by integrating electrocatalytic and enzymatic strategies

Alkaline phosphatase (ALP) is an important biomarker that reflects osteoblast activity and bone growth. Accurately detecting ALP activity is of pivotal clinical significance for the diagnosis and differentiation of bone system diseases. In this work, an enhanced bipolar electrode electrochemiluminescence (BPE-ECL) biosensor based on enzyme catalysis and electrocatalysis was proposed for ultrasensitive detection of ALP in osteoblasts. Carbon nitride nanosheets (CNNS) were utilized as electrocatalysts to facilitate the electrochemical reaction of bipyridine ruthenium (Ru(bpy)32+) and tripropylamine (TPrA) in the reporting cell. Meanwhile, in the sensing cell, the target ALP catalyzed the conversion of p-aminophenyl phosphate monohydrate into p-aminophenol (p-AP). The p-AP was subsequently oxidized at the anode of the driving electrode, producing electrons and increasing the Faradaic current of BPE. The dual-signal amplification strategy, combining electrocatalysis and enzyme catalysis, resulted in a 10-fold enhancement of the ECL intensity of Ru(bpy)32+/TPrA. The BPE-ECL biosensor achieved ultrasensitive detection of ALP with a detection limit as low as 1.9×10−6 U/L, and was successfully applied to monitor ALP activity in osteoblast cells. Additionally, a portable smartphone imaging was developed for the visual detection of ALP. This research introduces an innovative BPE-ECL biosensor for the monitoring of ALP activity and point-of-care testing (POCT) in osteoblasts in clinical settings.

High-Energy-Density All-V2O5 Battery.

Symmetrical batteries hold great promise as cost-effective and safe candidates for future battery technology. However, they realistically suffer low energy density due to the challenge in integrating high specific capacity with high voltage plateau from the limited choice of bipolar electrodes. Herein, a high-voltage all-V2O5 symmetrical battery with clear voltage plateau is conceptualized by decoupling the cathodic/anodic redox reactions based upon the episteme of V2O5intercalation chemistry. As the proof-of-concept, a hierarchical V2O5-carboncomposite (VO-C) bipolar electrode with boosted electron/ion transport kinetics is fabricated, which shows high performance as both cathode and anode in their precisely clamped working potential windows. Accordingly, the symmetrical full-battery exhibits a high capacity of 174 mAh g-1 along with peak voltage output of above 2.9V at 0.5C, remarkable capacity retention of 81% from 0.5C to 10C, and good cycling stability of 70% capacity retention after 300 cycles at 5C. Notably, its energy density reaches 429Wh kg-1 at 0.5C estimated by the cathode mass, which outperforms most of the existing Li/Na/K-based symmetrical batteries. This study leaps forward the performance of symmetrical battery and provides guidance to extend the scope of future battery designs.

Muscle activity during multi-step descent

BackgroundPrevious step studies have shown mechanical variances across steps in descent; however, muscle activity differences have not been examined across steps in a staircase. The purpose of this study was to quantify differences in muscle activity during step descent between step strategies (step-over-step and step-match) and across steps. MethodsTwenty-five individuals descended a seven-step staircase at self-selected pace (rise: 15.5 cm) in both descent types. Muscle activity was recorded with bipolar electrodes placed on the right tibialis anterior, peroneals, medial gastrocnemius, rectus femoris, and biceps femoris. Two-way Repeated Measures ANOVA tests were conducted for co-activation (ankle: tibialis anterior/medial gastrocnemius; knee: rectus femoris/biceps femoris) and integrated EMG in the lead and trail limbs. ResultsResults showed muscle activity is dependent on the step number for both descent strategies. ConclusionsBetween strategies, lead limb step-match co-activation began the staircase high then decreased for both ankle and knee, while step-over-step activity was the opposite. Trail limb co-activation was more similar beginning high for both joints in step-over-step and the knee in step-match. Across steps, this study supports previous findings of differences between entry and exit steps compared to middle stairs. Additionally, differences were found between mid-staircase steps. These differences in both descent strategies counters previous assumptions of ‘steady-state’ step descent, which may have implications for individuals dealing with lower extremity musculoskeletal issues. Patients may benefit by training on their most encountered staircase length, and researchers must recognize the challenge of generalizing across step studies of varying step number.

Induced electric wireless effects on energy storage: Bipolar electrochemistry effects on Cu/Zn batteries performance

Immersed conducting materials in an electrolyte undergo polarization in presence of electric fields, resulting in a dipole where opposite poles of the material become an anode and cathode, where electrochemical reactions may occur at sufficiently induced potentials. Such induction phenomena lower significantly the resistance of the electrochemical cell. This work shows how in a Cu/Zn battery, it also yields lower overpotentials, and enhanced charge capacity and power, especially at high currents. The outcome of such bipolar electrochemistry, depends on the specific configuration of the bipolar electrodes within the electric field, and the possible reactions at the bipolar electrode for the specific redox system chosen. For the largest induced dipole tested, specific capacities may be increased by 40 % and volumetric capacities may double. It is of great significance that, with appropriate configurations, the capacity of a specific battery may be greatly enhanced, allowing also to reduce the number of cells in a stack to maintain the same performance.

Effect of interfacial contact properties on the structural dynamics of PEMFC based on fractal theory and virtual material

The vibration from the road inevitably causes the microscopic dynamic contact of the contact interface inside the proton exchange membrane fuel cell (PEMFC), and the dynamic characteristics of the contact interface have an obvious influence on the dynamic behavior of the whole stack. In this paper, the normal and tangential contact between bipolar plate (BP) and membrane electrode assembly (MEA) is investigated by fractal theory, and the variation of contact stiffness with fractal dimension, characteristic length and loading force is studied comprehensively. Then, through the virtual material method, a dynamic model of the fuel cell stack reflecting the contact characteristics is established. It is found that the natural frequencies of the stacks considering the contact stiffness are lower than those not considering it. The larger the contact stiffness corresponding to the fractal dimension and characteristic length, the higher the natural frequency of the stack, and the effect of fractal parameters on the surface roughness is explored. Increasing the total clamping force can increase the stack global modal frequency, but it will decrease the cell local modal frequency.

Electrochemical radiofluorination using a split-bipolar electrode

Electrochemical (radio)fluorination (ECF) is a versatile approach for nucleophilic radiofluorination of electron-rich compounds such as thioether derivatives. However, ECF generally requires high concentrations of supporting salts, which leads to low molar activity (Am) of the final product due to undesired contamination with [19F]F– ions. Here, we demonstrate the first example of radiofluorination using a split bipolar electrode (s-BPE) platform with low concentration of supporting salt. Under optimal reaction conditions, the ECF of methyl (methylthio)acetate (MMTA) using s-BPEs provided [18F]F-MMTA with radiochemical conversion of up to 70 % and high molar activities (28–43 GBq/μmol; 0.74–1.1 Ci/μmol), with approximately 5 mM of tetrabutylammonium perchlorate as supporting electrolyte.

Local ionic transport enables selective PGM-free bipolar membrane electrode assembly

Bipolar membranes in electrochemical CO2 conversion cells enable different reaction environments in the CO2-reduction and O2-evolution compartments. Under ideal conditions, water-splitting in the bipolar membrane allows for platinum-group-metal-free anode materials and high CO2 utilizations. In practice, however, even minor unwanted ion crossover limits stability to short time periods. Here we report the vital role of managing ionic species to improve CO2 conversion efficiency while preventing acidification of the anodic compartment. Through transport modelling, we identify that an anion-exchange ionomer in the catalyst layer improves local bicarbonate availability and increasing the proton transference number in the bipolar membranes increases CO2 regeneration and limits K+ concentration in the cathode region. Through experiments, we show that a uniform local distribution of bicarbonate ions increases the accessibility of reverted CO2 to the catalyst surface, improving Faradaic efficiency and limiting current densities by twofold. Using these insights, we demonstrate a fully platinum-group-metal-free bipolar membrane electrode assembly CO2 conversion system exhibiting <1% CO2/cation crossover rates and 80-90% CO2-to-CO utilization efficiency over 150 h operation at 100 mA cm−2 without anolyte replenishment.

Differences of interference myogram patterns from forearm muscles at different variants of the hand grip

Background. Most modern bioprostheses use two sensors located on the flexor and extensor muscles of the hand and fingers to register muscle activity, which severely limits the functionality of the device and complicates switching between grips. One of the solutions to this problem is to use an array of more sensors to recognize different grips using a neural network.Aim. To evaluate the possibility in principle of using an array of 8 sensors for recognizing different grips.Materials and methods. Research was conducted on 23 healthy volunteers, whose surface myograms were recorded at 13 different grips. An array of surface-type electroneuromyographic sensors (n = 8) with bipolar electrodes and electroneuromyographic signal amplification factor of 2000 times, myograph and software are of own development were used as a technical base for the research.Results. For most subjects, the differences in the investigated parameters when comparing grips with each other reached thousands of percent, especially when comparing the product of frequency and mean amplitude. In some pairs the differences were less significant and amounted to less than 400 %. The proportion of pairs with reliable differences varies from subject to subject when comparing the product of frequency and mean amplitude and ranges from 71 to 98 %. The average value for the whole group is 87 %. When comparing frequency only, the variation ranges from 67 to 93 %, with an average of 78 %.Conclusion. For most subjects, the majority of grips are confidently differentiated from each other. Due to pronounced individual peculiarities, the decision to use this or that parameter to control the bioprosthesis for a definite person is individual and should be made after a thorough neurophysiological research. Some people will require training in order to develop a new motor stereotype.

Development of integrated packaged single fuel cell short stack based on titanium metal plates for mobile power generation

Bipolar plates (BPPs) and membrane electrode assemblies (MEAs) are the key components for proton exchange membrane fuel cells (PEMFCs), they are alternately arranged to construct a compact stack with high power generation. This stacking method may introduce several issues, such as the difficulties in maintenance, imprecise assembly and sealing. This paper presents a novel integrated packaged single fuel cell that employs titanium metal bipolar plates to construct a short stack with superior sealing performance and working reliability. To predict the performance of integrated packaged single cell, numerical model was developed to analyze the mass transfer of O2, H2 and H2O within the cell, revealing a uniform distribution of reactants and current. A short stack was manufactured with 10 layers of single cells, it retains excellent sealing properties and consistent output across a range of pressure conditions, with a leakage rate deviation lower than 0.03 mL/(min·cell) and membrane current density variation less than 5%. Finally, the electrochemical performance of the integrated packaged short stack was tested, its maximum power is 886.67 mW/cm2. It can achieve a rated output power of 169.14 W and an energy density of 1684.97 mW/cm3. Thus, our developed short stack has high energy utilization efficiency for power generation, and is anticipated to provide a durable power source for drones, robots and new energy vehicles.

Computer modelling and vegetable bench test of a bipolar electrode array intended for use in high frequency irreversible electroporation treatment of skin cancer

Computer modelling and vegetable bench test of a bipolar electrode array intended for use in high frequency irreversible electroporation treatment of skin cancer

Diffusive Memristor with CuS Nanoparticles Embedded in Polymeric Film as Artificial Nociceptor.

The threshold behavior and the ion diffusion dynamics in diffusive volatile memristors have a very uncanny resemblance to the transduction process of biological nociceptors. Hence, the diffusive memristors are considered the most suited for making artificial nociceptive systems. To facilitate their widespread adoption, it is imperative to develop polymeric or organic-inorganic hybrid material-based diffusive memristors that are economical, biocompatible, and easily processable. In this study, we present a cluster-type polymeric diffusive memristor where copper is used as the active top electrode. The switching medium comprises copper(II) sulfide (CuS) nanoparticles embedded in poly(ethylene oxide) (PEO). The devices show electrochemical metalization (ECM)-type and bidirectional diffusive volatile memory with high nonlinearity (104) and turn-on slope (5.6 mV/dec). They reliably remain diffusive volatile with up to 10 wt % CuS in PEO and for a wide range of compliance (10-6 to 10-2 A) without transitioning to the bipolar nonvolatile type. The low reduction potential of CuS and optimal segmental dynamics of PEO work synergistically to ensure stable and reproducible diffusive memory. The CuS nanoparticles act as bipolar electrodes, undergoing local oxidation and reduction under the influence of the bias. The switching of resistance states in the CuS-PEO memristors is attributed to the formation of cluster-type filaments between CuS nanoparticles within the PEO matrix supported by the participation of copper ions from the top Cu electrode. The observation of low filament temperature and the independence of on-state resistance with respect to the device area and temperature further corroborate the cluster-type filament in CuS-PEO memristors. Using a 5 wt % CuS-based device, an artificial nociceptor is realized, which successfully mimics most of the nociceptive plasticities such as threshold, relaxation, no adaptation, and sensitization.

Bipolar electrochemical growth of conductive microwires for cancer spheroid integration: a step forward in conductive biological circuitry

The field of bioelectronics is developing exponentially. There is now a drive to interface electronics with biology for the development of new technologies to improve our understanding of electrical forces in biology. This builds on our recently published work in which we show wireless electrochemistry could be used to grow bioelectronic functional circuitry in 2D cell layers. To date our ability to merge electronics with in situ with biology is 3D limited. In this study, we aimed to further develop the wireless electrochemical approach for the self-assembly of microwires in situ with custom-designed and fabricated 3D cancer spheroids. Unlike traditional electrochemical methods that rely on direct electrical connections to induce currents, our technique utilises bipolar electrodes that operate independently of physical wired connections. These electrodes enable redox reactions through the application of an external electric field. Specifically, feeder electrodes connected to a power supply generate an electric field, while the bipolar electrodes, not physically connected to the feeder electrodes, facilitate the reduction of silver ions from the solution. This process occurs upon applying a voltage across the feeder electrodes, resulting in the formation of self-assembled microwires between the cancer spheroids.Thereby, creating interlinked bioelectronic circuitry with cancer spheroids. We demonstrate that a direct current was needed to stimulate the growth of conductive microwires in the presence of cell spheroids. Microwire growth was successful when using 50 V (0.5 kV/cm) of DC applied to a single spheroid of approximately 800 µm in diameter but could not be achieved with alternating currents. This represents the first proof of the concept of using wireless electrochemistry to grow conductive structures with 3D mammalian cell spheroids.

Design and Synthesis of D‐A Polymer as Cathode Material for Na‐Based Dual‐Ion Batteries with Excellent Cycling Performance

AbstractOrganic bipolar electrodes can undergo both n‐type and p‐type reactions for energy storage due to numerous active sites, which can usually deliver a high theoretical specific capacity. Herein, a new bipolar polymer cathode material PQPZ is designed and synthesized. The electron‐donating phenazine group undergoes a two‐electron redox reaction which can store anions, the electron‐withdrawing phenanthraquinone can store sodium‐ions through a two‐electron redox reaction. Notably, as a bipolar cathode material for sodium‐ion batteries, PQPZ exhibits a reversible specific capacity of up to 270 mAh g−1 in the voltage range of 1.0–4.0 V (vs. Na+/Na) and achieves a high energy density of 696 Wh kg−1 in a half‐cell. A capacity retention rate of 90% is obtained after 300 cycles at a current density of 0.5C. More excitingly, even after being cycled for 10000 cycles at 10C, the PQPZ electrode shows an average decay rate as low as 0.0036% per cycle, manifesting a very stable cycling performance. In addition, PQPZ also shows excellent performances when tested at −10 °C, making it promising in practical applications. Considering the bipolar character of PQPZ, symmetric batteries are also successfully constructed, fulfilling the “ready‐to‐charge” property without a pre‐activation process. The results reveal the potential application of PQPZ in practical use.

Bipolar Textile Composite Electrodes Enabling Flexible Tandem Solid-State Lithium Metal Batteries.

A majority of flexible and wearable electronics require high operational voltage that is conventionally achieved by serial connection of battery unit cells using external wires. However, this inevitably decreases the energy density of the battery module and may cause additional safety hazards. Herein, a bipolar textile composite electrode (BTCE) that enables internal tandem-stacking configuration to yield high-voltage (6 to 12V class) solid-state lithium metal batteries (SSLMBs) is reported. BTCE is comprised of a nickel-coated poly(ethylene terephthalate) fabric (NiPET) core layer, a cathode coated on one side of the NiPET, and a Li metal anode coated on the other side of the NiPET. Stacking BTCEs with solid-state electrolytes alternatively leads to the extension of output voltage and decreased usage of inert package materials, which in turn significantly boosts the energy density of the battery. More importantly, the BTCE-based SSLMB possesses remarkable capacity retention per cycle of over 99.98% over cycling. The composite structure of BTCE also enables outstanding flexibility; the battery keeps stable charge/discharge characteristics over thousands of bending and folding. BTCE shows great promise for future safe, high-energy-density, and flexible SSLMBs for a wide range of flexible and wearable electronics.