Hierarchical electrodes with superior cycling performance using porous material based on cellulose nanofiber as flexible substrate.

The development and application of flexible electrodes with extended cycle life have long been a focal point in the field of energy research. In this study, positively charged polyethylene imine (PEI) and conductive polymer poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate) (PEDOT:PSS) with negative charge were alternately deposited onto a cellulose nanofiber (CNF) porous material utilizing pressure gradient-assisted layer-by-layer (LbL) self-assembly technology. The flexible substrate, characterized by a three-dimensional porous structure reinforced with stiff CNF, not only facilitated high charge storage but also enhanced the electrode's cycling life by reducing the volume changes of PEDOT:PSS. Furthermore, the exceptional wettability of PEI by the electrolyte could promote efficient charge transport within the electrode. The electrode with 10 PEI/PEDOT:PSS bilayer exhibits a capacitance of 63.71 F g-1 at the scan rate of 5 mV s-1 and a remarkable capacitance retention of 128 % after 3000 charge-discharge cycles. The investigation into the nanoscale layers of the LbL multilayer structure indicated that the exceptional cyclic performance was primarily attributed to the spatial constraints imposed by the rigid porous substrate layered structure on the deformation of PEDOT:PSS. This work is expected to make a significant contribution to the development of electrodes with high charge storage capacity and ultra-long cycling life.

Anode glow discharge electrolysis synthesis of flower-like α-MnO2 nanospheres: structure, formation mechanism, and supercapacitor performance.

A novel green synthesis strategy-anode glow discharge electrolysis (AGDE) was employed for one-step preparation of a-MnO2 in 2 g L-1 KMnO4 solution, in which Pt needle and carbon rod were regarded as anode and cathode, respectively. The optimal preparation condition is 400 V for 60 min and the power consumption is below 45 W. The XRD, Raman spectra, XPS and EPR proved that a-MnO2 with structural defects (oxygen vacancies) is obtained. SEM and TEM revealed that a-MnO2 shows a flower-like nanospheres with a diameter of 165 nm, which is assembled by many nanosheets. A possible formation mechanism is that the MnO2 is generated via the reduction of MnO4- by H· and eaq- in plasma-liquid interface. Electrochemical test found that MnO2 nanospheres exhibit a specific capacitance of 365 F g-1 at 1 A g-1, and capacity retention of 79.8% after 10,000 cycles at 5 A g-1. The assembled asymmetric supercapacitor shows the maximum energy density of 23.1 Wh kg-1 at power density of 1.89 kW kg-1. In brief, AGDE is a simple, facile and green technique for the synthesis of a-MnO2 without adding extra chemicals, and prepared a-MnO2 can be considered as an excellent candidate of electrode materials for supercapacitor.

[An efficient and practical electrode optimization method for transcranial electrical stimulation].

Transcranial electrical stimulation (TES) is a non-invasive neuromodulation technique with great potential. Electrode optimization methods based on simulation models of individual TES field could provide personalized stimulation parameters according to individual variations in head tissue structure, significantly enhancing the stimulation accuracy of TES. However, the existing electrode optimization methods suffer from prolonged computation times (typically exceeding 1 d) and limitations such as disregarding the restricted number of output channels from the stimulator, further impeding their clinical applicability. Hence, this paper proposes an efficient and practical electrode optimization method. The proposed method simultaneously optimizes both the intensity and focality of TES within the target brain area while constraining the number of electrodes used, and it achieves faster computational speed. Compared to commonly used electrode optimization methods, the proposed method significantly reduces computation time by 85.9% while maintaining optimization effectiveness. Moreover, our method considered the number of available channels for the stimulator to distribute the current across multiple electrodes, further improving the tolerability of TES. The electrode optimization method proposed in this paper has the characteristics of high efficiency and easy operation, potentially providing valuable supporting data and references for the implementation of individualized TES.

Solid-state Ru(bpy)32+ electrochemiluminescence sensor for trace detection of fenpropathrin using loofah sponge-like carbon nanofibers and CdS.

Loofah sponge-like carbon nanofibers (LF-Co,N/CNFs) were utilized as a carrier for Ru(bpy)32+, and then combined with CdS to create a novel solid-state electrochemiluminescence sensor capable of detecting trace amounts of fenpropathrin. LF-Co,N/CNFs, obtained through the high-temperature pyrolysis of ZIF-67 coaxial electrospinning fibers, were characterized by a loofah-like morphology and exhibited a significant specific surface area and porosity. Apart from serving as a carrier, LF-Co,N/CNFs also functioned as a luminescence accelerator, enhancing the system's luminescence efficiency by facilitating electron transmission and reducing the transmission distance. The inclusion of CdS in the luminescence reaction, in conjunction with Ru(bpy)32+, further boosted the sensor's luminescence signal. The resulting sensor demonstrated a satisfactory signal, with fenpropathrin causing significant quenching of the ECL signal. Under optimized conditions, a linear relationship between the signal quench value and fenpropathrin concentration in the range 1 × 10-12 to 1 × 10-6 M was observed, with a detection limit of 3.3 × 10-13 M (S/N = 3). This developed sensor is characterized by its simplicity, sensitivity, and successful application in detecting fenpropathrin in real samples. The study not only presents a straightforward detection platform for fenpropathrin but also introduces new avenues for the rapid determination of various food contaminants, thereby expanding the utility of carbon fibers in electrochemiluminescence sensors.

Quantum Confinement and End-Sealing Effects for Highly Sensitive and Stable Nitrogen Dioxide Detection: Homogeneous Integration of Ti3C2Tx-Based Flexible Gas Sensors.

The real-time and room-temperature detection of nitrogen dioxide (NO2) holds significant importance for environmental monitoring. However, the performance of NO2 sensors has been hampered by the trade-off between the high sensitivity and stability of conventional sensitive materials. Here, we present a novel fully flexible paper-based gas sensing structure by combining a homogeneous screen-printed titanium carbide (Ti3C2Tx) MXene-based nonmetallic electrode with a MoS2 quantum dots/Ti3C2Tx (MoS2 QDs/Ti3C2Tx) gas-sensing film. These precisely designed gas sensors demonstrate an improved response value (16.3% at 5 ppm) and a low theoretical detection limit of 12.1 ppb toward NO2, which exhibit a remarkable 3.5-fold increase in sensitivity compared to conventional Au interdigital electrodes. The outstanding performance can be attributed to the integration of the quantum confinement effect of MoS2 QDs and the conductivity of Ti3C2Tx, establishing the main active adsorption sites and enhanced charge transport pathways. Furthermore, an end-sealing effect strategy was applied to decorate the defect sites with naturally oxygen-rich tannic acid and conductive polymer, and the formed hydrogen bonding network at the interface effectively mitigated the oxidative degradation of the Ti3C2Tx-based gas sensors. The exceptional stability has been achieved with only a 1.8% decrease in response over 4 weeks. This work highlights the innovative design of high-performance gas sensing materials and homogeneous gas sensor techniques.

Stabilizing the Interphase in an Ultra-High-Nickel Cathode Enabling High-Performance Lithium-Ion Batteries.

High-nickel (Ni ≥ 90%) cathodes which have a high specific capacity hold great potential for next-generation lithium-ion batteries (LIBs). However, their practical application is restricted by their high interfacial reactivity because of the presence of residual lithium (Li) compounds on the surface. Herein, the LiNi0.9Co0.06Mn0.04O2 (NCM90) cathode is surface-modified with sulfur (S) via a simple and feasible dry mixing and low-temperature heat treatment, converting the residual lithium compound on the surface into inactive lithium sulfate (Li2SO4). This induces the formation of a stable inorganic enriched electrode-electrolyte interface on the cathode surface and inhibits the occurrence of side reactions, ultimately inhibiting lattice collapse and the dissolution of transition metal ions. After modifying, the capacity retention rates of NCM90/Li and NCM90/graphite cells are both greatly enhanced after long cycling. This work provides a new idea for the rational design of the electrode-electrolyte interface of high-nickel cathodes.

Unlocking high-efficiency charge storage: Co-assembled nanoparticles of lignin and polyaniline molecules.

Redox-active lignin rich in phenolic hydroxyl groups is an ingenious charge storage material. However, its insulating nature limits the storage/release of electrons and requires the construction of electron transfer channels within it. Herein, nanoparticles (PANI/DKL-NPs) are prepared by co-assembly via π-π interactions between conducting polyaniline (PANI) and demethylated Kraft lignin (DKL) molecules for the first time, and rapid electron transfer inside DKL is achieved. The co-assembled PANI/DKL-NPs consist of interpenetrating structures of PANI and DKL at the molecular scale, and the content of PANI molecules interspersed within them is controllable. Meanwhile, the extensive and abundant mesoporous structure in nanoscale PANI/DKL-NPs facilitates ion transport and electron storage. Based on this favorable microstructure, the specific capacitance of PANI/DKL-NPs at 1 A·g-1 is as high as 532 F·g-1, which is 780 % and 90.68 % higher compared to DKL-NPs and PANI-NPs, respectively. Meanwhile, the rate performance of PANI/DKL-NPs is significantly enhanced than that of DKL-NPs (33.11 %) and comparable to that of PANI-NPs (more than 69 %). Furthermore, the symmetric supercapacitor (PANI/DKL-NPs//PANI/DKL-NPs) assembled from it achieves a high energy density of 27.49 Wh·kg-1 at 400 W·kg-1 power density, and superb flexibility and mechanical stability. Therefore, the co-assembly of DKL and PANI will effectively stimulate the energy storage potential of lignin, providing a practical pathway to promote the development of biopolymers in energy storage.

Two birds with one stone: Bimetallic ZnCo2S4 polyhedral nanoparticles decorated porous N-doped carbon nanofiber membranes for free-standing flexible anodes and microwave absorption.

Cost-efficient material with an ingenious design is important in the engineering applications of flexible energy storage and electromagnetic (EM) protection. In this study, bimetallic ZnCo2S4 (ZCS) polyhedral nanoparticles homogenously embedded in the surface of porous N-doped carbon nanofiber membranes (ZCS@PCNFM) have been fabricated by electrospinning technique combined with carbonization and hydrothermal processes. As a self-assembled electrode for lithium-ion batteries (LIBs), the bimetallic ZCS nanoparticles possess rich redox reactions, good electrical conductivity, and pseudocapacitive properties, while the three-dimensional (3D) multiaperture architecture of the nanofiber film not only shortens the transfer spacing of lithium ions and electrons but also effectively tolerates the volume variation during lithiation and delithiation cycles. Benefiting from the above merits, the ZCS@PCNFM electrode exhibits good cycle performance (662.3 mA h/g at 100 mA/g after 100 cycles), superior rate capacity (401.3 mA h/g at 1 A/g) and an extremely high initial specific capacity of 1152.2 mAh/g at 100 mA/g. Meanwhile, depending on the hierarchical nanostructure and multi-component heterogeneous interface effects constructed by 3D inlaid architecture, the ZCS@PCNFM nanocomposite exhibits fascinating microwave absorption (MA) characteristics with a superhigh reflection loss (RL) of -49.7 dB at a filling content of only 20 wt% and corresponding effective absorption bandwidth (EAB, RL<-10 dB) of 5.2 GHz ranging from 12.8 to 18.0 GHz at 2.2 mm.

Optimizing microplastic treatment in the effluent of biological nutrient removal processes using electrocoagulation: Taguchi experimental design.

Microplastics (MPs) have become one of the most critical environmental pollution problems in recent years. Due to the growing abundance of MPs in aquatic environments, extensive research has been conducted and continues to be ongoing to develop effective treatment methods. In this study, the removal of MPs in the effluent of biological wastewater treatment plant (WWTP) was investigated by electrocoagulation (EC) process with aluminum electrodes. Using Taguchi design, the importance of process variables such as pH, current density, and reaction time were evaluated by Analysis of Variance (ANOVA). Statistically, according to F and p values, the most effective parameter for microplastic (MP) removal was current density, followed by pH and reaction time. The R2 value of the created model was found to be above 98%. According to Taguchi results, the optimum process conditions were determined as pH 9, current density 1.905 mA/cm2, and reaction time 15 min and 99% MP removal efficiency was obtained. Under these optimum conditions, the process cost was calculated as 0.049 $/m3 wastewater, considering energy and electrode consumption. As a result of visual analyses, fiber, film, pellet, amorphous, and undefined forms were dominant in WWTP effluent, while only fiber structures were observed after treatment with EC. In this study, it was concluded that the EC process is an alternative treatment method that can be integrated into wastewater treatment plant effluent to achieve MP removal at very low cost and high efficiency. In addition, as a result of this study, it was observed that the EC process can also be used in MP removal by applying it to real wastewater.

An ITO free All Tungsten-Based Electrochromic Energy Storage Device as Smart Window.

Excessive electricity usage in buildings, notably for heating and cooling, accounts for over 30% of energy consumption, creating a pressing need for energy-saving solutions. Electrochromic Smart Windows (ECSW) aims to reduce energy use while maintaining comfort but faces high costs due to materials like tin-doped indium oxide (ITO) and thick electrochromic films. Moreover, achieving full opacity in the colored state of ECSW is a bottleneck for the industry to overcome privacy concerns. Herein, efforts are directed toward finding cost-efficient alternatives, with all-tungsten-based mesh networks showing promise due to enhanced stability. This newly developed ITO-free, all-tungsten ECSW displays minimal transmittance (≈3%) in the colored state using only 260 nm thick sub-stoichiometric tungsten oxide (WO3-x) film within a lithium-ion-based electrolyte. The ECSW device of size (25 cm2) also demonstrates areal capacitance of ≈13 mF cm-2 to power a liquid crystal display (LCD) for ≈25 min, showcasing its energy storage capabilities. Additionally, to confirm scalability and cost-effectiveness, a larger 15 × 15 cm2 ECSW utilized a single hybrid electrode, highlighting the potential for reducing costs when scaling up production processes. This advancement represents a significant stride toward accessible and energy-efficient smart window technology, offering broader applicability within modern architectural practices.

Thyroid cartilage needle vs. endotracheal tube electrodes in EBSLN monitoring during thyroidectomy.

During thyroidectomy, both needle electrodes (NE) and endotracheal tube electrodes (ETE) can be used. Incomplete contact of the endotracheal tube electrode with the vocal cords, endotracheal tube electrode may hinder an optimal outcome and even result in an inability to obtain an electromyography wave while neuromonitoring the external branch of the superior laryngeal nerve (EBSLN). There is no study that compares NE and ETE for EBSLN monitoring. Therefore, this study compares NE and ETE recordings during EBSLN monitoring. Twenty-six consecutive patients undergoing total thyroidectomy were included in this study. Intraoperative neuromonitoring was performed simultaneously with both NEs and ETEs. Pre-resection (V1, R1, and S1) and post-resection (V2, R2, and S2) amplitudes and latencies were recorded for both types of electrodes. The Mann-Whitney U test was used for statistical analysis. Twenty-one women and five men were included, and 52 nerves at risk were evaluated. The mean amplitudes for right S1 (314 vs. 168 µV, p = 0.009) and right S2 (428 vs. 161 µV, p: 0.001) and for left S1 (346 vs. 229 µV, p: 0.017) and left S2 (413 vs. 229 µV, p: 0.009) were statistically higher for the NE group. All amplitudes obtained using NEs, except on the left for V1, R1, V2, and R2, were statistically higher than those obtained using ETEs. There was no loss of signal or vocal cord palsy in the patients. There were no needle-related complications. EBSLN monitoring using NE is a safe alternative to ETE. With NE, higher amplitudes were obtained. Level of evidence: Level 3.

Electroanalytical Strategies for Local pH Sensing at Solid-Liquid Interfaces and Biointerfaces.

Obtaining analytical information about chemical species at interfaces is fundamentally important to improving our understanding of chemical reactions and biological processes. pH at solid-liquid interfaces is found to deviate from the bulk solution value, for example, in electrocatalytic reactions at surfaces or during the corrosion of metals. Also, in the vicinity of living cells, metabolic reactions or cellular responses cause changes in pH at the extracellular interface. In this review, we collect recent progress in the development of sensors with the capability to detect pH at or close to solid-liquid and bio interfaces, with spatial and time resolution. After the two main principles of pH detection are presented, the different classes of molecules and materials that are used as active components in these sensors are described. The review then focuses on the reported electroanalytical techniques for local pH sensing. As application examples, we discuss model studies that exploit local pH sensing in the area of electrocatalysis, corrosion, and cellular interfaces. We conclude with a discussion of key challenges for wider use of this analytical approach, which shows promise to improve the mechanistic understanding of reactions and processes at realistic interfaces.

Comparative study of two MIP-based electrochemical sensors for selective detection and quantification of the antiretroviral drug lopinavir in human serum.

Thermal polymerization (TP) and electropolymerization (EP) are the two methods used in this study to explore the molecular imprinting process. To detect the antiviral medication lopinavir (LPV), an inhibitor of enzyme HIV-1 protease that is co-formulated with ritonavir (RTV) to extend its half-life in the body, with greater precision, these methods were merged with an electrochemical sensor. The sensors were created on glassy carbon electrodes (GCE) based on molecularly imprinted polymers (MIP) using TP with methacrylic acid (MAA) functional monomer and EP with p-aminobenzoic acid (PABA) functional monomer. Fourier transform infrared spectroscopy (FT-IR), scanning electron microscopy (SEM), and electrochemical methods were utilized to examine the technical features of the suggested sensors. For both approaches, the necessary optimization investigations were carried out. Different LPV concentrations, ranging from 1.0 pM to 17.5 pM in drug solution and commercial human serum samples, were used to validate the analytical efficiency of the two sensors and compare their electroanalytical behaviour. For TP-LPV@MIP/GCE and EP-LPV@MIP/GCE, the corresponding limit of detection (LOD) was 2.68 × 10-13 M (0.169 pg mL-1) and 1.79 × 10-13 M (0.113 pg mL-1) in standard solutions, and 2.87 × 10-13 M (0.180 pg mL-1) and 2.91 × 10-13 M (0.183 pg mL-1) in serum samples. For the measurement of LPV in tablet form and serum samples, the proposed TP-LPV@MIP/GCE and EP-LPV@MIP/GCE sensors provide good recovery, demonstrating 99.85-101.16 % and 100.36-100.97 % recovery, respectively. The imprinting factor was utilized to demonstrate the selectivity of the suggested sensors by utilizing several anti-viral drugs that are structurally comparable to LPV. Additionally, the constructed sensors were examined for the potential impacts of interferences and the stability during the storage.

Polyelectrolyte Additive-Modulated Interfacial Microenvironment Boosting CO2 Electrolysis in Acid.

Acidic CO2 electrolysis offers a promising strategy to achieve high carbon utilization and high energy efficiency. However, challenges remain in suppressing the competitive hydrogen evolution reaction (HER) and improving product selectivity. High concentrations of potassium ions (K+) can suppress HER and accelerate CO2 reduction, but they still inevitably suffer from salt precipitation problems. In this study, we demonstrate that the sulfonate-based polyelectrolyte, polystyrene sulfonate (PSS), enables to reconstruct the electrode-electrolyte interface to significantly enhance the acidic CO2 electrolysis. Mechanistic studies reveal that PSS induces high local K+ concentrations through electrostatic interaction between PSS anions and K+. In situ spectroscopy reveals that PSS reshapes the interfacial hydrogen-bond (H-bond) network, which is attributed to the H-bonds between PSS anions and hydrated proton as well as the steric hindrance of the additive molecules. This greatly weakens proton transfer kinetics and leads to the suppression of undesirable HER. As a result, a Faradaic efficiency of 93.9% for CO can be achieved at 250 mA cm-2, simultaneous with a high single-pass carbon efficiency of 72.2% on commercial Ag catalysts in acid. This study highlights the important role of the electrode-electrolyte interface induced by polyelectrolyte additives in promoting electrocatalytic reactions.

Enhancing Conductivity in Silicon Heterojunction Solar Cells with Silver Nanowire-Assisted Ti3C2Tx MXene Electrodes for Cost-Effective and Scalable Photovoltaics.

Silicon heterojunction (SHJ) solar cells have set world-record efficiencies among single-junction silicon solar cells, accelerating their commercial deployment. Despite these clear efficiency advantages, the high costs associated with low-temperature silver pastes (LTSP) for metallization have driven the search for more economical alternatives in mass production. 2D transition metal carbides (MXenes) have attracted significant attention due to their tunable optoelectronic properties and metal-like conductivity, the highest among all solution-processed 2D materials. MXenes have emerged as a cost-effective alternative for rear-side electrodes in SHJ solar cells. However, the use of MXene electrodes has so far been limited to lab-scale SHJ solar cells. The efficiency of these devices has been constrained by a fill factor (FF) of under 73%, primarily due to suboptimal charge transport at the contact layer/MXene interface. Herein, a silver nanowire (AgNW)-assisted Ti3C2Tx MXene electrode contact is introduced and explores the potential of this hybrid electrode in industry-scale solar cells. By incorporating this hybrid electrode into SHJ solar cells, 9.0 cm2 cells are achieved with an efficiency of 24.04% (FF of 81.64%) and 252 cm2 cells with an efficiency of 22.17% (FF of 76.86%), among the top-performing SHJ devices with non-metallic electrodes to date. Additionally, the stability and cost-effectiveness of these solar cells are discussed.

Unraveling the Fluoride-Induced Interface Reconstruction Across Lead-Based Hierarchical MnO2 Anode in Zinc Electrowinning.

Although the hierarchical manganese dioxide film electrode shows promise as a durable and catalytically active anode for zinc electrowinning, it often fails and deactivates when it is exposed to fluoride-rich environments. The lack of understanding regarding the mechanism behind fluoride-induced irreversible interface reconstruction hinders their practical application in large-scale energy-saving and pollution-reduction efforts. Here, we conducted multidimensional operando investigations to gain insights into the dynamic evolution across the film electrode interface with temporal and spatial resolution. Our findings reveal that electroosmosis of F- initially triggers structural collapse and subsequent reconstruction of [MnO6] units, followed by interaction with the spontaneous oxide film at the surface of lead substrate. Experimental studies and theoretical calculations indicate that F- facilitates the irreversible transformation of γ-MnO2 into more stable yet protective catalytic dual-defective α-MnO2. Additionally, lower levels of F- at the interface promote a change in microenvironmental pH within porous PbSO4, triggering the development of microporous corrosion-resistant ß-PbO2 as the dominant phase. The combined effects of MnO2 and interphase evolution effectively explain the abnormally elevated oxygen evolution overpotential. Then, the proposed appropriate application scenarios based on the corrosion behavior will serve as a practical guide for the implementation of the hierarchical manganese dioxide film electrode.

EEG-based emotion recognition using graph convolutional neural network with dual attention mechanism.

EEG-based emotion recognition is becoming crucial in brain-computer interfaces (BCI). Currently, most researches focus on improving accuracy, while neglecting further research on the interpretability of models, we are committed to analyzing the impact of different brain regions and signal frequency bands on emotion generation based on graph structure. Therefore, this paper proposes a method named Dual Attention Mechanism Graph Convolutional Neural Network (DAMGCN). Specifically, we utilize graph convolutional neural networks to model the brain network as a graph to extract representative spatial features. Furthermore, we employ the self-attention mechanism of the Transformer model which allocates more electrode channel weights and signal frequency band weights to important brain regions and frequency bands. The visualization of attention mechanism clearly demonstrates the weight allocation learned by DAMGCN. During the performance evaluation of our model on the DEAP, SEED, and SEED-IV datasets, we achieved the best results on the SEED dataset, showing subject-dependent experiments' accuracy of 99.42% and subject-independent experiments' accuracy of 73.21%. The results are demonstrably superior to the accuracies of most existing models in the realm of EEG-based emotion recognition.

Electroretinograms Recorded with Skin Electrodes from Post-Vitrectomy Silicone Oil Filled Eyes with Proliferative Diabetic Retinopathy.

Purpose: To determine the physiological status of the retina by electroretinography (ERG) using skin electrodes and the RETevalTM system in eyes that had undergone pars plana vitrectomy (PPV) with silicone oil (SO) tamponade. The vitrectomy was performed for a retinal detachment and proliferative diabetic retinopathy (PDR). Design: Retrospective case series. Methods: ERGs were recorded with the RETevalTM system (LKC Technologies Inc. Gaithersburg, MD; Welch Allyn, Inc. Skaneateles Falls, NY) from eight eyes with PDR before and after the SO removal. The amplitudes and implicit times of the a- and b-waves of the ERGs before the SO removal were compared to that after the SO removal. Results: ERGs were recordable in four eyes before and after the SO removal and the a- and b-amplitudes improved in three eyes and worsened in one eye after the SO removal. In the remaining four eyes, ERGs were non-recordable both before and after the SO removal. Conclusion: These results indicate that ERGs picked up by skin electrodes can be used to assess the physiology of the retina in eyes with a SO tamponade. The flat ERGs in the SO-filled eye indicated the presence of diffuse retinal damage which was confirmed by the flat ERGs after the SO removal.

There has been an increasing number of reports on evaluating the retinal function using electroretinography (ERG) with skin electrodes. The main advantage of this system is the ability to record ERGs with a skin electrode that does not touch the cornea and ocular surface. This reduces the risk of infection especially in the postoperative period and in clinical situations where infection is suspected. In addition, there have been only a few reports evaluating the function of the retina by ERG in SO-filled eyes. We recorded ERGs with the RETeval (LKC Technologies Inc. Gaithersburg, MD; Welch Allyn Inc. Skaneateles Falls, NY) device, a relatively new ERG recording system that uses skin electrodes and is less invasive. We recorded ERGs from eight SO-filled eyes with proliferative diabetic retinopathy (PDR). In 4 SO filled eyes, the amplitudes increased in three eyes after the SO removal. In the other four eyes, ERGs were non-recordable before and after the SO removal. These results suggest that the RETeval system that uses skin electrodes can be used to assess the retinal function in PDR eyes with a SO tamponade. We suggest that the absence of ERGs in the SO filled eyes was not due to the electrical non-conductive effects of SO but may indicate the presence of diffuse retinal damage which was confirmed after the SO removal.

Solid electrochemiluminescence sensor by immobilization luminol in Zn-Co-ZIF CNFs for sensitive detection of procymidone in vegetables.

A solid-state electrochemiluminescence (ECL) sensor was fabricated by immobilizing luminol, a classical luminescent reagent, on a Zn-Co-ZIF carbon fiber-modified electrode for the rapid and sensitive detection of procymidone (PCM) in vegetable samples. The sensor was created by sequentially modifying the glassy carbon electrode with Zn-Co-ZIF carbon fiber (Zn-Co-ZIF CNFs), Pt@Au NPs, and luminol. Zn-Co-ZIF CNFs, prepared through electrospinning and high-temperature pyrolysis, possessed a large specific surface area and porosity, making it suitable as carrier and electron transfer accelerator in the system. Pt@Au NPs demonstrated excellent catalytic activity, effectively enhancing the generation of active substances. The ECL signal was significantly amplified by the combination of Zn-Co-ZIF CNFs and Pt@Au NPs, which can subsequently be diminished by procymidone. The ECL intensity decreased proportionally with the addition of procymidone, displaying a linear relationship within the concentration range 1.0 × 10-13 to 1.0 × 10-6 mol L-1 (R2 = 0.993). The sensor exhibited a detection limit of 3.3 × 10-14 mol L-1 (S/N = 3) and demonstrated outstanding reproducibility and stability, making it well-suited for the detection of procymidone in vegetable samples.

Safety assessment of coronary arteries during left bundle branch area pacing.

BACKGROUND: This study aimed to assess the safety of left bundle branch area pacing (LBBAP) by measuring the distance from the tip of the electrode to the nearby coronary artery with a nine-partition grid method. METHODS: From January 2019 to October 2020, patients who underwent LBBAP and postoperative coronary angiography in the Second Affiliated Hospital of Nanchang University were included in the study. The patients' fluoroscopic images of LBBAP and coronary angiography were collected and analyzed. Changes in the ST­T segment in the electrocardiogram (ECG), serum troponin, and myocardial enzyme profiles were observed before and after the LBBAP procedure. RESULTS: A total of 50 patients were included in this study, of whom 46 patients underwent implantation with a pacemaker and 4 patients received an implantable cardioverter defibrillator (ICD). The pacing electrodes were confined to the posterior-middle (PM), median (M), Posterior inferior (PI), and middle inferior (MI) positions of the two-dimensional nine-square grid or in the junction area of the above positions, and were concentrated in the rectangle formed by the line of the center points of the four positions. The average vertical distances from the electrode tip to the left anterior descending branch artery (LAD), posterior descending branches (PD) and the left posterior ventricular branches (PL) were 19.69 ± 8.72 mm, 26.09 ± 8.02 mm, and 21.11 ± 7.86 mm, respectively; the minimum was 5.28 mm, 9.51 mm, and 8.69 mm, respectively. Coronary angiography in all patients showed no significant injury to the ventricular septal branch; however, we observed elevated serum troponin and changes in ST­T segment in ECG. CONCLUSION: The study demonstrates that pacing electrodes in LBBAP can be safely implanted over a wide range. Coronary arteries are likely to be safe when the pacing electrodes are located within the rectangle formed by the line connecting the PM, M, PI, and MI zone centroids. The left bundle branch can be quickly captured and the safety of the coronary artery can be improved by locating the electrode in the posterior-mid zone. The potential risk of injury to the LAD from the electrode is greater compared with the PD.