Electrochemical Workstation Research Articles

Preparation of amorphous TiO2 films by RF magnetron sputtering: Process optimization and effect of sputtering pressure on electrochromic properties

In this study, radio frequency (RF) magnetron sputtering was utilized to fabricate Titanium dioxide (TiO2) thin films at a room temperature. Scanning electron microscopy, energy dispersive spectroscopy, X-ray diffraction, atomic force microscopy, X-ray photoelectron spectroscopy, electrochemical workstation, and UV–Vis spectrophotometry were employed to analyze and characterize the microstructure, compositional components, and electrochromic properties of the films. The main focus is on exploring the microstructure and electrochromic properties of films produced under diverse sputtering pressures. The results show that the TiO2 films fabricated at a sputtering pressure of 1.2 Pa exhibit the most desirable surface morphology, with an optical modulation amplitude of up to 49.18 % (@550 nm), coloring time of 1.28 s, bleaching time of 0.79 s, and a coloration efficiency of 21.07 cm2/C. After 1000 cyclic voltammetry tests, the Q decay rate is 51.75 %. Electrochemical impedance spectroscopy (EIS) measurements reveal that TiO2 films prepared under these process parameters have lower charge transfer resistance and ion diffusion impedance, which facilitate ion injection and extraction.

Wearable Patch Biosensor through Electrothermal Film-Stimulated Sweat Secretion for Continuous Sweat Glucose Analysis at Rest.

Wearable patch biosensors for noninvasive and continuous diabetes management through sweat glucose analysis present a promising prospect. However, how to obtain sweat samples safely and effectively remains a huge challenge, especially in a resting state. In this work, we propose an innovative wearable patch biosensor through a heat-stimulated approach for sweat collection. A silver nanowire-loaded electrothermal film was designed as the heat source to stimulate sweat glands for sweat secretion. Subsequently, the secreted sweat sample was transported and enriched through microfluidic channels, which was continuously and sensitively analyzed by a Prussian blue and glucose oxidase comodified glucose electrochemical biosensor. Under optimal conditions, its sensitivity could achieve 14 μM sweat glucose within 15 min, which was 17 min shorter than that without heating. The specificity, reproducibility, and accuracy were also adequate. To achieve on-body perspiration monitoring of human subjects, the wearable patch biosensor was integrated with a portable electrochemical workstation, a temperature controller, and a power source. The glucose concentration was presented on a smartphone. Results showed that the glucose concentration in sweat detected by the wearable biosensor presented a highly consistent trend with the blood glucose measured by a blood glucose meter throughout the day with normal meals. Compared with other conventional sweat stimulation strategies, the simple device and safe principle made it more suitable for individuals who were sedentary or at rest. This work provides a new approach to realizing wearable patch biosensors for personalized health monitoring.

Preparation of PTFE-TIO2-GO/EP superhydrophobic costing and its performance study

For many years, the issue of microbial adhesion has presented difficulties in both daily life and business. In this paper, superhydrophobic coatings were produced by adding epoxy resin (EP), butyl acetate, titanium dioxide (TiO2) nanoparticles, polytetrafluoroethylene micropowder (PTFE), and graphene oxide (GO) sequentially into a mug and mixing well, and then modifying the microscopic particles by using perfluorooctyltriethoxysilane (POTS), and lastly producing the superhydrophobic coatings applied via spraying on the aluminum sheet surface. The micro morphology of the samples was analysed by SEM and EDS, the molecular makeup of the samples was analysed by FTIR and the molecular stability, mechanical stability and algae resistance were tested, and finally the the rust unwillingness of the coatings was investigated by using an electrochemical workstation (Tafel and EIS). The outcomes demonstrated that the best GO to nanoparticle mass ratio of 10% was chosen to achieve a contact angle of 167.5° and a sliding angle of 2.5°. The coating contact angle was still superior to 150° after 7 days of immersion in strong acids and bases as well as 3.5 wt% Nacl and after 8 hours of immersion in boiling water. After 800 abrasion tests the contact angle was still 150.6°. Algae resistance tests showed that the coatings had good resistance to algae adhesion.

An oriented self-assembly biosensor with built-in error-checking for precise midkine detection in cancer diagnosis and prognosis evaluation

Midkine (MDK) is a neurotrophic growth factor highly expressed during embryogenesis, currently recognized as a multifaceted factor in cancer progression and drug resistance. MDK has demonstrated greater accuracy than existing biomarkers. Serum MDK is a valuable indicator for the non-invasive early detection of tumors. It dynamically changes following surgical tumor excision and prior to recurrence, facilitating prognosis and treatment response evaluation. However, existing methods struggle to achieve the sensitivity required for clinical applications. Herein, we developed a triple-mode biosensor with oriented self-construction and built-in error-checking for rapid, sensitive, and convenient MDK detection. The sensor construction adhered to the principle of achieving oriented and strong covalent connections to ensure high sensitivity. Biosynthesized quantum dots (BQDs) were introduced to orient antibodies, enhancing the exploration of active binding sites and significantly increasing antibody-capturing ability. To further enhance sensitivity and signal amplification, Au@Pt nanorods-Ab2 (MF-Probe) were used as multifunctional probes, incorporating an error-checking mechanism to minimize false results. Detection was feasible using an electrochemical workstation, a microplate reader, and even a mobile phone. The sensor exhibited a wide linear range from 5 fg/mL to 100 ng/mL and a low limit of detection (LOD) of 1.620 fg/mL. It accurately distinguished MDK levels in the serum of healthy donors and cancer patients. Compared to existing ELISA kits, it exhibited a lower LOD and a more sensitive response to trace MDK, suggesting it is a promising tool for cancer diagnosis and prognostic evaluation.

Microstructure and characteristics of Zn and Mg-doped LiNbO3 materials for electrochromic devices

In this investigation, polycrystalline targets of lithium niobate (LN), zinc-doped lithium niobate (Zn:LN), and magnesium-doped lithium niobate (Mg:LN) were synthesized utilizing the Hot Isostatic Pressing (HIP) and Cold Isostatic Pressing (CIP) sintering technique. Subsequently, amorphous thin films of LN, Zn:LN, and Mg:LN and electrochromic devices were fabricated via radio frequency (RF) magnetron sputtering. Comprehensive characterization of the microstructure and optoelectronic properties of the targets, films and devices was conducted employing scanning electron microscopy, X-ray diffraction, spectrophotometry, atomic force microscopy, and an electrochemical workstation. Studies have shown that doping with zinc and magnesium enhances the sintering quality of ceramics, reducing lithium vacancies in polycrystalline lithium niobate ceramics. Zinc doping increases the resistance of lithium niobate, whereas magnesium doping introduces a secondary phase that decreases the resistance. The resistances of LN, Zn:LN, and Mg:LN polycrystalline ceramics are 8.35 GΩ, 9.80 GΩ, and 7.61 GΩ, respectively. The doping process refines the growth of the target and film particles, enhancing the microstructural quality. Notably, the ionic conductivity of the Mg:LN film escalates to 1.7 × 10−5 S/cm. Using doped lithium niobate thin films as electrolytes, the electrochromic devices showed a 38 % increase in coloration efficiency and a 46 % improvement in bleaching efficiency, significantly enhancing device performance.

Ce-Doped Iron Oxide Anticorrosive Coatings: Effect of c(Ce4+):c(Fe3+) Ratio on Structure, Morphology, and Coating Anticorrosion Performance

Utilizing hydrothermal methods, Ce-doped iron oxide nanoparticles were synthesized from precursor solutions under different c(Ce4:c(Fe3+) precursor solutions. The effects of the c(Ce4+):c(Fe3+) ratio in the precursor solutions on the nanoparticle morphology and nanoparticle structure of the Ce-doped iron oxide were investigated using X-Ray diffraction, transmission electron microscopy, and scanning electron microscopy. Fourier transform infrared spectroscopy (FTIR) was used to examine the bond energy strength of the Ce-doped iron oxide nanoparticles. The electrochemical properties of the Ce-doped iron oxide nanoparticles were tested using an electrochemical workstation and a saltwater immersion resistance test. The corrosion resistance of Ce-doped iron oxide coatings at different c(Ce4+):c(Fe3+) ratios was systematically analyzed, uncovering corrosion resistance mechanisms and self-healing capabilities. The results show that as the c(Ce4+):c(Fe3+) ratio decreases, the lattice constants of the samples increase along with the average grain size. Both smaller and larger c(Ce4+):c(Fe3+) ratios are detrimental to lattice distortion in α-Fe2O3. The reduced number of valence electrons provided by cerium ions in Ce-doped iron oxide hinders the generation of holes and exerts a minor influence on the crystal band structure, leading to weaker electrochemical stability. The Ce-doped iron oxide coating prepared at a c(Ce4+):c(Fe3+) ratio of 1:60 readily generates a higher number of reactive hydroxyl radicals during corrosion, thus exhibiting enhanced self-healing capabilities and corrosion resistance.

Redox Activity of Co Species in the Active Sites of CoNx/CoOx Facilitates Oxygen Electrocatalysis for Zn-Air Batteries.

Developing efficient bifunctional oxygen electrocatalysts is crucial for enhancing the performance of rechargeable Zn-air batteries (ZABs). In this study, cobalt/cobalt oxides embedded in N-doped carbon nanofibers (Co/CoOx/NCNFs) were synthesized through a combination of electrospinning and annealing processes. The resulting Co/CoOx/NCNFs catalysts feature abundant CoNx and CoOx active species, leveraging the large specific surface area of nanofibers to facilitate oxygen reduction reaction (ORR) and oxygen evolution reaction (OER). The optimized Co/CoOx/NCNFs-0.1 achieved a half-wave potential (vs. RHE) of 0.82 V and required only 429 mV to reach 10 mA cm-2 in a typical three-electrode system with 0.1 M KOH using an electrochemical workstation equipped with a pine instruments rotator, outperforming the Pt/C+RuO2. The assembled ZABs exhibited high specific capacity (771 mAh gZn -1), substantial power density (981.6 mWh gZn -1), and long-term stability (>325 h). In situ Raman spectroscopy confirmed that the electrocatalytic processes involve the redox activity of Co (II and III) species derived from abundant CoNx and CoOx, elaborating the origin of the catalysts' exceptional oxygen electrocatalysis performance. This work not only presents a straightforward and effective approach for producing bifunctional oxygen electrocatalysts in ZABs but also sheds light on the catalytic mechanisms underlying ORR and OER for CoNx/CoOx-based oxygen electrocatalysts.

A vertical/horizontal graphene-based microneedle plant sensor for on-site detection of indole-3-acetic acid in vegetables

Plant hormones are important regulators of crop growth and production. In this study, an in situ electrochemical sensor was successfully built using flat microelectrodes with horizontally and vertically grown graphene to detect the plant regulator indole-3-acetic acid (IAA) in plants. Vertical and horizontal graphene layers were prepared by electron-assisted hot-filament chemical vapor deposition. Vertical graphene nanosheets were grown on a horizontal graphene layer as sensing electrodes, and a microneedle sensor was assembled by combining Pt and Ti microelectrodes. The vertical/horizontal graphene (VHG) microneedle sensor can rapidly detect IAA levels in various plants in situ over a wide pH range of 4.0–9.0 and concentration range of 1–100 μM, with a minimum detection limit of 0.21 μM (3σ/S). Subsequently, this microneedle sensor was used to determine the IAA content in different tissues of cucumber and cauliflower stems with satisfactory results. The combination of VHG microelectrode arrays and small electrochemical workstations is useful for constructing portable, low-cost, on-site, and fast electrochemical sensing platforms for plant growth monitoring.

Synergistic Effect of Polyurethane on Pore-Sealing and Lubrication of Microarc Oxidation Coating.

Microarc oxidation (MAO) is a widely used surface treatment technology. However, its processing inevitably leads to the presence of micropores, microcracks, and other defects in the MAO coating. These defects lead to suboptimal tribological performance and diminished corrosion resistance of the MAO coating. Thus, this study proposed a new pore-sealing method with environmental protection and high efficiency. Polyurethane reactive (PUR) composite coating was prepared on the surface of MAO coating. The sealing effect of the PUR sample was analyzed using scanning electron microscopy (SEM). The molecular structure and elemental changes of the coating were analyzed using X-ray photoelectron spectroscopy (XPS). The tribological properties were analyzed using a tribological testing machine, and the corrosion resistance was tested using an electrochemical workstation. The test results show that the lubricity and corrosion resistance of PUR sample are improved significantly compared with MAO coating. When the mass fraction of PUR is 3 wt %, the PUR sample shows the best lubrication performance, and the coefficient of friction decreases by 70.8%. Compared with the traditional sealing technology, this experimental method is simple and low-cost and has a wide application prospect, which promotes the development of MAO technology.

The Dependence of Electrochemical Behavior and Discharge Performance on the Zn/Gd Ratio of Mg-Li-Zn-Gd Anodes for Mg-Air Batteries

In this study, the electrochemical performance and discharge behavior of Mg-Li-Zn-Gd alloys with α-Mg and β-Li-based anode material are investigated, with the aim to improve the anode performance of Mg-air batteries. The experimental anode alloys with detailed Mg-8Li-xZn-yGd (x = 1, 2, 3; y = 1, 2, 3 wt.%) components are prepared, and extrusion deformation is carried out on these alloys. Simultaneously, scanning electron microscope (SEM), X-ray diffractometer (XRD), electrochemical workstation, and constant current discharge systems are applied for microstructure characterization, corrosion, and discharge performance testing. The results show that the experimental alloys are composed of an α-Mg and β-Li dual matrix, with W-Mg3Gd2Zn3, Mg3Gd, and MgLiZn second phases. Meanwhile, extrusion deformation promotes the recrystallization process through the particle-induced nucleation mechanism. The corrosion resistance is improved with the increasing Zn/Gd ratio, and the extruded Mg-8Li-2Zn-1Gd (LZG821) alloy exhibits the optimum corrosion resistance, with a corrosion rate of 0.493 mm·year−1. In addition, the extruded Mg-8Li-1Zn-1Gd (LZG811) alloy has the optimal discharge performance, with a discharge specific capacity of 1371.04 mA·g−1 at a current density of 40 mA∙cm−2, and its anode efficiency reaches nearly 70%. The poorer discharge properties of the Mg-8Li-2Zn-1Gd (LZG821) and Mg-8Li-2Zn-3Gd (LZG823) alloys are attributed to their refined grains, which could bring severe intergranular corrosion while increasing the grain boundary density.

Atomic-scale insight on nanostructures and electrochemical properties of (NiCrCo)82Ti9Al9 high-entropy alloy coatings by density functional theory calculations

(NiCrCo)82Ti9Al9 high−entropy alloy was attached to act as coating material by combining of laser cladding and laser remelting. In this study, the electrochemical properties of obtained HEA coatings were comparatively investigated using an electrochemical workstation, and the corrosion mechanism was revealed by the density functional theory calculations. The results show that the laser cladded HEA coating is mainly consisted of face-centered and body-centered cubic structures, and the face-centered cubic structure of the laser cladded HEA coating is transferred to the amorphous structure by laser remelting, which provides the stronger anti−corrosion capability compared with the face-centered cubic structure of HEA coating.

CoOX composite Pr0.4Sr0.6Co0.2Fe0.8O3-δ perovskite was used to obtain an IT-SOFC cathode with high electrocatalytic activity

The advancement and application of mesophilic solid oxide fuel cells (IT-SOFCs) rely heavily on enhancing cathode materials to achieve greater efficiency. In this paper, Pr0.4Sr0.6Co0.2Fe0.8O3-δ (PSFC) and transition metal oxide CoOx were selected as cathode materials, which not only combined the high catalytic activity of Pr6O11 but also took advantage of the structural stability and economy of Fe-based perovskite. The samples underwent analysis using X-ray diffraction (XRD), field emission scanning electron microscopy (FE-SEM), high-resolution transmission electron microscopy (HR-TEM), and X energy dispersion spectrometer (EDS) for structural examination. The electrochemical workstation was used to test the conductivity of the material and the stability of the cell. The results indicate that an appropriate amount of CoOX composite can effectively enhance the level of oxygen vacancies, thereby enhancing the ORR activity of the cathode. Among these composites, Pr0.4Sr0.6Co0.2Fe0.8O3-δ-CoOx-I exhibits the fastest rate of oxygen exchange at the surface and the best electrochemical performance. At 700 °C, the polarization resistance ASR of Pr0.4Sr0.6Co0.2Fe0.8O3-δ-CoOx-I is 0.0749 Ω cm2; In single-cell fuel mode with NiO-YSZ as anode, YSZ electrolyte, and GDC as cell layer, the peak power density (PDD) is 0.97W cm−2. The PSCF-CoOx composite cathode holds promise as a high electrocatalytic active material for Solid Oxide Fuel Cells (SOFCs).

An In2O3/In2S3 photoanode-driven whole-cell biocathode sensor for sensitive detection of nitrate

Whole-cell biocathode sensor is a new form of self-regenerable biosensor and promising for environmental monitoring especially in the scenario with low organic substrate. However, external power supply such as electrochemical workstation is required to drive the biocathode reaction, which greatly limits its application. Herein, a new strategy based on the visible-light-driven whole-cell biocathode was proposed and validated for self-powered sensitive detections. To be specific, 1-OH phenazine was selected as the optimal electron shuttle for a Shewanella oneidensis MR-1 inoculated biocathode, which efficiently mediate the cathodic reaction at an electrode potential below −0.6 V (vs. SCE). Meanwhile, an In2O3/In2S3 photoanode with nanoflower-like structure was fabricated to match the kinetic of the biocathode. The photo-driven biocathode reduction was convinced by comparing with the performance of biocathode in the conventional three-electrode system. With this basis, a self-powered whole-cell biocathode sensor was developed for nitrate detection. An extreme low limit of detection of 0.028 μM (S/N=3) and linear detection range of 0.1–20 μM was achieved. Moreover, this biocathode sensor also exhibited excellent selectivity, reusability, accuracy, stability and was reliable for the detection of complex environmental samples. Therefore, this work developed a new photo-driven whole-cell biocathode sensor with excellent detection capacity of nitrate, which opens up new prospects for the development of high-performance biosensors.

Graphene quantum dots based flexible planar micro-supercapacitors with different bending angles

The development of micro-electronic products and the increase in demand for portable devices have driven the research of planar micro-supercapacitors (PMSCs). Flexible PMSCs have the advantages of high energy and power density, stable cycling performance and good flexibility, which makes the flexible PMSCs valuable for the research in the field of wearable electronic devices. In this paper, graphene quantum dots were selected as the electrode material for the flexible devices and PET as the flexible substrate, and the flexible PMSCs with interdigital electrode width to gap ratio of 60 μm/60 μm were prepared using modified liquid-air interface self-assembly, photolithography and oxygen plasma etching. Cyclic voltammetry, galvanostatic charge-discharge, electrochemical impedance spectroscopy and cyclic stability were performed on the devices with the bending angles of 0°, 60°, 90°, 150° and 180°, respectively, using electrochemical workstation. Redox peaks appeared in the CV curves of the devices at the very low scan rates, indicating that redox reaction occurred and pseudocapacitance effect appeared. The area capacitance, energy density and power density of the devices decreased and the charging time was longer than discharging time after the bending angle was increased. After 10,000 cycles, the cyclic stability for the five bending angles was maintained at more than 71%. In short, the larger the bending angles, the greater the impact on some performance of the devices, and when the devices were placed in non-vacuum environment for too long, some performance after bending but better.

Investigation of corrosion resistance offered by the Fe-based clad layer under salt spray and electrochemical workstations

The present work aims to evaluate the electrochemical characteristics of the Fe–based alloy coating formed on the 27SiMn steel substrate under neutral salt spray and 3.5 wt% NaCl environments. By adopting the high-speed laser cladding technique, the Fe-based clad layer was fabricated to perform microstructural and electrochemical characterizations. The microstructure and phase of the coating were analyzed using a scanning electron microscope (SEM), electron backscatter diffraction (EBSD) and X-ray diffraction (XRD), and its corrosion performance was also discussed using the salt spray corrosion chamber and the electrochemical workstation. The results show that the microstructure of the coating surface contains equiaxed crystals and long dendritic crystals which arise due to the higher solidification rate after the cladding process. The Fe–based coating was rich in FeCr phase throughout its microstructure without the formation of the intermetallic compounds. Compared to the substrate, the corroded surface of the coating tends to be compact containing a few corrosion pits after different corrosion times, which is attributed to the formation of Cr oxide on it. The electrochemical tests on the potentiodynamic polarization curve (PPC) and electrochemical impedance spectrum (EIS) indicate that the corrosion resistance of the coating is superior to the substrate, presenting a higher corrosion potential (−0.298 V), lower passive current density (1.36 × 10−6 A•cm2), and higher charge transfer resistance (8.23 × 106 Ω·cm2). Additionally, the corrosion mechanism of coating in salt spray and electrochemical tests is the local pitting corrosion due to the autocatalytic effect on the localized region, which facilitates Cl− ions penetrating the coating and leads to the dissolution of Fe and Cr oxides.

Effect of Ni on the corrosion resistance and passivation characteristics of Ni-Mn-Ga-Gd shape memory alloys in sodium chloride solutions

This paper investigates the effect of different Ni contents on the corrosion and passivation behavior of Ni54+xMn25Ga20.9-xGd0.1 (x = 0, 1, 2, 3, 4) shape memory alloy in a 3.5 wt% NaCl solution. Using scanning electron microscope, electrochemical workstation, and X-ray photoelectron spectroscopy. The results indicate that the corrosion resistance of single-phase alloys initially increases and then decreases as the Ni content ranges from x = 0 to 3, with the best corrosion resistance observed at x = 2. The passive film of the alloy mainly consists of NiO, Ni(OH)2, and Ga2O3. Both NiO and Ga2O3 positively affect the corrosion resistance of the passive film. In the range of 54 to 57 at% Ni content, the alloy remains a single-phase alloy. The elements Ni and Ga work together in the passivation film and at a Ni content of 56 at% to reach equilibrium, which provides the best corrosion resistance for single phase alloys. When the Ni content reaches 58 at%, the second phase appears in the form of a nickel-rich phase. Typically, intergranular corrosion preferentially corrodes the second phase, but in this study, the second phase is a nickel-rich phase with some corrosion resistance, which improves the overall corrosion resistance of the alloy.

Theoretical design and synthesis of Co30Ni60/CC for high selective methanol oxidation assisted energy-saving hydrogen production

The integration of methanol oxidation reaction (MOR) with hydrogen evolution reaction (HER) represents an advanced approach to hydrogen production technology. Nonetheless, the rational design and synthesis of bifunctional catalysts for both MOR and HER with exceptional activity, stability and selectivity present formidable challenges. In this work, firstly, density functional theory (DFT) was utilized to design and evaluate material models with high performance for both MOR and HER. Secondly, guided by DFT, Co30Ni60/CC (CC, carbon cloth) composites with a leaf-like nanosheet structure were successfully fabricated via electrodeposition. In the MOR process, Ni acts as the predominant active center, while Co amplifies the electrochemically active surface area (ECSA) and enhances the selectivity of methanol oxidation. Conversely, in the HER process, Co serves as the primary active center, with Ni augmenting the charge transfer rate. The electrochemical results demonstrate that Co30Ni60/CC exhibits exceptional performance in both MOR and HER at a current density (j) of 10 mA cm−2, with peak potentials of 1.323 V and −95 mV, respectively. Additionally, it shows remarkable selectivity for the oxidiation of methanol to high value-added formic acid. Thirdly, following a 100 h chronopotentiometry (CP) test, the required potential demonstrates an increase of 4.9 % (MOR) and 8.1 % (HER), signifying the superior stability of Co30Ni60/CC compared to those reported in the literature. The exceptional performance of Co30Ni60/CC can be primarily attributed to that the leaf-like nanosheets structure not only exposes a plethora of active sites but also facilitates electrolyte diffusion, the monolithic structure prepared by electrodeposition enhances its stability, and the transfer of electrons from Co to Ni regulates its electronic structure, as corroborated by X-ray photoelectron spectroscopy (XPS) and density of states (DOS) analyses. Finally, at the same j, the voltage required by the Co30Ni60/CC||Co30Ni60/CC electrolytic cell, powered by an electrochemical workstation, is 198 mV lower than that required for alkaline water-splitting. Meanwhile, at higher j (100 mA cm−2), the electrolytic cell exhibits sustained and stable operation for 150 h, enabling high-efficiency hydrogen production and the synthesis of high value-added formic acid.

Catechol/m-Phenylenediamine Modified Sol-Gel Coating with Enhanced Long-Lasting Anticorrosion Performance on 3003 Al Alloy.

Aluminum alloys, characterized by their low density and high mechanical strength, are widely applied in the manufacturing sector. However, the application of aluminum alloys in extreme environments presents severe corrosion challenges. Sol-gel organic coating techniques have garnered significant attention due to their excellent stability, barrier properties, and cost-effectiveness, as well as their simpler processing. Nevertheless, conventional sol-gel coatings are unable to withstand the corrosive effects of high-chloride and high-halide ion environments such as marine conditions, owing to their inherent structural defects. Therefore, this study proposes the utilization of a simple method to synthesize catechol (CA) and meta-phenylenediamine (MPD)-derived catecholamine compounds to modify sol-gel coatings. Surface characteristics of the modified coatings were analyzed using Fourier-transform infrared spectroscopy (FT-IR), ultraviolet-visible (UV-Vis) spectroscopy, scanning electron microscopy (SEM), and X-ray photoelectron spectroscopy (XPS). The thickness of the modified coating was approximately 6.8 μm. The CA/MPD-modified substance effectively densifies the sol-gel coating, enhancing its corrosion protection performance. A 3.5 wt% NaCl solution was used to simulate a marine environment, and electrochemical impedance spectroscopy (EIS) was conducted using an electrochemical workstation to evaluate the coating's protective properties over a long-term period. The results indicate that the modified coating provides protection for 3003 aluminum alloy for a minimum of 30 days under corrosive conditions, outperforming unmodified sol-gel coatings in terms of corrosion resistance.

Preparation of porous (Mo2/3Y1/3)2AlC and its hydrogen evolution reaction performance

Porous (Mo2/3Y1/3)2AlC MAX phase ceramic was prepared by reaction sintering method using Mo, Y, Al, and graphite powder as raw materials. The influence of changes in Al content on the purity of the obtained samples was investigated using X-ray diffraction (XRD), scanning electron microscopy (SEM), Archimedes method, and bubble point method. The conditions for obtaining a pure phase were identified, and the transformation path of the phase during sintering and the mechanism of pore formation were provided. The linear sweep voltammetry (LSV) cure and cyclic voltammetry (CV) cure of MAX were tested using an electrochemical workstation. It can be calculated that MAX exhibits good hydrogen evolution reaction (HER) performance under alkaline conditions due to its high electrochemical active surface area (ECSA) of 373.2 and small Tafel slope of 41.7 ​mV·dec−1.

Ultrasensitive and multiplexed Gastric cancer biomarkers detection with an integrated electrochemical immunosensing platform

Developing immunosensing platforms capable of simultaneously detecting multiple cancer markers is crucial for clinical diagnosis and biomedical research. Here, we introduce a novel dual-mode electrochemical biosensing assay platform capable of detecting two gastric cancer biomarkers: pepsinogen I (PG I) and pepsinogen II (PG II). Methylene blue (MB) and Prussian blue (PB) were used as dual signal sources to label PG I and PG II, respectively. The platform integrates an ARM STM32F411 microcontroller and an AD5941 analog front-end, which not only facilitates cyclic voltammetry (CV) and differential pulse voltammetry (DPV) with efficacy comparable to commercial electrochemical workstations but also offers data collection and synchronous analysis capabilities, allowing simultaneous output of PG I and PGR (PG I/PG II) values. Equipped with an interactive screen for operational control and result display, the immunosensing platform provides linear detection ranges for PG I (5 pg/mL–100 ng/mL) and PG II (50 pg/mL–200 ng/mL), enabling rapid detection within 5 min. It demonstrates excellent sensitivity and selectivity when comparing serum samples from healthy individuals and gastric cancer patients. The dual-marker detection platform significantly enhances early diagnosis and screening of gastric cancer, offering substantial improvements over single-marker assays. Furthermore, this platform shows potential for detecting multiple biomarkers in various diseases, highlighting its utility for biomedical applications.