Search Results (4,373)

Lithium-ion batteries (LIBs) are pivotal for energy storage in electric vehicles and renewable systems, but how to effectively monitor their conditions and ensure their operational reliability is still a concern today. This study employs electrochemical impedance spectroscopy (EIS) to systematically investigate the evolution of impedance characteristics in nickel–cobalt–manganese oxide (NCM) lithium-ion batteries (LIBs) under varying states of charge (SOCs), states of health (SOHs), temperatures, and mechanical compression displacements. Results reveal that higher SOC and temperature reduce impedance by enhancing ion kinetics and interfacial activity, with $R_{ct}$ (charge transfer resistance) exhibiting a U-shaped dependence on SOC, minimized at 40–60%. As SOH declines from 100% to 80%, $R_{SEI}$ (SEI film resistance) and $R_{ct}$ increase progressively, reflecting SEI thickening and electrode degradation. Mechanical compression (0–8 mm) elevates all resistances, particularly $R_{ct}$ at high SOC, due to structural deformation and hindered diffusion. DRT (distribution of relaxation times) spectra highlight amplified low-frequency peaks with aging and low SOC, underscoring diffusion limitations. These findings elucidate multi-scale failure mechanisms, from interfacial polarization to structural instability, providing a framework for non-invasive health monitoring and lifetime prediction. Full article

Steels remain among the most widely used structural and engineering materials in modern infrastructure, energy systems, and industrial facilities. Their long-term reliability depends critically on the early detection of corrosion damage and microstructural degradation. This review surveys recent advances in two complementary families of non-destructive evaluation (NDE) methods: magnetic techniques, including magnetic Barkhausen noise (MBN), magnetic flux leakage (MFL), eddy current testing (ECT), and magnetic hysteresis analysis; and electrochemical methods including electrochemical impedance spectroscopy (EIS), linear polarization resistance (LPR), scanning vibrating electrode technique (SVET), and electrochemical noise (EN). Recent progress in sensor miniaturization, signal processing algorithms, and multi-technique integration is reviewed. Particular attention is given to the sensitivity of these methods to microstructural changes reported in the literature, including carbide dissolution, phase transformations, temper embrittlement, and sensitization in stainless steels, as well as to the conditions under which such sensitivity has been demonstrated. The potential synergy between magnetic and electrochemical monitoring is discussed as a possible pathway toward more robust, condition-based maintenance frameworks. Challenges related to field deployment, environmental interference, calibration, and data interpretation are identified, and future directions—including machine learning-assisted analysis and multi-physics sensor arrays—are outlined. Full article

To meet the demand for rapid detection of methylene blue residues in aquatic products, this study constructed a composite structure modified with silver nanoparticles on the surface of a glassy carbon sheet for precise detection. This composite film used the synergistic effect of the composite structure, which significantly enhanced the current response between the composite film and MB. The CV and EIS results demonstrated that this composite structure exhibited outstanding performance, endowing the composite film with the capability for sensitive detection of methyl blue. The results showed that the composite film detected methylene blue by differential pulse voltammetry, with a limit of detection as low as 1.6 nM. In the concentration range of 10 nM to 120 nM, the current intensity presented a good linear relationship with the concentration of MB. In addition, this composite film successfully identified methylene blue in aquatic products, with a recovery rate ranging from 81% to 113%. The results indicated that the composite film could be effectively applied to the sensitive detection of methylene blue in complex samples. This study provided a reliable and easy-to-construct electrochemical sensing platform for aquatic product safety monitoring. Full article

Steroid-resistant nephrotic syndrome (SRNS) in childhood frequently reflects monogenic podocytopathies in which immunosuppression is ineffective. Biallelic variants in MYO1E, encoding the class I myosin Myo1E, cause a distinctive form of focal segmental glomerulosclerosis (FSGS) often accompanied by “Alport-like” multilamination of the glomerular basement membrane (GBM). Early recognition has therapeutic and prognostic implications. A previously healthy 4-year-old boy presented with generalized edema and nephrotic-range proteinuria. Glucocorticoids induced no remission; sequential calcineurin inhibition (cyclosporine, then tacrolimus) and a single dose of ofatumumab yielded only transient, partial reductions in proteinuria. A first biopsy elsewhere showed FSGS with nonspecific IgM/C3 trapping; electron microscopy (EM) was not performed. At age 10, repeat biopsy with EM revealed ~30% segmental foot-process effacement, focal GBM thickening (to 1740 nm), irregular lamina densa multilamination, and lamellar duplications without immune-complex deposits—features highly suggestive of hereditary GBM disease. Targeted sequencing identified compound-heterozygous MYO1E variants segregating in trans: a canonical splice-donor change (c.2785+1G>A) and a frameshift (c.3094_3097del; p.Thr1032Profs*73). Each parent was an unaffected heterozygous carrier; the sibling was negative. Supportive therapy with ramipril was continued. At last follow-up (January 2025), renal function was normal (serum creatinine 0.5 mg/dL; creatinine clearance 122 mL/min) with stable sub-nephrotic proteinuria (0.52 g/day; 16 mg/m² per hour) and normotension. This case broadens clinicopathologic recognition of MYO1E-associated nephropathy and highlights the teaching point that Alport-like GBM changes are not pathognomonic for type IV collagen disorders but may signal defects in podocyte cytoskeletal anchoring. Full article

Bacterial and fungal infections, together with oxidative stress-mediated damage, remain major challenges in human health and in the protection of materials, highlighting the need for new multifunctional molecules that combine antioxidant and antimicrobial properties. In this context, a new chloropyridine-based derivative, N4,N4-bis((6-chloropyridin-3-yl)methyl)-N1,N1-diethylpentane-1,4-diamine (AMZ), was synthesized via a simple, catalyst-free N-alkylation of N1,N1-diethylpentane-1,4-diamine with 2-chloro-4-(chloromethyl)pyridine in acetonitrile at 55 °C, affording a 62% yield. The structure of AMZ was confirmed by melting point determination, ¹H and ¹³C NMR spectroscopy, and EI–MS analysis. Its antioxidant activity was evaluated using DPPH and FRAP assays with BHT as a reference standard, while antibacterial and antifungal activities were assessed via disk diffusion and microdilution methods to determine inhibition zones and MIC/MBC values. In silico investigations included drug-likeness and ADMET predictions, as well as molecular docking on catalase (PDB: 2CAG) and fungal CYP51 (PDB: 1EA1). AMZ exhibited dose-dependent radical scavenging in the DPPH assay, reaching 76.88 ± 3.20% inhibition at 1000 µg/mL, with an EC₅₀ of 26.03 ± 0.21 µg/mL, close to that of BHT (23.65 ± 0.22 µg/mL). In the FRAP assay, AMZ showed a higher reducing power than BHT at a low concentration (OD₅₀ µg/mL 0.177 ± 0.023 vs. 0.134 ± 0.017), although its FRAP EC₅₀ was higher (700.48 ± 22.54 vs. 400.16 ± 8.67 µg/mL). AMZ displayed broad-spectrum antimicrobial activity against Gram-positive and Gram-negative bacteria and fungi, with particularly strong effects on Bacillus subtilis (44.5 ± 0.5 mm; MIC/MBC 0.008 mg/mL) and Aspergillus niger (30 mm; MIC/MBC 0.030 mg/mL), in some cases comparable or superior to streptomycin and fluconazole. In silico analysis indicated that AMZ fulfilled major drug-likeness rules, showed high predicted intestinal absorption (91.14%), and was classified as non-AMES toxic, while docking predicted favorable binding to catalase and CYP51, in agreement with the experimental antioxidant and antifungal activities. These findings highlight the potential of AMZ as a multi-target pyridine-based lead compound that warrants further structural optimization and in vivo evaluation for applications in oxidative-stress-related and infectious conditions. Full article

The corrosion behavior and mechanism of Q235 steel during a two-year exposure to the subtropical marine atmospheric environment on an offshore platform in the East China Sea were investigated in this study. Methods including corrosion weight loss measurement, macro/micro-morphological observation (using a digital camera, SEM, and 3D-CLSM), composition analysis (XRD and XPS), and electrochemical tests (EIS and Tafel polarization curves) were employed to systematically examine corrosion kinetics, rust layer evolution, and electrochemical performance. The results indicated that the corrosion rate of Q235 steel initially increased and subsequently decreased with prolonged exposure, with the atmospheric corrosivity reaching CX level as defined (according to the ISO 9223 standard). The corrosion products transitioned from an early-stage rust layer predominantly consisting of γ-FeOOH to a later-stage layer primarily composed of α-FeOOH and Fe₃O₄. XPS analyses revealed that both the α*/γ* ratio and the Fe(II)/Fe(III) ratio increased over time, demonstrating a progressive improvement in the protective properties of the rust layer. The polarization resistance of the rust layer gradually rose, while the corrosion current density declined significantly, further confirming the enhanced stability and protective performance of the rust layer following long-term exposure. Chloride ions accumulated at defects within the rust layer, inducing local acidification, which played a key role in promoting the initiation and propagation of pitting corrosion. This study elucidated the corrosion behavior and mechanism of Q235 steel in the marine atmospheric environment of the East China Sea. Despite the increase in exposure time from 6 to 24 months, during which the electrochemical stability of the rust layer enhanced over time, it failed to prevent the initiation and propagation of severe localized corrosion—an issue of critical importance for load-bearing structures. The findings provide important theoretical and data support for service-life assessment and corrosion protection design of offshore photovoltaic steel structures. Full article

The flexible upper-limb exoskeleton robot (exosuit) is composed of fabrics, soft actuators and compliant force-transmitting structures, which provides assistance or rehabilitation training for the shoulders, elbows, wrists and hands. By realizing human–robot collaboration, this kind of system has the advantages of comfort, light weight and portability, thus promoting motor function recovery and neural plasticity. This review establishes a classification and comparison framework for flexible upper-limb exoskeletons based on the actuation modalities and systematically summarizes the research progress under different actuation modalities. The relevant literature published from 2015 to 2025 was retrieved from the EI, IEEE Xplore, PubMed and Web of Science databases. After screening according to the preset inclusion and exclusion criteria, a total of 64 original research papers meeting the criteria were finally included for analysis. According to the actuation modalities, the flexible upper-limb exoskeleton robot is classified, and all kinds of systems are summarized and compared. Motor–cable/tendon actuation and pneumatic/hydraulic actuation have advanced substantially and are approaching technical maturity for flexible upper-limb exoskeletons. Meanwhile, designs based on passive/hybrid mechanisms (e.g., elastic energy storage elements and clutches) and new intelligent material actuations are showing a diversified development trend. In the future, the development is expected to further focus on lightweight and compliance, and by integrating multimodal sensing and feedback control, motion intention recognition and human–robot interaction theories, actuation systems will be developed towards modularization, intelligence and high-power density, in order to achieve more comfortable, lighter and more effective flexible upper-limb exoskeleton systems. Full article

Physiologically relevant in vitro intestinal models are essential for studying key physiological processes, including barrier function, drug screening and gut-microbiota interactions. However, conventional 2D culture systems often fail to recapitulate structural and functional complexity. Here, we aimed to validate a 3D bioelectronic transmembrane platform, previously used for monitoring human intestinal epithelium and vascular endothelium, for modeling the rat small intestinal barrier in vitro. The device integrates a poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate) (PEDOT:PSS) scaffold supporting co-cultures of rat intestinal epithelial cells (IEC-6) and rat fibroblasts (208F), enabling real-time monitoring of barrier formation through electrical measurements using electrochemical impedance spectroscopy (EIS). Barrier formation was monitored over 21 days and exhibited a time-dependent increase in barrier resistance. The 3D platform was compared with traditional 2D insert-based cultures and ex vivo rat tissue using an Ethylene Glycol Tetraacetic Acid (EGTA)-induced calcium switch assay to evaluate barrier disruption and recovery. EGTA treatment and removal induced reversible barrier disruption in the 3D in vitro and ex vivo models, whereas 2D in vitro cultures showed limited recovery. These findings demonstrate that the 3D platform more faithfully recapitulates native tissue architecture and function, closely paralleling ex vivo responses. Our study highlights the importance of validating advanced 3D in vitro models and establishes this bioelectronic platform as a robust tool for drug screening, barrier studies, and preclinical gastrointestinal research. Full article

Lithium–sulfur (Li-S) batteries hold great promise for next-generation energy storage, offering high theoretical energy density and cost-effectiveness. However, challenges like sulfur’s low conductivity, polysulfide dissolution, and significant volume changes limit their practical application. This study addresses these issues by investigating porosity-engineered carbon hosts, specifically potassium hydroxide (KOH)-activated Black Pearl carbons (BP2000, BP1300, and BP800). Varying KOH-to-carbon ratios allowed precise tailoring of micro- and mesoporous structures, optimizing sulfur loading, electrolyte infiltration, and ion transport. Composites were characterized by TGA, NLDFT, SEM, XRD, and FTIR and electrochemically (cycling, CV, EIS). The KOH-modified BP2000 1:1 cathode, exhibiting the highest mesopore volume increase, demonstrated superior electrochemical performance, including enhanced cycling stability, rate capability, and reduced charge-transfer resistance. These findings emphasize the importance of optimizing pore distribution in carbon hosts for high-performance Li-S batteries and provide valuable insights for advanced energy storage material design. Full article

Biochar provides a porous scaffold, conductive carbon framework and redox-active surface functional that can promote microbial attachment and extracellular electron flow. However, how feedstock-dependent biochar properties regulate the biochar–cell interface and microbial metabolism during contaminant removal remains insufficiently understood. Here, biochar derived from rice husk, corn straw and corn cob was used to immobilize Pseudomonas chlororaphis for triclocarban removal in batch microcosms. Multiscale analyses, including scanning electron microscopy (SEM), fourier transform infrared spectroscopy (FTIR), X-ray photoelectron spectroscopy (XPS), cyclic voltammetry (CV), (electrochemical impedance spectroscopy (EIS) and liquid chromatography–mass spectrometryLC-MS, were combined to link the biochar structure, interface and extracellular metabolism signatures with triclocarban (TCC) removal. Compared with free cells, all composites enhanced TCC removal and exhibited altered interfacial functional-group features together with substantially reduced fitted charge-transfer resistance, indicating facilitated interfacial electron exchange. Untargeted metabolomics further revealed consistent remodeling of extracellular redox-associated metabolite signatures upon immobilization, with increased quinone/polyphenol-associated features and pathway-level shifts related to redox homeostasis. Among feedstocks, the corn cob composite showed the highest triclocarban removal. Overall, this work proposes an evidence-supported “structure–interface–metabolism” framework for interpreting how agricultural-residue biochars modulate biofilm interfaces and redox-related metabolic signatures to improve triclocarban removal, providing guidance for designing biochar-supported bioprocesses for halogenated micropollutants. Full article

Thermal energy storage (TES) systems are widely employed in concentrated solar power (CSP) applications as a means of storing and dispatching energy. Typical thermal fluids used in TES systems include molten salts, such as solar salt (a KNO₃–NaNO₃ eutectic), as well as other inorganic salts currently under consideration. While these molten nitrate, chloride, sulfate, and carbonate salts offer favourable thermal properties, they can induce significant corrosion of metallic containment materials, leading to reduced system efficiency and component lifetime. Despite extensive post-exposure studies, in situ electrochemical understanding of corrosion mechanisms in molten solar salt remains limited, particularly for emerging alloys such as FeCrAl. In this study, the in situ corrosion behaviour of structural alloys in molten solar salt was investigated using electrochemical impedance spectroscopy (EIS). Complementary post-exposure characterization was performed using destructive techniques, including scanning electron microscopy (SEM) and energy-dispersive X-ray spectroscopy (EDX), to assess microstructural and chemical changes. The materials evaluated were stainless steel SS316 and comparatively underexplored Kanthal FeCrAl alloys, exposed to molten solar salt (40 wt% KNO₃–60 wt% NaNO₃) at 545 °C. The electrochemical and microstructural analyses indicate that FeCrAl exhibits superior corrosion resistance associated with the formation of a more stable and protective oxide scale, compared to SS316 under the investigated conditions. This study provides new electrochemical evidence supporting the suitability of FeCrAl alloys for TES applications, while also indicating that SS316 may develop improved corrosion resistance over extended exposure durations, highlighting the importance of long-term performance assessment. Full article

Organic coatings are used as one of the most effective strategies for the corrosion protection of metals. Nowadays, due to environmental regulations, the use of water-based coatings has become essential compared to solvent-based ones. However, their application to magnesium alloys remains largely unexplored due to their high reactivity with water. In the present work, a phosphate-functionalized waterborne binder is applied to AZ31B magnesium alloy. The surface has been modified by four different pre-treatments, respectively: (i) mechanical grinding, (ii) pickling, (iii) conventional conversion treatment, and (iv) a novel conversion treatment based on layered double hydroxides (LDH). The most promising pre-treatments are selected to explore their synergy with a biobased waterborne binder, containing CeO₂ nanoparticles as a corrosion inhibitor. The morphology and composition of the different systems are studied, prior to and after corrosion tests in NaCl solution, by scanning electron microscopy (SEM) and energy-dispersive X-ray spectroscopy (EDS). Results obtained by electrochemical impedance spectroscopy (EIS) in NaCl solution have revealed not only that LDH performs better than the conventional conversion treatment but also the synergy between LDH pre-treatment and CeO₂ nanoparticles when two organic layers are used. Full article

In this study, the structural and electrochemical performance of Nb₂CT_x MXene-based composite electrodes modified with activated carbon (AC) derived from food waste was systematically investigated for supercapacitor applications. Three composites with Nb₂CT_x:AC mass ratios of 90:10 (MXAC1), 80:20 (MXAC2), and 70:30 (MXAC3) were prepared and comparatively evaluated. SEM/EDS, XRD, HR-TEM, XPS, and BET analyses revealed that, in the MXAC2 composite, activated carbon was homogeneously distributed between the MXene layers, effectively suppressing restacking and promoting the formation of a hierarchical micro/mesoporous structure. XPS results confirmed the preservation of the Nb–C framework and the enrichment of surface functional groups (–O, –OH, and –F). BET analysis demonstrated that MXAC2 possesses an optimized pore architecture that facilitates efficient ion diffusion. Electrochemical measurements revealed that the MXAC2 electrode exhibited the highest specific capacitance at all scan rates and current densities. At 5 mV·s⁻¹, MXAC2 achieved a specific capacitance of 651.84 F·g⁻¹ and maintained a substantial capacitance even at a high current density of 4 A·g⁻¹. EIS analysis confirmed the very low charge transfer resistance (0.023 Ω) and enhanced capacitive behavior for MXAC2. Additionally, MXAC2 has high cycle stability, demonstrating 82.15% capacitive retention and 92.45% coulombic efficiency after 10000 cycles. These results indicate that food waste-derived AC-optimized Nb₂CT_x MXene composite materials are a strong candidate for sustainable and high-performance supercapacitor electrodes. Full article

This study introduces a novel anticorrosion coating for copper based on an epoxy matrix reinforced with a berberine-loaded graphene oxide (BBR@GO) nanocomposite. The BBR@GO was synthesized via a simple, non-covalent functionalization method, leveraging π-π stacking interactions between the planar berberine molecule and the graphene oxide surface. The successful loading of berberine was confirmed by Fourier-transform infrared (FTIR) spectroscopy, thermogravimetric analysis (TGA), and energy-dispersive X-ray spectroscopy (EDS). The BBR@GO nanocomposite was incorporated into an epoxy resin at 0.1 wt.% loading and applied to a copper substrate. The corrosion protection performance of the BBR@GO/EP coating was systematically evaluated in 3.5 wt.% NaCl solution for 27 days using electrochemical impedance spectroscopy (EIS) and potentiodynamic polarization (PDP). The BBR@GO/EP coating exhibited a total impedance of 5.31 × 10⁸ Ω·cm² after 27 days, which was 17 times higher than the pure epoxy (EP) coating. The corrosion current density (i_corr) was reduced to 2.59 × 10⁻⁸ A·cm⁻², a four-fold decrease compared to the EP coating. Post-immersion analysis confirmed the excellent durability of the BBR@GO/EP coating and the retention of berberine within the matrix. The enhanced performance is attributed to the synergistic effect of the physical barrier provided by the well-dispersed GO nanosheets and the inhibitive action of the retained berberine molecules at the coating–metal interface. Full article

Monitoring the concentration of doxorubicin (DOX) was critical for tumor treatment, but existing methods failed to cross cell membrane. Here, an electrochemical platform for intracellular DOX detection in MCF-7 cells based on membrane-permeation strategy was developed. A modified gold electrode was prepared via electrodepositing AuNPs and assembling SH-DNA. Concurrently, the silica nanosphere/gold nanocluster-circular transmembrane peptide (SiO₂/AuNCs-iRGD) composite nanoparticles with membrane permeability, tumor targeting, and imaging capability were synthesized. After co-incubation of SiO₂/AuNCs-iRGD with MCF-7 cells and DOX, followed by co-incubation with the DNA-modified electrode, intracellular DOX intercalated into the DNA backbone, and redox-generated electrons were transferred to the electrode to produce a concentration-correlated electrochemical signal. The modification of the electrode, the morphology of the composite nanoparticles and the detection process were characterized by means of SEM, TEM, CV, EIS, DPV, fluorescence spectroscopy and laser confocal imaging. Under the optimized conditions, the proposed method exhibited a wide detection range of 0.05–300 μmol/L, with a detection limit of 0.01 μmol/L. Moreover, the modified electrode demonstrated satisfactory regenerability, and the proposed method showed excellent reproducibility and stability. The development platform could offer a new strategy for real-time assessment of drug concentration within cultured breast cancer cells in vitro. Full article