Search Results (24)

Electrocatalytic glycerol oxidation to formic acid (FA) offers a sustainable route for biomass valorization, yet non-noble metal catalysts generally suffer from sluggish C-C bond cleavage and poor product selectivity. Here we report an amorphous nickel–cobalt oxyhydroxide bearing both metal and oxygen vacancies (D-NiCoO_xH_y-V_Cr,O), grown on nickel foam via one-step electrodeposition followed by electrochemical activation with Cr doping. The coexistence of the dual vacancies is experimentally confirmed by X-ray photoelectron spectroscopy (XPS), which reveals elevated Ni³⁺/Co³⁺ ratios and reduced lattice oxygen, and by electron paramagnetic resonance (EPR), which shows a markedly enhanced signal at g = 2.003. Building on prior Cr-leaching approaches in single-metal nickel oxides, this work extends dual-vacancy engineering to an amorphous bimetallic NiCo oxyhydroxide and correlates the defect structure with glycerol-induced interfacial responses, charge-transfer behavior, and product selectivity. The catalyst delivers 200 mA cm⁻² at 1.31 V vs. RHE and achieves 100% Faradaic efficiency for formate at 1.32 V vs. RHE. In situ electrochemical impedance spectroscopy further reveals a significantly reduced charge-transfer resistance. These results establish Cr-assisted dual-vacancy engineering in amorphous bimetallic oxyhydroxides as a promising strategy for selective biomass electrooxidation. Full article

The growing deployment of green hydrogen technologies is increasing pressure on freshwater resources, motivating the exploration of alternative water sources that do not compete with human consumption. In this work, the direct use of untreated produced water from the Shushufindi 78 oil well (Ecuador) as an electrolyte for the hydrogen evolution reaction (HER) was experimentally evaluated. A comprehensive physicochemical characterization combined with electrochemical techniques, electrochemical impedance spectroscopy (EIS), and gas chromatography (GC-TCD) was performed to correlate electrolyte composition with electrochemical performance. Despite the high salinity and complex composition of the electrolyte, hydrogen production was achieved without pretreatment. Quantitative GC-TCD analysis yielded 10.29 µmol of H₂ after 4 h of electrolysis under non-optimized laboratory conditions, corresponding to a faradaic efficiency of 43.8%. These results demonstrate the feasibility of direct hydrogen generation from untreated produced water under realistic operating conditions. Additional experiments conducted in a membrane separated H-type electrolyzer evaluated mixtures of produced water and KOH, the electrolyte commonly employed in alkaline water electrolysis. Hydrogen production increased significantly under alkaline conditions, with the PW 10% + KOH 90% electrolyte exhibiting the highest hydrogen yield and faradaic efficiency among the investigated systems. Electrochemical impedance spectroscopy revealed that KOH addition reduced solution resistance and improved ionic transport, while differences in interfacial behavior were observed depending on electrolyte composition. The combined electrochemical and chromatographic results demonstrate that untreated produced water can be directly utilized for hydrogen production and can also be partially integrated into alkaline electrolysis systems without compromising electrochemical performance. These findings highlight the potential of produced water as a non-conventional water resource for sustainable hydrogen generation and industrial wastewater valorization. Full article

The escalating threat of infectious diseases necessitates the development of diagnostic technologies that are not only rapid and sensitive but also deployable at the point of care. Electrochemical impedance spectroscopy (EIS) has emerged as a leading technique for the label-free detection of pathogens, offering a unique combination of sensitivity, non-invasiveness, and adaptability. This review provides a comprehensive overview of the design and application of EIS-based biosensors tailored for pathogen detection, focusing on critical components such as biorecognition elements, electrode materials, nanomaterial integration, and surface immobilization strategies. Special emphasis is placed on the mechanisms of signal generation under Faradaic and non-Faradaic modes and how these underpin performance characteristics such as the limit of detection, specificity, and response time. The application spectrum spans bacterial, viral, fungal, and parasitic pathogens, with case studies highlighting detection in complex matrices such as blood, saliva, food, and environmental water. Furthermore, integration with microfluidics and point-of-care systems is explored as a pathway toward real-world deployment. Emerging strategies for multiplexed detection and the utilization of novel nanomaterials underscore the dynamic evolution of the field. Key challenges—including non-specific binding, matrix effects, the inherently low ΔR_ct/decade sensitivity of impedance transduction, and long-term stability—are critically evaluated alongside recent breakthroughs. This synthesis aims to support the future development of robust, scalable, and user-friendly EIS-based pathogen biosensors with the potential to transform diagnostics across healthcare, food safety, and environmental monitoring. Full article

Zearalenone (ZEA), a potent mycotoxin commonly found in contaminated grains, presents a serious threat to food safety and public health. Conventional detection methods, including culture-based assays and laboratory-bound analytical tools, are often time-consuming, require specialized infrastructure, and lack portability, limiting their utility for rapid, on-site screening. In response, this study introduces a compact, real-time electrochemical sensing platform for the swift and selective detection of ZEA in corn flour matrices. Utilizing a non-faradaic, label-free approach based on Electrochemical Impedance Spectroscopy (EIS), the sensor leverages ZEA-specific antibodies to achieve rapid detection within 5 min. The platform demonstrates a low detection limit of 0.05 ng/mL, with a broad dynamic range from 0.1 ng/mL to 25.6 ng/mL. Reproducibility tests confirm consistent performance, with both inter- and intra-assay variation remaining under a 20% coefficient of variation (%CV). Comparative evaluation with standard benchtop systems underscores its accuracy and field applicability. This portable and user-friendly device provides a powerful tool for real-time mycotoxin monitoring, offering significant potential for improving food safety practices and enabling point-of-need testing in resource-limited settings. Full article

A sustainable reaction of electrocatalytic nitrate conversion in ammonia production (NO₃RR) occurring under ambient conditions is currently of prime interest, as well as urgent research due to the real potential replacement of the environmentally unfavorable Haber–Bosch process. Herein, a series of electrocatalysts based on two-component cobalt alloys was synthesized using low-cost non-noble metals Co, Fe, Cr, and also Si. The samples of electrocatalysts were characterized and studied by the following methods: SEM, EDX, XRD (both transmission and reflection), UV–VIS spectroscopy, optical microscopy, linear (and cyclic) voltammetry, chronoamperometry, and electrochemical impedance spectroscopy. Beyond that, the determination of electrochemically active surface area was also carried out for all samples of electrocatalysts. Unexpectedly, the sample having an intermetallic compound (IMC) of the composition Co₂Si turned out to be the most highly effective. The highest Faradaic efficiency (FE) of 80.8% at E = −0.585 V (RHE) and an ammonia yield rate of 22.3 µmol h⁻¹ cm⁻² at E = −0.685 V (RHE) indicate the progressive role of IMC as the main active component of the electrocatalyst. Thus, this study demonstrates the promise and enormous potential of IMC as the main component of highly efficient electrocatalysts for NO₃RR. This work can serve primarily as a starting point for future studies of electrocatalytic conversion reactions in the production of ammonia using IMC catalysts containing non-noble metals. Full article

A time-dependent electrochemical impedance spectroscopy (EIS) model is presented using the finite element method (FEM) to simulate a 2D interdigitated electrode in an aqueous NaCl electrolyte. Developed in COMSOL Multiphysics, the model incorporates ion transport, electric field distribution, Stern layer effects, and electrode sheet resistance, governed by the Poisson and Nernst–Planck equations. This model can predict the transient current response to an applied excitation voltage, which gives information about the dynamics of the electrochemical system. The simulation results are compared with the experimental data, reproducing key features of the measurements. The transient current response indicates the need for multiple excitation cycles to stabilize the impedance measurement. At low frequencies (<1 kHz), the voltage drop at the Stern layer is significant, while at higher frequencies (>100 kHz), the voltage drop due to sheet resistance dominates. Moreover, the amplitude of the excitation voltage influences the EIS measurement, higher amplitudes (above 0.1 V) lead to non-linear impedance behavior, particularly at low ion concentrations. Discrepancies at low frequencies suggest that Faradaic processes may need to be incorporated for improved accuracy. Overall, this model provides quantitative insights for optimizing EIS sensor design and highlights critical factors for high-frequency and low-concentration conditions, laying the foundation for future biosensing applications with functionalized electrodes. Full article

Direct testing of pesticide contaminants in drinking water is a challenge. Portable and sensitive sensor platforms are desirable to test water contaminants directly at farm and consumer levels. In this study, we have demonstrated the feasibility of an electrochemical sensor for the direct detection of paraquat (PQ) in drinking water samples. An immunoassay-based sensing platform was fabricated using PQ-specific antibody immobilized on the surface of the electrochemically reduced graphene oxide (rGO) modified screen-printed carbon electrode (rGO-SPCE). Using non-faradaic electrochemical impedance spectroscopy (EIS) as a detection tool, the sensor platform demonstrated a dynamic response for PQ concentration in drinking water ranging from 0.05 ng/mL to 72.9 ng/mL (0.19 to 243.8 nM), with a coefficient of determination (r²) of 0.997 and a limit of detection of 0.05 ng/mL (0.19 nM). Percentage recovery within ±20% error was obtained, and the sensor cross-reactivity test showed a selective response against glyphosate antigen. With the flexibility to use single-frequency EIS and low sample volume, the developed sensor demonstrated testing in water samples directly without any sample pre-processing. This low-volume electroanalytical sensor platforms can be translated into portable testing tools for the detection of various water contaminants. Full article

Due to rapid industrialization, novel water-quality monitoring techniques for the detection of highly toxic and hazardous heavy metal ions are essential. Herein, a hybrid noble nanoparticle/DNAzyme electrochemical biosensor is proposed for the simultaneous and label-free detection of Pb²⁺ and Cr³⁺ in aqueous solutions. The sensor is based on the combination of a two-dimensional naked-platinum nanoparticle film and DNAzymes, whose double-helix configuration disassembles into smaller fragments in the presence of target-specific heavy metal ions. The electrochemical behavior of the fabricated sensor was investigated with non-faradaic electrochemical impedance spectroscopy (EIS), resulting in the successful detection of Pb²⁺ and Cr³⁺ well below their maximum permitted levels in tap water. So far, there has been no report on the successful detection of heavy metal ions utilizing the non-faradaic electrochemical impedance spectroscopy technique based on advanced nanomaterials paired with DNAzymes. This is also one of the few reports on the successful detection of chromium (III) via a sensor incorporating DNAzymes. Full article

The determination of the electrochemically active surface area (ECSA) of a catalyst layer (CL) of a non-precious metal catalyst is of fundamental importance in optimizing the design of a durable CL for anion exchange membrane (AEM) water electrolysis, but has yet to be developed. Traditional double layer capacitance (C_dl), measured by cyclic voltammetry (CV), is not suitable for the estimation of the ECSA due to the nonconductive nature of Ni-based oxides and hydroxides in the non-Faradaic region. This paper analyses the applicability of electrochemical impedance spectroscopy (EIS) compared to CV in determining capacitances for the estimation of the ECSA of AEM-based CLs in an aqueous KOH electrolyte solution. A porous electrode transmission line (TML) model was employed to obtain the capacitance–voltage dependence from 1.0 V to 1.5 V at 20 mV intervals, covering both non-Faradic and Faradic regions. This allows for the identification of the contribution of a NiFe-layered double hydroxide (LDH) catalyst and supports in a CL, to capacitances in both non-Faradic and Faradic regions. A nearly constant double layer capacitance (Q_dl) observed in the non-Faradic region represents the interfaces between catalyst supports and electrolytes. The capacitance determined in the Faradic region by EIS experiences a peak capacitance (Q_F), which represents the maximum achievable ECSA in an AEMCL during reactions. The EIS method was additionally validated in durability testing. An approximate 30% loss of Q_F was noted while Q_dl remained unchanged following an eight-week test at 1 A/cm² constant current density, implying that Q_F, determined by EIS, is sensitive to and therefore suitable for assessing the loss of ECSA. This universal method can provide a reasonable estimate of catalyst utilization and enable the monitoring of catalyst degradation in CLs, in particular in liquid alkaline electrolyte water electrolysis systems. Full article

Drawing inspiration from the several thousand beautiful Pysanky egg art of Ukraine, we have developed a novel material, Aptamer–Gold Nanoparticles (AuNPs)@ZIF-8, that can be used for building sensitive and highly stable POC biosensors for longitudinal health mapping. Here, we demonstrate a sensitive and specific novel electrochemical biosensor, made of a novel synthesized in situ encapsulated aptamer-AuNPs@ZIF-8 composite, for monitoring levels of creatinine (0.1–1000 μg/mL). In this work, we have reported the synthetic protocol for the first-of-a-kind in situ encapsulation of aptamer and AuNPs together in a ZIF-8 matrix, and explored the characteristic properties of this novel material composite using standard analytical techniques and its application for biosensor application. The as-synthesized material, duly characterized using various physicochemical analytical methods, portrays the characteristics of the unique encapsulation strategy to develop the first-of-a-kind aptamer and AuNP encapsulation. Non-faradaic Electrochemical Impedance Spectroscopy (EIS) and Chronoamperometry were used to characterize the interfacial electrochemical properties. The biosensor performance was first validated using artificial urine in a controlled buffer medium. The stability and robustness were tested using a real human urine medium without filtration or sample treatment. Being versatile, this Ukrainian-art-inspired biosensor can potentially move the needle towards developing the next generation of sample-in-result-out robust POC diagnostics. Full article

The ability to bridge ionic and electronic transport coupled with large volumetric capacitance renders organic electrochemical transistors (OECTs) ideal candidates for bioelectronic applications. Adopting ionic-liquid-based solid electrolytes extends their applicability and facilitates large-area printable productions. However, OETCs employing solid electrolytes tend to show a pronounced hysteresis in the transfer curve. A detailed understanding of the hysteresis is crucial for their accurate characterizations and reliable applications. Here, we demonstrated fully photopatternable poly(3,4-ethylenedioxythiophene):tosylate (PEDOT:Tos)- based OECTs incorporating the ionic liquid [EMIM][EtSO₄] in a solid electrolyte (SE). The PEDOT:Tos films deposited through vapor phase polymerization (VPP) were annealed for different durations after the polymerization step. Upon rinsing with ethanol and the deposition of the SE, the OECTs made of these films showed impressive bias stress stability under prolonged operation cycles, a high switching ratio, a low threshold voltage, and a high transconductance. Furthermore, by taking transfer measurements with different sweep rates, we revealed two distinct regimes of hysteresis: kinetic hysteresis and non-kinetic hysteresis. We observed pronounced changes in these regimes after annealing. Finally, impedance spectroscopy exhibited that the PEDOT:Tos turned from a Faradaic to a non-Faradaic response through annealing, explaining the observed hysteresis changes in both regimes. Full article

Low-cost anion exchange membrane (AEM) water electrolysis is a promising technology for producing “green” high-purity hydrogen using platinum group metal (PGM)-free catalysts. The performance of AEM electrolysis depends on the overall overvoltage, e.g., voltage losses coming from different processes in the water electrolyzer including hydrogen and oxygen evolution, non-faradaic charge transfer resistance, mass transfer limitations, and others. Due to the different relaxation times of these processes, it is possible to unravel them in the frequency domain by electrochemical impedance spectroscopy. This study relates to solving and quantifying contributions to the total polarization resistance of the AEM water electrolyzer, including ohmic and charge transfer resistances in the kinetically controlled mode. The high-frequency contribution is proposed to have non-faradaic nature, and its conceivable nature and mechanism are discussed. The characteristic frequencies of unraveled contributions are provided to be used as benchmark data for commercially available membranes and electrodes. Full article

The performance of an anion exchange membrane water electrolyzer under various operational conditions (including voltage, KOH-supporting electrolyte concentration, and flow rate) is studied using conventional time-domain technics and electrochemical impedance spectroscopy (EIS). The water electrolyzer EIS footprint, depending on the variation in operational conditions, is studied and discussed, providing valuable data on the faradaic and non-faradaic processes in MEA, considering their contribution to the total polarization resistance. The distribution of the AEMWE cell voltage contributions is valuable to accessing the key directions in the system performance improvement. Full article

Despite their high sensitivity and their suitability for miniaturization, biosensors are still limited for clinical applications due to the lack of reproducibility and specificity of their detection performance. The design and preparation of sensing surfaces are suspected to be a cause of these limitations. Here, we first present an updated overview of the current state of use of capacitive biosensors in a medical context. Then, we summarize the encountered strategies for the fabrication of capacitive biosensing surfaces. Finally, we describe the characteristics which govern the performance of the sensing surfaces, along with recent developments that were suggested to overcome their main current limitations. Full article

An environmentally friendly hydrogel based on gelatin has been investigated as a gel polymer electrolyte in a symmetric carbon-based supercapacitor. To guarantee the complete sustainability of the devices, biomaterials from renewable resources (such as chitosan, casein and carboxymethyl cellulose) and activated carbon (from coconut shells) have been used as a binder and filler within the electrode, respectively. The electrochemical properties of the devices have been compared by using cyclic voltammetry, galvanostatic charge/discharge curves and impedance spectroscopy. Compared to the liquid electrolyte, the hydrogel supercapacitors show similar energy performance with an enhancement of stability up to 12,000 cycles (e.g., chitosan as a binder). The most performant device can deliver ca. 5.2 Wh/kg of energy at a high power density of 1256 W/kg. A correlation between the electrochemical performances and charge storage mechanisms (involving faradaic and non-faradaic processes) at the interface electrode/hydrogel has been discussed. Full article