Anodic Stripping Research Articles

Electrochemical immunosensor based on phages/CdSe nanoparticles as tracers to quantify clomazone in water

Clomazone, an herbicide used worldwide, contaminates river and lakes, as well as surface and ground water. Therefore, there is great interest in developing new analytical tools for detecting environmental pollutants that are simple, highly sensitive and provide an extended analytical range. This work describes a disposable, highly sensitive and reproducible electrochemical immunosensor based on a non-competitive and enzyme-free immunoassay to quantify clomazone in water samples. A specific clone of recombinant phage particles labelled with CdSe nanoparticles, which form a trivalent complex with the clomazone/monoclonal antibody anti clomazone immuno-complex, was used as tracer. Clomazone was determined indirectly by square wave anodic stripping voltammetry through the anodic oxidation of Cd previously deposited in an accumulation step from the reduction of Cd2+ ions released from CdSe nanoparticles. An excellent analytical performance, with a limit of detection and a midpoint sensitivity of 0.038 ng mL−1 and 1.34 ng mL−1, respectively, were found. The limit of detection was 60-fold lower than the limit of detection obtained using the same antibody and un-label phage in an optimized non-competitive ELISA. The developed electrochemical immunosensor was successively used to assay undiluted river water samples, where very good recoveries percentages were reached. The very low limit of detection achieved with the electrochemical immunosensor allows it to be used as an important environmental tool for the determination of clomazone.

Evaluation of Performance and Longevity of Ti-Cu Dry Electrodes: Degradation Analysis Using Anodic Stripping Voltammetry

This study aimed to investigate the degradation of dry biopotential electrodes using the anodic stripping voltammetry (ASV) technique. The electrodes were based on Ti-Cu thin films deposited on different polymeric substrates (polyurethane, polylactic acid, and cellulose) by Direct Current (DC) magnetron sputtering. TiCu0.34 thin films (chemical composition of 25.4 at.% Cu and 74.6 at.% Ti) were prepared by sputtering a composite Ti target. For comparison purposes, a Cu-pure thin film was prepared under the same conditions and used as a reference. Both films exhibited dense microstructures with differences in surface topography and crystalline structure. The degradation process involved immersing TiCu0.34 and Cu-pure thin films in artificial sweat (prepared following the ISO standard 3160-2) for different durations (1 h, 4 h, 24 h, 168 h, and 240 h). ASV was the technique selected to quantify the amount of Cu(II) released by the electrodes immersed in the sweat solution. The optimal analysis conditions were set for 120 s and −1.0 V for time deposition and potential deposition, respectively, with a quantification limit of 0.050 ppm and a detection limit of 0.016 ppm. The results showed that TiCu0.34 electrodes on polyurethane substrates were significantly more reliable over time compared to Cu-pure electrodes. After 240 h of immersion, the TiCu0.34 electrodes released a maximum of 0.06 ppm Cu, while Cu-pure electrodes released 16 ppm. The results showed the significant impact of the substrate on the electrode’s longevity, with cellulose bases performing poorly. TiCu0.34 thin films on cellulose released 1.15 µg/cm2 of copper after 240 h, compared to 1.12 mg/cm2 from Cu-pure films deposited on the same substrate. Optical microscopy revealed that electrodes based on polylactic acid substrates were more prone to corrosion over time, whereas TiCu thin-film metallic glass-like structures on PU substrates showed extended lifespan. This study underscored the importance of assessing the degradation of dry biopotential electrodes for e-health applications, contributing to developing more durable and reliable sensing devices. While the study simulated real-world conditions using artificial sweat, it did not involve in vivo measurements.

Preferential Stripping Analysis of Post-Transition Metals (In and Ga) at Bi/Hg Films Electroplated on Graphene-Functionalized Graphite Rods

In this study, we introduce a novel electrochemical sensor combining reduced graphene oxide (rGO) sheets with a bismuth–mercury (Bi/Hg) film, electroplated onto pencil graphite electrodes (PGEs) for the high-sensitivity detection of trace amounts of gallium (Ga3+) and indium (In3+) in water samples using square wave anodic stripping voltammetry (SWASV). The electrochemical modification of PGEs with rGO and bimetallic Bi/Hg films (ERGO-Bi/HgF-PGE) exhibited synergistic effects, enhancing the oxidation signals of Ga and In. Graphene oxide (GO) was accumulated onto PGEs and reduced through cyclic reduction. Key parameters influencing the electroanalytical performance, such as deposition potential, deposition time, and pH, were systematically optimized. The improved adsorption of Ga3+ and In3+ ions at the Bi/Hg films on the graphene-functionalized electrodes during the preconcentration step significantly enhanced sensitivity, achieving detection limits of 2.53 nmol L−1 for Ga3+ and 7.27 nmol L−1 for In3+. The preferential accumulation of each post-transition metal, used in transparent displays, to form fused alloys at Bi and Hg films, respectively, is highlighted. The sensor demonstrated effective quantification of Ga3+ and In3+ in tap water, with detection capabilities well below the USEPA guidelines. This study pioneers the use of bimetallic films to selectively and simultaneously detect the post-transition metals In3+ and Ga3+, highlighting the role of graphene functionalization in augmenting metal film accumulation on cost-effective graphite rods. Additionally, the combined synergistic effects of Bi/Hg and graphene functionalization have been explored for the first time, offering promising implications for environmental analysis and water quality monitoring.

Efficient biosorption of Zn(II), Cd(II), and Pb(II) by Aspergillus brasiliensis in industrial wastewater coupled with electrochemical monitoring via sensor enhanced with modified silver nanoparticles.

This work investigates the use of Aspergillus brasiliensis, this particular species of Aspergillus, as a biosorbent for the first time. It is employed to biosorption Zn(II), Cd(II), and Pb(II) and combines the biosorption experiments with electrochemical measurements for in situ analysis. For the experiments, a batch system was employed with the dead biomass. In order to determine the biosorption capacity, the impact of several operational parameters was examined, including pH, temperature, agitation speed, contact time, and initial metal concentration, and the optimum values were 5, 30°C, 150rpm, 2h, and 150ppm, respectively. Using 0.2g biomass in 100mL solution, the maximal uptake of Zn(II), Cd(II), and Pb(II) at ideal conditions was determined to be 33.67, 24.51, and 36.76, respectively. The Langmuir and Freundlich isotherm model was studied for the biosorption process. An electrochemical sensor using nanomaterials is designed and constructed to monitor the concentration of these metals. The silver nanoparticles functionalized with thiosemicarbazide and 6-mercaptohexanoic acid (mercaptohexanoylhydrazinecarbothioamide-coated silver nanoparticles, MHHC-AgNPs) linked to the carboxylated multi-walled carbon nanotubes (MWCNTs) were utilized for glassy carbon electrode modification (MHHC-AgNPs/MWCNTs/GCE). The concentration range of Zn(II) is 0.7-173µg/L, Cd(II) is 1.18-293µg/L, and Pb(II) is 2.17-540µg/L. The detection limits for Zn(II), Cd(II), and Pb(II) are 0.036µg/L, 0.15µg/L, and 0.16µg/L, respectively. Under optimized conditions, these results were obtained using the differential pulse anodic stripping voltammetry method (DPASV). The successful detection of Zn(II), Cd(II), and Pb(II) was achieved by effectively preventing interference from other common ions. It was effectively employed for measuring ions in industrial wastewater, and the results obtained aligned with those acquired from an atomic absorption spectrometer (AAS). Thus, Aspergillus brasiliensis species, along with this electrochemical sensor, can be used to remediate and monitor environmental pollution, Zn(II), Cd(II), and Pb(II), successfully.

All-solid-state electrochemical marine sensors based on Na3V2(PO4)3@Na4Zr2Si3O12 solid-state reference electrodes

In this study, Na4Zr2Si3O12 (NZS) solid electrolyte was prepared using an elevated-temperature solid-state method. After heating under supercritical conditions (i.e., 400 °C and 40 MPa), the structure and performance stability of the as-fabricated NZS solid electrolyte were evaluated applying scanning electron microscopy (SEM), X-ray diffraction (XRD), and electrochemical impedance spectroscopy (EIS). A new all-solid-state reference electrode, combining Na3V2(PO4)3(NVP) with NZS (NVP@NZS), was developed, and its electrochemical properties were investigated. The prepared reference electrode demonstrated steady potential in both simulated seawater and buffer solutions across a range of pH values and different salt solutions. The reference electrode, integrated with an Ir/IrO2 working electrode, was used to construct an all-solid-state potentiometric pH sensor. This sensor demonstrated a strong linear related response when measuring the pH of both aqueous solutions and simulated seawater samples. Additionally, an ion sensor based on anodic stripping voltammetry, constructed with the assembled solid-state reference electrode, a platinum counter electrode, and a gold-mercury working electrode, was utilized to measure Cu2+ and S2− ions in both aqueous solutions and simulated seawater samples. These all-solid-state electrochemical sensors, incorporating the NVP@NZS solid-state reference electrode, demonstrated a small detection threshold, excellent linear correlation (R2 > 0.99), and a broad detection range, making them well-suited for chemical analysis in challenging marine environments.

MXene quantum dots/polyethylenimine/covalent organic framework nanocomposite for selective determination of Hg2+ in water samples using differential pulse anodic stripping voltammetry

MXene quantum dots/polyethylenimine/covalent organic framework nanocomposite for selective determination of Hg2+ in water samples using differential pulse anodic stripping voltammetry

Producing Activated Biochar from the Reuse of Discarded Coffee Grounds with Enhanced Adsorptive Features Explored Towards the Stripping Voltammetric Sensing of Copper (II)

AbstractThis work aims to allocate coffee grounds waste to the production of biochar from pyrolysis under different temperatures (350 °C and 500 °C), to add value to it. The resulting materials were characterized by immediate, elemental, thermogravimetric analysis, SEM, FT‐IR, XRD and Raman spectroscopy. Additionally, the need to activate the biochar produced for the desired use was evaluated. The obtained biochars were applied in electroanalysis in the manufacture of modified carbon paste electrodes. This choice was made due to the possibility of reaching a high sensitivity towards the determination of Cu2+ ions. The differential pulse adsorptive anodic stripping voltammetry technique was applied to perform the Cu2+ determination and, in this case, several parameters were optimized, including biochar’ percentage, pH of pre‐accumulation step and reduction/stripping step, pre‐accumulation time, potential and time of reduction of adsorbed‐Cu2+. From this, the proposed modified electrode showed a linear voltammetric response towards Cu2+ in the range of 66.1 to 3997.3 ppb, with a limit of detection of 31.8 ppb, in addition to having been satisfactorily applied in the analysis of water samples (recoveries close to 100 %). Thus, demonstrating the potential for reuse of discarded coffee grounds for the preparation of activated biochar with outstanding electrochemical performance.

Mercury Detection in Novel Foods by a Smart Pocket Sensor

AbstractMercury is one of the most well‐known toxic contaminants of natural and anthropogenic origin in aquatic ecosystems that can bioaccumulate in vegetal and animal organisms. In this work, we propose a smart detection system for Hg(II) ions by square wave anodic stripping voltammetry at nanocomposite graphite screen‐printed electrodes, as an analytical tool to be applied in food quality control. The nanocomposite surfaces were obtained by the modification of screen‐printed graphite electrodes with poly(l‐aspartic acid) and gold nanoparticles and were characterized by means of electrochemical techniques. An exhaustive study of the experimental conditions involved both in the electropolymerization and in the voltammetric stripping measurements was addressed to develop a reliable method capable of measuring Hg(II) concentration in the low μg/L range, both in conventional and drop configurations. The sensor was integrated in a smart setup, comprising a Sensit Smart pocket instrument connected to a smartphone, thus proving its applicability for in situ analysis due to its cost‐effectiveness. The analytical significance of the developed sensor was assessed by detecting Hg(II) in novel food samples.

Highly sensitive and specific electrochemical biosensor for direct detection of hepatitis C virus RNA in clinical samples using DNA strand displacement

Hepatitis C virus (HCV) is a common blood-borne infection that can lead to long-term illnesses such as hepatocellular cancer and liver cirrhosis. Early diagnosis is crucial for effective management, as no vaccine is available for preventing HCV infection. However, the high cost and complexity of current molecular diagnostic tools hinder efforts to achieve early diagnosis and prevent transmission, particularly in resource-limited settings. We developed a novel electrochemical biosensor for point-of-care testing (POCT) of HCV RNA. The sensor utilizes a strand displacement method, where the target RNA displaces a gold nanoparticle-labeled reporter probe (AuRP) from a pre-hybridized duplex with a magnetic nanoparticle (MNP)-labeled capture probe. The amount of displaced AuRP, detected using differential pulse anodic stripping voltammetry (DPASV), is directly proportional to the target RNA concentration. The biosensor exhibited excellent analytical performance, with a detection limit of 4 fM for synthetic targets and 43 ng/µL for RT-PCR products. Importantly, it successfully detected HCV RNA directly in clinical plasma samples without the need for RNA extraction or amplification. The sensor was used to analyze 30 RNA samples from HCV-positive patients, 20 cDNA samples from viral RNA, 30 HCV-positive plasma samples, and 22 HCV-negative plasma samples. The sensor results show good concordance with the RT-PCR results, demonstrating the sensor’s potential for detecting HCV in clinical samples.

Electroanalytical Studies on Codeposition of Cobalt with Ruthenium from Acid Chloride Baths

The aim of this study was to systematically analyze the influence of potential and the Co(II)–Ru(III) molar ratio on the electrochemical behavior of the Co–Ru system during codeposition from acidic chloride electrolytes. The equilibrium speciation of the baths was investigated spectrophotometrically and compared with theoretical calculations based on the stability constants of Co(II) and Ru(III) complexes. The codeposition of the metals was characterized using electroanalytical methods, including cyclic voltammetry, chronoamperometry, and anodic stripping linear voltammetry. The alloys obtained at different potentials were analyzed for their elemental composition (EDS, mapping), phase composition (XRD), and surface morphology (SEM). The morphology and composition of the alloys were mainly dependent on the deposition potential, which controlled the cobalt incorporation. Ruthenium–rich alloys were produced at potentials of −0.6 V and −0.7 V (vs. SCE). In these conditions, cobalt anomalously codeposited due to the formation of the CoOH+ intermediate, triggered by the intense hydrogen evolution on the ruthenium sublayer. Bulk cobalt electrodeposition began at a potential of around −0.8 V, resulting in the formation of cobalt-rich alloys. The early stages of the electrodeposition were investigated using different nucleation models. A transition from 2D progressive nucleation to 3D instantaneous nucleation at around −0.8 V was identified as being caused by cobalt incorporation. This was well correlated with electroanalytical data, partial polarization curves of alloy deposition, elemental mapping analysis, and the structure of the deposits.

Synthesis of a triazine based COF and its application for the establishment of an electrochemical sensor for the simultaneous determination of Cd2+ and Pb2+ in edible specimens using Box-Behnken design

The study presented here describes the characterization and synthesis of a triazine-based covalent organic framework using different analytical procedures such as scanning electron microscopy, X-ray diffraction, energy dispersive X-ray spectroscopy, cyclic voltammetry, Brunauer-Emmett-Teller analysis, and electrochemical impedance spectroscopy. The synthesized COF was then utilized as an electrocatalytic modifier for the selective and sensitive determination of Pb2+ and Cd2+ at nanomolar levels via square wave anodic stripping voltammetry. A Plackett-Burman design was employed to screen operational parameters influencing the sensitivity of the electroanalytical method, followed by optimization of the significant variables using Box-Behnken design. A linear response over 1.0–110.0 nmol L−1 and 5.0–300.0 nmol L−1 range for Pb2+ and Cd2+, with detection limits of 1.1 and 1.8 nmol L−1, respectively. Furthermore, the selectivity of the presented electrode over different species was evaluated with no significant interference found. The sensor was applied effectively to determine of Pb2+ and Cd2+ ions in samples.

Determination of silver ions in distilled water by stripping voltammetry at a Nafion-coated gold electrode in combination with quartz crystal microbalance and electrochemical impedance spectroscopy

Here, we propose a stripping voltammetric method for Ag+ ion determination in distilled water utilizing screen-printed Au electrodes coated with Nafion (Nafion/Au screen-printed electrodes). The concentration of Ag+ in pure water was determined by linear sweep voltammetry (LSV) after silver deposition on the Nafion/Au electrode. The anodic stripping peak current increased linearly with the concentration of Ag+ ion in the range from 1 ppm to 22 ppm. The LSV oxidative peak current was increased by extending the silver deposition time from 300 s to 500 s. Repetitive LSV measurements revealed satisfactory reproducibility of the Nafion/Au screen-printed electrodes. The detection mechanism was elucidated by recording mass changes of the Nafion/Au electrode with a quartz crystal microbalance (QCM), and by determining changes in the low-frequency capacitance of the Nafion/Au electrode by electrochemical impedance spectroscopy (EIS). The observed changes in mass and capacitance confirmed Ag+ accumulation and release processes at the Nafion/Au electrodes, in good agreement with stripping voltammetry. The combination of stripping voltammetry, QCM and EIS allowed a detailed characterization of the ion transfer, deposition and stripping processes at the Nafion/Au electrodes in presence of Ag+ ions. The Nafion/Au screen-printed electrode enabled voltammetric determination of low Ag+ concentrations in distilled water, without any sample pretreatment nor addition of supporting electrolyte.

Signal-Boosted Electrochemical Lateral Flow Immunoassay for Early Point-of-Care Detection of Liver Cancer Biomarker.

The early diagnosis of cancer in a point-of-need manner is of great significance, yet it remains challenging to achieve the necessary sensitivity and speed. Traditional lateral flow immunoassay (LFIA) methods are limited in accuracy and quantification, restricting their suitability for home-based applications. Thus, we explored a new and user-friendly electrochemical LFIA (e-LFIA) test strip to detect α-fetoprotein (AFP), a diagnostic marker for liver cancer. The specific electrochemical immunoprobe utilized in this e-LFIA test strip is characterized by significant signal boosting, resulted from the loading Ag shell into a gold nanoparticle (AuNP)-coated dendritic mesoporous silica nanoscaffold (DMSN). Leveraging the distinct electrochemical characteristics of Ag anodic stripping and the high volume-to-surface area ratio of DMSNs, the developed DMSNs/AuNPs@Ag-based e-LFIA test strip is capable of detecting AFP at a low concentration of 0.85 ng/mL within a rapid 20 min timespan, both of these values are smaller than those in current clinical testing. Furthermore, we utilized homemade screen-printed electrodes in this sensing prototype and demonstrated the high versatility and reliability of this e-LFIA device. We envision that this DMSNs/AuNPs@Ag-based e-LFIA holds substantial potential for the early diagnosis of liver cancer and household health monitoring.

Nitrogen functionalized biomass derived mesoporous carbon nanomaterials for electrochemical detection of lead (II) ions

This study has explored the sustainable solution after designing an economical metal-free biomass-derived nanocarbon for the selective sensing of lead. The nitrogen and sulfur-rich mesoporous nanocarbon is designed through a facile hydrothermal-assisted thermal annealing method. The high-temperature treatment gave nanocarbon unique carbon dot decorated layered morphology, while nitrogen and sulfur precursor thiourea and melamine strengthened the nanomaterial stability, sensitivity, and selectivity toward lead metal ions. The high specific surface area of mesoporous nanocarbon viz., 1671.93 m2/g with the pore width and pore volume of 2.02 nm and 0.476 cm3/g has enhanced the conductivity of as-synthesized sensor, which helps in increasing sensitivity toward lead. The high conductivity was also confirmed through cyclic voltammetry, where an 80 % increment in current was observed in the case of the modified electrode when compared with bare GCE. The differential pulse normal voltammetry and differential pulse anodic stripping voltammetry were performed to calculate the detection limit, where an excellent detection limit of 22 nM was obtained from the DPASV technique. Moreover, the nanomaterial was also tested for detecting lead in tap water. The as-synthesized nanocomposite is highly efficient and selective for the detection of lead. This study will motivate the researchers to engineer sustainable and efficient devices for sensing metal pollutants.

Non-enzymatic g-C3N4 supported CuO derived-biochar based electrochemical sensors for trace level detection of malathion

Malathion (MALA), a widely used insecticide, even at trace levels exhibits deleterious effects towards respiratory tracts, and nervous system, necessitating its detection. Herein, we have offered non-enzymatic trace level monitoring of MALA using g-C3N4 supported CuO-derived biochar. The present B-CuO/g-C3N4 based electrochemical sensor is synthesized using hydrothermal approach followed by calcination at high temperature. The result unveiled the strong <pi-pi> interactions, high charge separation efficiency, significant porosity leading to excellent electrochemically active surface area 9.88 × 10−5 cm2 with least charge transfer resistance (RCT) value of 35.2 K Ω. The B-CuO/g-C3N4 based nanocomposite offered excellent complex formation ability with MALA and square wave anodic stripping voltametric method (SWASV) generates an enhanced electrochemical signal due to oxidation of MALA. Following all necessary optimizations, the sensor was capable to exhibit limit of detection (LOD) value of 1.2 pg mL−1 with R2 = 0.968. The modified biosensor offered its potential towards detection of MALA in apple and tomato samples with a recovery ranging from 87.64 to 120.59%. This novel B-CuO/g-C3N4 ternary nanocomposite provides non-enzymatic detection of MALA having excellent electrochemical properties and hence opens new pathways for exploring the use of biochar in other electrochemical applications.

Surface-Initiated Reversible Addition-Fragmentation Chain Transfer Polymerization (SI-RAFT) to Produce Molecularly Imprinted Polymers on Graphene Oxide for Electrochemical Sensing of Methylparathion.

A nonenzymatic redox-responsive sensor was put forward for the detection of methylparathion (MP) by designing globular nanostructures of molecularly imprinted polymers on graphene oxide (GO@MIPs) via surface-initiated reversible addition-fragmentation chain transfer polymerization (SI-RAFT). Fourier transform infrared (FTIR) spectroscopy, field emission scanning electron microscopy (FESEM), and small-angle X-ray scattering (SAXS) studies have confirmed the successful formation of receptor layers of MIPs on RAFT agent-functionalized GO sheets. The electrochemical signal with an amplified current response was attained because of the enhanced diffusion rate of ions at the interface provided by widening the pore size of the MIP film. The analytical response of GO@MIPs, validated by recording square-wave anodic stripping voltammetry (SWASV) at varying MP concentrations, followed the linear response between 0.2 and 200 ng/mL. Under optimized conditions, the sensor exhibited a limit of detection of 4.25 ng/mL with high selectivity over other interfering ions or molecules. The anti-interfering ability and good recovery (%) in food samples directed the use of the proposed sensor toward real-time monitoring and also toward future mimicking of surfaces.

Nanoporous Gold-Modified Screen-Printed Electrodes for the Simultaneous Determination of Pb2+ and Cu2+ in Water.

In this study, nanoporous gold (NPG) was deposited on a screen-printed carbon electrode (SPCE) by the dynamic hydrogen bubble template (DHBT) method to prepare an electrochemical sensor for the simultaneous determination of Pb2+ and Cu2+ by square wave anodic stripping voltammetry (SWASV). The electrodeposition potential and electrodeposition time for NPG/SPCE preparation were investigated thoroughly. Scanning electron microscopy (SEM) and energy-dispersive X-ray diffraction (EDX) analysis confirmed successful fabrication of the NPG-modified electrode. Electrochemical characterization exhibits its superior electron transfer ability compared with bare and nanogold-modified electrodes. After a comprehensive optimization, Pb2+ and Cu2+ were simultaneously determined with linear range of 1-100 μg/L for Pb2+ and 10-100 μg/L for Cu2+, respectively. The limits of detection were determined to be 0.4 μg/L and 5.4 μg/L for Pb2+ and Cu2+, respectively. This method offers a broad linear detection range, a low detection limit, and good reliability for heavy metal determination in drinking water. These results suggest that NPG/SPCE holds great promise in environmental and food applications.

Exploring the synchronized effect of MWCNT/X-manganate (X-Cu, Zn) nanocomposite for the sensitive and selective electrochemical detection of Hg(II) and Pb(II) in water.

The presence of heavy metal ions in the environment is a long-lasting problem that requires the simultaneous detection of Hg(II) and Pb(II) which is both vital and challenging. This present study examines a simplified and effective approach for synthesizing multi-walled carbon nanotube-copper manganese oxide (MWCNT-CuMn2O4) and multi-walled carbon nanotube-zinc manganese oxide (MWCNT-ZnMn2O4) nanocomposites for electrochemical detection of heavy metal ions. The nanocomposites MWCNT-CuMn2O4 and MWCNT-ZnMn2O4 exceptional electrochemical performance was evaluated using Square Wave Anodic Stripping Voltammetry (SWASV). The fabricated MWCNT-ZnMn2O4 demonstrated lower values of Electrochemical Impedance Spectroscopy (EIS) with charge transfer resistance (Rct) of approximately 34.13 Ω. Remarkably, the MWCNT-ZnMn2O4 electrochemical sensor exhibited the widest linear ranges of 0.5-10μM with sensitive detection limits (0.011μM for Hg(II) and 0.014μM for Pb(II)). Interestingly, the MWCNT-ZnMn2O4 sensor showed excellent capability in detecting Hg(II) and Pb(II) in real water samples with a recovery percentage of 94.1% and 91.3%. Overall, the MWCNT-ZnMn2O4 modified GCE showcased superior selectivity, sensitivity, reproducibility, stability, and repeatability.

Magnetic Porous Hydrogel-Enhanced Wearable Patch Sensor for Sweat Zinc Ion Monitoring.

Wearable sensors for sweat trace metal monitoring have the challenges of effective sweat collection and the real-time recording of detection signals. The existing detection technologies are implemented by generating enough sweat through exercise, which makes detecting trace metals in sweat cumbersome. Generally, it takes around 20 min to obtain enough sweat, resulting in dallied and prolonged detection signals that cannot reflect the endogenous fluctuations of the body. To solve these problems, we prepared a multifunctional hydrogel as an electrolyte and combined it with a flexible patch electrode to realize real-time monitoring of sweat Zn2+. Such hydrogel has magnetic and porous properties, and the porous structure of hydrogel enables a fast absorption of sweat, and the magnetic property of the addition of fabricated Fe3O4 NPs not only improves the conductivity but also ensures the adjustable internal structures of the hydrogel. Such a sensing platform for sweat Zn2+ monitoring shows a satisfied linear relationship in the concentration range of 0.16-16 µg/mL via differential pulsed anodic striping voltammetry (DPASV) and successfully detects the sweat Zn2+ of four volunteers during exercise and resting, displaying a promising path for commercial application.

Co-electrodeposition of poly(Eriochrome black T) and copper oxide nanocomposite on the graphenized pencil electrode for enhanced anodic stripping voltammetric analysis of cadmium and lead in water samples

In this study, poly(Eriochrome Black T) /copper oxide nanocomposites were simultaneously electrodeposited on a graphenized pencil electrode (GPE/PEBT/CuO) for sensitive determination of Cd2+ and Pb2+ in water samples. Active surface area of the prepared electrode was remarkably increased in comparison with GPE/Cu and GPE/PEBT. Under the optimized conditions including accumulation time of 200 s, accumulation voltage of −1.0 V and pH 6, the prepared GPE/PEBT/CuO was utilized for Cd2+ and Pb2+ determination by differential pulse anodic stripping voltammetry with good linearity in the concentration range of 7.8–78 µg/L and 22–220 µg/L, detection limit of 1.8 µg/L and 6.85 µg/L and sensitivity of 0.1081 µA µg−1 L and 0.0394 µA µg−1 L respectively. The method was properly utilized for Cd2+ and Pb2+ detection in tap and river water samples with satisfactory results.