Electrochemical Sensor Applications Research Articles

Synthesis of strontium oxide nanoparticlesby probe sonication method: Its photocatalytic activity and electrochemical sensor studies

In this paper, we report on the synthesis of strontium oxide nanoparticles (SONPs) using a novel probe sonication method. Powder X-ray diffraction (PXRD) was used to characterize the physicochemical properties of the prepared materials, which confirmed that the average SrO crystallite size was 43 ​nm. The Kubelka-Monk function of diffuse reflectance spectroscopy (DRS) was used to confirm the average energy gap of SONPs (4.06 ​eV). SONPs have been successfully used in conjunction with inventive photocatalysts to remove dyes such as Methylene Blue (MB) and Acid Green (AG). MBand AG dyes were used as standard dyes to investigate the photocatalytic properties of NPs when exposed to UV light and sunlight.These nanometal oxides photodegrade methylene blue (87.70%) and acid green (71.20%) dyes with remarkable efficiency when exposed to UV light. These nanometal oxides demonstrated superior sensitivity when paracetamol was used as an analyte in cyclic voltammetry tests at various scan speeds (10 ​mV/s to 50 ​mV/s). As a result, SONPs may be useful in photocatalytic activity and electrochemical sensor applications.

MIL-88B(Fe)-NH2: an amine-functionalized metal-organic framework for application in a sensitive electrochemical sensor for Cd2+, Pb2+, and Cu2+ ion detection.

We propose here an electrochemical platform for multi-heavy metal ion detection in water based on MIL-88B(Fe)-NH2, an amine-functioned metal-organic framework (MOF) for modifying the surface of a glassy carbon electrode (GCE). Herein, MIL-88B(Fe)-NH2 with abundant functionalized amine groups can play the role of capture sites for the enrichment of metal ions before electrochemical oxidation sensing. MIL-88B(Fe)-NH2 was synthesized under optimized conditions through a solvothermal method and characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), transition electron microscopy (TEM), Fourier-transform infrared spectroscopy (FT-IR), cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS) techniques. MIL-88B(Fe)-NH2 was then drop-casted on GCE to electrochemically determine the Cd2+, Pb2+ and Cu2+ ion concentrations by differential pulse voltammetry (DPV). The electrochemical sensor exhibits excellent electrochemical performance toward Cd2+, Pb2+ and Cu2+ ions in the large linear ranges of 0.025-1.000 μM, 0.3-10.0 μM and 0.6-10.0 μM with limits of detection that are 2.0 × 10-10 M, 1.92 × 10-7 M and 3.81 × 10-7 M, respectively. The fabricated sensor also shows high reliability and good selectivity. This MIL-88B(Fe)-NH2 application strategy is promising for the evaluation of various heavy metal ions in water.

Robust method for uniform coating of carbon nanotubes with V2O5 for next-generation transparent electrodes and Li-ion batteries.

Composites comprising vanadium-pentoxide (V2O5) and single-walled carbon nanotubes (SWCNTs) are promising components for emerging applications in optoelectronics, solar cells, chemical and electrochemical sensors, etc. We propose a novel, simple, and facile approach for SWCNT covering with V2O5 by spin coating under ambient conditions. With the hydrolysis-polycondensation of the precursor (vanadyl triisopropoxide) directly on the surface of SWCNTs, the nm-thick layer of oxide is amorphous with a work function of 4.8 eV. The material recrystallizes after thermal treatment at 600 °C, achieving the work function of 5.8 eV. The key advantages of the method are that the obtained coating is uniform with a tunable thickness and does not require vacuuming or heating during processing. We demonstrate the groundbreaking results for two V2O5/SWCNT applications: transparent electrode and cathode for Li-ion batteries. As a transparent electrode, the composite shows stable sheet resistance of 160 Ω sq-1 at a 90% transmittance (550 nm) - the best performance reported for SWCNTs doped by metal oxides. As a cathode material, the obtained specific capacity (330 mA h g-1) is the highest among all the other V2O5/SWCNT cathodes reported so far. This approach opens new horizons for the creation of the next generation of metal oxide composites for various applications, including optoelectronics and electrochemistry.

Fabrication and application of a 3D-rGO electrochemical sensor for SO2 detection in ionic liquids.

Sulfur dioxide (SO2) is a common atmospheric pollutant. Currently, most of the detection methods are based on chemical reactions and optical absorption principles. However, these methods have some limitations in their detection range and accuracy, especially in complex environments. In this work, sulfur dioxide was absorbed by an ionic liquid, and a new electrochemical sensor based on 3D-rGO/CB was developed for electrochemical detection. Specifically, carbon black (CB) nanoparticles were incorporated with graphene oxide (GO) sheets using spray drying technology to form a highly porous and interconnected 3D-GO/CB microsphere structure. Then, the 3D-rGO/CB/GCE electrochemical sensor was fabricated by electrochemical reduction of the composite material onto a glassy carbon electrode (GCE) surface and used to detect sulfur dioxide in ionic liquids. The results demonstrated that the sensor had excellent conductivity and mass transfer preferable performance catalytic activity for SO2 in ionic liquids, and a linear detection range of 100-3500 ppm. Besides, the detection limit was 52.3 ppm (S/N = 3). Moreover, it had high selectivity, stability, and repeatability. This work significantly contributed to the development of advanced electrochemical sensors with improved performance for detecting SO2 in ionic liquids and has a potential application prospect in the field of electrochemical gas detection.

Application of Molecularly Imprinted Electrochemical Biomimetic Sensors for Detecting Small Molecule Food Contaminants.

Environmental chemical contaminants in food seriously impact human health and food safety. Successful detection methods can effectively monitor the potential risk of emerging chemical contaminants. Among them, molecularly imprinted polymers (MIPs) based on electrochemical biomimetic sensors overcome many drawbacks of conventional detection methods and offer opportunities to detect contaminants with simple equipment in an efficient, sensitive, and low-cost manner. We searched eligible papers through the Web of Science (2000-2022) and PubMed databases. Then, we introduced the sensing mechanism of MIPs, outlined the sample preparation methods, and summarized the MIP characterization and performance. The classification of electrochemistry, as well as its advantages and disadvantages, are also discussed. Furthermore, the representative application of MIP-based electrochemical biomimetic sensors for detecting small molecular chemical contaminants, such as antibiotics, pesticides, toxins, food additives, illegal additions, organic pollutants, and heavy metal ions in food, is demonstrated. Finally, the conclusions and future perspectives are summarized and discussed.

Stretchable Electrochemical Sensors: From Electrode Fabrication to Cell Mechanotransduction Monitoring†

Comprehensive SummaryElectrochemical sensing faces huge challenges in characterizing the transient release of biochemical molecules from deformed cells, due to the severely mechanical mismatch between rigid electrodes and soft cells. In recent years, the emergence of stretchable electrochemical sensors has made a breakthrough by complying with the deformation of living cells and simultaneous monitoring of mechanically evoked biochemical signals. This review first summarizes two fundamental strategies for the fabrication of stretchable electrodes from the points of structure and material. Next, recent progresses in construction of functionalized interface to improve the performance of stretchable electrochemical sensors are presented. Then, the application of stretchable electrochemical sensors in real‐time monitoring of biomolecules released by mechanically sensitive cells is introduced. Finally, some perspectives and challenges of stretchable electrochemical sensors regarding cell detection are discussed. What is the favorite and original chemistry developed in your research group?The design and construction of electrochemical sensing platform for real‐time monitoring of life activities.What is the most important personality for scientific research?Innovative spirit, strong curiosity and persistence.How do you supervise your students?Encourage students to think much and eager to innovate.What are your hobbies?I like music and playing badminton.Who influences you mostly in your life?My family and collaborators.Could you please give us some advices on improving Chinese Journal of Chemistry?Focusing on the originality of the manuscript.

Novel synthesis of Cu2ZnAl2O4 nanostructures for photocatalytic and electrochemical sensor applications

Hybrid nanostructured materials currently offer a potential approach for a variety of applications due to improvements in their physio-chemical characteristics. Techniques for XRD, TEM-HRTEM, SAED, and UV-DRS were used to characterize the Cu2ZnAl2O4 (CZA) material. Without any secondary phases and with an average crystallite size of 40 ​nm, X-ray diffraction pattern examination demonstrates the increased crystalline structure. A highly crystalline, polydisperse CZA nanostructure was visible using TEM-HRTEM and SAED. The CZA nanostructure's light-absorbing behavior is presented by UV-DRS analysis, which found that the predicted bandgap energy was 5.0 ​eV. In this article, we describe an easy chemical synthesis of a hybrid CZA nanostructure that works well as a catalyst to break down the acid red 88 (AR-88) dye under UV, sunlight, and low light conditions. Additionally, it was studied to determine how to modify the working electrode's surface to enable the detection of lead and tin metal ions. With 93.1% of degradation and comparison work on decolorizing AR-88 dye in the presence of both sunlight and darkness, CZA nanostructure was looked at as a potential catalyst for the decolorization of AR-88 dye. By using graphite electrode paste and cyclic voltammetry to analyze the synthesized sample in 1 ​N KCl, it was discovered that it had outstanding redox reaction and lead and tin detection capabilities.

Using 3D printed magnetic platform as support for screen printed electrode applied for p-toluenediamine detection in biological fluid and water samples

The present work reports the development and application of a new electrochemical sensor for the determination of low concentration levels of p-toluenediamine (PTD) in biological fluids and surface water samples. The proposed sensor was developed using a 3D-printed magnetic device as platform for carbon screen printed electrode (CSPE) modified by magnetic nanoparticles functionalized with carboxylic groups and l-cysteine (MNP-CA-CYS). The results obtained from the morphological and electrochemical characterizations of the sensing platform enabled us to confirm the success of the sensor functionalization with l-cysteine and to have a better understanding of the electrochemical behavior and preconcentration of PTD on the electrode surface. PTD oxidation occurred at 0.24V on MNP-CA-CYS and the mechanism recorded an increase of 51.0% in anodic peak current. Under optimized conditions, the square wave voltammograms obtained for the electrode modified by 40.0 μL MNP-CA-CYS suspension at 1.0 mg mL−1, with accumulation time of 3 min, presented an analytical curve with linear range of 8.00 × 10−7 to 8.00 × 10−5 mol L−1, represented by the equation Iap = (0.383 ± 0.011)[PTD] - (8.112 ± 0.07) × 10−8 (R2 = 0.9994), and detection and quantification limits of 8.53 × 10−8 and 2.56 × 10−7 mol L−1, respectively. Finally, the proposed method was validated through comparison with high performance liquid chromatography coupled to diode array detector (HPLC-DAD) technique and was successfully applied for PTD determination in samples of surface water, tap water, fetal bovine serum and artificial urine.

Electrochemical monitoring of 4-chlorophenol as a water pollutant via carbon paste electrode amplified with Fe3O4 incorporated cellulose nanofibers (CNF)

A crucial problem that needs to be resolved is the sensitive and selective monitoring of chlorophenol compounds, especifically 4-chlorophenol (4-CP), one of the most frequently used organic industrial chemicals. In light of this, the goal of this study was to synthesize Fe3O4 incorporated cellulose nanofiber composite (Fe3O4/CNF) as an amplifier in the development of a modified carbon paste electrode (CPE) for 4-CP detection. Transmission electron microscopy (TEM) was used to evaluate the morphology of the synthesized nanocatalyst, while differential pulse voltammetry (DPV), electrochemical impedance spectroscopy (EIS), and linear sweep voltammetry (LSV) techniques were implemented to illuminate the electrochemical characteristics of the fabricated sensor. The ultimate electrochemical sensor (Fe3O4/CNF/CPE) was used as a potent electrochemical sensor for monitoring 4-CP in the concentration range of 1.0 nM–170 μM with a limit of detection value of 0.5 nM. As a result of optimization studies, 8.0 mg Fe3O4/CNF was found to be the ideal catalyst concentration, whereas pH = 6.0 was chosen as the ideal pH. The 4-CP's oxidation current was found to be over 1.67 times greater at ideal operating conditions than it was at the surface of bare CPE, and its oxidation potential decreased by about 120 mV. By using the standard addition procedure on samples of drinking water and wastewater, the suggested capability of Fe3O4/CNF/CPE to detect 4-CP was further investigated. The recovery range was found to be 98.52–103.66%. This study paves the way for the customization of advanced nanostructure for the application in electrochemical sensors resulting in beneficial environmental impact and enhancing human health.

Recent advances in development of electrochemical biosensors for the detection of biogenic amines.

Biogenic amines (BAs) are widely found in food as a consequence of diverse factors including free amino acid availability, microbial production of decarboxylases, and variations in processing and storage conditions. Hence, BAs are considered as an important marker for determining the freshness and quality of food. Owing to the documentation of BAs in different dietary products, their numerous negative impacts on human health have reported to be a serious concern in past few decades. Therefore, the quantification of these chemical species in food becomes crucial as it can immensely contributes toward control of new episodes on food intoxication in humans. In this line, various chromatographic and colorimetric methods have been developed to detect BAs. However, these methods are in use from a longer time, still are limited by high cost, lengthy procedures, huge infrastructure and skilled personnel requirements that hinder their on-field application. In pursuit of a reliable method offering accurate detection of BAs, this review presents the state-of-the-art of electrochemical strategies for BAs sensing in food. The core of the review discusses about the widely employed electrochemical transducers, such as amperometric, potentiometric, impedimetric and conductometric-based BAs biosensors with significant findings of research work conducted previously. The application of electrochemical sensors to analyze BAs in different fields including food systems (fermented and non-fermented types) and smart packaging systems has been reviewed. Moreover, existing challenges and further available prospects for the development of rapid, facile, and sensitive electrochemical strategies for on-site determination of BAs have also been discussed.

Preparation of a Highly Sensitive Electrochemical Aptasensor for Measuring Epirubicin Based on a Gold Electrode Boosted with Carbon Nano-Onions and MB.

Epirubicin is prescribed as an essential drug for treating breast, prostate, uterine, and gastrointestinal cancers. It has many side effects, such as heart failure, mouth inflammation, abdominal pain, fever, and shortness of breath. Its measurement is necessary by straightforward and cheap methods. The application of aptamer-based electrochemical sensors is accounted as a selective option for measuring different compounds. In this work, a thiol-modified aptamer was self-assembled on the surface of the gold electrode (AuE) boosted with carbon nano-onions (CNOs), and coupled with methylene blue (MB) as an electroactive tracker to achieve a sensitive and selective aptasensor. In the absence of the epirubicin, CNOs binds to the aptamer through a π-π interaction enhancing the MB electrochemical signal. When epirubicin binds to the aptamer, the adsorption of CNOs and MB to the aptamer is not well established, so the electrochemical signal is reduced, consequently, the epirubicin value can be measured. The prepared aptasensor demonstrated an excellent sensitivity with a curve slope of 0.36 μI/nM, and 3 nM limit of detection in the linear concentration range of 1-75 nM. The prepared aptasensor was accurately capable of measuring epirubicin in blood serum samples.

Novel Electrochemical Sensor Application for Dopamine and Preparation of N-rGO Micro-regionally Constrained WS2 Nanocomposite

Dopamine is an important neurotransmitter for organisms and affects their function, so monitoring and detecting dopamine levels are essential. Sensitivity and selectivity of electrochemical sensors for the detection of dopamine usually rely on hybrid nanocomposites. In this context, we designed a micro-regionally restricted hybrid nanocomposite by modulating the micro-nano structure. Using functional groups on nitrogen-doped reduced graphene oxide (N-rGO) to restrict the random growth of tungsten disulfide nanosheets, we obtained a 2D layered material with bidirectional structural support to achieve high specific surface and high activity for application in robust and novel dopamine electrochemical sensors. A facile electrochemical sensor for dopamine detection was fabricated by modifying a screen-printed carbon electrode with the nanocomposite. The sensor exhibits excellent performance of dopamine detection in the wide range of 1 μmol l−1–100 μmol l−1 with a detection limit of 0.2 μmol l−1 and a high sensitivity of 0.56 μA μmol−1 l−1. The optimized sensor shows a good selectivity, satisfactory long-term stability and reproducibility towards DA and a separation of peak potential of 142 mV with uric acid. In addition, the prepared sensor provides favorable recovery in human serum and artificial cerebrospinal solution (aSCF), indicating great potentials in electrochemical detection and biological sensing applications.

One-step synthesized biogenic nanoparticles using Linum usitatissimum: Application of sun-light photocatalytic, biological activity and electrochemical H2O2 sensor

This study aimed to synthesize Ag NPs as a green catalyst for photocatalytic activity and to examine their biological activities. It was determined that they have high activity in catalytic and biological activities. The green synthesis which is an environmentally friendly and inexpensive method was used to synthesize Ag-NPs using Linum usitatissimum as a reducing agent. Transmission electron microscopy (TEM), infrared to Fourier transform infrared (FTIR) spectroscopy, UV-Visible (UV–Vis) spectroscopy, and X-ray diffraction (XRD) were used to characterize the Ag NPs. In UV–Vis examination, Ag-NPs had intense peaks in the 435 nm region. The antibacterial activity of Ag NPs was investigated, and Ag NPs showed a high lethal effect against S. aureus, E. coli, B. subtilis, and MRSA. In addition, Ag NPs were tested for anticancer activity against the HT-29 colon cancer cell line, MDA-MB-231 breast cancer cell line, healthy cell line L929-Murine Fibroblast cell Lines, and MIA PaCa-2 human pancreatic cancer cell line at various concentrations (1–160 μg/mL) and showed a high anticancerogenic properties against MDA-MB-231 cells. Ag NPs showed the ability of DNA cleavage activity. Also, the antioxidant activity of Ag NPs against DPPH was found to be 80% approximately. Furthermore, the photocatalytic activity of Ag NPs against methylene blue (MB) was determined to be 67.13% at the 180th min. In addition, it was observed that biogenic Ag NPs have high electrocatalytic activity for hydrogen peroxide (H2O2) detection. In the sensor based on Ag NPs, linearity from 1 μM to 5 μM was observed with a detection limit (LOD) of 1.323 μM for H2O2. According to these results, we conclude that the biogenic Ag NPs synthesized using Linum usitatissimum extract can be developed as an efficient biological agent as an antibacterial and anticancer also can be used as a photocatalyst for industrial wastewater treatment to prevent wastewater pollution.

GO/ZnO nanocomposite - as transducer platform for electrochemical sensing towards environmental applications

Graphene Oxide-Zinc Oxide (GO-ZnO) – a new nanomaterial that has queued the interest of researchers. Their intriguing promising physical and electrochemical features of electrode material have led to its widespread use in electrochemical sensor applications. GO-ZnO based nanomaterial were extensively exploited in the construction of electrochemical sensors due to their adaptability and distinct qualities. On understanding the structural role of these materials, their modification processes are critical for realizing their full potential. The advancement of technology on new concepts and strategies has revolutionized the field of sensor devices with high sensitivities and selectivity. These tools can test a range of contaminants quickly, accurately, and affordably while performing automated chemical analysis in complicated matrices. This paper highlights the electrochemical transducer surface for sensing various analytes and current research activity on GO-ZnO nanocomposite. Additionally, we talked about current developments in GO-ZnO nanostructured composites to identify relevant analytes (i.e., Nitrophenols, Antibiotic Drugs, Biomolecules). While being used in the laboratory, the majority of produced systems have proven to bring about excellent gains. Their monitoring application still has a long way to go before it is fixed due to problems like technological advancements and multifunctional strategies to get around the challenges for improving the sensing systems.

Preparation and Application of Electrochemical Horseradish Peroxidase Sensor Based on a Black Phosphorene and Single-Walled Carbon Nanotubes Nanocomposite.

To design a new electrochemical horseradish peroxidase (HRP) biosensor with excellent analytical performance, black phosphorene (BP) nanosheets and single-walled carbon nanotubes (SWCNTs) nanocomposites were used as the modifier, with a carbon ionic liquid electrode (CILE) as the substrate electrode. The SWCNTs-BP nanocomposite was synthesized by a simple in situ mixing procedure and modified on the CILE surface by the direct casting method. Then HRP was immobilized on the modified electrode with Nafion film. The electrocatalysis of this electrochemical HRP biosensor to various targets was further explored. Experimental results indicated that the direct electrochemistry of HRP was realized with a pair of symmetric and quasi-reversible redox peaks appeared, which was due to the presence of SWCNTs-BP on the surface of CILE, exhibiting synergistic effects with high electrical conductivity and good biocompatibility. Excellent electrocatalytic activity to trichloroacetic acid (TCA), sodium nitrite (NaNO2), and hydrogen peroxide (H2O2) were realized, with a wide linear range and a low detection limit. Different real samples, such as a medical facial peel solution, the soak water of pickled vegetables, and a 3% H2O2 disinfectant, were further analyzed, with satisfactory results, further proving the potential practical applications for the electrochemical biosensor.

Atomic-scale interfacial engineering enables high-performance electrochemical glucose detection

Developing noble-metal free electrocatalysts with high sensitivity is critical for the large-scale application of electrochemical glucose sensors. This work reports an atomic-scale interfacial engineering strategy to construct highly-active electrocatalyst for glucose detection. Ni(OH)2 nanosheets are decorated with an ultra-thin layer of Co9S8 using the atomic layer deposition (ALD) technique. After in-situ reconstruction, we obtain Ni@Co heterostructure composed of Ni hydroxide nanosheets and CoOx clusters, which exhibits outstanding electrochemical glucose sensing performance. Combining synchrotron-based X-ray adsorption spectroscopy, in situ Raman Spectroscopy, intermittent electrochemical measurements and density functional theory (DFT) calculations, we find that the presence of surface CoOx not only lowers the valence state of Ni, but also facilitates the deprotonation of Ni(OH)2 to form NiOOH active species for glucose oxidation. The approach used in this work can be adapted to synthesizing high-performance electrocatalysts for other energy and environmental devices.

Efficient lock-in CuO/WON heterostructures tailored for highly sensitive electrochemical detection of hazardous herbicide diuron in fruit juices and aqua region

A micro-nano lock-in heterostructure has attracted significant attention for electrochemical sensor application due to its high specific surface area, more exposed active sites, and fast ion transport. Despite these advantages, here we prepared lock-in hetero structured tungsten oxynitride (WON) with a flower of CuO architecture by using the impregnation method. The tungsten oxynitride (WON) was prepared from the doping of nitrogen over the lattice of WO3 via a reactive NH3 gas etching process which turns WO3 nanoflakes (NFs) into the WON etched nanoflakes (EFs). The EFs act as cages to hold the hydrothermally prepared CuO micro flowers (MFs) and forms a new type of ‘lock-in’ heterostructure. This structure enables the stable and faster charge transfer between the CuO MFs and WON EFs, resulting in an efficient electrochemical performance towards the detection of diuron herbicide. The prepared CuO/WON were subjected to physiochemical characterizations such as X-ray diffraction (XRD), Raman spectroscopy, and X-ray photoelectron spectroscopy (XPS). The morphological and elemental information was interpreted by field-emission scanning electron microscopy (FESEM) combined with EDX and mapping analysis. Then, CuO/WON/GCE sensor electrode exhibited a wide diuron (DU) detection range of about 0.01–764.4 µM. Moreover, the estimated limit of detection and sensitivity from the slope of DU detection is 5.5 nm and 0.445 µM µA−1 cm−2 respectively. The practical applicability of the sensor electrodes was tested in the DU-added grape juice, orange juice, tap water, and river water samples.

Synthesis and Characterization of High Entropy Alloy 23Fe-21Cr-18Ni-20Ti-18Mn for Electrochemical Sensor Applications.

High entropy alloys (HEA) are one of the modern-era alloys accelerating with greater velocity because of their excellent properties and different applications. In the present paper, we have successfully fabricated HEA (23Fe-21Cr-18Ni-20Ti-18Mn) powders by ball milling the elemental Fe, Cr, Ni, Ti, and Mn powders for 15 h. The advancement of the milling process and phase transformation of HEAs were studied by using X-ray diffraction (XRD) and scanning electron microscope (SEM). The crystallite size and the lattice strain of the HEA were calculated by using the Williamson-Hall (W-H) equation and the values were found to be 7 nm and 0.0176%, respectively. Similarly, the true lattice parameter was calculated using the Nelson-Riley (N-R) extrapolation method, and the value was found to be 3.544 Å. We have successfully investigated the electrochemical response of 15 h ball milled 23Fe-21Cr-18Ni-20Ti-18Mn HEA powders to determine the ascorbic acid (AA) using cyclic voltammetry. We have modified the carbon paste electrode with ball milled HEA of concentrations 0, 2, 4, 6, 8, and 10 mg, and among them, 8 mg HEA modified carbon paste electrode (HEA-MCPE) depicted the highest current sensitivity. We reported the effect of modifier concentration, analyte concentration, scan rate, and pH on the oxidation peak of AA. The electrochemical active surface area of carbon paste and MCPE was calculated using the Nernst equation and the values were found to be 0.0014 cm2 and 0.0027 cm2, respectively. The fabricated HEA-MCPE showed excellent current sensitivity, stability, anti-fouling, and selectivity.

Nano- and Microsensors for In Vivo Real-Time Electrochemical Analysis: Present and Future Perspectives.

Electrochemical nano- and microsensors have been a useful tool for measuring different analytes because of their small size, sensitivity, and favorable electrochemical properties. Using such sensors, it is possible to study physiological mechanisms at the cellular, tissue, and organ levels and determine the state of health and diseases. In this review, we highlight recent advances in the application of electrochemical sensors for measuring neurotransmitters, oxygen, ascorbate, drugs, pH values, and other analytes in vivo. The evolution of electrochemical sensors is discussed, with a particular focus on the development of significant fabrication schemes. Finally, we highlight the extensive applications of electrochemical sensors in medicine and biological science.

Direct interfacial growth of Sr–CeO2 nanoparticles on carbon nanofibers and their multidisciplinary applications

Cerium oxide (CeO2) and carbon nanofibers (CNF) based material have been widely used for supercapcitor, optoelectronic as well and electrochemical sensor applications due to their interesting physicochemical properties. Present article reports the facile hydrothermal synthesis of Sr–CeO2/CNF electrode material under subcritical reaction conditions. Different analytical techniques including X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR), UV–Visible spectroscopy, X-ray photoelectron spectroscopy (XPS), Brunauer-Emmett-Teller (BET), Scanning electron microscopy (SEM), Energy dispersive X-ray spectroscopy (EDX), and Transmission electron microscopy (TEM) were used for the chractrization of nanocomposite. XRD and XPS results confirm the formation of Sr–CeO2/CNF having cubic fluorite structure. In addition, morphological studies shows formation of dot like morphology of Sr–CeO2 nanoparticals embedded on CNF nanorods. Surface area analysis indicated that synthesized material is mesoporous in nature and exhibited high surface area of 38.45 m2/g. The optical absorption concludes that the band gap values lies between 2.1 and 3.15 eV, suitable for optoelectronic applications. Moreover, the electrochemical study of 5 wt% Sr–CeO2/CNF exhibits substantial specific capacitance of 192 Fg-1 with 95.4% good cyclic stability at 5000 cycles. The composite electrode exhibit energy density and power density of 96 WhKg−1and 1440 WKg−1at 0.8 Ag-1 current density suggesting a good electrode material for supercapacitor. Finally, the nanocomposite was also studied for cyclic voltammetric electrochemical detection of Harmaline (HAR) showing good sensitivity with Limit of detection (LOD) and Limit of quantification (LOQ) of 0.82 μg mL−1 and 2.48 μg mL−1 respectively.