The nanostructured dysprosium oxide ( Dy2O3) was synthesized by the co-precipitation method and incorporated with graphitic carbon nitride (g-C3N4) using the ultrasonication method. The resultant product is denoted as Dy2O3/ g-C3N4 nanocomposite which was further used for electrochemical sensing of riboflavin (RF). The physicochemical properties of Dy2O3/ g-C3N4 nanocomposite were examined using several characterization techniques. The obtained results exhibit the nanocomposite formation with the preferred elemental compositions, functional groups, crystalline phase and desired surface morphology. The electrocatalytic performance of Dy2O3/ g-C3N4 nanocomposite was scrutinized with a glassy carbon electrode (GCE) via differential pulse voltammetry (DPV) and cyclic voltammetry (CV) techniques with the conventional three-electrode system. The modified electrode distributes more active surface area suggesting high electrocatalytic activity for the RF detection with two linear ranges (0.001–40 μM and 40–150 μM), a low detection limit of 48 nM and sound sensitivity (2.5261 μA μM−1 cm− 2). Further, the designed sensor possesses high selectivity, excellent stability, repeatability and reproducibility. Finally, the fabricated sensor was successfully estimated for the detection of RF in actual food sample analysis using honey and milk with better recovery.

Black phosphorus (BP) is incorporated in the electrochemical detection of uric acid (UA) to form few layers of BP nanosheets (BPNS)-modified glassy carbon electrodes (BPNS/GCE), investigated by means of ultrasound-assisted liquid-phase exfoliation. We find a significant increase in the peak current magnitude and positive potential shift in the electrochemical response of BPNS/GCE, which may be attributed to the larger specific surface area and good charge transfer ability of BPNS. Further, the electrochemical response of BPNS/GCE is evaluated under different conditions to achieve the optimal conditions. UA detection using differential pulse voltammetry (DPV) shows linear response within the range of 1–1000 μM with a detection limit of 0.33 μM. This work reveals new applications of BP nanomaterials in the electrochemical sensing, thereby promoting further advancement in terms of practical applications of two-dimensional nanomaterials.

A simple and one-pot synthetic procedure using two different sources has been demonstrated to prepare heteroatoms doped reduced graphene oxide such as nitrogen-doped reduced graphene oxide (N-RGO) and sulfur-doped reduced graphene oxide (S-RGO). The N-RGO has been hydrothermally synthesized using urea as nitrogen precursor, wherein the S-RGO has been synthesized using dimethyl sulfoxide (DMSO) as sulfur precursor. The successful N-doping, S-doping and other physicochemical properties of N-RGO and S-RGO have been confirmed with different spectroscopic and electrochemical techniques. The results indicated that doping into the graphene structure exhibits a high conductivity and a better transfer of charge. Moreover, heteroatoms doped graphene (N-RGO and S-RGO) and graphene-related materials (RGO) have been applied for the individual detection of uric acid (UA). Interestingly, the N-RGO exhibited a lower limit of detection (LOD, S/N = 3) of 2.7 10– 5 M for UA (10–1000 μM) compared with undoped RGO and S-RGO. Furthermore, the simultaneous detection of UA in the presence of Xanthine (XA) has been demonstrated a wide linear range of detection for UA: 10–1000 μM, with unchanged concentration of XA to be 200 μM, and exhibited a low limit of detection of 8.7 10− 5 M ( S∕N = 3) for UA. This modified sensor based on N-RGO has revealed a high selectivity and reproducibility thanks to its large surface area, high catalytic properties, and chemical structure. Indeed, the practical applicability of the proposed sensor has been evaluated in milk samples even in the presence of high concentrations of UA with satisfactory results.

In this research, reduced graphene oxide/polypyrrole (rGO/PPy) particles were synthesized and used to measure the amount of dopamine (DA) electrochemically. The obtained rGO/PPy particle was characterized by Fourier Transform Infrared Spectrophotometer (FTIR), UV–Visible Spectrophotometer (UV–Vis), and X-Ray Diffraction Diffractometry (XRD). To investigate the DA sensor performance, cyclic voltammetry (CV) and differential pulse voltammetry (DPV) were used to acquire electrochemical measurements of the sensor. Current values of 1.65 and 5.9 mA were observed in the CV at 0.2 mM and 1.2 mM concentrations of target molecule, respectively. Under optimized conditions, the linear calibration plots were found to exhibit significant sensitivity in the linear range of 0.2 and 1.2 mM, with a corresponding detection limit of 0.061 μM for DA. The results obtained were similar to the sensor results of DA made using precious metals. This work was a demonstration of the feasibility of high-sensitivity electrochemical analysis with conductive carbon materials without the use of precious metals. It was also observed that the cost-effective rGO/PPy exhibited a very high potential for DA detection.

In zinc-air batteries, the gel polymer electrolyte (GPE) is an important factor for improving performance. The rigid physical properties of polyvinyl alcohol reduce ionic conductivity, which degrades the performance of the batteries. Zinc acetate is an effective additive that can increase ionic conductivity by weakening the bonding structure of polyvinyl alcohol. In this study, polymer electrolytes were prepared by mixing polyvinyl alcohol and zinc acetate dihydride. The material properties of the prepared polymer electrolytes were analyzed by Fourier-transform infrared spectroscopy (FT-IR), scanning electron microscopy (SEM), X-ray diffraction (XRD), and thermogravimetric analysis (TGA). Also, Electrochemical impedance spectroscopy was used to calculate ionic conductivity. The electrolyte resistances of GPE, 0.2 GPE, 0.4 GPE, and 0.6 GPE were 0.394, 0.338, 0.290, and 0.213 Ω, respectively. In addition, 0.6 GPE delivered 0.023 S/cm high ionic conductivity. Among all of the polymer electrolytes tested, 0.6 GPE showed enhanced cycle life performance and the highest specific discharge capacity of 11.73 mAh/cm2 at 10 mA. These results verified that 0.6 GPE improves the performance of zinc-air batteries.

In this study, the performances of H2S, NH3, and HCl sensors for real-time monitoring in small emission facilities (4, 5 grades in Korea) were evaluated at high concentration conditions of those gases. And the proper approach for the collection of reliable measurement data by sensors was suggested through finding out the effect on sensor performances according to changes in temperature and humidity (relative humidity, RH) settings. In addition, an assessment on sensor data correction considering the effects produced by environmental settings was conducted. The effects were tested in four different conditions of temperature and humidity. The sensor performances (reproducibility, precision, lower detection limit (LDL), and linearity) were good for all three sensors. The intercept (ADC0) values for all three sensors were good for the changes of temperature and humidity conditions. The variation in the slope value of the NH3 sensor showed the highest value, and this was followed by the HCl, H2S sensors. The results of this study can be helpful for data collection by enabling the more reliable and precise measurements of concentrations measured by sensors.

The potentiostatic titration method is one of the effective methods for determining the total uranium assay in high-concentration uranium samples. A notable approach is the Devies-Grey titration method, which was first reported in 1964. In the U sample treatment process of this method, the reduction of U(VI) by Fe(II) is initially a non-spontaneous reaction based on the reduction potentials of the two half-reactions. However, in a high-concentration phosphoric acid medium, the reduction potential of Fe(II) is enhanced, simultaneously increasing the reduction potential of U(VI). As a result, the redox reaction becomes spontaneous due to these dual effects. On the other hand, the reaction kinetics can elucidate why nitric acid does not oxidize U(IV) during the oxidation of Fe(II) to Fe(III). Furthermore, the role of Mo(VI)/Mo(V) as a redox enhancer, employed alongside nitric acid, can be comprehended through electrochemical means. Similarly, the function of V(IV) as an electrochemical enhancer, aiding the action of the Cr(VI) titrant, becomes understandable. Grasping the various phenomena that manifest during the titration process is imperative for refining existing titration methods and pioneering new ones.

Molten Salt Reactor (MSR) is one of the 4th generation nuclear power systems which is its verified technology in physically and chemically. Among the various salts used for MSR system, the eutectic composition of NaCl-MgCl2 system maintains the liquid state at around 450°C, in the same time, it has high solubility for nuclear fuel chlorides. This characteristic has high advantage for lowering the operating temperature for the MSR, which could reduce the problem of hightemperature corrosion by salt for structural materials significantly. In particular, since MgCl2 has the similar standard reduction potential with nuclear fuel, is used as a surrogate for, many basic researches have been conducted for verifying characteristic of MgCl2. It is well-known that main short-advantage of MgCl2 is hygroscopic properties. MgCl2 changes to MgCl2-xH2O state easily by absorbing moisture in air condition. The hydrated MgCl2 is producing MgOHCl by thermally decomposing at high temperature, the formed MgOHCl corrodes structural materials, even small amount of MgOHCl gives significant damage. Therefore, the purification of MgCl2 has been required for long-term operation of MSR using MgCl2 as a base salt. In this study, the purification of eutectic composition salt for NaCl-MgCl2 has been mainly performed by considering its thermodynamic properties and electrochemical characteristic, and the experimental results have been discussed.

Molten chloride salts have received considerable research attention as potential nuclear fuel and coolant candidates for molten salt reactors. However, there are several challenges, especially for structural materials due to the selective dissolution of chromium (Cr) in the molten chloride salts environment. Understanding the compatibility of uranium (U), which is used as nuclear fuel in molten salt reactors, with Cr in molten chloride salts is critical for designing the molten salt reactor structure. Therefore, in this study, the cyclic voltammetry (CV) was used to investigate the electrochemical behaviors of U and Cr. The diffusion coefficients and formal potentials were obtained. The electrochemical properties of uranium and chromium were investigated by CV in molten NaCl-MgCl2 salt at 600°C. Tungsten rods for working and counter electrode, and Ag/AgCl for reference electrode were utilized in this experiment. UCl3 made from the chemical dissolution of U rods and CrCl2 (Sigma-Aldrich, 99.99%) were used. Diffusion coefficients (D) of U and Cr were calculated by measuring reduction peak current of U3+/U and Cr2+/Cr from CV curves and using the Berzins-Delahay equation; D (U3+/U) = 3.0×10-5 cm2s-1 and D (Cr2+/Cr) = 3.3×10-5 cm2s-1. The formal potentials were also calculated by using the reduction peak potential obtained from CV results; E0’ (U3+/U) = -1.173 V and E0’ (Cr2+/Cr) = -0.321 V. The ionization tendency was investigated by comparing each reduction peak potential. The reduction peak potential Ep,c was increasing order of Ep,c (U3+/U) < Ep,c (Cr2+/Cr) < Ep,c (U4+/U3+). It can be seen that in the presence of U4+ and Cr metals, the Cr in the alloy can dissolve into Cr2+, but in the presence of U3+ and Cr metals, the Cr in the alloy does not dissolve into Cr2+. By analyzing the CV curve, diffusion coefficients and formal standard potentials were obtained. The result of comparing reduction peak potentials suggests that the nuclear fuel using U4+ should be inhibited to prevent the selective dissolution of Cr.

Heavy metal wastewater containing cobalt (Co2+) has received more attention as an environment issue, which is released from electroplating processes, battery materials industries, nuclear power plants, etc. Especially, cobalt exposed to high-temperature and high-pressure environment during the operation of a nuclear power plant to form corrosion products and forming a chalk river unidentified deposit (CURD) along with radioactive materials generated in cooling water pipes. Cobalt present in the oxide film is mainly Co-60, which emits radiation and causes increased radiation exposure to workers, and efficient management is essential. In this study, we demonstrated the performance of copper hexacyanoferrate (CuHCF) electrodes in a capacitive deionization (CDI) system for Co2+ ions removal. The structure and chemical status of CuHCF used as an electrode material were characterized, and electrochemical properties were evaluated. This study showed that Co2+ ions could be efficiently removed in aqueous solutions using CuHCF electrodes. It has been experimentally shown that the ion removal mechanism is driven by the insertion of Co2+ ions within the CuHCF lattice channels. The deionization capacities in 20 and 50 mg-Co2+ L-1 aqueous solutions were 141.62 and 156.85 mg g-1, respectively, and the corresponding charge efficiencies (Λ) were 0.55 and 0.68, respectively. Thus, we suggest that an electrochemically driven process using CuHCF can usefully remove Co2+ ions from wastewater.

MicroRNAs (miRNAs) are emerging materials as ideal biomarkers for noninvasive cancer detection in the early phase. In this article, a simple and label-free electrochemical miRNA biosensor was developed. A single-stranded DNA (ss-DNA) probes were successfully mapped to f-MWCNT and hybridized with the target miR-141 sequence. The optimum peak points of the obtained hybridization were determined using Cyclic Voltammetry (CV) and Differential Pulse Voltammetry (DPV) methods. Significant peaks were observed in the results, depending on miR-141 at different concentrations. The linear relationship (ν) between redox peak currents (Ip) and scanning rate indicated that electron transfer (ET) between miR-141 and the electrode surface was accomplished successfully. In DPV measurements, miR-141 was measured with a low detection limit (LOD) in the 1.3–12 nM concentration range, and the LOD and limit of quantification (LOQ) results were found to be 3 and 9.1 pM, respectively. Besides, selectivity test was investigated for the biosensor using different target analytes and a significant difference in value was observed between the peak currents of miR-141, and other target molecules. This developed strategy has been found to detect miR-141 sensitively, selectively and without tags, and its integration into mobile devices has been successfully carried out.

In this work, norepinephrine (NE) was determined by an electrochemical sensor represented by a carbon paste electrode boosted using nitrogen-doped porous carbon (NDPC) derived from Spirulina Platensis microalga anchored CoFe2O4@ NiO and 1-Ethyl-3-methylimidazolium acetate (EMIM Ac) ionic liquid. The morphological characteristics of the catalyst were recorded by field emission scanning electron microscope (FE-SEM) images. Moreover, the electrochemical behavior of norepinephrine on the fabricated electrode was checked using various voltammetric methods. All tests were done at pH 7.0 as the optimized condition in phosphate buffer solution. The results from linear sweep voltammetry revealed that the electro-oxidation of norepinephrine was diffusion, and the diffusion coefficient value was obtained by chronoamperometry (D⁓6.195 × 10– 4). The linear concentration of the modified electrode was obtained from 10 to 500 μM with a limit of detection of 2.26 μM using the square wave voltammetry (SWV) method. The sensor selectivity was investigated using various species, and the results from stability and reproducibility tests showed acceptable values. The sensor's efficiency was tested in urine and pharmaceutical as real samples with recovery percentages between 97.1% and 102.82%.

Aurantii Fructus Immature (AFI) and Aurantii Fructus (AF) are two important traditional Chinese herbs. As the harvesting time varies, the medicinal value of the plants is not uniform. Consequently, it has been difficult to quickly recognize them within the realm of traditional Chinese medicine. Separation and detection technologies are employed in combination to create fingerprints for identification. We proposed the utilization of graphene-assisted electrochemical fingerprint technology to acquire fingerprints of two varieties of medicinal materials. Simultaneously, we also obtained their fingerprints through HPLC. Two fingerprint recognition technologies were compared for their effectiveness. The findings demonstrate that the signals obtained through electrochemical fingerprinting have a higher recognition rate.

This work describes Ni–Ce–Cu metallic–organic framework (MOF) for the detection of non-essential amino acid l-cysteine. The tri-metallic Ni–Ce–Cu MOF was synthesized via a solvothermal method. The cyclic voltammetry and the differential pulse voltammetry techniques were used to examine the electrochemical detection of l-cysteine. The Ni–Ce–Cu MOF shows an oxidation peak in PB solution at pH 3.0 between the potential range of 0.0 and 0.7 V and strong electro-catalytic activity toward the oxidation of l-cysteine across a wide linear range of 0.1 to 250 nM and low detection limit (LOD) was calculated of 1.56 nM. The analysis of l-cysteine in milk and egg yolk samples showed with recovery range of 96.75–103.5% and 97.78–99.43% with RSD% of 2.3–3.2% and 2.7–7.2%, respectively. These results show the Ni–Ce–Cu MOF has high selectivity for l-cysteine detection in milk and egg samples.

In the present investigation, a new electrochemical sensor based on carbon paste electrode was applied to simultaneous determine the tramadol, olanzapine and acetaminophen for the first time. The CuO/reduced graphene nanoribbons (rGNR) nanocomposites and 1-ethyl 3-methyl imidazolinium chloride as ionic liquid (IL) were employed as modifiers. The electrooxidation of these drugs at the surface of the modified electrode was evaluated using cyclic voltammetry (CV), differential pulse voltammetry (DPV), electrochemical impedance spectroscopy (EIS) and chronoamperometry. Various techniques such as scanning electron microscopy (SEM) with energy dispersive X-Ray analysis (EDX), X-ray diffraction (XRD) and fourier-transform infrared spectroscopy (FTIR), were used to validate the structure of CuO-rGNR nanocomposites. This sensor displayed a superb electro catalytic oxidation activity and good sensitivity. Under optimized conditions, the results showed the linear in the concentration range of 0.08–900 μM and detection limit (LOD) was achieved to be 0.05 μM. The suggested technique was effectively used to the determination of tramadol in pharmaceuticals and human serum samples. For the first time, the present study demonstrated the synthesis and utilization of the porous nanocomposites to make a unique and sensitive electrode and ionic liquid for electrode modification to co-measurement of these drugs.

Phytohormones (plant hormones) are a class of small-molecule organic compounds synthesized de novo in plants. Although phytohormones are present in trace amounts, they play a key role in regulating plant growth and development, and in response to external stresses. Therefore, the analysis and monitoring of phytohormones have become an important research topic in precision agriculture. Among the various detection methods, electrochemical analysis is favored because of its simplicity, rapidity, high sensitivity, and in-situ monitoring. Graphene and graphene-like carbon materials have abundant sources, exhibiting large specific surface area, and excellent physicochemical properties. Thus, they have been widely used in the preparation of electrochemical biosensors for phytohormone detection. In this paper, the research advances of electrochemical sensors based on graphene and graphene-like carbon materials for phytohormone detection have been reviewed. The properties of graphene and graphene-like carbon materials are first introduced. Then, the research advances of electrochemical biosensors (including conventional electrochemical sensors, photoelectrochemical sensors, and electrochemiluminescence sensors) based on graphene and graphene-like carbon materials for phytohormone detection is summarized, with emphasis on their sensing strategies and the roles of graphene and graphene-like carbon materials in them. Finally, the development of electrochemical sensors based on graphene and graphene-like carbon materials for phytohormone detection is prospected.