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.

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 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.

In this work, a nanocomposite containing gold (Au) nanofibers decorated iron-metal–organic framework (Fe-MOF) was successfully synthesized for electrochemical detection of acetaminophen (AAP). The as-synthesized Au@Fe-MOF nanocomposite was confirmed by various characterization techniques. Morphological analysis showed that the Au nanofibers with an average size of less than 10 nm were dispersed on the Fe-MOF. Cyclic voltammetric analysis showed that the Au@Fe-MOF nanocomposite showed well-defined redox peaks with higher current than that of GCE and Fe-MOF. The Au@Fe-MOF/ GCE exhibited a linear range, sensitivity, and detection limit of 0.5–18 μM, 4.95 μM/μA/cm2, and 0.12 μM, respectively. The Au@Fe-MOF/GCE showed a very low response for the interference materials. The real sample analysis revealed that the Au@Fe-MOF/GCE showed good recovery towards the AAP in urine and paracetamol. Therefore, the developed sensor can be used for quality control of AAP.

Pentachlorophenol (PCP), as one of the common pesticide and preservatives, is easily accumulated in living organisms. Considering the high toxicity of PCP, the development of an effective and sensitive inspection method to determine the residual trace amounts of PCP continues to be a significant challenge. Herein, a convenient and sensitive electrochemical sensor is constructed by modifying glassy carbon electrode with cerium dioxide ( CeO2) nanoparticles anchored graphene ( CeO2-GR) to detect trace PCP. Benefiting from the two-dimensional lamellar structural advantages, the extraordinary electron-transfer properties, as well as the intensive coupling effect between CeO2 nanoparticles and graphene, the afforded CeO2- GR electrode nanomaterial possesses excellent electrocatalytic activity for the oxidation of PCP. Under the optimum synthetic conditions, the PCP oxidation peak currents of developed CeO2– GR sample exhibit a wide linear range of 5–150 μM. Moreover, the corresponding detection limit of PCP on the CeO2– GR electrode is as low as 0.5 μM. Apart from providing a promising electrochemical sensor, this work, most importantly, promotes an efficient route for the construction of highly active sensing electrode materials.

The central theme of this work is the synthesis of single-walled carbon nanotubes (SWCNTs) through the chemical vapor deposition method (CVD). Single-walled carbon nanotubes are synthesized using catalyst-chemical vapor deposition of acetylene at 750 °C temperature. X-ray diffraction study gives a characteristic peak (002) at 26.55° corresponding to the existence of carbon nanotube confirms that the particles are crystalline in nature and hexagonal phase. An SEM and HRTEM outcome gives surface morphology of SWCNTs. The elemental composition was confirmed by EDAX. The ideal concentration of single-walled carbon nanotubes was used to design a novel electrochemical sensor for determining paracetamol (PA) using cyclic voltammetry. Electrochemical determination of paracetamol is described using a single-walled carbon nanotube modified carbon paste electrode (SWCNT/MCPE). The SWCNT/MCPE was used in this study to detect paracetamol electrochemically at pH 7.2 in a 0.2 M PBS with a scan rate of 50 mV s− 1. A single-walled nanotube modified carbon paste electrode was used to develop a sensitive and selective electrochemical technique for the detection of PA. The SWCNT/MCPE showed excellent electrocatalytic activity towards the oxidation of paracetamol in phosphate buffer solution. Therefore, with increased oxidation currents, the voltammetric responses of paracetamol at the bare carbon paste electrode are organized within cyclic voltammetric peaks.

Cerium oxide decorated on nickel hydroxide anchored on reduced graphene oxide (Ce-Ni(OH)2/rGO) composite with hexagonal structures were synthesized by facile hydrothermal method. Fourier transform infrared spectroscopy (FT-IR), highresolution transmission electron microscopy with selected area diffraction (HRTEM-SAED), scanning electron microscopy (SEM), energy dispersive spectroscopy (EDS), X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), Brunauer– Emmett–Teller (BET) surface area analysis and electrochemical technology were used to characterize the composite. Due to its unique two-dimensional structures and synergistic effect among Ce2O3, Ni(OH)2 and rGO components indicated twodimensional hexagonal nano Ce-Ni(OH)2/rGO composite is promising electrode material for improved electrochemical H2O2 sensing application. From 50 to 800 μM, the H2O2 concentration was linearly proportional to the oxidation current, with a lower detection of limit of 10.5 μM (S/N = 3). The sensor has a higher sensitivity of 0.625 μA μM−1 cm− 2. In addition, the sensor demonstrated high selectivity, repeatability and stability. These findings proved the viability of the synthetic method and the potential of the composites as a H2O2 sensing option.

The electrochemical type gas sensor has the advantage of being easy to use due its small size, and it is also relatively inexpensive. However, its output can easily vary depending on temperature and humidity conditions. Therefore, it is important to ascertain the exact output characteristics of a sensor according to the measuring environment in order to improve measurement accuracy for any set of given conditions. The purpose of this study is to obtain basic information about the output characteristics of a sensor that is used both indoor and outdoor according to the variation in temperature and humidity conditions in order to improve the accuracy of the sensor. To achieve this result, a calibration curve was made using ammonia standard gas and the calibration factor was calculated using the calibration curve and the measuring accuracy was confirmed with regard to the ammonia sensor. Based on the test results, the variation of the sensor output value was large in relation to temperature and humidity variation. It was found that the output value from the sensor at higher temperature and humidity conditions was also higher. However, the measuring accuracy of the sensor could be improved by more than 10% by applying the calibration factor and an average accuracy of more than 97% could be achieved. It is anticipated that the result of this study can be used as basic data to obtain more accurate results using electrochemical sensors for a given set of temperature and humidity conditions, and therefore, it can also be considered that the reliability and applicability of electrochemical sensors can be improved.

This study was carried out to investigate the response characteristics of a hydrogen sulfide electrochemical gassensor for several wastewater odors. At first, it was found that bubbling sampling method was superior toheadspace sampling method in terms of sensor sensitivity. High correlation between odor concentration and sensorresults was shown for two wastewater which were r=0.977 for food-waste recycling wastewater and r=0.997for food industry wastewater. On the other hand, no correlation (r=0.258) was found for plating wastewater,because hydrogen sulfide was not the main odorant for that.