scholarly journals Cu(I) Coordination Complex Precursor for Randomized CuOx Microarray Loaded on Carbon Nanofiber with Excellent Electrocatalytic Performance for Electrochemical Glucose Detection

Sensors ◽  
2019 ◽  
Vol 19 (24) ◽  
pp. 5353
Author(s):  
Sorina Motoc ◽  
Carmen Cretu ◽  
Otilia Costisor ◽  
Anamaria Baciu ◽  
Florica Manea ◽  
...  

A homoleptic ionic Cu(I) coordination complex that was based on 2,2′-biquinoline ligand functionalized with long alkyl chains (Cu(I)–C18) was used as a precursor to modify a carbon nanofiber paste electrode (Cu–C18/CNF). Randomized copper oxide microelectrode arrays dispersed within carbon nanofiber paste (CuOx/CNF) were obtained by electrochemical treatment of Cu–C18/CNF while using cyclic voltammetry (CV). The CuOx/CNF exhibited high electrocatalytic activity towards glucose oxidation at +0.6 V and +1.2 V vs. Ag/AgCl. Infrared Spectroscopy (FTIR) and scanning electron microscopy (SEM) characterized the electrodes composition. Cyclic voltammetry (CV), square wave-voltammetry (SWV), and multiple-pulsed amperometry (MPA) techniques provided optimized conditions for glucose oxidation and detection. A preconcentration step that involved 10 minutes accumulation at open circuit potential before SWV running led to the lowest limit of detection and the highest sensitivity for glucose detection (5419.77 µA·mM−1·cm−2 at + 1.1 V vs. Ag/AgCl) vs. Cu-based electrodes reported to date in literature.

2019 ◽  
Vol 0 (0) ◽  
Author(s):  
T. Venu Gopal ◽  
Tukiakula Madhusudana Reddy ◽  
P. Shaikshavali ◽  
G. Venkataprasad ◽  
P. Gopal

Abstract A small scale of environmentally hazardous 4-aminophenol can show significant impact on human health. Hence, in the present work, we have designed L-Valine film (Vf) modified carbon paste electrode (Vf/CPE) for the determination of 4-aminophenol. Herein, a facile in-situ L-Valine film was developed by electrochemical polymerization method onto the surface of bare carbon paste electrode (BCPE) with the help of cyclic voltammetry (CV) technique. A two-folds of electrochemical peak current enhancement was achieved at Vf/CPE in comparison with BCPE towards the determination of 4-aminophenol in optimum pH 7.0 of phosphate buffer solution (PBS). This was achieved due to the large surface area and conductive nature of Vf/CPE, which was concluded through the techniques of cyclic voltammetry and electrochemical impedance spectroscopy (EIS). The effect of pH of buffer and scan rate studies were successfully studied. Morphological changes of BCPE and Vf/CPE was studied with the help of scanning electron microscopy (SEM). The formation of Vf on CPE was also analyzed by Fourier transform infrared (FTIR) spectra. Under the optimized conditions, the limit of detection (LOD) and limit of quantification (LOQ) values of 4-aminophenol were estimated with the aid of chronoamperometry (CA) technique and was found to be 9.8 μM and 32 μM, respectively. Finally the proposed method was found to have satisfactory repeatability, reproducibility and stability results with low relative standard deviation (RSD) values.


Author(s):  
Mahmoud Fatehy Abdalqader Altahan ◽  
Eric Achterberg ◽  
Asmaa Galal ◽  
Magdi Abdel Azzem

Abstract Here we describe a new electrochemical sensor for PO4 3− detection in seawater. In this work, we prepared a carbon paste electrode (CPE) modified with molybdate and pretreated in 0.1 M NaOH using cyclic voltammetry (CV). The modified CPE was employed for the determination of PO4 3− in artificial seawater (35 g/L NaCl) acidified with sulfuric acid to pH 0.8. An additional cleaning step (cyclic voltammetry (CV)) of 10 cycles in 0.1 M NaOH at −0.5 to 0.5 V was required between PO4 3− determinations to dissolve the phosphomolybdic complex formed on the surface of the working electrode. Electrochemical impedance spectroscopy (EIS) results confirmed that the molybdate-modified CPE (molybdate/CPE) exhibited a low charge-transfer resistance (Rct) toward PO4 3−, and showed an improved analytical performance for different concentrations of PO4 3−. A calibration plot in the range of 0.01–5 µM with a limit of detection (LOD) of 0.003 µM was obtained. The proposed electrode demonstrated good precision (4.3% and 5.8%) for concentrations of 5 and 0.2 µM, respectively. The proposed method was employed to analyze PO4 3− in seawater samples on a research cruise in the North Sea, with results in close agreement to those obtained using conventional colorimetric measuremen


2012 ◽  
Vol 600 ◽  
pp. 234-237 ◽  
Author(s):  
Cai Yu Lu ◽  
Jian Fei Xia ◽  
Zong Hua Wang ◽  
Yan Zhi Xia ◽  
Fei Fei Zhang

A nonenzymatic electrochemical sensor was fabricated for glucose detection based on gold nanoparticles graphene/carbon nanotube nanohybrids (AuNPs-GH/CNT), which were synthesized through in situ reduction procedure. Cyclic voltammetry (CV) and amperometry were used to evaluate the catalytic activity of the AuNPs-GH/CNT-Nafion modified electrode towards glucose. It was founded that AuNPs-GH/CNT-Nafion modified electrode showed remarkable enhanced electrocatalytic activity towards the oxidation of glucose under optimized conditions. The sensors exhibited linear behavior in the concentration range from 5 μM to 1 mM for the quantification of glucose with a limit of detection of 1.5 μM.


Author(s):  
Zulkarnain Zulkarnain ◽  
Suprapto Suprapto ◽  
Taslim Ersam ◽  
Fredy Kurniawan

<p><em>A novel selective and sensitive electrochemical sensor for insulin detection has been fabricated and investigated. The electrochemical sensor was made from a mixture of silica gel, chitosan and nickel hydroxide (Ni(OH)<sub>2</sub>) nanoparticles, which was mounted on a silver wire and covered by a glass tube (silica gel/chitosan/Ni(OH)<sub>2 </sub>nanoparticles paste electrode). The </em><em>sensor</em><em> was characterized using cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS). The anodic and cathodic currents of the silica gel/chitosan paste electrode with Ni(OH)<sub>2 </sub>are 580 </em><em>m</em><em>A and -750 </em><em>m</em><em>A, respectively. Without Ni(OH)<sub>2</sub>, however, the currents are 150 </em><em>m</em><em>A and -250 </em><em>m</em><em>A, respectively. The sensitivity and limit of detection of the silica gel/chitosan/Ni(OH)<sub>2 </sub>nanoparticle paste electrode for insulin detection are 5573 × 10<sub>­</sub><sup>5</sup>pA/pMcm<sup>2</sup> and 0.25 pM, respectively. The sensor also shows good reproducibility of measurement for 35 days with an RSD of 0.29%. The fabricated</em><em> electrodes</em><em> also show good reproducibility, with an RSD of 1.39%.</em></p>


Sensors ◽  
2019 ◽  
Vol 19 (6) ◽  
pp. 1332 ◽  
Author(s):  
Sorina Motoc ◽  
Florica Manea ◽  
Corina Orha ◽  
Aniela Pop

The requirements of the Water Framework Directive to monitor diclofenac (DCF) concentration in surface water impose the need to find advanced fast and simple analysis methods. Direct voltammetric/amperometric methods could represent efficient and practical solutions. Fullerene–carbon nanofibers in paraffin oil as a paste electrode (F–CNF) was easily obtained by simple mixing and tested for DCF detection using voltammetric and amperometric techniques. The lowest limit of detection of 0.9 nM was achieved by applying square-wave voltammetry operated under step potential (SP) of 2 mV, modulation amplitude (MA) of 10 mV, and frequency of 25 Hz, and the best sensitivity was achieved by four-level multiple pulsed amperometry (MPA) that allowed in situ reactivation of the F–CNF electrode. The selection of the method must take into account the environmental quality standard (EQS), imposed through the “watchlist” of the Water Framework Directive as 0.1 µg·L−1 DCF. A good improvement of the electroanalytical parameters for DCF detection on the F–CNF electrode was achieved by applying the preconcentration step for 30 min before the detection step, which assured about 30 times better sensitivity, recommending its application for the monitoring of trace levels of DCF. The electrochemical behavior of F–CNF as a pseudomicroelectrode array makes it suitable for practical application in the in situ and real-time monitoring of DCF concentrations in water.


2021 ◽  
Vol 12 (3) ◽  
pp. 2843-2851

In the present study, an electrochemical sensor for the determination of Cu(II) ions in aqueous solutions was introduced. This study proposes an electrochemical method using the calyx [6]arene-TiO2 nanocomposite modified carbon paste electrode (calyx[6]arene-TiO2/CPE) for the determination of metal Cu2+ ion. Calyx[6]arene-TiO2 were synthesized using the hydrolysis method as the Cu-binding ionophore. The electrode surface was studied by scanning electron microscopy (SEM), and the reduction and oxidation processes were studied by cyclic voltammetry (CV) techniques. The effect of modifier composition, scan rate, variation concentration, repeatability, and type of supporting electrolyte on the determination of metal ions was investigated. The best composition was 0.005 g calyx[6]arene-TiO2 in the carbon paste electrode with a scan rate of 0.5 V/s. The modified electrodes showed good performance for Cu2+ ion detection. Under optimum experimental conditions, a linear range for metal Cu(II) ions was from 0.1, 0.3, 0.5, 0.8, and 1.0 ppm with respective currents of 500, 550, 600, 700, and 800 µA. The limit of detection (LOD) for metal Cu2+ ions is found to be 0.022 ppm with a relative standard deviation (%RSD) of 0.011%.


2021 ◽  
Vol 11 (1) ◽  
Author(s):  
K. Chetankumar ◽  
B. E. Kumara Swamy ◽  
S. C. Sharma ◽  
S. A. Hariprasad

AbstractIn this proposed work, direct green 6 (DG6) decorated carbon paste electrode (CPE) was fabricated for the efficient simultaneous and individual sensing of catechol (CA) and hydroquinone (HY). Electrochemical deeds of the CA and HY were carried out by cyclic voltammetry (CV) and differential pulse voltammetry (DPV) at poly-DG6-modfied carbon paste electrode (Po-DG6-MCPE). Using scanning electron microscopy (SEM) studied the surface property of unmodified CPE (UCPE) and Po-DG6-MCPE. The decorated sensor displayed admirable electrocatalytic performance with fine stability, reproducibility, selectivity, low limit of detection (LLOD) for HY (0.11 μM) and CC (0.09 μM) and sensor process was originated to be adsorption-controlled phenomena. The Po-DG6-MCPE sensor exhibits well separated two peaks for HY and CA in CV and DPV analysis with potential difference of 0.098 V. Subsequently, the sensor was practically applied for the analysis in tap water and it consistent in-between for CA 93.25–100.16% and for HY 97.25–99.87% respectively.


Surfaces ◽  
2021 ◽  
Vol 4 (3) ◽  
pp. 191-204
Author(s):  
Edwin S. D’Souza ◽  
Jamballi G. Manjunatha ◽  
Chenthattil Raril ◽  
Girish Tigari ◽  
Huligerepura J. Arpitha ◽  
...  

A modest, efficient, and sensitive chemically modified electrode was fabricated for sensing curcumin (CRC) through an electrochemically polymerized titan yellow (TY) modified carbon paste electrode (PTYMCPE) in phosphate buffer solution (pH 7.0). Cyclic voltammetry (CV) linear sweep voltammetry (LSV) and differential pulse voltammetry (DPV) approaches were used for CRC detection. PTYMCPE interaction with CRC suggests that the electrode exhibits admirable electrochemical response as compared to bare carbon paste electrode (BCPE). Under the optimized circumstances, a linear response of the electrode was observed for CRC in the concentration range 2 × 10−6 M to 10 × 10−6 M with a limit of detection (LOD) of 10.94 × 10−7 M. Moreover, the effort explains that the PTYMCPE electrode has a hopeful approach for the electrochemical resolution of biologically significant compounds. Additionally, the proposed electrode has demonstrated many advantages such as easy preparation, elevated sensitivity, stability, and enhanced catalytic activity, and can be successfully applied in real sample analysis.


Proceedings ◽  
2021 ◽  
Vol 68 (1) ◽  
pp. 18
Author(s):  
Sutthima Sriprasertsuk ◽  
John R. Varcoe ◽  
Carol Crean

Reduced graphene oxide (rGO) fibre electrodes and their ability to sense paracetamol (as model drug) were studied. rGO was electrodeposited onto carbon fibre by two different approaches: potentiostatic deposition and cyclic voltammetry (CV) in the presence of graphene oxide solution. Carbon fibre electrodes coated with rGO (after five CV cycles) could sense paracetamol with an oxidation peak at 0.62 V (vs. Ag/AgCl). The limit of detection of this fibre sensor was found to be 36.3 µM with a linear range of 50–500 µM of paracetamol (R2 = 0.9901).


2002 ◽  
Vol 14 (1) ◽  
pp. 71-77 ◽  
Author(s):  
Wilson T. Lopes da Silva ◽  
Christine Thobie-Gautier ◽  
Maria O. O. Rezende ◽  
Nabil El Murr

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