Electrochemical Treatment of Graphene

2019 ◽  
Vol 799 ◽  
pp. 197-202
Author(s):  
Alexander Usikov ◽  
Mike Puzyk ◽  
Sergey Novikov ◽  
Iosif Barash ◽  
Oleg Medvedev ◽  
...  

Treatment of graphene/SiC dies in inorganic electrolytes (KOH, KCl and Na2SO4) is discussed. An electrochemical method based on the cyclic voltammetry in a conventional three-electrode cell with Ag/AgCl reference electrode, a platinum counter electrode, and the graphene/SiC dies as working electrode (anode) is used for the treatment. It was observed either partial oxidation of graphene or its complete dissolution with the formation of CO2. The treatment performed resulted in the deterioration of the graphene films and change of the graphene-die resistivity depending on the range of the scanning potential applied to the graphene/SiC dies.

2020 ◽  
Vol 24 (3) ◽  
pp. 39-54
Author(s):  
Kätlin Pitman ◽  
Jaak Nerut ◽  
Merlin Raud ◽  
Timo Kikas

AbstractThere is need to rapidly measure biochemical oxygen demand (BOD) to estimate organic pollution in wastewater. Biosensors are able to estimate BOD values within 5–30 minutes, but they have some limitations that can be overcome with biosensor-array. This work used sensor-array, which consists of 8 × 3 electrodes. The working electrode was inner Pt circle electrode, counter electrode was a Pt band electrode and the reference electrode was a silver wire. The potentiostat was used to record cyclic voltammetry and chronoamperometry. The pumping speed was set at 1.5 cm3 min−1 or higher, to avoid the interference. Next, sensor-array was tested to measure different oxygen amounts and calibrated accordingly. Lastly, Pseudomonas putida membranes were calibrated and used to estimate BOD value. The calibration gave linear range up to 85 mg L−1 of BOD and sensitivity from 0.0018 to 0.0068. Real industrial wastewater, from lignocellulosic bioethanol production, was used to test the biosensor-array. It underestimated BOD values from 8 to 37 %. This biosensor-array allows to measure BOD value in less than 15 minutes.


2014 ◽  
Vol 14 (2) ◽  
pp. 109-115
Author(s):  
Riyanto Riyanto ◽  
Ahmad Safarudin

Preparation and application of platinum composite microelectrode (PCM) for the routine analysis of acetaminophen in pharmaceutical products has been carried out. This electrode was prepare by Pt powder and PVC in 4 mL tetrahydrofuran (THF) solvent and swirled flatly to homogeneous followed by drying in an oven at 100 °C for 3 h. The mixture was placed in 0.5 cm diameter stainless steel mould and pressed at 10 ton/cm2. The cyclic voltammetry were performed in a three electrodes system using PCM as a working electrode, an Ag/AgCl (saturated KCl) as reference electrode and platinum wire as the counter electrode. Electroanalysis of acetaminophen was performed in 0.1 M H2SO4 as an electrolyte. The result of the study showed that the correlation of determination using PCM electrode for electroanalysis acetaminophen was R2 = 0.999. Precision, recovery, LOD and LOQ of the PCM towards acetaminophen were found to be 1.04%, 100.54%, 19.52 mg/L and 65.08 mg/L, respectively. As a conclusion, the methods can be used for routine analysis of acetaminophen in pharmaceutical product. Simplicity of sample preparation and use of low cost reagents are the additional benefit of this method.


Author(s):  
Alhasan H ◽  
Alahmadi N ◽  
Wadhawan J

Introduction: Chlorophyll is a light harvesting pigment, which absorbs light in the visible spectrum of sunlight and promotes electron transfer, Chlorophyllin (CHL) is One of the most important derivative molecules of chlorophyll. Nowadays, chlorophyll pigment and its derivatives are utilised in organic photosynthetic solar cells for their desirable photovoltaic properties. Cyclic voltammetry (CV) is an essential technique. It is extensively used to study electroactive species to interpret the intermediates of reactions, supply information about the thermodynamics of oxidation-reduction reactions and elucidate the kinetics of electron transfer reactions. Materials and Methods: Prior to the electrochemical study, the working gold (Au) electrode surface was prepared by immersing it in the various concentrations of chlorophyllin for a period time. The electrolyte was degassed by using N2 for approximately 30 minutes inside a Faraday cage before any electrochemical experiment was performed. A three electrode system was used with, Ag/AgCl as a reference electrode, graphiteas a counter and the working electrode (Au). Results and Discussion: As a route to develop new chemical systems for artificial photosynthesis, this work reports the effectiveness of different parameters in transferring electrons between chlorophyllin (CHL) pigment and the working electrode surface (gold). These parameters such as the adsorption time, the electrolyte nature and concentration and chlorophyllin concentration are investigated. The use of chlorophyllin as a redox mediator is examined, with a gold electrode being employed. The importance of gold electrode surface preparation in determining the mechanism of redox is described, and the environment of adsorption process of the different concentrations of chlorophyllin on the surface of the gold electrode has been elucidated in this study. Conclusiones: The electrochemical method showed that the cyclic voltammetry responses of studied adsorption chlorophyllin pigment on the gold electrode were more efficient. In addition, the redox reaction was successful electrochemically in aqueous solution thanthe organic solution. It was suggested that electrons reduce to the chlorophyllin pigment by adding active species in the bulk solution homogeneous transfer. Finally, detections of chl on spinach leaves using various methods are reported.


KOVALEN ◽  
2021 ◽  
Vol 7 (2) ◽  
pp. 109-120
Author(s):  
Rahmiani Gani ◽  
Syarifah Rabiatul Adawiah ◽  
Arfiani Nur

Hydrogen production by water electrolysis can be optimalized by improve the working electrode. Stainless steel as working electrode was coated with graphene and polyaniline by using cyclic voltammetry method with Ag/AgCl as reference electrode and Pt as counter electrode. Coated electrodes were characterized by SEM-EDS and cyclic voltammetry method. Furthermore, the synthesized electrode was applied for water electrolysis by adding 1- 5 g/L NaHCO3. The characterization data showed that Stainless steel/Graphene-Polyaniline electrode can be synthesized by using cyclic voltammetry. The coating process was conducted at sweeping rate 10 mV/s on voltage -0.2 to 0.8 V for 10 cycles. The voltammograms showed that the highest cathodic peak current of electrolysis obtained at 0.491 mA by addition 2 g NaHCO3 on SS/G-PANi0,5 electrode, and the highest anodic peak current obtained at 0.191 mA by addition 2 g NaHCO3 on SS/G-PANi0,5 electrode. Based on the overpotential data, the smallest average potential difference of H+ adsorption obtained by SS/G-PANi1,0 electrode, and the smallest average potential difference of H+ desorption obtained by SS/G-PANi0,5 electrode. Keywords: Stainless steel, hydrogen production, electroplating, electrocatalyst, electrolysis


Sensors ◽  
2022 ◽  
Vol 22 (2) ◽  
pp. 558
Author(s):  
Erican Santiago ◽  
Shailu Shree Poudyal ◽  
Sung Y. Shin ◽  
Hyeun Joong Yoon

A graphene oxide (GO)-based cortisol biosensor was developed to accurately detect cortisol concentrations from sweat samples at point-of-care (POC) sites. A reference electrode, counter electrode, and working electrode make up the biosensor, and the working electrode was functionalized using multiple layers consisting of GO and antibodies, including Protein A, IgG, and anti-Cab. Sweat samples contact the anti-Cab antibodies to transport electrons to the electrode, resulting in an electrochemical current response. The sensor was tested at each additional functionalization layer and at cortisol concentrations between 0.1 and 150 ng/mL to determine how the current response differed. A potentiostat galvanostat device was used to measure and quantify the electrochemical response in the GO-based biosensor. In both tests, the electrochemical responses were reduced in magnitude with the addition of antibody layers and with increased cortisol concentrations. The proposed cortisol biosensor has increased accuracy with each additional functionalization layer, and the proposed device has the capability to accurately measure cortisol concentrations for diagnostic purposes.


2014 ◽  
Vol 172 ◽  
pp. 105-116 ◽  
Author(s):  
Happiness V. Ijije ◽  
Richard C. Lawrence ◽  
Nancy J. Siambun ◽  
Sang Mun Jeong ◽  
Daniel A. Jewell ◽  
...  

The electrochemical deposition and re-oxidation of solid carbon were studied in CO32− ion-containing molten salts (e.g. CaCl2–CaCO3–LiCl–KCl and Li2CO3–K2CO3) at temperatures between 500 and 800 °C under Ar, CO2 or N2–CO2 atmospheres. The electrode reactions were investigated by thermodynamic analysis, cyclic voltammetry and chronopotentiometry in a three-electrode cell under various conditions. The findings suggest that the electro-reduction of CO32− is dominated by carbon deposition on all three tested working electrodes (Ni, Pt and mild steel), but partial reduction to CO can also occur. Electro-re-oxidation of the deposited carbon in the same molten salts was investigated for potential applications in, for example, direct carbon fuel cells. A brief energy and cost analysis is given based on results from constant voltage electrolysis in a two-electrode cell.


2010 ◽  
Vol 7 (3) ◽  
pp. 284-287
Author(s):  
Ani Mulyasuryani ◽  
Qonitah Fardiyah ◽  
Rizki Sugiri

The iodate-selective electrode based on the principle of precipitation reaction could be made by coating the platinum wire with silver iodate (AgIO3). In this research was carried out optimization the iodate-selective electrode using chitosan membrane as an AgIO3 support. The AgIO3 were added in the 2 mL 1% chitosan solution, is 0.5 to 2.5 % (w/v). The thickness of the membrane used is 6 to 12 µm. The electrode cell potential is measured against Ag/AgCl electrode as a reference electrode. The optimum electrode performance was at 2.0 % of AgIO3 with thickness a membrane of 10 µm. The iodate-selective electrode has a Nernstian factor is 52.96 mV/decade and a response time of 10 seconds. The concentration range was determined from 10-3 M to 10-1 M and the detection limit is 1.12 x 10-5 M.   Keywords:  Ion Selective Electrode, Iodate, Chitosan Membrane


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.


2020 ◽  
Vol 56 (27) ◽  
pp. 3879-3882 ◽  
Author(s):  
Xu Hun ◽  
Xiaoli Xiong ◽  
Jiawang Ding ◽  
Wei Qin

The photocurrent at a working electrode coated with a ZnSe/r-GO composite can be modulated by a polymeric membrane ion-selective electrode that works as a reference electrode.


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