Electrochemical impedance spectroscopy study of electron transfer at poly(3,4-ethylenedioxythiophene) containing gold nanoparticles coating

2011 ◽  
Vol 76 (12) ◽  
pp. 1433-1445
Author(s):  
Stelian Lupu

Electrochemical impedance spectroscopy (EIS) was used for characterization of electron transfer in various redox probes, such as the redox couple ferrocyanide-ferricyanide, ferrocene, ferrocenemethanol, and the poly(3,4-ethylenedioxythiophene) (PEDOT) conducting polymer containing gold nanoparticles. The PEDOT coating was deposited onto platinum (Pt) and glassy carbon (GC) electrodes by galvanostatic electrochemical polymerization from an aqueous solution containing 10–2 M EDOT and 10–1 M LiClO4 as supporting electrolyte. The PEDOT-Au nanoparticles composite coating was prepared by droplet deposition of Au nanoparticles on top of the Pt/PEDOT and GC/PEDOT modified electrodes. The pure PEDOT and PEDOT-Au nanoparticles composite coatings were investigated using EIS and cyclic voltammetry (CV) in 10–1 M LiClO4 solution containing various redox probes. The impedance spectra were recorded at the formal redox potential of the redox probes. The charge transfer resistance (Rct), solution resistance (Rs), exchange current density (i0), standard rate constant (k0), and double-layer capacitance (Cdl) were calculated from the EIS data.

Coatings ◽  
2021 ◽  
Vol 11 (2) ◽  
pp. 113
Author(s):  
Jacob Ress ◽  
Ulises Martin ◽  
Juan Bosch ◽  
David M. Bastidas

The protection of mild steel by modified epoxy coating containing colophony microencapsulated corrosion inhibitors was investigated in this study. The corrosion behavior of these epoxy coatings containing colophony microcapsules was studied by electrochemical analysis using cyclic potentiodynamic polarization and electrochemical impedance spectroscopy. The microcapsule coating showed decreased corrosion current densities of 2.75 × 10−8 and 3.21 × 10−8 A/cm2 along with corrosion potential values of 0.349 and 0.392 VSCE for simulated concrete pore solution and deionized water with 3.5 wt.% NaCl, respectively, indicating improved corrosion protection in both alkaline and neutral pH. Electrochemical impedance spectroscopy analysis also showed charge transfer resistance values over one order of magnitude higher than the control sample, corroborating the electrochemical corrosion potential and current density testing results. Overall, the use of colophony microcapsules showed improved corrosion protection in simulated concrete pore solution and DI water solutions containing chloride ions.


Sensors ◽  
2021 ◽  
Vol 21 (3) ◽  
pp. 788
Author(s):  
Hien T. Ngoc Le ◽  
Sungbo Cho

Aggregation of amyloid-β (aβ) peptides into toxic oligomers, fibrils, and plaques is central in the molecular pathogenesis of Alzheimer’s disease (AD) and is the primary focus of AD diagnostics. Disaggregation or elimination of toxic aβ aggregates in patients is important for delaying the progression of neurodegenerative disorders in AD. Recently, 4-(2-hydroxyethyl)-1-piperazinepropanesulfonic acid (EPPS) was introduced as a chemical agent that binds with toxic aβ aggregates and transforms them into monomers to reduce the negative effects of aβ aggregates in the brain. However, the mechanism of aβ disaggregation by EPPS has not yet been completely clarified. In this study, an electrochemical impedimetric immunosensor for aβ diagnostics was developed by immobilizing a specific anti-amyloid-β (aβ) antibody onto a self-assembled monolayer functionalized with a new interdigitated chain-shaped electrode (anti-aβ/SAM/ICE). To investigate the ability of EPPS in recognizing AD by extricating aβ aggregation, commercially available aβ aggregates (aβagg) were used. Electrochemical impedance spectroscopy was used to probe the changes in charge transfer resistance (Rct) of the immunosensor after the specific binding of biosensor with aβagg. The subsequent incubation of the aβagg complex with a specific concentration of EPPS at different time intervals divulged AD progression. The decline in the Rct of the immunosensor started at 10 min of EPPS incubation and continued to decrease gradually from 20 min, indicating that the accumulation of aβagg on the surface of the anti-aβ/SAM/ICE sensor has been extricated. Here, the kinetic disaggregation rate k value of aβagg was found to be 0.038. This innovative study using electrochemical measurement to investigate the mechanism of aβagg disaggregation by EPPS could provide a new perspective in monitoring the disaggregation periods of aβagg from oligomeric to monomeric form, and then support for the prediction and handling AD symptoms at different stages after treatment by a drug, EPPS.


2009 ◽  
Vol 2009 ◽  
pp. 1-15 ◽  
Author(s):  
Minna Toivola ◽  
Janne Halme ◽  
Lauri Peltokorpi ◽  
Peter Lund

Effects of aging and cyclically varying temperature on the electrical parameters of dye solar cells were analyzed with electrochemical impedance spectroscopy. Photoelectrode total resistance increased as a function of time due to increasing electron transport resistance in theTiO2film. On the other hand, photoelectrode recombination resistance was generally larger, electron lifetimes in theTiO2were film longer, and charge transfer resistance on the counter electrode was smaller after the temperature treatments than before them. These effects correlated with the slower deterioration rate of the temperature-treated cells, in comparison to the reference cells.


Chemosensors ◽  
2020 ◽  
Vol 8 (2) ◽  
pp. 27
Author(s):  
Georg Christoph Brunauer ◽  
Oliver Spadiut ◽  
Alfred Gruber ◽  
Christoph Slouka

Electrochemical impedance spectroscopy is a powerful tool in life science for cell and pathogen detection, as well as for cell counting. The measurement principles and techniques using impedance spectroscopy are highly diverse. Differences can be found in used frequency range (β or α regime), analyzed quantities, like charge transfer resistance, dielectric permittivity of double layer capacitance and in off- or online usage. In recent contributions, applications of low-frequency impedance spectroscopy in the α regime were tested for determination of cell counts and metabolic burden in Escherichia coli and Saccharomyces cerevisiae. The established easy to use methods showed reasonable potential in the lab scale, especially for S. cerevisiae. However, until now, measurements for cell counts in food science are generally based on Thoma cell counting chambers. These microscopic cell counting methods decelerate an easy and quick prediction of yeast viability, as they are labor intensive and result in a time delayed response signal. In this contribution we tested our developed method using low frequency impedance spectroscopy locally at an industrial brewery propagation site and compared results to classic cell counting procedures.


Energies ◽  
2019 ◽  
Vol 12 (23) ◽  
pp. 4507 ◽  
Author(s):  
Yusuke Abe ◽  
Natsuki Hori ◽  
Seiji Kumagai

Lithium-ion batteries (LIBs) using a LiFePO4 cathode and graphite anode were assembled in coin cell form and subjected to 1000 charge-discharge cycles at 1, 2, and 5 C at 25 °C. The performance degradation of the LIB cells under different C-rates was analyzed by electrochemical impedance spectroscopy (EIS) and scanning electron microscopy. The most severe degradation occurred at 2 C while degradation was mitigated at the highest C-rate of 5 C. EIS data of the equivalent circuit model provided information on the changes in the internal resistance. The charge-transfer resistance within all the cells increased after the cycle test, with the cell cycled at 2 C presenting the greatest increment in the charge-transfer resistance. Agglomerates were observed on the graphite anodes of the cells cycled at 2 and 5 C; these were more abundantly produced in the former cell. The lower degradation of the cell cycled at 5 C was attributed to the lowered capacity utilization of the anode. The larger cell voltage drop caused by the increased C-rate reduced the electrode potential variation allocated to the net electrochemical reactions, contributing to the charge-discharge specific capacity of the cells.


2014 ◽  
Vol 18 (08n09) ◽  
pp. 642-651 ◽  
Author(s):  
Audacity Maringa ◽  
Tebello Nyokong

We report on the electrodeposition of gold nanoparticles ( AuNPs ) on a glassy carbon electrode (GCE) followed by deposition of nickel tetrasulfonated phthalocyanine ( NiTSPc ) film by electropolymerization (poly- NiTSPc -GCE) to form Poly- NiTSPc / AuNPs -GCE. The presence of the gold nanoparticles caused a lowering of the anodic and cathodic peak separation (ΔE p ) of ferricyanide from 126 mV on poly- NiTSPc to 110 mV on poly- NiTSPc / AuNPs . The electrooxidation of nitrite improved on modified electrodes compared to GCE, with the latter giving E p = 0.78 V and the modified electrodes gave E p = 0.62 V or 0.61 V. Poly- NiTSPc / AuNPs -GCE had higher currents compared to poly- NiTSPc -GCE. This indicates the enhancement effect caused by the AuNPs . Electrochemical impedance spectroscopy and chronoamperometric studies also showed that poly- NiTSPc / AuNPs -GCE was a better electrocatalyst than poly- NiTSPc -GCE or AuNPs -GCE.


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