scholarly journals A Combinatorial Electrochemical Biosensor for Sweat Biomarker Benchmarking

2019 ◽  
Vol 25 (1) ◽  
pp. 25-32 ◽  
Author(s):  
Antra Ganguly ◽  
Paul Rice ◽  
Kai-Chun Lin ◽  
Sriram Muthukumar ◽  
Shalini Prasad
Keyword(s):  
Electrochemical Sensors ◽  
Electrochemical Impedance ◽  
Flexible Substrate ◽  
Chloride Ion ◽  
Charge Transfer Resistance ◽  
Open Circuit ◽  
Label Free ◽  
Transfer Resistance ◽  
Disease Biomarker ◽  
Sweat Chloride

Misclassification of an acute disease condition as chronic and vice versa by electrochemical sweat biomarker sensors can cause significant psychological, emotional, and financial stress among patients. To achieve higher accuracy in distinguishing between a chronic condition and an acute condition, there is a need to establish a reference biomarker to index the actual chronic disease biomarker of interest by combinatorial sensing. This work provides the first technological proof of leveraging the chloride ion content in sweat for a combinatorial sweat biomarker benchmarking scheme. In this scheme, the sweat chloride ion has been demonstrated as the reference/indexing biomarker, while sweat cortisol has been studied as the disease biomarker of interest. Label-free affinity biosensing is achieved by using a two-electrode electrochemical system on a flexible substrate suitable for wearable applications. The electrochemical stability of the fabricated electrodes for biosensing applications was studied by open-circuit potential measurements. Attenuated total reflectance–Fourier transform infrared spectroscopy spectra validate the crosslinker–antibody binding chemistry. Concentration-dependent analyte–capture probe binding induces a modulation in the electrical properties (charge transfer resistance and double-layer capacitance) at the electrode–sweat buffer interface, which are transduced by nonfaradaic electrochemical impedance spectroscopy (EIS). Calibration dose responses for the sensor for cortisol (5–200 ng/mL) and chloride (10–100 mM) detection were evaluated in synthetic (pH 6) and pooled human sweat ( R2 > 0.95). The variation in the cortisol sensor response due to fluctuations in sweat chloride levels and the significance of reporting normalized biomarker levels were demonstrated to further emphasize the need for biomarker benchmarking in electrochemical sensors.

Breast cancer detection using charge sensors coupled to DNA monolayer

2015 ◽  
Vol 1793 ◽  
pp. 19-26
Author(s):  
Marina R. Batistuti ◽  
Marcelo Mulato ◽  
Paulo R. Bueno
Keyword(s):  
Breast Cancer ◽  
Dna Sequence ◽  
Dna Sequences ◽  
Electrochemical Impedance ◽  
Redox System ◽  
Charge Transfer Resistance ◽  
Label Free ◽  
Self Assembled Monolayer ◽  
Transfer Resistance ◽  
Complementary Dna

ABSTRACTWe report the development of a label-free biosensors based on DNA hybridization, using cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS). This study uses DNA sequences based on microRNA related with breast cancer. The biosensor was fabricated by immobilizing a self-assembled monolayer of single-stranded 23-mer oligonucleotide (ssDNA) via a thiol linker on gold work electrodes. Residual binding places were filled with 6 -mercaptohexanol (MCH). The electrode was electrochemicaly characterized in the presence of a redox system ferri/ferrocyanide. Different concentrations of complementary DNA sequence for hybridization were incubated; an increase of charge transfer resistance (Rct) was observed, used as sensor parameter and correlated with concentrations of complementary DNA sequence. A debate was presented on the effect of the MgCl2 influence on ssDNA immobilization solution.

Effect of pyrite on the electrochemical behavior of chalcopyrite at different potentials in pH 1.8 H2SO4

2019 ◽  
Vol 43 (11-12) ◽  
pp. 493-502
Author(s):  
Qingyou Liu ◽  
Shuai Wang ◽  
Miao Chen ◽  
Yi Yang
Keyword(s):  
Electrochemical Impedance ◽  
Saturated Calomel Electrode ◽  
Surface Characteristics ◽  
Charge Transfer Resistance ◽  
Open Circuit ◽  
Electrochemical Dissolution ◽  
Passive Region ◽  
Transfer Resistance ◽  
Electrochemical Behaviors ◽  
Passive Resistance

Chalcopyrite is the most abundant, but also one of the most refractory, copper sources. One way to enhance chalcopyrite’s electrochemical dissolution is by mixing it with pyrite. To understand how and to what extent pyrite affects chalcopyrite’s electrochemical dissolution at different potentials, the electrochemical behaviors of chalcopyrite, pyrite, and chalcopyrite–pyrite couples in pH 1.8 H2SO4 were studied by potentiodynamic and electrochemical impedance spectroscopy. Potentiodynamic curves showed their different electrochemical reaction states and electrode surface characteristics. From open-circuit potential to 470 mV (vs saturated calomel electrode), chalcopyrite–pyrite was passivated with Cu1− xFe1− yS2 [Formula: see text]; from 470 to 580 mV, trans-passive dissolution occurred, and in the passive region, Cu1− xFe1− yS2 transformed into Cu1− x− zS2; from 580 to 700 mV was an active region; and a pseudo-passive region was formed with CuS when the potential was above 700 mV. The smaller charge transfer resistance and passive resistance, as well as the smaller inductive relaxation, revealed how and to what extent the coupled pyrite accelerated the electrochemical dissolution of chalcopyrite.

scholarly journals Multi-Leg TiO2 Nanotube Photoelectrodes Modified by Platinized Cyanographene with Enhanced Photoelectrochemical Performance

Catalysts ◽  
2020 ◽  
Vol 10 (6) ◽  
pp. 717 ◽  
Author(s):  
Mahdi Shahrezaei ◽  
Seyyed Mohammad Hossein Hejazi ◽  
Yalavarthi Rambabu ◽  
Miroslav Vavrecka ◽  
Aristides Bakandritsos ◽  
...  
Keyword(s):  
Charge Transfer ◽  
Recombination Rate ◽  
Electrochemical Impedance ◽  
Charge Transfer Resistance ◽  
Open Circuit ◽  
Transfer Time ◽  
Photoelectrochemical Performance ◽  
Transfer Resistance ◽  
Photocurrent Spectroscopy ◽  
Photogenerated Electrons

Highly ordered multi-leg TiO2 nanotubes (MLTNTs) functionalized with platinized cyanographene are proposed as a hybrid photoelectrode for enhanced photoelectrochemical water splitting. The platinized cyanographene and cyanographene/MLTNTs composite yielded photocurrent densities 1.66 and 1.25 times higher than those of the pristine MLTNTs nanotubes, respectively. Open circuit VOC decay (VOCD), electrochemical impedance spectroscopy (EIS), and intensity-modulated photocurrent spectroscopy (IMPS) analyses were performed to study the recombination rate, charge transfer characteristics, and transfer time of photogenerated electrons, respectively. According to the VOCD and IMPS results, the addition of (platinized) cynographene decreased the recombination rate and the transfer time of photogenerated electrons by one order of magnitude. Furthermore, EIS results showed that the (platinized) cyanographene MLTNTs composite has the lowest charge transfer resistance and therefore the highest photoelectrochemical performance.

The influence of membrane electrode assembly’s pressing on PEM fuel cell’s performance

2021 ◽  
Vol 0 (0) ◽  
Author(s):  
Federico Perdomo ◽  
Matilde Abboud ◽  
Erika Teliz ◽  
Fernando Zinola ◽  
Verónica Díaz
Keyword(s):  
Electrochemical Impedance ◽  
Linear Sweep Voltammetry ◽  
Membrane Electrode Assembly ◽  
Charge Transfer Resistance ◽  
Open Circuit ◽  
Polymeric Membrane ◽  
Membrane Electrode ◽  
Transfer Resistance ◽  
Supported Platinum Catalysts ◽  
Different Temperatures

Abstract The performance of a fuel cell depends on multiple factors, one of the most important being the preparation of the membrane electrode assembly (MEA). In the present work, MEAs constituted by gas diffuser electrodes (GDE) were pressed with carbon supported platinum catalysts. As solid electrolyte, a commercial polymeric membrane from Nafion was used, which was pressed at two GDE with loads of 5 and 1.5 mg/cm2 of catalyst at different temperatures and pressures for a fixed period of time. The assembly was characterized electrochemically using linear sweep voltammetry and electrochemical impedance spectroscopy at three different potentials. Also, the behavior when reversing the supply of hydrogen and oxygen to the GDE was studied. The results of the study showed a great dependence of the charge transfer resistance with the temperature, being secondary the dependence with the pressure in the range of temperature and pressure analyzed. Likewise, changes were observed in the open circuit potential after varying the temperature, pressure and catalyst load, hence affecting its maximum power and efficiency at that point.

Improved photovoltaic properties of nano-flake-based mesoporous dip-SILAR prepared BiOI electrochemical cell by tuning post-annealing treatment time at 100°C

2021 ◽  
Vol 06 ◽  
Author(s):  
MD Matiur Rahman ◽  
Shinya Kato ◽  
Tetsuo Soga
Keyword(s):  
Annealing Time ◽  
Treatment Time ◽  
Electrochemical Impedance ◽  
Short Circuit ◽  
Annealing Treatment ◽  
Charge Transfer Resistance ◽  
Open Circuit ◽  
Photovoltaic Properties ◽  
Transfer Resistance ◽  
Post Annealing

Background: This research article reports on the post-annealing treatment time effect on the dip-successive ionic layer adsorption and reaction (SILAR) prepared nano-flake-based mesoporous BiOI electrochemical cell's photovoltaic properties. Objective: Our study clarifies that the post-annealing time has a significant impact on the photovoltaic behavior and the nano-flake morphology. Methods: At 100°C for 90mins post-annealing treatment condition, the surface morphology converted into a connected uniform crystallized flaky structure, which improves the effective surface area and reduces the BiOI/ electrolyte charge transfer resistance confirmed via electrochemical impedance spectroscopy (EIS) analysis. Therefore, the maximum photovoltaic properties (short-circuit current density, Jsc = 1.83mA/cm2, open-circuit voltage, Voc = 0.48V and efficiency = 0.28%) have been observed. However, without annealing and beyond 90mins of post-annealing time, the film quality and crystallinity decreased as a consequence of photovoltaic properties the degraded. Results and Conclusion: So, our investigation finding is 90mins is the optimal post-annealing treatment duration for the dip-SILAR prepared nano-flake-based mesoporous BiOI electrochemical photovoltaic cell at 100°C post-annealing temperature.

scholarly journals Preparation of Nano-Ag-TiO2 Composites by Co-60 Gamma Irradiation to Enhance the Photocurrent of Dye-Sensitized Solar Cells

2019 ◽  
Vol 2019 ◽  
pp. 1-8
Author(s):  
Le Thanh Nguyen Huynh ◽  
Viet Hai Le ◽  
Thanh Long Vo ◽  
Thi Kim Lan Nguyen ◽  
Quoc Hien Nguyen ◽  
...  
Keyword(s):  
Solar Cells ◽  
Charge Transfer ◽  
Electrochemical Impedance ◽  
Dye Sensitized Solar Cells ◽  
Energy Conversion Efficiency ◽  
Charge Transfer Resistance ◽  
Open Circuit ◽  
Transfer Resistance ◽  
Dye Sensitized ◽  
Sensitized Solar Cells

Nano-silver-titanium dioxide (Ag-TiO2) composites were prepared from commercial TiO2 (P25, Degussa) and silver nitrate (AgNO3) by gamma Co-60 irradiation method with various initial concentrations of AgNO3. The nano-AgTiO2 composites are utilized as the photoanode for dye-sensitized solar cells (DSCs). Under full sunlight illumination (1000 W/m2, AM 1.5), the efficiency of DSCs has improved significantly despite the Ag content of below 1%. The DSC—assembled with 0.75 Ag-TiO2 (0.75% Ag) photoanode—showed that the photocurrent was significantly enhanced from 8.1 mA.cm−2 to 9.5 mA.cm−2 compared to the DSCs using bared TiO2 photoanode. The unchanged open-circuit voltage resulted in the overall energy conversion efficiency to be increased by 25% from 3.75% to 4.86%. Electrochemical impedance spectroscopy (EIS) analysis showed that the charge transfer resistance is reduced when increasing Ag content, demonstrating that the charge transfer at TiO2/dye interface was enhanced in the presence of silver nanoparticles.

Quantitative Determination of Triiodothyronine by Electrochemical Impedance Spectroscopic Biosensor Using Gold Nanoparticle-Modified Electrode

2020 ◽  
Vol 20 (11) ◽  
pp. 7163-7168
Author(s):  
Huynh Vu Nguyen ◽  
Anna Go ◽  
Min-Ho Lee
Keyword(s):  
Quantitative Determination ◽  
Gold Nanoparticle ◽  
Modified Electrode ◽  
Electrochemical Impedance ◽  
Low Cost ◽  
Charge Transfer Resistance ◽  
Impedance Change ◽  
Label Free ◽  
Transfer Resistance

A label-free electrochemical impedimetric immunosensor for the detection of Triiodothyronine—a thyroid hormone that functions as the biomarker for monitoring for thyroid dysfunction was developed. The gold nanoparticle-modified electrode was employed to achieve the sensitive determination of Triiodothyronine at a low concentration level. The gold nanoparticle layer on the gold electrode was generated by chronoamperometry method and its resulting characteristics were investigated by scanning electron microscopy. Redox probe [Fe(CN)6]3−/4− and electrochemical impedance spec-troscopy was used for both evaluation of the immobilization of anti-Triiodothyronine antibody on the electrode surface and quantitative determination of target Triiodothyronine in different concentrations. The electrode with absorbed antibodies showed significant changes in charge transfer resistance upon binding the antigen, which resulted in an increase in normalized impedance change as the addition of antigen concentrations over a dynamic linear range of 0.01–100 ng/ml. These results indicated that the proposed immunosensor could be a potential alternative method for determination of Triiodothyronine in clinics with the advantage of low cost and less time-consuming.

scholarly journals An Electrochemical Immunosensor Based on a Self-Assembled Monolayer Modified Electrode for Label-Free Detection of α-Synuclein

Sensors ◽  
2020 ◽  
Vol 20 (3) ◽  
pp. 617 ◽  
Author(s):  
Chuang-Ye Ge ◽  
Md. Mahbubur Rahman ◽  
Wei Zhang ◽  
Nasrin Siraj Lopa ◽  
Lei Jin ◽  
...  
Keyword(s):  
Dynamic Range ◽  
Electrochemical Impedance ◽  
Charge Transfer Resistance ◽  
Label Free ◽  
Serum Samples ◽  
Self Assembled Monolayer ◽  
Electrochemical Impedance Spectra ◽  
Transfer Resistance ◽  
Label Free Detection ◽  
Self Assembled

This research demonstrated the development of a simple, cost-effective, and label-free immunosensor for the detection of α-synuclein (α-Syn) based on a cystamine (CYS) self-assembled monolayer (SAM) decorated fluorine-doped tin oxide (FTO) electrode. CYS-SAM was formed onto the FTO electrode by the adsorption of CYS molecules through the head sulfur groups. The free amine (–NH2) groups at the tail of the CYS-SAM enabled the immobilization of anti-α-Syn-antibody, which concurrently allowed the formation of immunocomplex by covalent bonding with α-Syn-antigen. The variation of the concentrations of the attached α-Syn at the immunosensor probe induced the alternation of the current and the charge transfer resistance (Rct) for the redox response of [Fe(CN)6]3−/4−, which displayed a linear dynamic range from 10 to 1000 ng/mL with a low detection limit (S/N = 3) of ca. 3.62 and 1.13 ng/mL in differential pulse voltammetry (DPV) and electrochemical impedance spectra (EIS) measurements, respectively. The immunosensor displayed good reproducibility, anti-interference ability, and good recoveries of α-Syn detection in diluted human serum samples. The proposed immunosensor is a promising platform to detect α-Syn for the early diagnose of Parkinson’s disease, which can be extended for the determination of other biologically important biomarkers.

Study on Cu Passivation Film’s Forming Condition in HEDP Electrolyte with BTA and Chloride Ion

2013 ◽  
Vol 274 ◽  
pp. 471-474 ◽  
Author(s):  
Jin Hu Wang ◽  
Wen Jie Zhai
Keyword(s):  
Electrochemical Impedance ◽  
Processing Condition ◽  
Linear Sweep Voltammetry ◽  
Chloride Ion ◽  
Charge Transfer Resistance ◽  
Threshold Potential ◽  
Transfer Resistance ◽  
Passivation Film ◽  
Anodic Potential ◽  
Cu Passivation

The influence of corrosion inhibitor BTA, chloride ion and anodic potential on the formation of copper passivation film was studied in the electrolyte of 18wt% HEDP by using Linear Sweep Voltammetry (LSV) and electrochemical impedance spectroscopy (EIS). The results show that the increase of BTA concentration contributes to the formation of surface passivation film, and the chloride ion can promote the formation of the Cu passivation film at low concentrations but break it down when its concentration exceeds a certain limit. For each electrolyte there is a threshold anodic potential maintaining good passivation: the interfacial charge transfer resistance increases with the anodic potential when it is below the threshold potential and decreases when it is above the threshold potential. Smooth surface can be obtained by ECMP at the optimal processing condition.

scholarly journals Galvanic Corrosion Study between Tensile-Stressed and Non-Stressed Carbon Steels in Simulated Concrete Pore Solution

Metals ◽  
2022 ◽  
Vol 12 (1) ◽  
pp. 98
Author(s):  
Zheng Dong ◽  
Chuanqing Fu ◽  
Amir Poursaee
Keyword(s):  
Charge Transfer ◽  
Tensile Stress ◽  
Electrochemical Impedance ◽  
Pore Solution ◽  
Charge Transfer Resistance ◽  
Open Circuit ◽  
Carbon Steels ◽  
Cyclic Polarization ◽  
Transfer Resistance ◽  
Low Frequencies

The present study investigated the galvanic effect between tensile-stressed and non-stressed carbon steels, in addition to the influence of the tensile stress on the passivation and corrosion behavior of steel in a simulated concrete pore solution. Three different levels of tensile stress, ranging from elastic to plastic stress on the surface, were applied by adjusting the displacement of C-shape carbon steel rings. Different electrochemical measurements including the open circuit potential (OCP), the electrochemical impedance spectroscopy (EIS), the zero-resistance ammetry (ZRA), and the cyclic polarization were performed. Based on the results of EIS, the tensile stress degraded the resistance of the oxide film in moderate frequencies while enhancing the charge transfer resistance in low frequencies during passivation. As corrosion propagated, the stressed steel yielded a similar charge transfer resistance to or an even lower charge transfer resistance than the non-stressed steel, especially in the case of plastic tensile stress. The galvanic effect between the tensile-stressed and non-stressed steels increased the chloride threshold value of the tensile-stressed steel, although the susceptibility to pitting corrosion was exhibited after being corroded.

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