scholarly journals Parallel 1024-ch Cyclic Voltammetry on Monolithic CMOS Electrochemical Detector Array

2019 ◽  
Author(s):  
Kevin A. White ◽  
Geoffrey Mulberry ◽  
Brian N. Kim

AbstractLarge-scale microelectrode arrays offers enhanced spatiotemporal resolution in electrophysiology studies.. In this paper, we discuss the design and performance of an electrochemical detector array which is capable of 1024-ch parallel cyclic voltammetry (CV) as well as other electrochemical measurements. The electrochemical detector is fabricated using a custom-designed CMOS chip which integrates both the circuity and on-chip microelectrode array, to operate and record from electrochemical measurements. For parallel 1024-ch recordings, 1024 capacitor-based integrating transimpedance amplifiers (TIA) are designed and integrated. The TIA design features the bipolar capabilities for measuring both negative and positive electrochemical currents due to reduction and oxidation of molecules. The resulted dynamic range of this TIA is −700 pA – 1968 pA. CV can be used to examine the quality of electrochemical electrodes by measuring the double-layer capacitance. Double-layer capacitance forms at the electrode-electrolyte interface and is a function of the effective area of the electrode. Thus, a contaminated electrode can have smaller effective area resulting in smaller double-layer capacitance. Using the parallel CV capability of the monolithic CMOS device, the double layer capacitance of all 1024 electrodes are simultaneously measured to examine the status of the electrodes’ surface in real time. The initial measurement of the electrode array showed a mean capacitance of 466 pF. After plasma treatment to remove contamination on the electrode’s surface, the increased capacitance was 1.36nF nearly tripling the effective surface area. We have successfully developed of 1024-ch electrochemical detector array using the monolithic CMOS sensor. The CV functionality was validated by measuring the double-layer capacitance of the on-chip electrode array. This method can accelerate the characterization of a massive electrode array before analytical experiments to provide well-controlled electrochemical electrodes, which is crucial in conducting reliable electrochemical measurements.

2021 ◽  
Author(s):  
Dulce M. Morales ◽  
Marcel Risch

Discovery of electrocatalytic materials for high-performance energy conversion and storage applications relies on the adequate characterization of their intrinsic activity, which is currently hindered by the dearth of a protocol for consistent and precise determination of double layer capacitance (C<sub>DL</sub>). Herein, we propose a seven-step method that aims to determine C<sub>DL</sub> reliably by scan rate-dependent cyclic voltammetry. The method considers three aspects that strongly influence the outcome of the analysis: measurement settings, data collection, and data processing. To illustrate the proposed method, two systems were studied: a resistor-capacitor electric circuit and a glassy carbon disk in an electrochemical cell. With these studies it is demonstrated that when any of the mentioned aspects of the procedure are neglected, substantial deviations of the results are observed with misestimations as large as 61% in the case of the investigated electrochemical system. Moreover, we propose allometric regression as a more suitable model than linear regression for the determination of C<sub>DL</sub> for both the ideal and the non-ideal systems investigated. We stress the importance of assessing the accuracy of not only highly specialized electrochemical methods, but also of those that are well-known and commonly used as it is the case of the voltammetric methods. The methodology proposed herein is not limited to the determination of C<sub>DL</sub>, but can be effectively applied to any other voltammetry-based analysis that aims to deliver quantitative results.


2017 ◽  
Vol 7 (2) ◽  
pp. 89
Author(s):  
Francisco Prieto Garcia ◽  
Judith Callejas Hernandez ◽  
Judith Prieto Mendez ◽  
Yolanda Marmolejo Santillan

<p><span lang="EN-US">Anode (Al and Fe) and cathode (graphite and Ti/RuO<sub>2</sub>) materials have been tested for electrocoagulation (EC) and purification of the acid whey. The electroactive areas (EA) of electrodes were calculated by the double layer capacitance method. Experiments were performed by cyclic voltammetry, chronoamperometry and polarization experiments. Among cathodic materials, the Ti/RuO<sub>2</sub> electrode showed higher EA (2167 cm<sup>2</sup>) than graphite (1560 cm<sup>2</sup>). The Fe anode was found more stable than Al with greater charge transfer carried out in less time. Correlation of these results with those obtained during preliminary tests confirmed high removals (79 %) in 8 h. For the Al electrode, 24 h were required to achieve efficiency of 49 %.</span></p>


2020 ◽  
Author(s):  
Dulce M. Morales ◽  
Marcel Risch

Discovery of electrocatalytic materials for high-performance energy conversion and storage applications relies on the adequate characterization of their intrinsic activity, which is currently hindered by the dearth of a protocol for consistent and precise determination of double layer capacitance (C<sub>DL</sub>). Herein, we propose a seven-step method that aims to determine C<sub>DL</sub> reliably by scan rate-dependent cyclic voltammetry. The method considers three aspects that strongly influence the outcome of the analysis: measurement settings, data collection, and data processing. To illustrate the proposed method, two systems were studied: a resistor-capacitor electric circuit and a glassy carbon disk in an electrochemical cell. With these studies it is demonstrated that when any of the mentioned aspects of the procedure are neglected, substantial deviations of the results are observed with misestimations as large as 61% in the case of the investigated electrochemical system. Moreover, we propose allometric regression as a more suitable model than linear regression for the determination of C<sub>DL</sub> for both the ideal and the non-ideal systems investigated. We stress the importance of assessing the accuracy of not only highly specialized electrochemical methods, but also of those that are well-known and commonly used as it is the case of the voltammetric methods. The methodology proposed herein is not limited to the determination of C<sub>DL</sub>, but can be effectively applied to any other voltammetry-based analysis that aims to deliver quantitative results.


2020 ◽  
Author(s):  
Dulce M. Morales ◽  
Marcel Risch

Discovery of electrocatalytic materials for high-performance energy conversion and storage applications relies on the adequate characterization of their intrinsic activity, which is currently hindered by the dearth of a protocol for consistent and precise determination of double layer capacitance (C<sub>DL</sub>). Herein, we propose a seven-step method that aims to determine C<sub>DL</sub> reliably by scan rate-dependent cyclic voltammetry. The method considers three aspects that strongly influence the outcome of the analysis: measurement settings, data collection, and data processing. To illustrate the proposed method, two systems were studied: a resistor-capacitor electric circuit and a glassy carbon disk in an electrochemical cell. With these studies it is demonstrated that when any of the mentioned aspects of the procedure are neglected, substantial deviations of the results are observed with misestimations as large as 61% in the case of the investigated electrochemical system. Moreover, we propose allometric regression as a more suitable model than linear regression for the determination of C<sub>DL</sub> for both the ideal and the non-ideal systems investigated. We stress the importance of assessing the accuracy of not only highly specialized electrochemical methods, but also of those that are well-known and commonly used as it is the case of the voltammetric methods. The methodology proposed herein is not limited to the determination of C<sub>DL</sub>, but can be effectively applied to any other voltammetry-based analysis that aims to deliver quantitative results.


2020 ◽  
Vol 20 (8) ◽  
pp. 4395-4402 ◽  
Author(s):  
Kevin A. White ◽  
Geoffrey Mulberry ◽  
Brian N. Kim

Author(s):  
Xiangdong Zeng ◽  
Kun Zhou ◽  
Shijie Xian ◽  
Linting Jiang

Abstract The extraction of double-layer capacitance (DLC) is proposed using the electrochemical impedance spectroscopy (EIS) technique. By the concept of the frequency-dependent DLC, the DLC of polyaniline (PANI)-coated platinum wire is separated from the total capacitance at different DC potentials. The high conducting oxidized PANI is less frequency dependent. The DLC at the frequency of 1 Hz is the same as that of separation from the faradic current by cyclic voltammetry technology, exhibiting S-shaped curve at different DC potential. The process of the oxidation of PANI during the electrochemical impedance measurement is similar to the diffusion control.


Nanophotonics ◽  
2019 ◽  
Vol 9 (8) ◽  
pp. 2377-2385 ◽  
Author(s):  
Zhao Cheng ◽  
Xiaolong Zhu ◽  
Michael Galili ◽  
Lars Hagedorn Frandsen ◽  
Hao Hu ◽  
...  

AbstractGraphene has been widely used in silicon-based optical modulators for its ultra-broadband light absorption and ultrafast optoelectronic response. By incorporating graphene and slow-light silicon photonic crystal waveguide (PhCW), here we propose and experimentally demonstrate a unique double-layer graphene electro-absorption modulator in telecommunication applications. The modulator exhibits a modulation depth of 0.5 dB/μm with a bandwidth of 13.6 GHz, while graphene coverage length is only 1.2 μm in simulations. We also fabricated the graphene modulator on silicon platform, and the device achieved a modulation bandwidth at 12 GHz. The proposed graphene-PhCW modulator may have potentials in the applications of on-chip interconnections.


Author(s):  
Maximilian Schalenbach ◽  
Yasin Emre Durmus ◽  
Shay A. Robinson ◽  
Hermann Tempel ◽  
Hans Kungl ◽  
...  

2021 ◽  
Vol 125 (10) ◽  
pp. 5870-5879
Author(s):  
Maximilian Schalenbach ◽  
Yasin Emre Durmus ◽  
Shay A. Robinson ◽  
Hermann Tempel ◽  
Hans Kungl ◽  
...  

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