Description
The attached file is an updated version of a simple cyclic voltammetry (CV) simulator written in Microsoft Excel.^{1 }The spreadsheet supports up to four chemical species that can each undergo up to four redox processes. The calculations assume that the first process is a charge transfer. Experimental CVs with up to 10,000 data points can be copied/pasted into the spreadsheet for comparison to the simulation. The spreadsheet can be operated in protected mode or unprotected and modified as needed. The spreadsheet is provided with no guarantee and it may not be suitable for all applications. System requirements: Microsoft Windows 8.1 Office software or later. New version (v_18) uploaded to website on 9/21/19.
Potentials
List your formal redox potential (E^{o}') values in decreasing order if reduction occurs during the forward sweep.^{2 }Reverse this order if oxidation occurs during the forward sweep. Set the E^{o}' values of unused peaks beyond the switching potential (E_{2}) in the order noted above to exclude them from the model. Set the starting potential (E_{1}) value greater than the switching potential (E_{2}) if reduction occurs during the forward sweep. Reverse this order if oxidation occurs during the forward sweep.
Software updates
Incorporated separate diffusion coefficients for all subspecies on 9/20/19. Previous versions of this spreadsheet used “common” diffusion coefficients for members of the same redox couple to simplify the calculations. This update provides better control of the diffusion coefficients.
Improved the diffusion profile graphics on 6/4/19. The spreadsheet now automatically recognizes when symmetry in the model generates the same species on the forward and return sweeps and avoids graphing the same species twice.
Added a Total simulation graphic to the Import data page to help users optimize the background parameters on 5/31/18. First, copy/paste your experimental data into the Import data page. Then adjust the Offset parameter to zero the baseline of your CV. Next, click on the Species 1 tab to begin your simulation. You can then return to the Import data page at any time to optimize your Gain and Offset parameters based on your simulation.
Incorporated the Saul’yev RL variant to simulate Fick’s Second Law of Diffusion on 1/8/17. This method can calculate thinner reaction layers than the combined Taylor series that was used previously.^{3 }Reducing the variable x_{Scale}_{ }reduces the length of the diffusion grids and places the concentration points closer to the working electrode surface. However, using diffusion grids that are too short or long will distort your simulations, so adjust this parameter only as needed.
Separated the equations involving the number of electrons in the rate-determining step from the total number of electrons transferred on 12/22/16. The number of electrons in the rate-determining step (n_{a}) now controls the peak width.^{2} The total number of electrons transferred (n) now controls the total current.
Spreadsheet variables
Several variables from the original spreadsheet were renamed to incorporate new features. The following table describes the variables that are used in the newest version of the spreadsheet. Numbers in the spreadsheet that appear as subscripts in parentheses after a variable indicate which subspecies the variable is operating on.
Variable | Definition | Value and/or unit(s) |
Gain | Amplification factor for the experimental background | Unitless multiplier |
Offset | Constant added to the experimental current | A |
E^{o}ˊ | Formal potential for a redox couple | V |
n | Total number of electrons transferred per species (controls total peak area) | Unitless |
n_{a} | Number of electrons transferred in the rate determining step (controls peak width) | Unitless |
k^{o} | Standard heterogeneous rate constant for an electron transfer | cm/s |
a | Transfer coefficient for a redox couple | ≈ 0.5 (unitless) |
D | Diffusion coefficient for a subspecies | ≈ 1 x 10^{-5} cm^{2}/s |
C_{Bulk} | Concentration of the bulk solution | mol/cm^{3} |
E_{1} | Starting potential of the CV experiment | V |
E_{2} | Switching potential of the CV experiment | V |
v | Scan rate used during the CV experiment | V/s |
A | Surface area of the working electrode | cm^{2} |
T | Temperature of the sample during experiment | K |
x_{Scale} | Compress or expand x-axes of diffusion grids | Percentage (%) |
k_{R1} | Rate constant for a first-order homogeneous reaction that removes a species from electron transfer cycle | s^{-1} |
k_{R2} | Rate constant for second-order homogeneous reaction that removes a species from electron transfer cycle | cm^{3}/mol•s |
Bug report
Bug in the diffusion profile graphics was corrected on 6/26/19. Bug in the data selection process was corrected on 4/25/16. Bug in the Import data graphics corrected on 12/31/15. Bug in the concentration calculations of the 4^{th} redox couple oxidized form corrected on 12/8/15. Bug in the time increment calculations was corrected on 11/16/15.
References cited
1. J. H. Brown, J. Chem. Educ., 2016, 93 (7), 1326–1329. DOI: 10.1021/acs.jchemed.6b00052.
2. A. J. Bard, L. R. Faulkner, Electrochemical Methods: Fundamentals and Applications, Wiley: New York, 1980, ISBN: 0-471-05542-5.
3. D. Britz, Digital Simulation in Electrochemistry 3^{ed} ed., Springer: Berlin, 2010, ISBN: 978-3-642-06307-7.