Differential Pulse Voltammetry (DPV)
Differential pulse voltammetry performs a potential scan using constant-amplitude pulses superimposed on a stepped potential baseline. The current is measured continuously at a high sampling rate to capture the electrochemical response.
Optional OCV measurement and start ramp features ensure safe operation of the test specimen, with customizable scan rates for the initial ramp phase. Integration times for both pulse and step currents can be optimized during post-measurement analysis.
Parameter Description
Parameter |
Name |
Description |
Unit |
|---|---|---|---|
E start |
start potential |
starting DC potential |
V |
E step |
step potential |
potential of each step for the staircase function |
V |
E pulse |
pulse potential |
potential of each pulse added to the staircase potenial |
V |
E end |
end potential |
maximum DC potential of the last step and pulse |
V |
t settle |
settle time |
settling time at E start before the first DPV step and pulse is stimulated |
s |
t step |
step duration |
duration of each step of the staircase |
s |
t pulse |
pulse duration |
duration of each pulse |
s |
I range |
current range |
expected maximum absolute current value for fixed current range selection (autoranging is disabled) |
A |
ODR |
output data rate |
number of measurement points per second |
\(\frac{1}{s}\) |
I min |
minimum current |
minimum current limit for premature determination |
A |
I max |
maximum current |
maximum current limit for premature determination |
A |
A Start Phase Potentiostatic can be enabled or disabled before the method is executed.
Measurement Result
The measurement records voltage and current as functions of time, with specific sampling at two critical points: immediately before pulse application and at the end of each pulse. The integration times for both pulse and step currents can be adjusted later in the Zahner Analysis software. The difference between these current measurements is plotted against potential, creating a derivative-like response compared to linear sweep or normal pulse voltammetry.
This differential approach produces characteristic peak-shaped curves, where peak height typically correlates directly with analyte concentration in solution. Integration times for current sampling can be fine-tuned during data analysis to optimize signal quality and analytical precision.
Note
Important: The peak potential does not correspond to the redox potential! The relationship is: E peak = E½ - E pulse / 2, where E½ is the formal potential.
Custom Experiment Builder
This experiment is a combination of the following blocks: