Potentiodynamic and cyclic polarization scans are electrochemical experiments used to study corrosion. A potentiodynamic scan sweeps the potential across a range and measures the current response, revealing characteristics like the corrosion potential and passivation region. A cyclic polarization scan additionally reverses the potential sweep, exposing changes to the surface from the initial reactions. The scans can detect low currents precisely and identify phenomena like pitting corrosion and repassivation from the current-potential curves.
Potentiodynamic and cyclic polarization scans are electrochemical experiments used to study corrosion. A potentiodynamic scan sweeps the potential across a range and measures the current response, revealing characteristics like the corrosion potential and passivation region. A cyclic polarization scan additionally reverses the potential sweep, exposing changes to the surface from the initial reactions. The scans can detect low currents precisely and identify phenomena like pitting corrosion and repassivation from the current-potential curves.
Potentiodynamic and cyclic polarization scans are electrochemical experiments used to study corrosion. A potentiodynamic scan sweeps the potential across a range and measures the current response, revealing characteristics like the corrosion potential and passivation region. A cyclic polarization scan additionally reverses the potential sweep, exposing changes to the surface from the initial reactions. The scans can detect low currents precisely and identify phenomena like pitting corrosion and repassivation from the current-potential curves.
A quite popular experiment performed with Gamry A cyclic polarization scan is performed like a Instruments’ potentiostats is the Potentiodynamic Scan potentiodynamic scan, but with an addition: the voltage and its sibling, Cyclic Polarization. These experiments is swept across a range, but then reversed back to the are often used to study corrosion at a surface. This starting potential. This allows a return to the original Application Note examines these two types of potential. The surface is likely to be changed by the experiments. See our Application Note “Getting Started reactions during the scan, so often the data from the with Electrochemical Corrosion Measurement” for the return voltage sweep do not superimpose upon the data basics. Potentiodynamic scans are discussed in the from the forward sweep. ASTM G59 standard, while cyclic polarization scans are discussed in the ASTM G61 standard. Scanning Parameters The ASTM method recommends a scan rate of 0.1667 Potentiodynamic Method mV/s. Faster scan rates often result in distorted data, In this type of scan, the potential drives the reaction at because the sample cannot remain relatively stable. the anode or cathode. What we observe is the overall change in the rate of reaction (the current). That is, the Data potentiostat records the applied current to the cell that A typical set of potentiodynamic data may be plotted provides the increase in potential. The potential where like this (Figure 2): the total anodic current equals the total cathodic current is the open-circuit potential (Eoc). (See Figure 1.)
Fig. 2. Potentiodynamic scan of 430 stainless steel alloy
in 1 N H2SO4.
Interestingly, the independent variable (potential) is
plotted on the vertical axis, while the dependent Fig. 1. Corrosion process showing anodic and cathodic variable (measured current) is on the horizontal axis. components of total current. This scan of a stainless-steel sample in sulfuric acid can be interpreted as follows: The potential is swept across a range and the current is measured. For an anodic scan, researchers often start slightly cathodic of the open-circuit potential, and for a cathodic scan, the starting point is often slightly anodic. Figure 5 demonstrates no pitting:
Fig. 5. Cyclic polarization showing no pitting.
Fig. 3. Various important potentials, currents, and regions indicated by colors, from Fig. 2. Another cyclic polarization plot (Figure 6) reveals pitting without repassivation: As the voltage is increased from about –550 mV, the current drops in the cathodic region (purple) to a minimum at the Ecorr, then rises again in the activity region (green) where oxidation of the metal occurs. A maximum is reached at the passivation potential, Epp. The current drops again in the transition region (yellow) and then remains at a fairly constant, low level in the passivity region (pink). Breakdown of the surface, which may be pitting or dissolution at the surface, initiates just above 600 mV. Note the area around Ecorr, which is similar to the Fig. 6. Cyclic polarization showing pitting without (expanded) idealized view in Figure 1. repassivation. Gamry Instruments’ potentiostats are sensitive enough to detect current down to picoamperes, as shown in Figure Yet another cyclic polarization data set (Figure 7) with 4. pitting and repassivation:
Fig. 4. Low-current potentiodynamic sweep of
austentitic stainless steel in de-aerated seawater using a Fig. 7. Pitting and repassivation seen in a sample Gamry Instruments Reference 600+™. undergoing cyclic polarization.
In Figure 4, there is no major electrochemical activity on
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