The corrosion behavior of a 7075-T6 Aluminum Alloy sample (AA7075-T6) and a low-Carbon low-Manganese microalloyed dual-phase steel sample (MADPS) were studied by electrochemical impedance spectroscopy (EIS) and potentiodynamic polarization (PP). The galvanic corrosion resulting from their assembly within a dissimilar joint, was studied by the zero-resistance ammeter technique (ZRA). The tests were conducted at room temperature and pressure (Mexico City) using an aqueous solution of 3% NaCl as electrolyte (pH 5.3) and without deaereating the solution. All tests were repeated more than twice to check the reproducibility. Electrochemical impedance spectroscopy (EIS) and potentiodynamic polarization were conducted using a BioLogic VMP3 potentiostat with EC-Lab software. The samples were pasted to the side of an acrylic cell. Circular sections of 1 cm² on top of the samples were cut off from the cell to allow electrolyte contact. A typical three-electrode cell arrangement was used, with the samples connected as working electrode (WE), an Ag/AgCl (3.5 M KCl) electrode as the reference electrode (RE), and a platinum wire or mesh as counter electrode (CE). The samples were allowed to contact the electrolyte during 1 h before each electrochemical measurement to allow open circuit potential (OCP) stabilization. Impedance measurements were performed in the frequency range from 100 kHz to 10 mHz, with a 10 mV voltage amplitude from the OCP, acquiring the data at a resolution of 10 points per decade. Potentiodynamic polarization curves were carried out with a potential scanning rate of 0.5 mV/s from - 250 mV to +250 mV vs. (Ag/AgCl) to ensure steady-state conditions. The zero-resistance ammeter (ZRA) technique was conducted using the BioLogic VMP3 potentiostat. The galvanic couple was set in a coplanar configuration with the samples contacting each other along one of their sides. The samples were pasted to the bottom of the acrylic cell. The MADP-steel sample was connected as WE, while the AA was connected as CE, and an Ag/AgCl (3.8M KCl) was employed as RE (set at a height of 4 mm from the samples surface). The galvanic current and the galvanic potential were measured every 0.5 s during 4 h. The galvanic current was further divided by the electrode area to calculate the galvanic current density.