Hydrogen fuel cells are an essential source of electrical energy for heavy-duty mobile applications. However, before being assembled into vehicles, they must undergo conditioning procedures to ensure optimal performance. The conditioning process is especially interesting for automotive manufacturers as it can improve the performance of fuel cell stacks to meet their required rated power without the need to change materials. Voltage recovery (VR) is an electrochemical process referring to a (re-)conditioning of the fuel cell's electrode. [1][2][3] This step is typically carried out during initial conditioning and durability testing to recover any reversible losses before performance testing. The term "recovery" used in this work refers explicitly to the in situ electrochemical conditioning of the fuel cell electrode to remove possible surface oxides (Pt-O) and impurities (e.g., sulfonate anions or solvents from the fabrication process). [2] There are several approaches for VR used on perfluorinated sulfonic acid (PFSA)based fuel cells, including 1) high current density operation under elevated temperatures and high back pressure, [4] 2) low potential (<0.2 V) at low temperature and oversaturated conditions, [1,[5][6][7] 3) current/voltage/reactant cycling/pulses, [8,9] 4) air braking/cathode starvation, [10] and 5) hydrogen pumping, [11] and combinations of these methods. [12,13] To achieve optimal fuel cell performance, selecting an appropriate recovery procedure is crucial. For fuel cells that use PFSA membranes and ionomers, VR procedures at very low cell voltages (<0.3 V) have been found to be effective in improving performance. The potential explanations range from surface oxide or contaminant removal to the restructuring of the membrane and electrode ionomer. [1,5] Low cell voltages are believed to facilitate the desorption of sulfonate anions (SO 3 À ) from catalyst sites, [6,14] which can impede the oxygen reduction reaction (ORR) and lead to lower kinetic activity and performance. [4] Oversaturated conditions, combined with higher water production rates at low potentials under H 2 /air, can lead to "flooding" of the catalyst layer, which can help reduce the adsorption of sulfonate groups on the catalyst surface. In addition to maximizing the performance, it is essential to reduce the conditioning duration to ramp up fuel cell production. [2] For more information on various VR conditions and their corresponding mechanisms, readers are directed to excellent review articles by Kocha and Pollet, [2] Christmann et al., [3] Choo et al., [6] and Mitzel et al. [4]