Implementing iridium oxide (IrO x) nanocatalysts can be a major breakthrough for oxygen evolution reaction (OER), the limiting reaction in polymer electrolyte membrane water electrolyser devices. However, this strategy requires developing a support that is electronically conductive, is stable in OER conditions, and features a large specific surface area and a porosity adapted to gas-liquid flows. To address these challenges, we synthesized IrO x nanoparticles, supported them onto doped SnO 2 aerogels (IrO x /doped SnO 2), and assessed their electrocatalytic activity towards the OER and their resistance to corrosion in acidic media by means of a flow cell connected to an inductively-coupled mass spectrometer (FC-ICP-MS). The FC-ICP-MS results show that the long-term OER activity of IrO x /doped SnO 2 aerogels is controlled by the resistance to corrosion of the doping element, and by its concentration in the host SnO 2 matrix. In particular, we provide quantitative evidence that Sb-doped SnO 2 type supports continuously dissolve while Tadoped or Nb-doped SnO 2 supports with appropriate doping concentrations are stable under acidic OER conditions. These results shed fundamental light on the complex