This work investigates various commercially available austenitic stainless steels and Ni-based alloys as possible metallic bipolar plates for high-temperature polymer electrolyte fuel cells (HT-PEFCs). The dynamic formation and depletion of passivation layers that depends strongly on applied potential was analyzed in 85 wt% phosphoric acid at RT and 130 • C by means of cyclic voltammetry and steady-state polarization. All materials showed a beneficial passivation in the potential window 0.3-1.2 V, which is mainly based on a stable inner Cr 2 O 3 layer, and a reduction of the passive layers at cathodic polarization. Alloy 2.4869 (Cronix 80) with 80 wt% Ni and 20 wt% Cr reveals the lowest corrosion rates of 16.1 μA cm −2 at 130 • C in the passive region at 0.6 V and a free corrosion potential E cor of 235 mV. The improvement of passivity was achieved by the dominant superficial Ni 3 (PO 4 ) 2 layer. Alloying additions Mo and Ti revealed a characteristic increase of passive current densities due to instability of these passivation components at 130 • C. Passivation based on Fe oxides and phosphates in stainless steels shows to be beneficial at RT, but less efficient at 130 • C.High-temperature polymer electrolyte fuel cells (HT-PEFCs) operate in the range of 120-180 • C and currently employ phosphoric acid doped polybenzimidazole membranes. This in turn represents a quite aggressive environment for the components of a fuel cell. Presently, bipolar plates are made of graphitic composite materials. Significant drawbacks are the apparent corrosion rates, a high effort of manufacturing and the uptake of phosphoric acid. Previous studies have demonstrated a wide range of corrosion current densities for different types of graphite up to the level of 1 mA cm −2 in ∼100 wt% H 3 PO 4 at 185-200 • C depending strongly on polarization, amount of binders or resins and heat-treatment.