“…Prior to all electrochemical measurements and accelerated degradation tests (ADTs), the electrolyte was de-aerated by purging with Ar, the supported monometallic Pt NPs were cleaned by potential cycling between 0.05 VRHE and 1.20 VRHE at a scan rate of 500 mV s -1 until a stable cyclic voltammograms (CVs) could be observed, the supported PtxIry alloy NPs and Pt -IrO2 nanocomposites were cleaned by potential cycling between 0.10 VRHE and 0.30 VRHE at a scan rate of 100 mV s -1 for 20 cycles (in order not to oxidize Ir to obtain the exact value of the ECSA originating from Pt as well as Ir; once Ir is oxidized, the CO stripping method for the Ir ECSA determination does not work as Ir oxide does not adsorb CO). 38 After cleaning, for each bimetallic catalyst layer the following automized measurement procedure was applied using a macro-script of the potentiostat software: CO stripping, Ir oxidation, CO stripping, ORR activity determination, OER activity determination, ADT treatment, ORR activity determination, OER activity determination, CO stripping. The activities are determined with respect to the metal mass (mass activity (MA)) as well as with respect to the electrochemically active surface area (specific activity (SA)).…”