We studied proton exchange membrane fuel cell membrane electrode assemblies ͑MEAs͒ degradation after fuel-cell operation. Anode and cathode pronounced degradation was monitored by chemical ͓energy dispersive spectrometry ͑EDS͒, X-ray photoelectron spectroscopy ͑XPS͔͒, physical ͓scanning electron microscopy ͑SEM͒, transmission electron microscopy͔, and electrochemical ͑ultramicroelectrode with cavity͒ techniques. Aged MEAs underwent severe redistribution of most elements ͑Pt, C, F͒, coupled to a dramatic change of Pt particles shape, mean particle size and density over the carbon substrate. Among the various scenarios for Pt redistribution, Pt dissolution into Pt z+ species and transport in the ionomer or the proton exchange membrane play important roles. The Pt z+ dissolution/transport is likely favored by activators/ligands ͑For SO x -containing species͒ originating from the alteration of the polymers contained in the MEA. From SEM observations, the source of Pt z+ species is the cathode, while EDS and XPS show some SO x -and F-containing species origin from the anode. Local chemical analyses ͑SEM-EDS and XPS͒ revealed the excess Pt monitored in aged MEAs is associated with F excess. For instrumental limitation concerns, we could not detect the S element, but SO x -containing species could also act as counter ions during Pt z+ transport within the MEA. Pt corrosion/ redistribution is associated with the decrease of Pt-active area as revealed by CO ad -stripping voltammograms.