Instability of Pt∕C Electrocatalysts in Proton Exchange Membrane Fuel Cells

Abstract

Equilibrium concentrations of dissolved platinum species from a Pt∕CPt∕C electrocatalyst sample in 0.5 M H2SO4H2SO4 at 80°C were found to increase with applied potential from 0.9 to 1.1 V vs reversible hydrogen electrode. In addition, platinum surface area loss for a short-stack of proton exchange membrane fuel cells (PEMFCs) operated at open-circuit voltage (∼0.95V)(∼0.95V) was shown to be higher than another operated under load (∼0.75V)(∼0.75V) . Both findings suggest that the formation of soluble platinum species (such as Pt2+Pt2+ ) plays an important role in platinum surface loss in PEMFC electrodes. As accelerated platinum surface area loss in the cathode (from 63 to 23m2∕gPt23m2∕gPt in ∼100h∼100h ) was observed upon potential cycling, a cycled membrane electrode assembly (MEA) cathode was examined in detail by incidence angle X-ray diffraction and transmission electron microscopy (TEM) to reveal processes responsible for observed platinum loss. In this study, TEM data and analyses of Pt∕CPt∕C catalyst and cross-sectional MEA cathode samples unambiguously confirmed that coarsening of platinum particles occurred via two different processes: (i) Ostwald ripening on carbon at the nanometer scale, which is responsible for platinum particle coarsening from ∼3∼3 to ∼6nm∼6nm on carbon, and (ii) migration of soluble platinum species in the ionomer phase at the micrometer scale, chemical reduction of these species by crossover H2H2 molecules, and precipitation of platinum particles in the cathode ionomer phase, which reduces the weight of platinum on carbon. It was estimated that each process contributed to ∼50%∼50% of the overall platinum area loss of the potential cycled electrode.