Degradation Mechanism of an IrO2 Anode Co-Catalyst for Cell Voltage Reversal Mitigation under Transient Operation Conditions of a PEM Fuel Cell

Abstract

IrO 2 is the most stable oxygen evolution reaction (OER) catalyst in acidic media and it has been widely used as co-catalyst to mitigate cell reversal damages in the anode of PEM fuel cells (PEMFCs). In this study, a mechanistic understanding of the degradation of an IrO 2 anode co-catalyst under transient operation of a PEMFC is provided. Thermogravimetric analysis (TGA) in reductive atmosphere (3.3 vol.% H 2 /Ar) shows that IrO 2 is not stable in H 2 containing atmosphere at operational temperatures of PEMFCs. By conducting a series of physical-chemical and electrochemical analyses, it is proven that H 2 under the operating conditions in a PEMFC anode can chemically reduce a few outer monolayers of the surface of IrO 2 nanoparticles to metallic Ir. The metallic Ir formed on the IrO 2 surface can then dissolve during fuel cell start-up/shut-down (SUSD) cycles. At least part of the dissolved Ir species formed in the anode electrode are shown to diffuse through the membrane to the cathode electrode, where they lead to a deterioration of the oxygen reduction reaction (ORR) activity of the Pt cathode catalyst. The consequences of Ir dissolution on the cell reversal tolerance of the anode are also discussed.