Universal Correlation between the Roughness Factor and PEMFC Performance Losses in Voltage Cycling Based Accelerated Stress Tests

Abstract

During operational lifetime, proton exchange membrane fuel cells (PEMFCs) suffer from high performance losses. For the year 2025, the U.S. Department of Energy (DoE) set the durability target for PEMFC light-duty transportation applications at 5,000 hours.1 To meet the automotive target, different aging protocols were established in order to simulate load cycle variations.2 It is well known that load or voltage cycling induces substantial catalyst degradation due to an increasing loss of electrochemically active surface area (ECSA), which is known to be a main driver for the resulting performance penalties.3 Thus, an increasing interest exists in developing accelerated stress test (AST) protocols that can sufficiently describe the degradation of the different components of a membrane electrode assembly (MEA) during automotive application using shorter measurement times.In this study, we report on a strategy to predict the performance degradation of an MEA, making use of a strongly accelerated voltage cycling based ASTs. For this, voltage cycling based ASTs were performed using 5 cm2 MEAs with a 0.1 mgPt cmMEA -2 loaded Pt/C catalyst (TEC10V20E, Tanaka) for both cathode and anode. Voltage cycling was done under H2/N2 (200/75 nccm) at 80 °C, 95% RH, and ambient pressure using square wave profiles with a constant lower potential limit (LPL) of 0.6 V and different upper potential limits (UPLs) of 0.85, 0.95, and 1.0 V, with LPL/UPL hold times of 1, 2, or 8 s. Full characterization of the MEA at beginning-of-life and after each set of voltage cycling intervals was performed by: i) measuring H2/O2 and H2/air polarization curves; ii) determining the ECSA by cyclic voltammetry and CO stripping; iii) conducting limiting current measurement to calculate the O2 transport resistance (R O2 total); and, iv) conducting electrochemical impedance spectroscopy (EIS) measurements under blocking conditions to quantify the proton conduction resistance in the cathode catalyst layer (R H+ cath).When the ECSA loss ranges between ≈20-85%, it was found that the ECSA decreases approximately linearly when plotted against the logarithm of the number of cycles (see fig. 1), exhibiting higher slopes for procedures with higher UPLs and longer hold times, in agreement with the results from previous studies.3, 4 In addition, a direct and AST protocol independent correlation between the loss in total available surface area, i.e., the roughness factor (rf ≡ ECSA × Pt-loading), and the individual loss contributions in H2/air performance curves, namely kinetic (mass/specific activity for the oxygen reduction reaction (ORR)) and O2 transport resistance contributions, was shown. This is due to the fact, that these individual voltage losses are not only highly affected by the cathode rf,3, 5 but that the Pt dissolution/redeposition mechanism seems to be identical for all of the here investigated voltage cycling ASTs, despite the largely varying UPLs and hold times. As a result, a universal correlation between the H2/air performance losses and the rf deterioration was found throughout all ASTs. The important corollary of this finding is that the data from quickly degrading voltage cycling ASTs (i.e., with high UPL) can be used to project the H2/air performance losses when cycling under less degrading conditions.