Numerical analyses on oxygen transport resistances in polymer electrolyte membrane fuel cells using a novel agglomerate model

Abstract

Characterizing oxygen transport resistances in different components of a polymer electrolyte membrane fuel cell (PEMFC) is essential to achieve better cell performance at high current under low Pt loading. In this work, a macroscopic three-dimensional model, together with a novel agglomerate model was proposed to analyze impacts of operating conditions on these resistances via limiting current strategy. By introducing a focusing factor obtained with lattice Boltzmann method at mesoscopic level, the structure-dependent local transport resistance in ionomer thin-film of the electrode was comprehensively captured and validated by existing experimental studies. Contributions of the cell components to the total transport resistance were dissected. Results show that the present agglomerate model could well reproduce the local transport behaviors of oxygen in catalyst layer by fully considering the detailed nanoscale diffusion and adsorption processes. A small mass fraction of oxygen was favored to minimize the relative deviation of the local transport resistance from its intrinsic one due to the water production and heat generation, which can reach 7% for the mass fraction of oxygen of 1%. Contribution of the in-plane diffusion of oxygen in the inactive electrode is around 1%. The total transport resistance increased with the absolute pressure, mainly due to the dominated molecular diffusion mechanism in gas channel and gas diffusion layer. Gas convection accounted for 26% of the oxygen transport resistance originated from gas channel. The transport resistance of catalyst layer increased significantly with the reduction of Pt loading, and decreased with relative humidity and operating temperature, particularly at high Pt loading.