Abstract

Numerical simulation of a direct methanol fuel cell (DMFC) operating under discharging conditions is challenged by the difficulties in modeling of complicated liquid–gas two-phase flows and coupled electrochemical kinetics. Under open-circuit conditions, the net electrochemical reactions in the DMFC anode cease, but, owing to the methanol concentration difference between the anode and cathode, the mass transport of methanol remains, creating a mass transport process of methanol in a single-phase liquid flow with no electrochemical reactions in the DMFC anode. Consequently, an accurate simulation of mass transport of methanol under such open-circuit conditions becomes possible. In this work, we performed a 3D numerical simulation of mass transport of methanol in the DMFC anode under open-circuit conditions and obtained the mass flux of methanol through the porous layer for different values of permeability. We also measured the mass flux of methanol permeation from the anode flow field to the cathode under open-circuit conditions. The comparison between the numerical and measured mass flux of methanol made it possible to in situ determine the permeability of the typical commercial porous layer. Using this in situ determined permeability, we then investigated numerically the effect of methanol feed rates on mass transport and found that the in-plane under-rib convection plays an important role, even at low methanol feed rate, to make the reactant evenly distributed over the entire catalyst layer.

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