The efficiency of polymer electrolyte fuel cells is closely linked to effective heat and water management. Evaporation of water in the gas diffusion layers (GDL) is an important process influencing water management and can even be used for evaporative cooling. In this study, evaporation rates in Toray-GDL materials are obtained for different temperatures, gas flow rates, carrier gases and water saturation levels. Evaporation rates are correlated with water distribution profiles in the GDL, obtained using X-ray tomographic microscopy imaging. The influence of temperature on the evaporation rates is predicted by considering the effect of temperature on vapor diffusion alone. However, changing the carrier gas type points to a deviation from diffusive-driven vapor transport, which could be due to entrainment of gas inside the GDL, among other factors. © The Author ( Polymer electrolyte fuel cells (PEFC) efficiently convert the chemical energy stored in hydrogen to electrical energy, with water and heat as the byproducts. PEFCs are therefore considered a key technology for future hydrogen-based energy scenarios, especially in the mobility and energy storage sectors, as the usage of renewable electricity gains momentum worldwide. The central component of PEFCs is the membrane-electrode-assembly (MEA), which consists of a membrane at the center that is coated with catalyst layers (CL) on both sides, which are contacted by gas diffusion layers (GDL). Water management in the MEA is a critical topic that is closely related to power density and durability of PEFCs.1 Water management (i.e. having maximum water content in the membrane and a minimum saturation in the porous layers) is a complex issue governed by the fluid and energy flows in the MEA. Most of this complexity arises from the fluxes of heat and water in the GDLs, which are difficult to localize and quantify.Gas diffusion layers are porous structures with porosities in the range of 70-85% and average pore sizes around 10-40 μm.2 The GDL materials have to provide maximum heat and electron conductivity in the solid structure while simultaneously ensuring high permeability of the reactant gases, product water and water vapor in the void. At low operating-temperatures or high current densities, gas transport in the pore space can be significantly hindered by liquid water occupying pore space, especially at the cathode side. Consequently, oxygen transport to the cathode CL is significantly affected, which in turn reduces fuel cell performance or efficiency.