Ceramic carbon electrodes (CCEs) have demonstrated their ability to function as proton exchange membrane fuel cell electrodes under low relative humidity (RH) conditions. Small quantities of sulfonated silane in the catalyst layer produced electrodes with high surface area, porosity, and water retention which improved catalytic activity and proton conductivity. The purpose of this work was to investigate the mechanisms that facilitate enhanced performance of CCE electrodes under different RH conditions. Differences in transport phenomena related to membrane, electrode, and reactant concentration components were measured and compared for standard Nafion-based and CCE cathode catalyst layers using oxygen, air, helox (21% O 2 in He), and 4% O 2 in N 2 . Membrane electrode assemblies were characterized via cyclic voltammetry and electrochemical impedance spectroscopy. CCE cathodes displayed decreased resistance related protonic and electronic transport when relative humidity was lowered, and both types of electrodes suffered limitations due to oxygen transport losses where the oxygen also undergoes reduction in the catalyst layer. Remarkably, at 20% RH there was no change in performance at lower oxygen concentrations or mass transport loss observed for the CCE cathodes, indicating that the overall oxygen transport (through the gas diffusion layer and ionomer) is enhanced using this type of electrode structure. The performance output of an individual proton exchange membrane fuel cell (PEMFC), or a fuel cell stack, is dependent on many internal and external factors. Temperature, relative humidity, gas composition and flow, flow field design, and distribution of materials in the catalyst layer can all have a profound effect on the power output of a given membrane electrode assembly (MEA).1,2 Operation conditions are dynamic and changes to these conditions can manifest in the performance profile. Some of the most useful information can come from examination of polarization (I-V) curves as they are collected in the operating fuel cell environment; that is, when oxidant is present. It is essential to monitor performance losses and identify their sources in order to design and evaluate a viable catalyst layer. With the knowledge that gas transport is restricted, or that catalytic sites are unavailable, comes the ability to modify the catalyst layer or reaction conditions to mitigate loss and maintain reliable performance.There are a number of intrinsic losses associated with general fuel cell operation. The most basic of these losses are activation polarization losses, which are due to slow reaction kinetics at the electrodes as the hydrogen oxidation reaction (HOR) and oxygen reduction reaction (ORR) will never reach theoretical efficiencies.1,3 The more efficient these reactions are (i.e., the greater the exchange current density), the lower the activation losses will be. Ohmic (or resistive) losses result from the ability of the ionomer material to transport protons through the membrane and catalyst layers, as well as ...