A one dimensional (1-D), isothermal model for a direct methanol fuel cell (DMFC) is presented. This model accounts for the kinetics of the multi-step methanol oxidation reaction at the anode. Diffusion and crossover of methanol are modeled and the mixed potential of the oxygen cathode due to methanol crossover is included. Kinetic and diffusional parameters are estimated by comparing the model to data from a 25 cm2 DMFC. This semi-analytical model can be solved rapidly so that it is suitable for inclusion in real-time system level DMFC simulations.
The effect of silicone on the catalytic activity of Pt for oxygen reduction and hydrogen adsorption was studied using di-phenyl siloxane as a source compound at a rotating disc electrode (RDE). Di-phenyl siloxane did not affect the catalytic activity of Pt when it was injected into the electrolyte. However, it blocked the oxygen reduction reaction when it was premixed with the catalyst. Proton transport was not blocked in either case. We postulate that di-phenyl siloxane induces hydrophobicity and causes local water starvation thereby blocking oxygen transport. Hence, the slow leaching of silicone seals in a fuel cell could cause silicon accumulation in the electrode, which will irreversibly degrade fuel cell performance by blocking oxygen transport to the catalyst sites.
Hydrogen peroxide (H2O2) formation rates in a proton exchange membrane (PEM) fuel cell anode and cathode were estimated as a function of humidity and temperature by studying the oxygen reduction reaction (ORR) on a rotating ring disc electrode (RRDE). Fuel cell conditions were replicated by depositing a film of Pt/Vulcan XC-72 catalyst onto the disk and by varying the temperature, dissolved O2 concentration and the acidity levels in hydrochloric acid (HClO4). The HClO4 acidity was correlated to ionomer water activity and hence fuel cell humidity. The H2O2 formation rates showed a linear dependence on oxygen concentration and square dependence on water activity. The H2O2 selectivity in ORR was independent of oxygen concentration but increased with decrease in water activity (i.e., decreased humidity). Potential dependent activation energy for the H2O2 formation reaction was estimated from data obtained at different temperatures.
The cross sections for the formation of five residual radionuclides (72Se, 97Zr, 112Pd, 125Sb, and 147Nb) from 40- to 200-MeV proton irradiation of thorium have been measured and are reported. The atomic masses of these fragments span the expected mass distribution of radionuclides formed by fission of the target nucleus. Especially in mass regions corresponding to transitions between different relaxation mechanisms employed by available models, these data are expected to be useful to the improvement of high-energy transport codes. The predictions of the event generators incorporated into the latest release of the Monte Carlo N-Particle code (MCNP6) are compared with data measured in this work in the hope that these results may be useful to the continued process of code verification and validation in MCNP6.
