| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 1277867 | International Journal of Hydrogen Energy | 2009 | 9 Pages |
Because of the different experimental conditions found in literature for the measurement of the electroactive area of Pt/C electrodes of proton exchange membrane fuel cells (PEMFC) by means of underpotential hydrogen adsorption (HUPD) voltammetry, specially concerning sweep rate and temperature, it was found necessary to perform an analysis of these parameters. With this aim, the electroactive area of PEMFC electrodes has been measured by means of HUPD voltammetry at different sweep rates and temperatures, in liquid electrolyte and solid polymer contact. Both configurations show that HUPD adsorption and desorption charges are strongly dependent on sweep rate voltage and temperature. The most common behaviour observed is a maximum in HUPD desorption charge, typically in the 100–10 mV s−1 sweep rate range, whereas HUPD adsorption charge shows continuous increase with decreasing sweep rate. The decrease of desorption charge at low sweep rates is attributed to adsorbing species related with carbon support reactivity. These processes are also responsible for the increase in desorption HUPD charge at low sweep rate. At high sweep rate, both adsorption and desorption HUPD charges decrease due to limiting diffusion of protons through the microporous electrode. As a consequence, it is found that the closest approximation to the real electroactive area (i.e. the area accessible to protons) corresponds to the maximum in the HUPD desorption charge in the range of 10–100 mV s−1 sweep rate. The influence of measuring temperature is also tested in the range 25 °C–80 °C. A dependence of the adsorption and desorption hydrogen charges is found, due to thermodynamic and kinetics factors. We observe that the processes competing with hydrogen adsorption, i.e. generation and adsorption of carbon species are enhanced with temperature, so a low measuring temperature is found as most appropriate.
