Fabrication and Cell Analysis of a Pt/SiO2 Platinum Thin Film Electrode
Platinum was deposited on a SiO2 nanofiber web (Japan Vilene Company, Ltd., 200 nm in fiber diameter and 6 mm in web thickness) by atomic layer deposition. An SEM image of the cross section of the Pt/ SiO2 nanofiber electrode is shown in Fig. 1. The SiO2 nanofibers are covered with a platinum thin film of 3 nm in thickness. Nafion membrane was sandwiched between the Pt/SiO2 nanofiber electrode as a cathode and a conventional Pt/C electrode as an anode to form an MEA. Note that no ionomer was impregnated on the Pt/SiO2 nanofiber electrode. Fuel cell polarization curves were obtained using 1 cm2 single-cell hardware with cross-flow flowfields under various conditions. The electrochemical surface area (ECSA), proton conductivity and oxygen transport resistance were analyzed by cyclic voltammetry, electrochemical impedance measurement, and diffusion-limited current measurement using diluted oxygen, respectively.
Polarization curves and analyzed results were shown in Fig. 2 and Table 1, respectively, in comparison with those of conventional Pt/C electrode. The Pt/SiO2 cell showed comparable performance to the Pt/C cell at 100% RH in spite of the much smaller ECSA. At 40% RH, however, the Pt/SiO2 cell showed lower performance than the Pt/C cell.
A transmission line model of the electrode was applied to the Pt/SiO2 nanofiber electrode to analyze the performance loss. By following the model, the reaction resistance was calculated using values of the cathode resistance and the ohmic resistance, which were obtained from slopes of the polarization curves and the proton conductivity, respectively. The analyzed results under various RH conditions are shown in Fig. 3. The reaction resistance significantly increases with decreasing RH, while the ohmic resistance increase is limited. This indicates that the performance loss of the Pt/SiO2 nanofiber electrode under dry condition is mainly due to the increase in the reaction resistance.
Oxygen transport resistance, performances in wet conditions, and the effects of ionomer impregnation on the Pt/SiO2 electrode will also be discussed.
 M. K. Debe, J. Electrochem. Soc., 2013, 160, F552