화학공학소재연구정보센터
Journal of the Electrochemical Society, Vol.156, No.5, B614-B619, 2009
Sputter-Deposited Pt PEM Fuel Cell Electrodes: Particles vs Layers
Platinum catalyst layers with Pt loadings w = 0.05-0.40 mg/cm(2) were deposited by magnetron sputtering from a variable deposition angle alpha onto gas diffusion layer (GDL) substrates and tested as cathode electrodes in proton exchange membrane (PEM) fuel cells using Nafion 1135 membranes and Teflon-bonded Pt-black electrode (TBPBE) anodes. Layers deposited at normal incidence (alpha = 0 degrees) are continuous and approximately replicate the rough surface morphology of the underlying GDL. In contrast, glancing angle deposition (GLAD) with alpha = 87 degrees and continuous substrate rotation yields highly porous layers consisting of vertically oriented Pt particles, 100-500 nm high and 100-300 nm wide, that are separated by 20-100 nm. The particle electrodes exhibit a higher (lower) mass-specific performance than the continuous-layer electrodes for a high (low) current density i. This is attributed to a higher porosity but lower overall electrochemically active surface area for the particles compared to the continuous layer. Increasing w in particle cells from 0.05 to 0.10 to 0.18 mg/cm(2) yields increasing potentials, but w = 0.40 mg/cm(2) causes a voltage drop at i > 0.4 A/cm(2), associated with the reduced pore density at large w. Comparison cells with a TBPBE cathode exhibit comparatively low Tafel slopes but a lower Pt mass specific performance than the sputtered catalysts. Quantitative analyses of kinetic and mass-transport losses in the polarization curves suggest a competing microstructural effect, favoring mass-transport performance and an efficient oxygen reduction reaction for particle and continuous layer electrodes, respectively. The overall results suggest that in addition to the well-known promise of sputter-deposited Pt catalysts as an approach to increase Pt utilization at low loading, GLAD provides the unique ability to control Pt porosity and to achieve efficient reactant flow for high-current-density operation. (C) 2009 The Electrochemical Society. [DOI: 10.1149/1.3097188] All rights reserved.