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We present a model of the cathode catalyst layer morphology before and after loading a porous catalyst support with Pt and ionomer. Support nanopores and catalyst particles within pores and on the support surface are described by size distributions, allowing for qualitative processes during the addition of a material phase to be dependent on the observed pore and particle size. A particular focus is put on the interplay of pore impregnation and blockage due to ionomer loading and the consequences for the Pt/ionomer interface, ionomer film thickness and protonic binding of particles within pores. We used the model to emulate six catalyst/support combinations from literature with different porosity, surface area and pore size distributions of the support as well as varying particle size distributions and ionomer/carbon ratios. Besides providing qualitatively and quantitatively accurate predictions, the model is able to explain why the protonically active catalyst surface area has been reported to not increase monotonically with ionomer addition for some supports, but rather decrease again when the optimum ionomer content is exceeded. The proposed model constitutes a fast translation from manufacturing parameters to catalyst layer morphology which can be incorporated into existing performance and degradation models in a straightforward way.
The effect of ionomer to carbon (I/C) weight ratio and relative humidity (RH) on cathode catalyst degradation was investigated by comprehensive in situ characterization. Membrane electrode assemblies (MEA) with I/C ratios of 0.5, 0.8 and 1.2 were subjected to an accelerated stress test performed at 40, 70 and 100% RH. The results show an increasing loss in electrochemical active surface area (ECSA) for both higher I/C ratios and RH during voltage cycling. To differentiate between ionomer and water connected ECSA, carbon monoxide stripping measurements were performed at varying RH. Before degradation, all MEAs show comparable total ECSA values, while higher I/C ratios lead to a larger fraction of ionomer connected ECSA. After degradation, ECSA measurements of the lowest I/C ratio showed a relatively higher loss of Pt in contact with ionomer than Pt in contact with water, while an opposite trend was observed for higher I/C ratios. H2 /N2 impedance measurements showed drastically increasing protonic catalyst layer resistances for decreasing RH especially at low I/C ratios, which might hinder Pt 2+ ion diffusion towards the membrane, hence decreasing the ECSA loss. Limiting current measurements show increasing molecular O 2 diffusion resistances at end of test for samples with higher I/C ratios and higher ECSA loss.
In this work, flatbed screen printing is evaluated regarding its capability to produce catalyst layers of PEM fuel cells. In the field of printed electronics, screen printing is regarded as robust and high-throughput coating technology. The possibility of in-plane structuring could be an additional degree of freedom, enabling more complex designs of catalyst layers in the future. In this study, process parameters are varied to investigate their effect on resulting layer thickness, homogeneity, and Pt-loading. With the usage of different screens, the Pt-loading can be adjusted. Additionally, two different pastes with and without water content are investigated. The catalyst paste without water showed a better process stability during printing and performed best under dry conditions (RH = 40%) and worst under wet conditions (RH = 100%) during electrochemical in-situ testing. Overall, the reproducibility of the CCM production process was verified. The viscosity of the catalyst paste with 19.55 wt% water in solvent was higher compared to the paste without water. Furthermore, a carbon paste (Pt-free) is developed in a similar viscosity range as the catalyst pastes. The main challenge of screen printing process development lies in the paste optimization to prevent evaporation effects over time, ensuring sufficient wetting of the paste on the substrate and sufficient fuel cell performance.
Kempten hat sich zu einer Drehscheibe für angehende Automobilingenieure entwickelt. Der ADAS-Master der Universität ist der weltweit einzige seiner Art. Sechs Studenten erzählen uns, warum sie vom automatisierten Fahren fasziniert sind, was sie von zukünftigen Arbeitgebern erwarten und wie sich der „Fahrspaß“ mit autonomen Autos verändern wird.