Dictating Pt-Based Electrocatalyst Performance in Polymer Electrolyte Fuel Cells, from Formulation to Application

Van Cleve, Tim; Khandavalli, Sunilkumar; Chowdhury, Anamika; Medina, Samantha; Pylypenko, Svitlana; Wang, Min; More, Karren L.; Kariuki, Nancy; Myers, Deborah J.; Weber, Adam Z.; Mauger, Scott A.; Ulsh, Michael J.; Neyerlin, Kenneth C.

doi:10.1021/acsami.9b17614

DOE OSTI · 1580098

Dictating Pt-Based Electrocatalyst Performance in Polymer Electrolyte Fuel Cells, from Formulation to Application

Van Cleve, Tim·Khandavalli, Sunilkumar·Chowdhury, Anamika·Medina, Samantha·Pylypenko, Svitlana·Wang, Min·More, Karren L.·Kariuki, Nancy·Myers, Deborah J.·Weber, Adam Z.·Mauger, Scott A.·Ulsh, Michael J.·Neyerlin, Kenneth C.

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Abstract

In this study, in situ electrochemical diagnostics designed to probe ionomer interactions with platinum and carbon were applied to relate ionomer coverage and conformation, gleaned from anion adsorption data, with O 2 transport resistance for low-loaded (0.05 mg Pt cm -2 ) platinum-supported Vulcan carbon (Pt/Vu)-based electrodes in a polymer electrolyte fuel cell. Coupling the in situ diagnostic data with ex situ characterization of catalyst inks and electrode structures, the effect of ink composition is explained by both ink-level interactions that dictate the electrode microstructure during fabrication and the resulting local ionomer distribution near catalyst sites. Electrochemical techniques (CO displacement and ac impedance) show that catalyst inks with higher water content increase ionomer (sulfonate) interactions with Pt sites without significantly affecting ionomer coverage on the carbon support. Surprisingly, the higher anion adsorption is shown to have a minor impact on specific activity, while exhibiting a complex relationship with oxygen transport. Ex situ characterization of ionomer suspensions and catalyst/ionomer inks indicates that the lower ionomer coverage can be correlated with the formation of large ionomer aggregates and weaker ionomer/catalyst interactions in low-water content inks. These larger ionomer aggregates resulted in increased local oxygen transport resistance, namely, through the ionomer film, and reduced performance at high current density. In the water-rich inks, the ionomer aggregate size decreases, while stronger ionomer/Pt interactions are observed. The reduced ionomer aggregation improves transport resistance through the ionomer film, while the increased adsorption leads to the emergence of resistance at the ionomer/Pt interface. Overall, the high current density performance is shown to be a nonmonotonic function of ink water content, scaling with the local gas (H 2 , O 2 ) transport resistance resulting from pore, thin film, and interfacial phenomena.

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30 DIRECT ENERGY CONVERSION 37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CHEMISTRY Pt/C catalyst inks in situ electrochemical diagnostics ink formulation and processing ionomer coverage oxygen transport resistance

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Van Cleve, Tim, Khandavalli, Sunilkumar, Chowdhury, Anamika, Medina, Samantha, Pylypenko, Svitlana, Wang, Min, More, Karren L., Kariuki, Nancy, Myers, Deborah J., Weber, Adam Z., Mauger, Scott A., Ulsh, Michael J., Neyerlin, Kenneth C.. 2019-11-19. Dictating Pt-Based Electrocatalyst Performance in Polymer Electrolyte Fuel Cells, from Formulation to Application. https://doi.org/10.1021/acsami.9b17614

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