(357c) Mass Transport Optimization in Direct Formic Acid Fuel Cell Catalyst Layer Via Pore-Former Templating
AIChE Annual Meeting
2021
2021 Annual Meeting
Transport and Energy Processes
Poster Session: Transport and Energy Processes Division
Tuesday, November 9, 2021 - 3:30pm to 5:00pm
In 2012, pore-former (lithium carbonate, LiCO3) was incorporated and removed from the anode catalyst layer forming ~10 μm pores. [2] Peaking at 17.5 wt% pore-former addition, the increase in porosity resulted in a reduction of the formic acid electrooxidation charge transfer. The increased porosity the disconnection between catalyst agglomerated and reduced the connected electrochemical surface area.
Previous work has been done with the addition of a smaller pore-former, MgO (~50 nm). [3] The intent of the smaller pore-former is to increase the porosity of the anode catalyst layer while retaining the connectivity of the agglomerates. The addition of 25 wt% pore-former increased the electrochemical surface area and cell performance by 293% and 86%, respectfully, compared to an anode catalyst layer with no pore-former. The present work aims study more variations in the wt% of pore-former (0-30 wt%), the effect of pore-former wt% on catalyst ink viscosity, and the effect of catalyst ink sonication with pore-former.
- Ma, Z., Legrand, U., Pahija, E., Tavares, R.J., and Boffito, C.D., From CO2 to Formic Acid Fuel Cells. 2021, 60(2), 803-815.
- Bauskar, A.S. and Rice, C.A., Impact of Anode Catalyst Layer Porosity on the Performance of a Direct Formic Acid Fuel Cell. 2012, 62, 36-41.
- Lam, S., Bixby, M.M., and Rice, C.A., Optimization of Mass Transport within Direct Formic Acid Fuel Cell Catalyst Layer via Pore Formers. 2020, 98, 355.