TY - JOUR
T1 - Improved Electrode Performance Using Fine-Tuned Poly(arylene piperidinium) Ionomers In Anion Exchange Membrane Fuel Cells
AU - Novalin, Timon
AU - Pan, Dong
AU - Nikolić, Nikola
AU - Eriksson, Björn
AU - Pérez-Trujillo , Juan Pedro
AU - Lagergren, Carina
AU - Lindbergh, Göran
AU - Jannasch, Patric
AU - Wreland Lindström, Rakel
PY - 2024
Y1 - 2024
N2 - Ionomers based on poly(arylene piperidinium)s with varying ion exchange capacities are evaluated in different combinations of anode and cathode electrodes in anion exchange membrane fuel cells. The operational conditions are chosen with an asymmetrical regime including a dry anode with 50% relative humidity at the inlet, and full humidification at the cathode. Polarization and impedance measurements are carried out in potentiostatic steps within 0.3–0.9 V and distribution of relaxation times analysis is utilized to deconvolute resistance contributions. The results show that the best cell performance is achieved with both electrodes utilizing an ionomer with the highest ion exchange capacity (IEC) of 2.79 meq g−1. Cells built exclusively from this ionomer achieved a peak power density of 1.01 W cm−2. Deconvolution of the resistance contributions revealed the impact of water content on the effective charge transfer resistance in both electrodes and a diffusion resistance associated with the movement of water from anode to cathode side. The higher conductivity and water uptake of the high IEC ionomer resulted in a reduction of both resistance contributions, leading to the highest performance under the conditions evaluated. These findings provide important insights into how to tailor the electrode layers for optimum fuel cell output.
AB - Ionomers based on poly(arylene piperidinium)s with varying ion exchange capacities are evaluated in different combinations of anode and cathode electrodes in anion exchange membrane fuel cells. The operational conditions are chosen with an asymmetrical regime including a dry anode with 50% relative humidity at the inlet, and full humidification at the cathode. Polarization and impedance measurements are carried out in potentiostatic steps within 0.3–0.9 V and distribution of relaxation times analysis is utilized to deconvolute resistance contributions. The results show that the best cell performance is achieved with both electrodes utilizing an ionomer with the highest ion exchange capacity (IEC) of 2.79 meq g−1. Cells built exclusively from this ionomer achieved a peak power density of 1.01 W cm−2. Deconvolution of the resistance contributions revealed the impact of water content on the effective charge transfer resistance in both electrodes and a diffusion resistance associated with the movement of water from anode to cathode side. The higher conductivity and water uptake of the high IEC ionomer resulted in a reduction of both resistance contributions, leading to the highest performance under the conditions evaluated. These findings provide important insights into how to tailor the electrode layers for optimum fuel cell output.
U2 - 10.1002/aenm.202403355
DO - 10.1002/aenm.202403355
M3 - Article
SN - 1614-6840
JO - Advanced Energy Materials
JF - Advanced Energy Materials
M1 - 2403355
ER -