TY - JOUR
AU - Evan F Johnson
AU - Rangachary Mukundan
AU - Adam Z Weber
AB - <p>
                    Understanding chemical degradation of the proton-exchange membrane in fuel cells is crucial for extending their lifetimes. Herein, various degradation reactions reported in literature are organized and analyzed, including direct radical generation and an indirect (Fenton) pathway. To understand the transport of dissolved H
                    <sub>2</sub>
                    and O
                    <sub>2</sub>
                    crossover gases as they relate to membrane degradation, an agglomerate-scale model is introduced, treating gas, ionomer, and catalyst as discrete phases. The model reveals a key phenomenon: at working potentials, dissolved gases are mostly consumed at the interface between the catalyst layer and the membrane, leaving little gas to cross the membrane. Under open-circuit conditions, dissolved gases are not consumed and can then cross the membrane. This explains high H
                    <sub>2</sub>
                    O
                    <sub>2</sub>
                    concentrations and degradation rates seen in experiments but not captured in previous models. Following mixed-potential theory, crossover gases supply the hydrogen-oxidation and oxygen-reduction reactions, which occur simultaneously on individual Pt particles comprising the Pt band in the membrane, forming reactive species (H
                    <sub>2</sub>
                    O
                    <sub>2</sub>
                    , OH·). Results show crossover gas almost entirely reacts on the Pt band, allowing little to reach the opposite electrode. Furthermore, the micro-scale geometry of the catalyst-layer/membrane interface impacts the gas crossover at working potentials, indicating that cell construction affects membrane durability.
                  </p>
BT - Journal of The Electrochemical Society
DA - 28/01/2026
DO - 10.1149/1945-7111/ae3648
IS - 2
N2 - <p>
                    Understanding chemical degradation of the proton-exchange membrane in fuel cells is crucial for extending their lifetimes. Herein, various degradation reactions reported in literature are organized and analyzed, including direct radical generation and an indirect (Fenton) pathway. To understand the transport of dissolved H
                    <sub>2</sub>
                    and O
                    <sub>2</sub>
                    crossover gases as they relate to membrane degradation, an agglomerate-scale model is introduced, treating gas, ionomer, and catalyst as discrete phases. The model reveals a key phenomenon: at working potentials, dissolved gases are mostly consumed at the interface between the catalyst layer and the membrane, leaving little gas to cross the membrane. Under open-circuit conditions, dissolved gases are not consumed and can then cross the membrane. This explains high H
                    <sub>2</sub>
                    O
                    <sub>2</sub>
                    concentrations and degradation rates seen in experiments but not captured in previous models. Following mixed-potential theory, crossover gases supply the hydrogen-oxidation and oxygen-reduction reactions, which occur simultaneously on individual Pt particles comprising the Pt band in the membrane, forming reactive species (H
                    <sub>2</sub>
                    O
                    <sub>2</sub>
                    , OH·). Results show crossover gas almost entirely reacts on the Pt band, allowing little to reach the opposite electrode. Furthermore, the micro-scale geometry of the catalyst-layer/membrane interface impacts the gas crossover at working potentials, indicating that cell construction affects membrane durability.
                  </p>
PB - The Electrochemical Society
PY - 2026
EP - 024504
T2 - Journal of The Electrochemical Society
TI - Membrane Degradation in PEM Fuel Cells: Part I. Modeling Gas Crossover and the Pt Band
UR - https://doi.org/10.1149/1945-7111/ae3648
VL - 173
SN - 0013-4651, 1945-7111
ER -