Electric Fields and Charge Separation for Solid Oxide Fuel Cell Electrodes

Activation losses at solid oxide fuel cell (SOFC) electrodes have been widely attributed to charge transfer at the electrode surface. The electrostatic nature of electrode-gas interactions allows us to study these phenomena by simulating an electric field across the electrode-gas interface, where we are able to describe the activation overpotential using density functional theory (DFT). The electrostatic responses to the electric field are used to approximate the behavior of an electrode under electrical bias and have found a correlation with experimental data for three different reduction reactions at mixed ionic-electronic conducting (MIEC) electrode surfaces (H2O and CO2 on CeO2; O-2 on LaFeO3). In this work, we demonstrate the importance of decoupled ion-electron transfer and charged adsorbates on the performance of electrodes under nonequilibrium conditions. Finally, our findings on MIEC-gas interactions have potential implications in the fields of energy storage and catalysis.

Automated summary

In this study, the activation losses at solid oxide fuel cell (SOFC) electrodes were investigated by simulating charge transfer using density functional theory (DFT). The electrostatic responses to the electric field were found to correlate with experimental data for different reduction reactions at mixed ionic-electronic conducting (MIEC) electrode surfaces. The study also highlighted the importance of decoupled ion-electron transfer and charged adsorbates on the performance of electrodes under nonequilibrium conditions. The findings have potential implications in energy storage and catalysis.