Electric Fields and Charge Separation for Solid Oxide Fuel Cell Electrodes.
basic_science · Level V
Where this comes from
- Record sourced from PubMed, PMID 36067488.
- Also identified by DOI 10.1021/acs.nanolett.2c02468 and PMC identifier 9523703.
- Licence recorded as CC BY.
- The licence permits redistribution, so the abstract is shown in full and the full text is available from the publisher.
Abstract
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 (H<sub>2</sub>O and CO<sub>2</sub> on CeO<sub>2</sub>; O<sub>2</sub> on LaFeO<sub>3</sub>). 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.