Publication | Closed Access
Nanocomposites: A New Opportunity for Developing Highly Active and Durable Bifunctional Air Electrodes for Reversible Protonic Ceramic Cells
164
Citations
49
References
2021
Year
EngineeringChemistryChemical EngineeringRepcc TechnologyHybrid MaterialsNew OpportunityHighly ActiveMaterials ScienceBattery Electrode MaterialsNovel NanocompositesAdvanced Electrode MaterialEnergy StorageElectrochemical CellElectrochemical ProcessElectrochemistryProton TransferElectrochemical Energy StorageBatteriesFunctional Materials
Abstract Reversible protonic ceramic cells (RePCCs) can facilitate the global transition to renewable energy sources by providing high efficiency, scalable, and fuel‐flexible energy generation and storage at the grid level. However, RePCC technology is limited by the lack of durable air electrode materials with high activity toward the oxygen reduction/evolution reaction and water formation/water‐splitting reaction. Herein, a novel nanocomposites concept for developing bifunctional RePCC electrodes with exceptional performance is reported. By harnessing the unique functionalities of nanoscale particles, nanocomposites can produce electrodes that simultaneously optimize reaction activity in both fuel cell/electrolysis operations. In this work, a nanocomposite electrode composed of tetragonal and Ruddlesden–Popper (RP) perovskite phases with a surface enriched by CeO 2 and NiO nanoparticles is synthesized. Experiments and calculations identify that the RP phase promotes hydration and proton transfer, while NiO and CeO 2 nanoparticles facilitate O 2 surface exchange and O 2‐ transfer from the surface to the major perovskite. This composite also ensures fast (H + /O 2‐ /e ‐ ) triple‐conduction, thereby promoting oxygen reduction/evolution reaction activities. The as‐fabricated RePCC achieves an excellent peak power density of 531 mW cm ‐2 and an electrolysis current of −364 mA cm ‐2 at 1.3 V at 600 °C, while demonstrating exceptional reversible operation stability of 120 h at 550 °C.
| Year | Citations | |
|---|---|---|
Page 1
Page 1