Abstract
A rapid in-situ nanodecoration strategy is developed to enhance the durability of nanostructured La0.6Sr0.4CoO3-δ (LSC) cathodes for solid oxide fuel cells. Cu nanoparticles (∼5 nm) are deposited onto nanoporous PLD-grown LSC surfaces via magnetron sputtering and subsequently oxidized to CuxO under 500 °C operating conditions. Initial electrochemical performance, including power density and polarization resistance, remains comparable between decorated and undecorated cells. However, the undecorated cathode exhibits rapid degradation, with resistance increasing from 1.6 to 3.25 Ω cm2 over 23 h. In contrast, the CuxO-decorated cathode stabilizes after an initial conditioning period, maintaining a resistance of 1.75 Ω cm2. The Cu nanoparticles retain their size during oxidation, indicating morphological stability. Constant-voltage operation reveals a >58% enhancement in current density over time for the decorated electrode. Impedance spectroscopy and distribution of relaxation times (DRT) analysis attribute the performance improvement to a marked reduction in charge transfer resistance. These results demonstrate a simple and scalable surface modification approach for improving the longevity and functionality of nanoporous oxide electrodes in electrochemical energy systems.
| Original language | English |
|---|---|
| Article number | 153837 |
| Journal | International Journal of Hydrogen Energy |
| Volume | 214 |
| DOIs | |
| Publication status | Published - 4 Mar 2026 |
Bibliographical note
Publisher Copyright:© 2026
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 7 Affordable and Clean Energy
Keywords
- Cathode
- Cu
- Degradation
- Pulsed laser deposition
- Solid oxide fuel cell
- Sputter
- Sr segregation
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