Investigation on Smbasrcofeo Double Perovskite as an Oxygen Electrode for Reversible Solid Oxide Fuel Cell
SSRN, ISSN: 1556-5068
2023
- 78Usage
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
Citation Benchmarking is provided by Scopus and SciVal and is different from the metrics context provided by PlumX Metrics.
Article Description
Solid oxide fuel cells (SOFCs) are contemplated as promising power generation systems due to their higher energy conversion efficiency, low emissions, and multi-fuel capability. It is crucial to develop reversible SOFC (RSOFC), which can produce hydrogen when operated as an electrolyzer and electricity when utilized as a power source. There has been a lot of interest in the development of reversible SOFC (RSOFC) as they can be operated in (i) fuel cell mode to produce electricity and (ii) electrolyzer mode to produce hydrogen. However, the conventional oxygen electrode degrades when operated in RSOFC mode. To address this issue, double perovskites have been explored as promising cathode electrodes in RSOFC with proton conducting electrolyte YSZ as the electrolyte. In the present study, SmBaSrCoFeO (SBSCF) double perovskite is explored as the oxygen electrode using YSZ as the electrolyte. The (SBSCF) has been successfully synthesized using a simple and cost-effective solution combustion technique as the oxygen electrode for RSOFC. The structural, morphological and electrical conductivity of SBSCF powder and the electrochemical performance of SOFC containing SBSCF as cathode material are discussed. The performance of the cell in the electrolyzer mode is also discussed.
Bibliographic Details
Elsevier BV
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