Electrochemical study reveals performance variations across modified perovskite electrodes in reversible solid oxide cells, indicating distinct reaction mechanisms across operating modes.
Influence of A-site deficiency and chemical composition of B-site (concentration of Ni, Mn, and Cr) on electrochemical performance of hydrogen electrode in (La 1-x Sr x ) y Cr 0.5-z Mn 0.5-w Ni z+w O 3-δ |(Sc 2 O 3 ) 0.10 (CeO 2 ) 0.01 (ZrO 2 ) 0.89 |La 0.8 Sr 0.2 FeO 3-δ reversible solid oxide fuel cell has been studied.Electrochemical characterization has been carried out in fuel cell and electrolysis regimes.Results indicate that in fuel cell regime most notable limiting steps were detected around 0.5 Hz frequency range and were attributed to gas-solid adsorption-desorption processes.pO 2 variation in the oxygen electrode compartment led to small variations in a total impedance of single cells but was not the limiting process.In electrolysis mode, the dissociative adsorption was shown as an important limiting stage and limitations in kinetic region of charge transfer step were remarkable.Increase of A-site deficiency caused a significant increase in high-frequency series resistance as well as some increase of total polarization resistance.Variation in B-site composition had a significant influence on electrochemical performance with very different frequency dependence of impedance.Highest current density values of 0.27 and 0.66 A cm -2 at unit cell potentials of 0.9 and 1.5 V, respectively, at 850°C were measured for La 0.75 Sr 0.25 Cr 0.3 Mn 0.5 Ni 0.2 O 3-δ (fuel cell mode) and (La 0.8 Sr 0.2 ) x Cr 0.49 Mn 0.49 Ni 0.02 O 3-δ (electrolysis mode) in hydrogen fuel gas with pH 2 O = 0.03 and 0.30 atm, respectively.
No takes yet. Share an insight, caveat, or question.
Maide et al. (2019) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: