Video Experimental Relacionado
Updated: May 13, 2026

High Temperature Fabrication of Nanostructured Yttria-Stabilized-Zirconia YSZ Scaffolds by In Situ Carbon Templating Xerogels
Published on: April 16, 2017
Actividad catalítica superior mejorada por la acidez del catión en cátodos de cobalto de perovskita para celdas de
Jingyi Ding1, Haixia Zhang1, Zhe Zhang2
1School of Materials and Environmental Engineering, Bohai University, Jinzhou, China.
Abstract:
Developing high-performance and durable cathodes is crucial for efficient reversible solid oxide cells (R-SOCs). While A-site cation effects on perovskite cathodes are well-established, the mechanistic role of B-site cation acidity in regulating oxygen reduction reaction (ORR) and CO2 reduction reaction (CO2RR) remains inadequately understood. This study systematically investigates the influence of B-site cation acidity in BaCo0.8M0.2O3- δ (M = Fe, Nb, and Ta) on electrochemical performance. Our findings reveal a direct correlation between dopant acidity and enhanced performance. Specifically, Fe doping (BCFO) leads to significant structural evolution with suppressed Jahn-Teller distortion, resulting in a lower Co4+/Co3+ ratio and increased oxygen vacancy concentration that promotes oxygen ion diffusion. At 800°C, BCFO achieves the highest peak power density in fuel cell mode (1520 mW·cm-2) and superior CO2 electrolysis current density (2.60 A·cm-2 at 1.3 V). Notably, a clear trend of performance enhancement with increasing dopant acidity is observed (BCFO > BCNO > BCTO). The superior performance of BCFO is attributed to its optimal metal-oxygen bond energy, balancing facile bond dissociation and formation. This work establishes B-site cation acidity as a predictive descriptor for the rational design of highly active and stable perovskite cathodes for advanced solid oxide fuel cells and electrolysis cells.
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