The effect of glass sealing stabilization on LSM–YSZ cathode poisoning and oxygen reduction reaction processes in solid oxide fuel cell

材料科学 氧化钇稳定氧化锆 硼 阴极 介电谱 固体氧化物燃料电池 电化学 氧化物 极化(电化学) 化学工程 氧化硼 电极 分析化学(期刊) 无机化学 复合材料 冶金 陶瓷 阳极 化学 立方氧化锆 物理化学 有机化学 工程类 色谱法
作者
Zahra Shomali,Parvin Alizadeh,Hamid Abdoli
出处
期刊:Journal of the American Ceramic Society [Wiley]
卷期号:108 (3) 被引量:3
标识
DOI:10.1111/jace.20206
摘要

Abstract The perovskite structure and electrochemical activity of (La 0.80 Sr 0.20 ) 0.95 MnO 3− x –(Y 2 O 3 ) 0.08 (ZrO 2 )0 .92 (LSM–YSZ) composite cathode can be significantly affected by volatile boron species originated from sealing glass–ceramics. Herein, we investigate the impact of doping the varying Er 2 O 3 content (ranging from 0 to 4%) into an aluminoborosilicate glass to mitigate boron volatilization, its interaction with the LSM–YSZ cathode and consequent effects on its electrochemical performance. The results reveal that the volatility of boron species can be significantly suppressed by introducing Er oxide into the glass network by enhancing the conversion of [BO 3 ] to [BO 4 ] units, thereby increasing the binding energy of boron and strengthening of the glass structure. Moreover, the electrocatalytic performance for the O 2 reduction reaction on the LSM–YSZ/8YSZ/LSM–YSZ symmetric cells is studied under open‐circuit conditions in the presence and absence of glass sealants. The analyses utilizing electrochemical impedance spectroscopy (EIS) and distribution of the relaxation times (DRT) analysis indicate that the electrocatalytic performance of LSM–YSZ cathodes can be enhanced in the presence of glass with 4% Er 2 O 3 (GE4). This enhancement in the electrocatalytic activity of the LSM–YSZ electrode for the oxygen reduction reaction (ORR) is attributed to formation of the thin layer on the electrode surface, leading to a notable reduction in the polarization resistance ( R p ) from 0.81 Ω cm 2 in the glass absence to 0.45 Ω cm 2 in the presence of GE4. However, DRT analysis demonstrates that the prolonged exposure of the cathode to GE4 causes a deterioration in cell performance primarily due to the blocking the cathode active sites, which impedes dominant cathode processes of oxygen dissociative adsorption/desorption and charge transfer and consequently reducing kinetics of the ORR.
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