...
首页> 外文期刊>Journal of Applied Electrochemistry >Comparison of the oxygen reduction mechanisms in a GBCO-SDC-impregnated cathode and a GBCO cathode
【24h】

Comparison of the oxygen reduction mechanisms in a GBCO-SDC-impregnated cathode and a GBCO cathode

机译:GBCO-SDC浸渍阴极和GBCO阴极氧还原机制的比较

获取原文
获取原文并翻译 | 示例
           

摘要

In this paper, a GdBaCo2O5+delta-Ce0.8Sm0.2O1.9 (GBCO-SDC) composite cathode was prepared by the impregnation method with GdBaCo2O5+delta (GBCO) as the impregnating phase and Ce0.8Sm0.2O1.9 (SDC) as the cathode skeleton. X-ray diffraction (XRD) analysis showed a good chemical compatibility between GBCO and SDC, and there were no obvious impurities at high temperature. The particle size of GBCO was approximately 80 nm. The continuous GBCO phase was deposited on the surface of porous SDC backbones, which greatly improved the electrochemical activity of the cathode. The polarization resistance of GBCO-SDC-impregnated cathode was 0.50 omega cm(2) at 600 degrees C, which was only 28.6% of that of pure GBCO cathode. The oxygen reduction reaction (ORR) at GBCO cathode mainly involved the adsorption-dissociation of oxygen molecules and charge-transfer process of oxygen atoms. The two ORR rate-controlling steps were the adsorption-dissociation process at 500-600 degrees C and the charge-transfer processes at 600-700 degrees C, respectively. The oxygen reduction reaction at GBCO-SDC-impregnated cathode mainly involved the diffusion of oxygen ions through the three phase boundaries and the charge transfer of oxygen atoms, in which the charge-transfer process was always the ORR rate-controlling step.
机译:本文通过用GdBaco2O5 + Delta(GBCO)为浸渍相和Ce0.8sm0.2O1.9(SDC )作为阴极骨架。 X射线衍射(XRD)分析显示GBCO和SDC之间的良好化学相容性,并且在高温下没有明显的杂质。 GBCO的粒度约为80nm。将连续的GBCO相沉积在多孔SDC骨架的表面上,这大大提高了阴极的电化学活性。 GBCO-SDC浸渍阴极的偏振电阻在600℃的600℃下为0.50ωcm(2),其仅为纯GBCO阴极的28.6%。 GBCO阴极的氧还原反应(ORR)主要涉及氧分子的吸附 - 氧原子的氧分子和电荷转移过程。两个ORR速率控制步骤是在500-600℃的吸附 - 解离过程,分别为600-700℃的电荷转移过程。 GBCO-SDC浸渍阴极处的氧还原反应主要涉及氧离子的扩散通过三相边界和氧原子的电荷转移,其中电荷转移过程始终是ORR速率控制步骤。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号