首页> 外文会议>European SOCF SOE Forum >Short stack and full system test using a ceramic A-site deficient strontium titanate anode
【24h】

Short stack and full system test using a ceramic A-site deficient strontium titanate anode

机译:使用陶瓷A现场缺乏钛酸锶阳极的短堆叠和全系统测试

获取原文

摘要

Doped strontium titanates have been widely studied as potential anode materials in solid oxide fuel cells (SOFCs). The high n-type conductivity that can be achieved in these materials makes them well suited for use as the electronically conductive component in SOFC anodes. This makes them a potential alternative to nickel, the presence of which is a major cause of degradation due to coking, sulphur poisoning and low tolerance to redox cycling. As the electrocatalytic activity of strontium titanates tends to be low, impregnation with oxidation catalysts, such as ceria and nickel is often required to obtain anode performances that can compete with Ni-YSZ cermets. Here the stability issues due to nickel should be reduced due to the small loadings and its non-structural function. In this study, a lanthanum and calcium co-doped A-site deficient strontium titanate (LSCTA-) was used as the anode material in cells with an active area of 100 cm~2. Cell performance was tested in both short (5 cell) stack configuration, as well as a full HEXIS Galileo system (nominally 1 kW AC). Various impregnates, such as nickel and ceria, were used in this approach with promising results. The system test initially produced 70% of the nominal output power and is to the authors’ knowledge the first all-oxide SOFC test on this scale. The strontium titanate backbone provides sufficient electronic conductivity to ensure acceptable ohmic losses. Power densities up to 200 mA/cm~2 could be obtained at 900°C, which compares well with Ni-cermet based anodes. Degradation is however severe at 900°C, due to impregnate coarsening, but operation at 850°C minimises this effect. Short stacks could be stably operated for 1600 hours with an output power of 100 mA/cm~2. Stacks are redox stable, but sulphur tolerance is determined by the electrocatalysts.
机译:掺杂的钛酸锶已被广泛地研究了固体氧化物燃料电池中的潜在阳极材料(SOFC)。在这些材料中可以实现的高N型导电性使其适合于在SOFC阳极中用作电子导电组分。这使得它们成为镍的潜在替代方案,其中存在是由于焦化,硫中毒和氧化还原循环低耐受性导致的主要原因。随着钛酸锶的电催化活性趋于低,通常需要浸渍催化剂,例如氧化铈和镍,以获得可以与Ni-Ysz金属陶瓷竞争的阳极性能。这里应该由于小的负载量及其非结构函数而导致镍引起的稳定性问题。在该研究中,使用钛酸镧和钙的钛酸钙钛酸锶(LSCTA-)作为阳极材料,其具有100cm〜2的活性面积。在短(5个单元)堆叠配置中测试细胞性能,以及全六角伽利略系统(名义上1 kW AC)。在这种方法中使用各种浸渍物,例如镍和二氧化铈,具有有前途的结果。系统测试最初生产了70%的标称输出功率,并是作者知识在此规模上的第一个全氧化物SOFC测试。钛酸锶骨架提供足够的电子电导率,以确保可接受的欧姆损失。在900℃下可以获得高达200mA / cm〜2的功率密度,其与基于Ni-Cermet的阳极孔很好。然而,由于浸渍粗化,降解在900℃下严重,但在850℃下的操作最小化了这种效果。短堆叠可以稳定运行1600小时,输出功率为100 mA / cm〜2。堆叠是氧化还原稳定的,但硫耐受由电催化剂确定。

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