降级(电信)
钙钛矿(结构)
材料科学
氧化物
渗透(HVAC)
阴极
化学工程
催化作用
氧气
多孔性
杂质
无机化学
化学
冶金
复合材料
工程类
电气工程
物理化学
有机化学
生物化学
作者
Han Gil Seo,Hyunseung Kim,WooChul Jung,Harry L. Tuller
标识
DOI:10.1016/j.apcatb.2024.124172
摘要
The major barrier to commercialization of solid oxide fuel cells (SOFCs) is to overcome long-term surface degradation during operation. Sr/Co-based perovskite cathodes have been recognized to suffer from two major sources of degradation: inherent Sr segregation and extrinsic Cr-impurities at the surface, respectively. Here, we demonstrate the ability to simultaneously reverse both surface degradation modes in SrTi0.65Fe0.35O3-δ (STF35), a model high performance perovskite cathode, via surface acid/base engineering via infiltration. The acidic nature of Cr-infiltration is found to induce surface electron depletion, while enhancing Sr segregation to the surface, leading to ~40% drop in SOFC peak power. Subsequent infiltration of basic Ca-additives is demonstrated to not only neutralize these detrimental effects, but ultimately lead to 160% enhancement in peak power, thereby enabling Co-free operation. This approach holds great promise for extending the operating lives, more generally, of materials and devices for which the catalytic oxygen/solid interface reaction is central.
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