钙钛矿(结构)
氧气
水煤气变换反应
离子键合
化学
材料科学
化学工程
无机化学
结晶学
催化作用
离子
有机化学
工程类
作者
Thattarathody Rajesh,R. Nandini Devi
出处
期刊:Journal of Molecular Catalysis A-chemical
[Elsevier]
日期:2014-12-01
卷期号:395: 534-542
被引量:6
标识
DOI:10.1016/j.molcata.2014.08.042
摘要
Abstract Pt doped and impregnated LaMnO 3 perovskites are synthesized at different temperatures and Pt and Mn states are compared in an attempt to get insight into extent of lattice incorporation of Pt in perovskite. Various characterization studies indicate that oxygen excess system like LaMnO 3 presents substantial resistance to B site doping with Pt. This behavior is different from other oxygen deficient perovskites like LaCoO 3 and LaFeO 3 in which lattice incorporation stabilizes the active species against sintering. Water gas shift reaction was used as a probe reaction to understand the effect of this difference in the activity. In case of LaMnO 3 , failure in lattice substitution leads to sintering and deactivation at high synthesis temperatures (≥700 °C) in both impregnated and doped samples. In doped samples, however, a strong interaction of Pt species with a persistent amorphous phase prevents sintering at lower synthesis temperature thereby enhancing the activity when compared to impregnated sample. The study reveals a possible mechanism in which only Pt(0) species is active with perovskite playing a minimal role in this system due to the resistance to lattice incorporation.
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