催化作用
氧化剂
铂金
烧结
化学工程
粒径
材料科学
色散(光学)
选择性催化还原
粒子(生态学)
贵金属
还原气氛
金属
纳米颗粒
废气
铂纳米粒子
无机化学
化学
纳米技术
冶金
有机化学
物理
海洋学
光学
工程类
地质学
作者
Andreas M. Gänzler,Maria Casapu,P. Vernoux,S. Loridant,F.J. Cadete Santos Aires,Thierry Épicier,Benjamin Betz,R. Hoyer,Jan‐Dierk Grunwaldt
标识
DOI:10.1002/ange.201707842
摘要
Abstract A dynamic structural behavior of Pt nanoparticles on the ceria surface under reducing/oxidizing conditions was found at moderate temperatures (<500 °C) and exploited to enhance the catalytic activity of Pt/CeO 2 ‐based exhaust gas catalysts. Redispersion of platinum in an oxidizing atmosphere already occurred at 400 °C. A protocol with reducing pulses at 250–400 °C was applied in a subsequent step for controlled Pt‐particle formation. Operando X‐ray absorption spectroscopy unraveled the different extent of reduction and sintering of Pt particles: The choice of the reductant allowed the tuning of the reduction degree/particle size and thus the catalytic activity (CO>H 2 >C 3 H 6 ). This dynamic nature of Pt on ceria at such low temperatures (250–500 °C) was additionally confirmed by in situ environmental transmission electron microscopy. A general concept is proposed to adjust the noble metal dispersion (size, structure), for example, during operation of an exhaust gas catalyst.
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