In situ observation of highly oxidized Ru species in Ru/CeO2 catalyst under propane oxidation

被引:19
作者
Bezkrovnyi, Oleksii [1 ]
Vorokhta, Mykhailo [2 ]
Pawlyta, Miroslawa [3 ]
Ptak, Maciej [1 ]
Piliai, Lesia [2 ]
Xie, Xianxian [2 ]
Dinhova, Thu Ngan [2 ]
Khalakhan, Ivan [2 ]
Matolinova, Iva [2 ]
Kepinski, Leszek [1 ]
机构
[1] Polish Acad Sci, W Trzebiatowski Inst Low Temp & Struct Res, Wroclaw, Poland
[2] Charles Univ Prague, Dept Surface & Plasma Sci, Fac Math & Phys, Holesovickach 2, Prague 18000 8, Czech Republic
[3] Silesian Tech Univ, Mat Res Lab, PL-44100 Gliwice, Poland
关键词
RAY PHOTOELECTRON-SPECTROSCOPY; CR; CAYAG CERAMICS; LOW-TEMPERATURE; CO OXIDATION; OXYGEN; NANOPARTICLES; REDUCTION; SUPPORT; PT/CEO2; OXIDES;
D O I
10.1039/d2ta02330j
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
In this work, we prepared a promising catalyst for propane oxidation composed of ruthenium supported on polycrystalline hollow CeO2 nanospheres. It was found that the Ru loading on the CeO2 support strongly improves its catalytic activity, decreasing the T-50 by about 200 degrees C (from 500 to about 300 degrees C). By utilizing several ex situ techniques (XRD, HR-STEM, Raman spectroscopy, ICP analysis) and in situ NAP-XPS, we investigated the effect of different pre-treatments (calcination, reduction, and C3H8 oxidation reaction) on the morphology, structure, and chemical state of the Ru/CeO2 catalyst. The correlations between the chemical state of ruthenium in the Ru/CeO2 catalyst and its activity in C3H8 oxidation received particular attention. Here, it is shown for the first time that the Ru/CeO2 interaction with an oxygen-rich atmosphere (C3H8 + O-2 (1 : 10)) at >= 300 degrees C results in ruthenium oxidation to volatile RuO4, leading to Ru evaporation/desorption from the outer surface and homogeneous high dispersion inside the powder catalyst.
引用
收藏
页码:16675 / 16684
页数:10
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