In situ generated catalyst: copper(ii) oxide and copper(i) supported on Ca2Fe2O5 for CO oxidation

被引:13
|
作者
Penkala, Bartosz [1 ,2 ]
Gatla, Suresh [3 ]
Aubert, Daniel [1 ]
Ceretti, Monica [2 ]
Tardivat, Caroline [1 ]
Paulus, Werner [2 ]
Kaper, Helena [1 ]
机构
[1] St Gobain CREE, CNRS, Lab Synth & Fonctionnalisat Ceram, UMR 3080, F-84306 Cavaillon, France
[2] Univ Montpellier, Inst Charles Gerhardt Montpellier, CNRS, UMR 5253,ENSCM, Pl Eugene Bataillon, F-34095 Montpellier 5, France
[3] European Synchrotron Radiat Facil, 71 Rue Martyrs,CS 40220, F-38043 Grenoble 9, France
关键词
CARBON-MONOXIDE OXIDATION; LOW-TEMPERATURE; PREFERENTIAL OXIDATION; MIXED OXIDES; REDUCTION; COMBUSTION; BEHAVIOR; H-2; CU; SCIENCE;
D O I
10.1039/c8cy00806j
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
Two sets of copper oxide-brownmillerite Ca2Fe2O5 catalysts are prepared and studied for CO oxidation. The first set of catalysts is prepared by classical wet impregnation of the Ca2Fe2O5 support. The second set is prepared by Ca2Fe2O5 B-site doping. The active catalyst species are generated during hydrogen treatment. The two sets of catalysts behave very differently in CO oxidation. The performance of the impregnated catalysts is independent of the Cu content, while the performance of the doped catalysts can be tuned by the copper content. The best performing catalyst is a doped-reduced catalyst with 40 mol% Cu. Detailed characterization of the catalysts is carried out using nitrogen physisorption, X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS) and in situ X-ray absorption fluorescence spectroscopy (XAFS).
引用
收藏
页码:5236 / 5243
页数:8
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