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CO-PROX reactions on copper Y2O3-ZrO2 catalysts prepared by a single step co-precipitation technique
被引:24
作者:

Marie, Olivier
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机构:
Normandie Univ, LCS, CNRS, ENSICAEN,UNICAEN, F-14000 Caen, France Normandie Univ, LCS, CNRS, ENSICAEN,UNICAEN, F-14000 Caen, France

Portier, Xavier
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机构:
Normandie Univ, UMR CNRS 6252, CEA, CIMAP,ENSICAEN, Caen, France Normandie Univ, LCS, CNRS, ENSICAEN,UNICAEN, F-14000 Caen, France

Korsunska, Nadiia
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机构:
Natl Acad Sci Ukraine, V Lashicaryov Inst Semicond Phys, 45 Pr Nauky, UA-03028 Kiev, Ukraine Normandie Univ, LCS, CNRS, ENSICAEN,UNICAEN, F-14000 Caen, France

Khomenkova, Larysa
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h-index: 0
机构:
Natl Acad Sci Ukraine, V Lashicaryov Inst Semicond Phys, 45 Pr Nauky, UA-03028 Kiev, Ukraine
Natl Univ Kyiv Mohyla Acad, 2 Skovorody Str, UA-04070 Kiev, Ukraine Normandie Univ, LCS, CNRS, ENSICAEN,UNICAEN, F-14000 Caen, France
机构:
[1] Normandie Univ, LCS, CNRS, ENSICAEN,UNICAEN, F-14000 Caen, France
[2] Normandie Univ, UMR CNRS 6252, CEA, CIMAP,ENSICAEN, Caen, France
[3] Natl Acad Sci Ukraine, V Lashicaryov Inst Semicond Phys, 45 Pr Nauky, UA-03028 Kiev, Ukraine
[4] Natl Univ Kyiv Mohyla Acad, 2 Skovorody Str, UA-04070 Kiev, Ukraine
关键词:
CO PROX;
Yttrium stabilized zirconia;
Copper active sites;
YTTRIA-STABILIZED ZIRCONIA;
PREFERENTIAL OXIDATION;
CARBON-MONOXIDE;
MIXED OXIDES;
COMPOSITE;
H-2;
TEMPERATURE;
CUO/CEO2;
PERFORMANCE;
GOLD;
D O I:
10.1016/j.apcatb.2020.119258
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:
Nano-sized CuYZr ternary oxides obtained through an original single step co-precipitation synthesis were submitted to an in depth characterization and further tested in the catalytic CO PROX reaction. The tetragonal phase was identified as the main one whatever the calcination temperature. The study of the copper distribution within the crystals through complementary STEM EDX chemical mapping, UV-vis and H-2 Thermo Programmed Reduction (TPR) analysis allowed the identification of at least three distinct sites. The PROX tests revealed interesting properties with CO conversion as high as 95 % and relatively high O-2 selectivity towards CO2 in the high temperature range. Finally, interesting relationships between relative abundance of copper sites and catalytic activity/selectivity were obtained allowing suggesting relevant active sites.
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