Scandium and copper co-doping effect on stability and activity to the NO direct decomposition of Ba3Y4O9

被引:6
作者
Fang, Siman [1 ]
Takagaki, Atsushi [2 ,3 ]
Watanabe, Motonori [1 ,2 ,3 ]
Song, Jun Tae [2 ,3 ]
Ishihara, Tatsumi [1 ,2 ,3 ]
机构
[1] Kyushu Univ, Grad Sch Integrated Frontier Sci, Dept Automot Sci, Nishi Ku, 744 Motooka, Fukuoka 8190395, Japan
[2] Kyushu Univ, Fac Engn, Dept Appl Chem, Nishi Ku, 744 Motooka, Fukuoka 8190395, Japan
[3] Kyushu Univ, Int Inst Carbon Neutral Energy Res WPI I2CNER, Nishi Ku, 744 Motooka, Fukuoka 8190395, Japan
基金
日本学术振兴会;
关键词
NO decomposition; Ba3Y4O9; Co-doping effect; CATION SEGREGATION; REACTION-MECHANISM; NITROGEN MONOXIDE; CATALYTIC PROCESS; REDUCTION; OXIDE; ADSORPTION; O-2; N-2; FE;
D O I
10.1016/j.apcata.2020.117743
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
Direct decomposition of NO on Ba3Y4O9 doped with Cu and Sc was studied and it was found that co-doping of Sc and Cu into Ba3Y4O9 was effective for increasing both lattice stability and NO decomposition activity. In particular, Ba3Y3Sc0.6Cu0.4O9 (10 % Cu and 15 % Sc doping) catalyst showed N-2 and O-2 yield of 90 % and 99 %, respectively, in NO decomposition reaction at 700 degrees C. Comparing with the pristine and single-metal doped system, the optimized catalyst showed superior long-term stability and increased activity under O-2, and water vapor co-existence conditions because of the increased stability of crystal structure, improved lattice oxygen mobility and weakened oxygen adsorption on the surface. TPD and in-situ FT-IR results suggested that the co-doping effect was assigned to the easier removal of surface NO2- or NO3- species which blocks the active site to NO decomposition.
引用
收藏
页数:9
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