Monomeric Fe Species in Square Planar Geometry Active for Low Temperature NH3-SCR of NO

被引:6
作者
Wierzbicki, Dominik [1 ,3 ]
Clark, Adam H. [1 ]
Kroecher, Oliver [1 ,2 ]
Ferri, Davide [1 ]
Nachtegaal, Maarten [1 ]
机构
[1] Paul Scherrer Inst, CH-5232 Villigen, Switzerland
[2] Ecole Polytech Fed Lausanne EPFL, Inst Chem Sci & Engn, CH-1015 Lausanne, Switzerland
[3] AGH Univ Sci & Technol, Fac Energy & Fuels, PL-30059 Krakow, Poland
基金
瑞士国家科学基金会;
关键词
SELECTIVE CATALYTIC-REDUCTION; OXIDATION-STATE; NITROGEN-OXIDES; PRE-EDGE; ZEOLITES; FE-ZSM-5; SITES; IDENTIFICATION; COORDINATION; PERFORMANCE;
D O I
10.1021/acs.jpcc.2c03480
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
Monomeric Fe species in zeolites are considered to be the active sites for the low temperature activity toward ammonia-assisted selective catalytic reduction of nitrogen oxides (NH3-SCR) in exhaust gases. Herein, we report on a preparation method to synthesize single-site Fe/ZSM-5 by combination of dealumination with the use of a bulky iron complex to introduce Fe. Transient in situ XAS experiments at the Fe K-edge under dynamic NH3-SCR reaction conditions demonstrated the involvement of all iron atoms in the redox cycle and, with that, suggest that Fe species in the studied Fe/ZSM-5 catalyst are monomers. Simulation of experimental X-ray absorption data revealed that the Fe species in the sample obtained by this approach adopt a square planar geometry, which changes into fivefold coordination at low temperature by strongly binding either NO or NH3 as the ligand. The presence of monomeric Fe species in this Fe/ZSM-5 conveys molecular level insights into the temperature-dependent NH3-SCR activity and might prove useful in the study of other reactions over monomeric Fe species, such as methane partial oxidation or dehydroaromatization reactions.
引用
收藏
页码:17510 / 17519
页数:10
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