Ru1/FeOx single-atom catalyst with dual active sites for water gas shift reaction without methanation

被引:54
作者
Sun, Li [1 ,2 ]
Cao, Liru [1 ,2 ]
Su, Yang [1 ]
Wang, Chaojie [1 ,2 ]
Lin, Jian [1 ]
Wang, Xiaodong [1 ]
机构
[1] Chinese Acad Sci, Dalian Inst Chem Phys, CAS Key Lab Sci & Technol Appl Catalysis, Dalian 116023, Peoples R China
[2] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
来源
APPLIED CATALYSIS B-ENVIRONMENT AND ENERGY | 2022年 / 318卷
基金
中国国家自然科学基金;
关键词
Ruthenium; Iron oxide; Dual active sites; Single atom catalyst; Water gas shift; LOW-TEMPERATURE; CO OXIDATION; HYDROGEN-PRODUCTION; SELECTIVE OXIDATION; MECHANISTIC ASPECTS; GOLD NANOPARTICLES; ALPHA-MOC; SUPPORT; AU; REDUCTION;
D O I
10.1016/j.apcatb.2022.121841
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
Ru-based catalysts are rarely considered for water gas shift (WGS) reaction due to either inferior activity or methanation side reaction. Here, Ru-1/FeOx single-atom catalyst is synthesized via a co-precipitation method, which can realize high CO conversion with low loading of 0.18 wt. % and stable specific rates with-3 times higher than Ru nanoparticles (NPs) with loading of 2.00 wt. % at 300 ?C. Moreover, it shows no formation of methanation byproducts even under CO2- and H-2-rich WGS stream which can occur on Ru NPs. Detailed characterizations demonstrate that Ru single atoms have stronger interaction with FeOx to form dual active sites for WGS reaction. The positive Ru1 species own rather weaker bonded CO* and the neighbored FeOx can help activate H2O to generate OH*, which then react facilely via an associative process. Meanwhile, the single atom Ru prohibits the dissociation of H-2 with low adsorption strength to avoid the methanation.
引用
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页数:12
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