High Activity of Au/γ-Fe2O3 for CO Oxidation: Effect of Support Crystal Phase in Catalyst Design

被引:136
作者
Zhao, Kunfeng [1 ,2 ,3 ]
Tang, Hailian [1 ,2 ,3 ,4 ]
Qiao, Botao [1 ]
Li, Lin [1 ]
Wang, Junhu [1 ,2 ,3 ]
机构
[1] Chinese Acad Sci, Dalian Inst Chem Phys, State Key Lab Catalysis, Dalian 116023, Peoples R China
[2] Chinese Acad Sci, Dalian Inst Chem Phys, Mossbauer Effect Data Ctr, Dalian 116023, Peoples R China
[3] Chinese Acad Sci, Dalian Inst Chem Phys, Lab Catalysts & New Mat Aerosp, Dalian 116023, Peoples R China
[4] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
基金
中国国家自然科学基金;
关键词
gold; CO oxidation; redox; gamma-Fe2O3; catalyst design; SINGLE-ATOM CATALYSIS; GAS SHIFT REACTION; LOW-TEMPERATURE; GOLD CATALYSTS; CARBON-MONOXIDE; SELECTIVE OXIDATION; FERRIC HYDROXIDE; OXIDE NANOPARTICLES; GROUP METALS; OXYGEN;
D O I
10.1021/cs5020496
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
Au/gamma-Fe2O3 and Au/alpha-Fe2O3 catalysts with identical size of Au nanoparticles, chemical state of Au species, and amount of surface OW group were prepared. The Au/gamma-Fe2O3 catalyst exhibited exceptionally high activity, regardless of the heat treatments. The COTPR, sequential pulse reaction, and in situ Raman spectra demonstrate that the much higher activity of Au/gamma-Fe2O3 originated from its higher redox property at low temperature. Systematic study shows that this higher-redox-property-based higher activity could be extended to gamma-Fe2O3-supported Pt-group metals and to other reactions that follow Mars-Van Krevelen mechanism. This finding may provide a new avenue for catalyst improvement or development by choosing the suitable crystal phase of the oxide support.
引用
收藏
页码:3528 / 3539
页数:12
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