Interface-Confined Ferrous Centers for Catalytic Oxidation

被引:930
作者
Fu, Qiang [1 ]
Li, Wei-Xue [1 ,2 ]
Yao, Yunxi [1 ]
Liu, Hongyang [1 ]
Su, Hai-Yan [1 ,2 ]
Ma, Ding [1 ]
Gu, Xiang-Kui [1 ,2 ]
Chen, Limin [1 ]
Wang, Zhen [1 ]
Zhang, Hui [3 ]
Wang, Bing [3 ]
Bao, Xinhe [1 ]
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, Ctr Theoret & Computat Chem, Dalian 116023, Peoples R China
[3] Univ Sci & Technol China, Hefei Natl Lab Phys Sci Microscale, Hefei 230026, Peoples R China
关键词
PREFERENTIAL OXIDATION; CARBON-MONOXIDE; CO OXIDATION; OXIDE LAYERS; FE; SURFACES; SITES; NANOPARTICLES; ADSORPTION; ZEOLITES;
D O I
10.1126/science.1188267
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Coordinatively unsaturated ferrous (CUF) sites confined in nanosized matrices are active centers in a wide range of enzyme and homogeneous catalytic reactions. Preparation of the analogous active sites at supported catalysts is of great importance in heterogeneous catalysis but remains a challenge. On the basis of surface science measurements and density functional calculations, we show that the interface confinement effect can be used to stabilize the CUF sites by taking advantage of strong adhesion between ferrous oxides and metal substrates. The interface-confined CUF sites together with the metal supports are active for dioxygen activation, producing reactive dissociated oxygen atoms. We show that the structural ensemble was highly efficient for carbon monoxide oxidation at low temperature under typical operating conditions of a proton-exchange membrane fuel cell.
引用
收藏
页码:1141 / 1144
页数:4
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