Identification of active sites in CO oxidation and water-gas shift over supported Pt catalysts

被引:991
|
作者
Ding, Kunlun [1 ]
Gulec, Ahmet [2 ]
Johnson, Alexis M. [1 ]
Schweitzer, Neil M. [3 ]
Stucky, Galen D. [4 ]
Marks, Laurence D. [2 ]
Stair, Peter C. [1 ,5 ]
机构
[1] Northwestern Univ, Dept Chem, Evanston, IL 60208 USA
[2] Northwestern Univ, Dept Mat Sci & Engn, Evanston, IL 60208 USA
[3] Northwestern Univ, Dept Chem & Biol Engn, Evanston, IL 60208 USA
[4] Univ Calif Santa Barbara, Dept Chem & Biochem, Santa Barbara, CA 93106 USA
[5] Argonne Natl Lab, Chem Sci & Engn Div, Argonne, IL 60439 USA
基金
美国国家科学基金会;
关键词
CARBON-MONOXIDE OXIDATION; INFRARED-SPECTRA; TEMPERATURE; PLATINUM; SINGLE; GOLD; FTIR; ATOM; ADSORPTION; PT/AL2O3;
D O I
10.1126/science.aac6368
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
Identification and characterization of catalytic active sites are the prerequisites for an atomic-level understanding of the catalytic mechanism and rational design of high-performance heterogeneous catalysts. Indirect evidence in recent reports suggests that platinum (Pt) single atoms are exceptionally active catalytic sites. We demonstrate that infrared spectroscopy can be a fast and convenient characterization method with which to directly distinguish and quantify Pt single atoms from nanoparticles. In addition, we directly observe that only Pt nanoparticles show activity for carbon monoxide (CO) oxidation and water-gas shift at low temperatures, whereas Pt single atoms behave as spectators. The lack of catalytic activity of Pt single atoms can be partly attributed to the strong binding of CO molecules.
引用
收藏
页码:189 / 192
页数:4
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