CO2 Hydrogenation Studies on Co and CoPt Bimetallic Nanoparticles Under Reaction Conditions Using TEM, XPS and NEXAFS

被引:100
作者
Alayoglu, Selim [1 ,2 ]
Beaumont, Simon K. [1 ,2 ]
Zheng, Fan [1 ,3 ]
Pushkarev, Vladimir V. [1 ,2 ]
Zheng, Haimei [3 ]
Iablokov, Viacheslav [4 ]
Liu, Zhi [5 ]
Guo, Jinghua [5 ]
Kruse, Norbert [4 ]
Somorjai, Gabor A. [1 ,2 ,3 ]
机构
[1] Univ Calif Berkeley, Dept Chem, Berkeley, CA 94720 USA
[2] Univ Calif Berkeley, Lawrence Berkeley Natl Lab, Div Chem Sci, Berkeley, CA 94720 USA
[3] Univ Calif Berkeley, Lawrence Berkeley Natl Lab, Div Mat Sci, Berkeley, CA 94720 USA
[4] Univ Libre Bruxelles, B-1050 Brussels, Belgium
[5] Univ Calif Berkeley, Lawrence Berkeley Natl Lab, Adv Light Source, Berkeley, CA 94720 USA
关键词
Cobalt nanoparticles; Silica support; NEXAFS; AP-XPS; Catalysis; FISCHER-TROPSCH SYNTHESIS; MEAN FREE PATHS; COBALT CATALYSTS; PLATINUM;
D O I
10.1007/s11244-011-9695-9
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Cobalt and platinum-cobalt bimetallic alloy nanoparticles of uniform size distribution where prepared and supported on MCF-17 to produce a controlled and well-characterized model catalyst which was studied under reaction conditions during CO2 hydrogenation. Near edge X-ray absorption fine structure (NEXAFS) spectroscopy was used to elucidate the oxidation state of the catalyst under reaction conditions while the effect of reducing H-2 gas on the composition and structure of the bimetallic PtCo nanoparticles was measured using ambient pressure X-ray photoelectron spectroscopy (AP-XPS) and environmental transmission electron microscopy (ETEM). NEXAFS indicates that Pt aids the reduction of Co to its metallic state under relevant reaction conditions, while AP-XPS and ETEM indicate that Pt is enriched at the surface by exchange with subsurface layers which become Pt deficient-in agreement with the "Pt-like'' selectivity seen during catalytic testing of these materials.
引用
收藏
页码:778 / 785
页数:8
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