Platinum/graphite nanofiber catalysts of various structure:: Characterization and catalytic properties

被引:20
作者
Baker, RTK
Rodriguez, N
Mastalir, A
Wild, U
Schlögl, R
Wootsch, A
Paál, Z
机构
[1] Hungarian Acad Sci, Inst Isotopes, Chem Res Ctr, H-1525 Budapest, Hungary
[2] Max Planck Gesell, Fritz Haber Inst, D-14195 Berlin, Germany
[3] Univ Szeged, Inst Organ Chem, H-6720 Szeged, Hungary
[4] Catlayt Mat LLC, Holliston, MA 01746 USA
关键词
D O I
10.1021/jp0400519
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
Platinum/graphite nanofiber (Pt/GNF) catalysts were prepared by impregnating three types of GNF (herringbone, H; ribbon, R; and platelet, P) with Pt salt dissolved in organic solvents. Electron microscopy showed small Pt particles (1.5-8 nm) in all catalysts. The ethanol-toluene solvent of the Pt salt corrupted the ordered nanofiber structure of Pt/GNF-P. Butanol solvent did not harm the nanofiber. Nevertheless, X-ray photoelectron spectroscopy (XPS) indicated that the structure of all three samples was essentially graphitic. Surface Pt enrichment was observed on Pt/GNF-H and depletion on the (corrupted) Pt/GNF-P. Catalytic properties were checked in the skeletal reactions of hexane in H-2 between 543 and 603 K. Both the activity and the formation of isomers were the most marked on Pt/GNF-H, where also the hydrogen migration to storage positions on the support was most pronounced. Repeated regeneration with oxygen did not alter the catalytic propensities. High isomerization selectivity is attributed to creating hydrogen-rich active sites on Pt by the back-migration of hydrogen retained by the nanofiber structure of the support. Product selectivities can be used as an indirect indicator for the hydrogen storage capacity of GNF samples.
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收藏
页码:14348 / 14355
页数:8
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