Tuning the oxidation of carbon monoxide using nanoassembled model catalysts

被引:95
作者
Heiz, U [1 ]
Sanchez, A [1 ]
Abbet, S [1 ]
Schneider, WD [1 ]
机构
[1] Univ Lausanne, Inst Phys Mat Condensee, CH-1015 Lausanne, Switzerland
关键词
D O I
10.1016/S0301-0104(00)00268-8
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
While the oxidation of CO has long been considered to be structure insensitive, nano-assembled model catalysts consisting of size-selected metal clusters (Au-n, Pt-n, Pd-n, and Rh-n, n = 1-20), supported on thin MgO(1 0 0) films, reveal distinct size-effects. When adding a single Pt atom to Pt-14,Pt- platinum clusters increase their reactivity by a factor of three. Rh-20 shows the highest reactivity of all the investigated clusters, oxidizing about 13 CO molecules per cluster at 350 K. While F-centers on MgO films transform Aug from an inert to an active catalyst, the reactivity of Pds is not suppressed when deposited on defect-poor films. These different catalytic properties are rationalized within simple frontier orbital models, whereas for AUg the reaction mechanism for the low temperature oxidation of CO is elucidated within first-principle calculations. (C) 2000 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:189 / 200
页数:12
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