Catalyst genesis studied by atomic force microscopy

被引:18
|
作者
Bird, DPC [1 ]
de Castilho, CMC [1 ]
Lambert, RM [1 ]
机构
[1] Univ Cambridge, Dept Chem, Cambridge CB2 1EW, England
基金
英国工程与自然科学研究理事会;
关键词
aluminum oxide; atomic force microscopy; catalysis; growth; surface structure; morphology; roughness; and topography; nucleation; silver; single crystal surfaces; surface chemical reaction;
D O I
10.1016/S0039-6028(99)01220-0
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
Atomic force microscopy has been used to study the genesis of realistic Ag-alpha-alumina model catalysts from an aqueous precursor (AgNO3), using conditions identical to those used in the synthesis of practical dispersed catalysts. The Various stages in the evolution of the final catalyst from the initially deposited precursor were successfully imaged. It is found that the structure of the alumina substrate exerts a dramatic influence on the structure and stability of the silver deposit. On Al2O3(0001), sintering in I bar oxygen at 780 K causes a quasi-2D network of metallic Ag to collapse to large well-formed hemispherical particles on the bare oxide surface. On Al2O3(11 (2) over bar 0), precursor decomposition leads initially to the formation of quasi-1D Ag nanowires that decorate the faceted step edges and extend for many hundreds of nanometres. This is entirely different from the behaviour of vacuum-deposited Ag. These nanowires are much more stable against sintering in 1 bar oxygen at 780 K. Their formation and stability suggest a particularly favourable wetting interaction between Ag and the (1 (1) over bar 02) plane of alpha-alumina. (C) 2000 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:L221 / L227
页数:7
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