Fluctuations and critical phenomena in catalytic CO oxidation on nanoscale Pt facets

被引:73
作者
Suchorski, Y
Beben, J
Imbihl, R
James, EW
Liu, DJ
Evans, JW
机构
[1] Leibniz Univ Hannover, Inst Phys Chem & Elektrochem, D-30167 Hannover, Germany
[2] Univ Wroclaw, Inst Phys Expt, PL-50204 Wroclaw, Poland
[3] Iowa State Univ, Ames Lab, Ames, IA 50010 USA
[4] Iowa State Univ, Dept Math, Ames, IA 50017 USA
关键词
D O I
10.1103/PhysRevB.63.165417
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Local fluctuations and fluctuation-induced transitions in catalytic CO oxidation are studied with field electron microscopy on the (112) facets of a [100]-oriented Pt field emitter tip. The reaction is investigated in the bistable range close to the cusp point (critical point) that terminates the bistability range in p(CO), T-parameter space. The amplitude and the spatial coherence of the fluctuations increase on approaching the critical point. The fluctuations are spatially well correlated on each flat (112) facet, but their correlation decays rapidly across stepped regions that terminate the flat facets. On smaller (112) facets, an onset of fluctuation-induced transitions is observed earlier (i.e., further away from the critical point) than for larger (112) facets. The behavior of the reaction system near the cusp point appears to be similar to that of an equilibrium system near the critical point. The observed fluctuations are mimicked in a simple reaction model for CO oxidation on surfaces that incorporates both rapid diffusion of adsorbed CO, and superlattice ordering of adsorbed immobile oxygen. The steady states of the model exhibit a cusp bifurcation, from a regime of bistability to one of monostability. The fluctuations increase near this cusp point, as in experiment. This behavior is analyzed via kinetic Monte Carlo simulations and analytic procedures, focusing on the consequences for fluctuation-induced transitions.
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页数:12
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