Dynamics of the dissociative adsorption of alkanes on Ir(110)

Journal Article · Mon Jun 01 00:00:00 EDT 1987 · J. Chem. Phys.; (United States)

DOI:https://doi.org/10.1063/1.452442· OSTI ID:6614014

Hamza, A V; Steinruck, H; Madix, R J

The dissociative adsorption of C/sub 1/--C/sub 4/ alkanes on Ir(110)--(1 x 2) was investigated using supersonic molecular beam techniques. Three regimes of reactivity were observed. At incident kinetic energies less than 100 kJ/mol the dissociative adsorption probability for propane and butane increased to about 0.6 with both decreasing surface temperature and decreasing translational energy of the incident molecule suggesting that activation occured via trapping of the alkane on the surface. At kinetic energies below 110 kJ/mol for butane, 90 kJ/mol for propane, 60 kJ/mol for ethane, 40 kJ/mol for methane, and at elevated surface temperatures the reaction probabilities for alkanes were independent of surface temperature and translational energy, but increased significantly with the molecular weight or carbon chain length of the incident alkane. This behavior indicates an unactivated reaction channel for each species except methane. At kinetic energies above 110 kJ/mol for butane, 90 kJ/mol for propane, 60 kJ/mol for ethane, and 40 kJ/mol for methane the initial dissociative sticking probability increased with increasing translational energy and was independent of surface temperature, indicating direct translational activation of the incident alkane. The translational energy required to activate the incident alkane via this channel increased with carbon number or molecular weight, indicative of energy transfer processes that dissipate energy in the reactive collision. The dissipative transfer of translational energy out of the reactive channel via a hard cube collision with the surface accounts qualitatively for the increase in the apparent activation barrier with increasing molecular weight in this activated channel.

• Research Organization: Department of Chemical Engineering, Stanford University, Stanford, California 94305
• OSTI ID: 6614014
• Journal Information: J. Chem. Phys.; (United States), Journal Name: J. Chem. Phys.; (United States) Vol. 86:11; ISSN JCPSA
• Country of Publication: United States
• Language: English

Related Subjects

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CHEMISTRY
400201* -- Chemical & Physicochemical Properties
ADSORPTION
ALKANES
BEAMS
COLLISIONS
DISSOCIATION
ELEMENTS
FLUID FLOW
HYDROCARBONS
IRIDIUM
METALS
MOLECULAR BEAMS
MOLECULE COLLISIONS
ORGANIC COMPOUNDS
PLATINUM METALS
SORPTION
SORPTIVE PROPERTIES
SUPERSONIC FLOW
SURFACE PROPERTIES
TRANSITION ELEMENTS
TRAPPING