2001The Journal of Physical Chemistry BRequires access

Physisorption of CO on the MgO(100) Surface

Zdenek Dohnálek, Greg A. Kimmel, Stephen A. Joyce, Patrick Ayotte, R. Scott Smith, Bruce D. Kay

Open publisher page 128 citations

Abstract

The ability to grow thin MgO(100) films of quality approaching that of vacuum-cleaved MgO(100) is demonstrated using low-energy electron diffraction and temperature-programmed desorption (TPD) of CO. Highly ordered MgO(100) surfaces are used to study the adsorption and desorption of CO. A linearly increasing sticking coefficient from 0.47 ± 0.03 to 0.90 is observed for relative CO coverages, θ, less than 0.8 monolayer (ML). For this coverage range, the total sticking coefficient is given by S MgO (1 − P CO ) + S CO P CO, where S MgO ( S CO ) is the sticking on the bare (CO-covered) MgO and P CO is the probability of striking the CO-covered surface. In TPD, the desorption of CO is dominated at very low coverages by desorption from sites influenced by defects. At intermediate coverages (0.25−0.8 ML) the CO desorbs via first-order desorption. At 0.8 ML where the monolayer peak saturates, the desorption energy is 17 ± 2 kJ/mol and the preexponential factor is 1 × 10 15±2 s -1 . The desorption energy increases linearly as coverage decreases due to repulsive interactions between adsorbed CO molecules. Above θ = 0.8 ML the adsorption occurs on fully-CO-covered MgO(100) surfaces, and further increases in θ are achieved by compression of the CO layer. The compression results in a sharp decrease in desorption energy, which, upon saturation of the first CO layer (θ = 1 ML) and the formation of a c(4×2) ordered phase, has a value of ∼9 kJ/mol.

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What this paper is about

The ability to grow thin MgO(100) films of quality approaching that of vacuum-cleaved MgO(100) is demonstrated using low-energy electron diffraction and temperature-programmed desorption (TPD) of CO. Highly ordered MgO(100) surfaces are used to study the adsorption and desorption of CO. A linearly increasing sticking coefficient from 0.47 ± 0.03 to 0.90 is observed for relative CO coverages, θ, less than 0.8 monolayer (ML). For this coverage range, the total sticking coefficient is given by S MgO (1 − P CO ) + S CO P CO, where S MgO ( S CO ) is the sticking on the bare (CO-covered) MgO and P CO is the probability of striking the CO-covered surface. In TPD, the desorption of CO is dominated at very low coverages by desorption from sites influenced by defects. At intermediate coverages (0.25−0.8 ML) the CO desorbs via first-order desorption. At 0.8 ML where the monolayer peak saturates, the desorption energy is 17 ± 2 kJ/mol and the preexponential factor is 1 × 10 15±2 s -1 . The desorption energy increases linearly as coverage decreases due to repulsive interactions between adsorbed CO molecules. Above θ = 0.8 ML the adsorption occurs on fully-CO-covered MgO(100) surfaces, and further increases in θ are achieved by compression of the CO layer. The compression results in a sharp decrease in desorption energy, which, upon saturation of the first CO layer (θ = 1 ML) and the formation of a c(4×2) ordered phase, has a value of ∼9 kJ/mol.

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Available abstract

The ability to grow thin MgO(100) films of quality approaching that of vacuum-cleaved MgO(100) is demonstrated using low-energy electron diffraction and temperature-programmed desorption (TPD) of CO. Highly ordered MgO(100) surfaces are used to study the adsorption and desorption of CO. A linearly increasing sticking coefficient from 0.47 ± 0.03 to 0.90 is observed for relative CO coverages, θ, less than 0.8 monolayer (ML). For this coverage range, the total sticking coefficient is given by S MgO (1 − P CO ) + S CO P CO, where S MgO ( S CO ) is the sticking on the bare (CO-covered) MgO and P CO is the probability of striking the CO-covered surface. In TPD, the desorption of CO is dominated at very low coverages by desorption from sites influenced by defects. At intermediate coverages (0.25−0.8 ML) the CO desorbs via first-order desorption. At 0.8 ML where the monolayer peak saturates, the desorption energy is 17 ± 2 kJ/mol and the preexponential factor is 1 × 10 15±2 s -1 . The desorption energy increases linearly as coverage decreases due to repulsive interactions between adsorbed CO molecules. Above θ = 0.8 ML the adsorption occurs on fully-CO-covered MgO(100) surfaces, and further increases in θ are achieved by compression of the CO layer. The compression results in a sharp decrease in desorption energy, which, upon saturation of the first CO layer (θ = 1 ML) and the formation of a c(4×2) ordered phase, has a value of ∼9 kJ/mol.

Key concepts: Desorption, Sticking coefficient, Monolayer, Sticking probability, Adsorption, Analytical Chemistry (journal), Physisorption, Saturation (graph theory)

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