ScholarWorks@숙명여자대학교

초록

Initial adsorption of CO molecules on Si(001) is investigated by using room-temperature (RT) scanning tunneling microscopy (STM) and density functional theory calculations. Theoretical calculations show that only one adsorption configuration of terminal-bound CO (T-CO) is stable and that the bridge-bound CO is unstable. All the abundantly observed STM features due to CO adsorption can be identified as differently configured T-COs. The initial sticking probability of CO molecules on Si(001) at RT is estimated to be as small as similar to 1 X 10(-4) monolayer/ Langmuir, which is significantly increased at high-temperature adsorption experiments implying a finite activation barrier for adsorption. Thermal annealing at 900 K for 5 min results in the dissociation of the adsorbed CO molecules with the probability of 60-70% instead of desorption, indicating both a strong chemisorption state and an activated dissociation process. The unique adsorption state with a large binding energy, a tiny sticking probability, and a finite adsorption barrier is in stark contrast with the previous low-temperature (below 100 K) observations of a weak binding, a high sticking probability, and a barrierless adsorption. We speculate that the low-temperature results might be a signature of a physisorption state in the condensed phase.

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