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Potential Energy Surface of Methanol Decomposition on Cu(110)

Journal Article · · Journal of Physical Chemistry. C
DOI:https://doi.org/10.1021/jp808211q· OSTI ID:951833

Combining the dimer saddle point searching method and periodic density functional theory calculations, the potential energy surface of methanol decomposition on Cu(110) has been mapped out. Each elementary step in the methanol decomposition reaction into CO and hydrogen occurs via one of three possible mechanisms: O-H, C-H or C-O bond scission. Multiple reaction pathways for each bond scission have been identified in the present work. Reaction pathway calculations were started from an initial (reactant) state with methanol adsorbed in the most stable geometry on Cu(110). The saddle point and corresponding final state of each reaction or diffusion mechanism were determined without assuming the reaction mechanism. In this way, the reaction paths are determined without chemical intuition. The harmonic pre-exponential factor of each identified reaction is calculated from a normal mode analysis of the stationary points. Then, using harmonic transition state theory, the reaction rate of each identified reaction pathway in the entire reaction network is obtained. The most favorable decomposition route for methanol on Cu(110) is found as follows: . The rate-limiting step in this route is the dehydrogenation of methoxy to formaldehyde. Our calculation results are in agreement with previous experimental observations and results. This work was supported by a Laboratory Directed Research and Development (LDRD) project of the Pacific Northwest National Laboratory (PNNL). The computations were performed using the Molecular Science Computing Facility in the William R. Wiley Environmental Molecular Sciences Laboratory (EMSL), which is a U.S. Department of Energy national scientific user facility located at PNNL in Richland, Washington.

Research Organization:
Pacific Northwest National Laboratory (PNNL), Richland, WA (US), Environmental Molecular Sciences Laboratory (EMSL)
Sponsoring Organization:
USDOE
DOE Contract Number:
AC05-76RL01830
OSTI ID:
951833
Report Number(s):
PNNL-SA-61917; 20691
Journal Information:
Journal of Physical Chemistry. C, Journal Name: Journal of Physical Chemistry. C Journal Issue: 11 Vol. 113; ISSN 1932-7447
Publisher:
American Chemical Society
Country of Publication:
United States
Language:
English

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