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Simulating CH4 physisorption on ionic crystals: Limitations of an atomic partial charge model
European Physical Journal D (2008)
  • Philip Stimac
  • Robert Hinde
Abstract

We use quantum chemical techniques to evaluate the electrostatic and polarization components of the interaction between a rigid CH4 molecule and a lattice of point charges representing the MgO(100) surface. We find that CH4 positioned above Mg adopts an edge-down configuration in which two H atoms are oriented downward towards the MgO(100) surface and point at O ions in the surface layer. The CH4–MgO(100) electrostatic interaction is substantially less favorable (but is still attractive) for the face-down configuration in which three H atoms point downward. Neither configuration is energetically favorable for CH4 molecules positioned above O ions. We show that for edge-down CH4 molecules above Mg, the electrostatic component of the CH4–substrate interaction varies considerably as the CH4 molecule rotates about the surface normal; the polarization component of the interaction, by contrast, is nearly constant during this rotation. We show that a point-charge model for the CH4 charge distribution, in which the C and H atoms carry effective partial charges, predicts that the CH4–surface electrostatic interaction should be more favorable for face-down CH4 molecules than for edge-down CH4 molecules, in disagreement with the quantum chemical results. We show that this is because the point-charge model poorly represents the high-order electric multipoles of CH4.

Publication Date
2008
Citation Information
Philip Stimac and Robert Hinde. "Simulating CH4 physisorption on ionic crystals: Limitations of an atomic partial charge model" European Physical Journal D Vol. 46 (2008)
Available at: http://works.bepress.com/robert_hinde/6/