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Short-Range Catalyst-Surface Interactions Revealed by Heterodyne Two-Dimensional Sum Frequency Generation Spectroscopy.
Heterodyne 2D sum frequency generation spectroscopy is used to study a model CO2 reduction catalyst, Re(diCN-bpy) (CO)3Cl, as a monolayer on a gold surface. We show that short-range interactions with the surface can cause substantial line-shape differences between vibrational bands from the same molecules. We explain this interaction as the result of couplings between CO vibrational modes of the catalyst molecules and the image dipoles on gold surface, which are sensitive to the relative distance between the molecule and the surface. Thus, by analysis of HD 2D SFG line-shape differences and polarization dependences of IR spectra, we can unambiguously determine the ensemble-averaged orientation of the molecules on the surface. The high sensitivity of HD 2D SFG spectra to short-range interactions can be applied to many other adsorbate-substrate interactions and therefore can serve as a unique tool to determine adsorbate orientations on surfaces
Short-Range Catalyst–Surface Interactions Revealed by Heterodyne Two-Dimensional Sum Frequency Generation Spectroscopy
Heterodyne
2D sum frequency generation spectroscopy is used to
study a model CO<sub>2</sub> reduction catalyst, ReÂ(diCN-bpy) (CO)<sub>3</sub>Cl, as a monolayer on a gold surface. We show that short-range
interactions with the surface can cause substantial line-shape differences
between vibrational bands from the same molecules. We explain this
interaction as the result of couplings between CO vibrational modes
of the catalyst molecules and the image dipoles on gold surface, which
are sensitive to the relative distance between the molecule and the
surface. Thus, by analysis of HD 2D SFG line-shape differences and
polarization dependences of IR spectra, we can unambiguously determine
the ensemble-averaged orientation of the molecules on the surface.
The high sensitivity of HD 2D SFG spectra to short-range interactions
can be applied to many other adsorbate–substrate interactions
and therefore can serve as a unique tool to determine adsorbate orientations
on surfaces