Under the local plasmonic excitation, the Raman images of a single molecule
can now reach sub-nanometer resolution. We report here a theoretical
description of the interaction between a molecule and a highly confined
plasmonic field. It is shown that when the spatial distribution of the
plasmonic field is comparable with the size of the molecule, the optical
transition matrix of the molecule becomes to be dependent on the position and
the spatial distribution of the plasmonic field, resulting in spatially
resolved Raman image of a molecule. It is found that the resonant Raman image
reflects the electronic transition density of the molecule. In combination with
the first principles calculations, the simulated Raman image of a porphyrin
derivative adsorbed on the silver surface nicely reproduces its experimental
counterpart. The present theory provides the basic framework for describing
linear and nonlinear responses of molecules under the highly confined plasmonic
field.Comment: 5 pages, 4 figures, Revised versio