Order,
disorder, and domains affect many of the functional properties
in self-assembled monolayers (SAMs). However, carrier transport, wettability,
and chemical reactivity are often associated with collective effects,
where conventional imaging techniques have limited sensitivity to
the underlying intermolecular coupling. Here we demonstrate vibrational
excitons as a molecular ruler of intermolecular wave function delocalization
and nanodomain size in SAMs. In the model system of a 4-nitrothiophenol
(4-NTP) SAM on gold, we resolve coupling-induced peak shifts of the
nitro symmetric stretch mode with full spatio-spectral infrared scattering
scanning near-field optical microscopy. From modeling of the underlying
2D Hamiltonian, we infer domain sizes and their distribution ranging
from 3 to 12 nm across a field of view on the micrometer scale. This
approach of vibrational exciton nanoimaging is generally applicable
to study structural phases and domains in SAMs and other molecular
interfaces.