The
ability to control the emission from single-molecule quantum
emitters is an important step toward their implementation in optoelectronic
technology. Phthalocyanine and derived metal complexes on thin insulating
layers studied by scanning tunneling microscope-induced luminescence
(STML) offer an excellent playground for tuning their excitonic and
electronic states by Coulomb interaction and to showcase their high
environmental sensitivity. Copper phthalocyanine (CuPc) has an open-shell
electronic structure, and its lowest-energy exciton is a doublet,
which brings interesting prospects in its application for optospintronic
devices. Here, we demonstrate that the excitonic state of a single
CuPc molecule can be reproducibly switched by atomic-scale manipulations
permitting precise positioning of the molecule on the NaCl ionic crystal
lattice. Using a combination of STML, AFM, and ab initio calculations, we show the modulation of electronic and optical bandgaps
and the exciton binding energy in CuPc by tens of meV. We explain
this effect by spatially dependent Coulomb interaction occurring at
the molecule–insulator interface, which tunes the local dielectric
environment of the emitter.