On the role of spectral diffusion in single-molecule spectroscopy

This paper reports on measurements of fluorescence excitation spectra of single impurity molecules of terrylene in n-decane at T=1.7 K. Spectra measured within the same spectral interval but at consecutive instants of time exhibit zero-phonon (ZP) lines of single impurity molecules of several species, differing in the behavior of the line shape and frequency in time. On the one hand, one observes stable ZP lines, well approximated with a Lorentzian. On the other, one sees spectral features with a profile varying from one spectrum to another, with only individual fragments of such a profile allowing the Lorentzian approximation; such features are interpreted assuming the presence of unstable impurity molecules, the ZP lines of which display small (a few tens of MHz) spectral jumps with a time interval of about 10 s. Such molecules exhibit a substantial decrease in the spectral jump frequency within a measurement period of the order of 5000 s, which is attributed to a decrease in the contribution due to spectral diffusion resulting from sample structure relaxation.