The control of light emission on the scale of individual quantum systems, like molecules or quantum dots, is a field of intense current research. One way to induce light emission from these systems is the local charge injection through the tip of a scanning tunnelling microscope (STM). Studies which employ this method have to address one basic question: Does the detected luminescence provide information precisely from the molecule into which charge is injected by the STM tip apex or are the luminescence properties determined by a larger volume?In this article, we focus on the investigation of organic nanocrystals and discuss the relation between the local excitation, the intermolecular coupling and the influence of the STM as a measuring instrument. Choosing pentacene as an organic emitter, we present results, which suggest that the STMinduced luminescence cannot be attributed simply to the emission by a single molecule. We discuss how information about locality can be obtained and comment on the present experimental limitations and possible future improvements.