📝 SummarXiv

Abstract

Accurate determination of electronic states with low density in the bandgap (in-gap states) is crucial for understanding and optimizing the performance of organic optoelectronic devices. In the device research field, photoelectron yield spectroscopy (PYS) has been widely used to evaluate such states, and its derivative is commonly employed to estimate the density of states (DOS). However, low-energy photons in PYS can generate excitons and anions in organic semiconductors, raising questions about whether derivative PYS spectra truly represent the DOS. Here, we applied hv-dependent high-sensitivity ultraviolet photoelectron spectroscopy with low-energy photons to probe the origin of photoelectrons in organic semiconductors. We show that PYS signals arise from the single-quantum external photoelectron effect (SQEPE) of in-gap states, from SQEPE of the singly occupied molecular orbital (SOMO) in anions, and biphotonic electron emission (BEE) effect via exciton fusions. Because the BEE signal masks the DOS, derivative PYS can misestimate the DOS of in-gap states. In contrast, constant final state yield spectroscopy (CFS-YS) can reliably determine the DOS. For example, in Tris(8-hydroxyquinoline) aluminum (Alq3), we observed BEE, and CFS-YS revealed the DOS of in-gap states and SOMO over six orders of magnitude. The direct determination of the SOMO DOS allowed us to clarify the role of Alq3 in the electron injection layer in organic light-emitting diodes. Moreover, the BEE process can act as both a carrier-generation and degradation pathway in organic optoelectronic devices. These findings demonstrate that CFS-YS provides a reliable method to determine the DOS of in-gap states and to probe exciton and/or anion interactions. We establish practical guidelines for determining the DOS of in-gap states for low-energy photon measurements, such as examining photon-flux dependence.