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Understanding the underlying physics of charge transport in organic semiconductors under illumination is important for the development of novel optoelectronic applications. We study the effects of monochromatic light in the visible spectrum on the channel of an organic thin-film transistor based on 2,8-difluoro-5,11-bis(triethylsilylethynyl) anthradithiophene. When the channel of the transistor was illuminated with red, green, or blue light, more charge carriers were measured than what exciton generation from photon absorption alone could provide, leading to a photon-to-charge-carrier conversion efficiency much larger than 100%. We explain this phenomenon using a model incorporating space-charge limited photocharges and enhanced hole injection from the source electrode due to lowering of the potential barrier by photogenerated electrons. 

Charge-transfer (CT) complexes are a promising class of materials for the semiconductor industry because of their versatile properties. This class of compounds shows a variety of phase transitions, which are of interest because of their potential impact on the electronic characteristics. Here temperature-dependent vibrational spectroscopy is used to study structural phase transitions in a set of organic CT complexes. Splitting and broadening of infrared-active phonons in the complex formed between pyrene and pyromellitic dianhydride (PMDA) confirm the structural transition is of the order-disorder type and complement previous x-ray diffraction (XRD) results. We show that this technique is a powerful tool to characterize transitions, and apply it to a range of binary CT complexes composed of polyaromatic hyrdocarbons (anthracene, perylene, phenanthrene, pyrene, and stilbene) and PMDA. We extend the understanding of transitions in perylene-PMDA and pyrene-PMDA, and show that there are no order-disorder transitions present in anthracene-PMDA, stilbene-PMDA and phenanthrene-PMDA in the temperature range investigated here.