Recent work on hybrid photovoltaic systems based on conjugated polymers and III-V compound semiconductors with relatively high power conversion efficiency revived fundamental questions regarding the nature of charge separation and transfer at the interface between organic and inorganic semiconductors with different degrees of delocalization. In this work, we studied photoinduced charge generation and interfacial transfer dynamics in a prototypical photovoltaic n-type GaAs (111)B and poly(3-hexyl-thiophene) (P3HT) bilayer system. Ultrafast spectroscopy and density functional theory calculations indicate the coexistence of electron and hole transfer at the GaAs/P3HT interface, leading to the generation of long-lived species and photoinduced absorption upon creation of hybrid interfacial states. This opens up new avenues for the use of low-dimensional III-V compounds (e.g., nanowires or quantum dots) in hybrid organic/inorganic photovoltaics, where advanced bandgap and density of states engineering may also be exploited as design parameters.
Keywords: III−V semiconductors; charge photogeneration; conjugated polymers; density functional theory (DFT); organic−inorganic charge-transfer systems; ultrafast transient spectroscopy.