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Iron pyrite (FeS 2 ) is a promising photovoltaic absorber because of its Earth abundance, high optical extinction, and infrared band gap ( E g = 0.95 eV), but its use has been hindered because of the difficulty of phase pure synthesis. Pyrite phase purity is a paramount concern, as other phases of iron sulfide have undesirable electronic properties. Here we report the synthesis of phase pure iron pyrite nanocrystals with cubic morphology and a mean dimension of 80 nm. Control over the nanocrystal shape was achieved using an unusual ligand, 1-hexadecanesulfonate. The particles were characterized via synchrotron X-ray spectroscopy, indicating an indirect band gap of 1.00 ± 0.11 eV and a valence bandwidth of nearly 1 eV. Transmission electron microscopy from early reaction stages suggests a nucleation and growth mechanism similar to solution precipitation syntheses typical of metal oxide nanocrystals, rather than the diffusion-limited growth process typical of hot-injection metal chalcogenide nanocrystal syntheses.
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Lucas et al. (2013) studied this question.
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