Shape-Programmed Nanofabrication: Understanding the Reactivity of Dichalcogenide Precursors

Abstract

Dialkyl and diaryl dichalcogenides are highly versatile and modular precursors for the synthesis of colloidal chalcogenide nanocrystals. We have used a series of commercially available dichalcogenide precursors to unveil the molecular basis for the outcome of nanocrystal preparations, more specifically, how precursor molecular structure and reactivity affect the final shape and size of II-VI semiconductor nanocrystals. Dichalcogenide precursors used were diallyl, dibenzyl, di-tert-butyl, diisopropyl, diethyl, dimethyl, and diphenyl disulfides and diethyl, dimethyl, and diphenyl diselenides. We find that the presence of two distinctively reactive C-E and E-E bonds makes the chemistry of these precursors much richer and interesting than that of other conventional precursors such as the more common phosphine chalcogenides. Computational studies (DFT) reveal that the dissociation energy of carbon-chalcogen (C-E) bonds in dichalcogenide precursors (R-E-E-R, E = S or Se) increases in the order (R): diallyl < dibenzyl < di-tert-butyl < diisopropyl < diethyl < dimethyl < diphenyl. The dissociation energy of chalcogen-chalcogen (E-E) bonds remains relatively constant across the series. The only exceptions are diphenyl dichalcogenides, which have a much lower E-E bond dissociation energy. An increase in C-E bond dissociation energy results in a decrease in R-E-E-R precursor reactivity, leading to progressively slower nucleation and higher selectivity for anisotropic growth, all the way from dots to pods to tetrapods. Under identical experimental conditions, we obtain CdS and CdSe nanocrystals with spherical, elongated, or tetrapodal morphology by simply varying the identity and reactivity of the dichalcogenide precursor. Interestingly, we find that precursors with strong C-E and weak E-E bond dissociation energies such as Ph-S-S-Ph serve as a ready source of thiol radicals that appear to stabilize small CdE nuclei, facilitating anisotropic growth. These CdS and CdSe nanocrystals have been characterized using structural and spectroscopic methods. An intimate understanding of how molecular structure affects the chemical reactivity of molecular precursors enables highly predictable and reproducible synthesis of colloidal nanocrystals with specific sizes, shapes, and optoelectronic properties for customized applications. D ialkyl dichalcogenides (RÀEÀEÀR;where R = alkyl or aryl, E = S, Se, or Te) recently re-emerged as highly versatile molecular precursors for the solution-phase synthesis of colloidal nanocrystals. Intriguingly, these dichalcogenides enable the isolation of metastable nanocrystalline phases with unusual composition and morphology. tBuÀEÀEÀtBu (E = S or Se) precursors allow the isolation of CuInE 2 and Cu 2 SnE 3 nanocrystals with metastable wurtzite phases. 1,2 A change in reaction solvent from oleylamine to squalene leads to CuInE 2 nanocrystals with the more stable chalcopyrite phase. 2,3 tBuÀSÀSÀtBu serves as precursor to In 2 S 3 nanorods 4 and Cu 2Àx S nanocrystals with a wide range of morpholog...

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Single-step synthesis of hyperbranched, luminescent Mn2+-doped ZnSe1−xSx nanocrystals using dichalcogenide precursors

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