Water-Dispersible Copper Sulfide Nanocrystals via Ligand Exchange of 1-Dodecanethiol.

Abstract

In colloidal Cu2–xS nanocrystal synthesis, thiols are often used as organic ligands and the sulfur source, as they yield high-quality nanocrystals. However, thiol ligands on Cu2–xS nanocrystals are difficult to exchange, limiting the applications of these nanocrystals in photovoltaics, biomedical sensing, and photocatalysis. Here, we present an effective and facile procedure to exchange native 1-dodecanethiol on Cu2–xS nanocrystals by 3-mercaptopropionate, 11-mercaptoundecanoate, and S2– in formamide under inert atmosphere. The product hydrophilic Cu2–xS nanocrystals have excellent colloidal stability in formamide. Furthermore, the size, shape, and optical properties of the nanocrystals are not significantly affected by the ligand exchange. Water-dispersible Cu2–xS nanocrystals are easily obtained by precipitation of the nanocrystals capped by S2–, 3-mercaptopropionate, or 11-mercaptoundecanoate from formamide, followed by redispersion in water. Interestingly, the ligand exchange rates for Cu2–xS nanocrystals capped with 1-dodecanethiol are observed to depend on the preparation method, being much slower for Cu2–xS nanocrystals prepared through heating-up than through hot-injection synthesis protocols. XPS studies reveal that the differences in the ligand exchange rates are due to the surface chemistry of the Cu2–xS nanocrystals, where the nanocrystals prepared via hot-injection synthesis have a less dense ligand layer due to the presence of trioctylphosphine oxide during synthesis. A model is proposed that explains the observed differences in the ligand exchange rates. The facile ligand exchange procedures reported here enable the use of high-quality colloidal Cu2–xS nanocrystals prepared in the presence of 1-dodecanethiol in various applications.