Exploiting Organometallic Chemistry to Functionalize Small Cuprous Oxide Colloidal Nanocrystals
Bradley E. Cowie, Kristian L. Mears, Mark S’ari, Ja Kyung Lee, Martha Briceno de Gutierrez, Curran Kalha, Anna Regoutz, Milo S. P. Shaffer, Charlotte K. Williams
Abstract
High Resolution Image Download MS PowerPoint Slide The ligand chemistry of colloidal semiconductor nanocrystals mediates their solubility, band gap, and surface facets. Here, selective organometallic chemistry is used to prepare small, colloidal cuprous oxide nanocrystals and to control their surface chemistry by decorating them with metal complexes. The strategy is demonstrated using small (3–6 nm) cuprous oxide (Cu 2 O) colloidal nanocrystals (NC), soluble in organic solvents. Organometallic complexes are coordinated by reacting the surface Cu–OH bonds with organometallic reagents, M(C 6 F 5 ) 2, M = Zn(II) and Co(II), at room temperature. These reactions do not disrupt the Cu 2 O crystallinity or nanoparticle size; rather, they allow for the selective coordination of a specific metal complex at the surface. Subsequently, the surface-coordinated organometallic complex is reacted with three different carboxylic acids to deliver Cu–O–Zn(O 2 CR’) complexes. Selective nanocrystal surface functionalization is established using spectroscopy (IR, 19 F NMR), thermal gravimetric analyses (TGA), transmission electron microscopy (TEM, EELS), and X-ray photoelectron spectroscopy (XPS). Photoluminescence efficiency increases dramatically upon organometallic surface functionalization relative to that of the parent Cu 2 O NC, with the effect being most pronounced for Zn(II) decoration. The nanocrystal surfaces are selectively functionalized by both organic ligands and well-defined organometallic complexes; this synthetic strategy may be applicable to many other metal oxides, hydroxides, and semiconductors. In the future, it should allow NC properties to be designed for applications including catalysis, sensing, electronics, and quantum technologies.