ABSTRACT
As the commercial display market grows, the demand for low-toxicity, highly emissive, and size-tunable semiconducting nanoparticles has increased. Indium phosphide quantum dots represent a promising solution to these challenges; unfortunately, they typically suffer from low inherent emissivity resulting from charge carrier trapping. Strategies to improve the emissive characteristics of indium phosphide often involve zinc incorporation into or onto the core itself and the fabrication of core/shell heterostructures. InP clusters are high fidelity platforms for studying processes such as cation exchange and surface doping with exogenous ions since these clusters are used as single-source precursors for quantum dot synthesis. Here, we examined the incorporation of zinc and gallium ions in InP clusters and the use of the resultant doped clusters as single-source precursors to emissive heterostructured nanoparticles. Zinc ions were observed to readily react with InP clusters, resulting in partial cation exchange, whereas gallium resisted cluster incorporation. Zinc-doped clusters effectively converted to emissive nanoparticles, with quantum yields strongly correlated with zinc content. On the other hand, gallium-doped clusters failed to demonstrate improvements in quantum dot emission. These results indicate stark differences in the mechanisms associated with aliovalent and isovalent doping and provide insight into the use of doped clusters to make emissive quantum dots.
ABSTRACT
Understanding and deconvoluting the different mechanisms involved in the synthesis of nanomaterials is necessary to make uniform materials with desirable function. In this study, in situ spectroscopic methods were used to study exchange reactions at the surface of indium phosphide clusters, revealing that the cluster surface lacks significant dynamics on the NMR time-scale at room temperature. The exchange of surface carboxylate ligands can be induced at elevated temperatures and with the addition of carboxylic acid and indium carboxylate. These studies suggest that carboxylate may be a key ingredient in promoting cluster dissolution to larger nanostructures. Toward this end, the evolution of InP clusters was examined by in situ UV-vis spectroscopy, revealing cluster dissolution and renucleation that is dramatically dependent on the concentration of carboxylate. In addition to the concentration of exogenous ligands, the rate of particle growth and final product distribution were dependent on temperature and initial cluster concentration. These results, taken together, suggest a mechanism of cluster evolution involving cluster dissociation to form multiple reactive monomer species that renucleate and grow to larger nanomaterials. Nonproductive monomer degradation is observed in the lower temperature regime (<200 °C), suggesting a critical temperature threshold for efficient cluster to quantum dot conversion.
