Spatially Confined Formation and Transformation of Nanocrystals within Nanometer-Sized Reaction Media

Abstract

CONSPECTUS: The extensive research performed in the past two decades has enabled the production of a range of colloidal nanocrystals, mostly through solution-based procedures that generate and transform nanostructures in bulk-phase solutions containing precursors and surfactants. However, the understanding and control of each nanocrystal (trans)formation step during the synthesis are still complicated because of the high complexity of this process, in which multiple diverse events such as nucleation, subsequent growth, attachment, and ripening occur simultaneously in bulk suspensions. Unlike well-established solution-based methods, solid-state reactions, which had been at the forefront of traditional inorganic materials chemistry, are quite rarely utilized in the realm of nanomaterials because of the high temperatures required for most solid-state reactions, as a result of which the clusters and NCs are prone to migrate through the bulk reaction medium and sinter together uncontrollably into large particles. We have been pursuing the "nanospace-confined approach" to explore the use of a variety of solid and hollow silica nanoparticles as either solid-state or solution-phase reaction media to carry out the syntheses and transformations of nanocrystals in a unique microenvironment, partitioning the reactants, intermediates, and transition states from the rest of the bulk reaction medium. Such nanoconfined systems have the potential not only to enable efficient and selective nanocrystal conversion chemistries but also to provide fundamental understanding pertaining to the synthetic evolution of nanostructures and transient mechanistic steps. The unique spaces with sizes of a few tens of nanometers inside nanoconfined systems offer the opportunity to observe and elucidate novel deconvoluted chemical phenomena that are impossible to investigate in bulk systems, and comprehensive understanding of nanoconfined chemistry can be implicated in explaining and controlling the macroscopic chemical behaviors. This Account describes our focused research on developing spatially confined platforms for nanocrystal syntheses and transformations, highlighting our diversity-oriented strategy, namely, the "postdecoration approach", which results in the evolution of new nanocatalytic sites in a preformed cavity for diversifying and controlling their morphologies, number, density and combinations. We discuss key examples of the "nanoconfined solid-state conversion approach" that involve novel reactions of nanocrystals within thermally stable solid silica nanospheres to synthesize and transform complex hybrid nanocrystals with increased complexity and functionality. In addition, an enlightening discussion of the examples of nanocrystal syntheses and conversions in nanoconfined solutions inside enclosed and exposed cavities of silica nanospheres is included. Finally, the important applications of nanospace-confined systems in various fields are also briefly discussed.