Multimetallic post-synthetic modifications of copper selenide nanoparticles.

In this report, we investigate the addition of two metal cations, simultaneously and sequentially to CuSe nanoparticles. The metal combinations (Ag-Au, Ag-Pt, Hg-Au and Hg-Pt) are chosen such that one metal adds to the structure cation exchange and the other adds to the structure metal deposition when added individually to CuSe nanoparticles. Surprisingly, we find that for each metal combination, across all three synthesis routes, cation exchange and metal deposition products are obtained without deviation from the outcomes seen in the binary metal systems. However, within those outcomes the data show several types of heterogeneities in the morphologies formed including extent and composition of cation exchange products as well as the extent and composition of the metal deposited products. Taken together, these results suggest a hierarchical control for nanoheterostructure morphologies where the pathways of cation exchange or metal deposition in post-synthetic modification of CuSe exhibit relatively general outcomes as a function of metal, regardless of synthetic approach or metal combination. However, the detailed composition and interface populations of the resulting materials are more sensitive to both metal identities and synthetic procedure ( order of reagent addition), suggesting that certain principles of metal chalcogenide post-synthetic modification are excitingly robust, while also revealing new avenues for both mechanistic discovery and structural control.