Herein, we report the colloidal synthesis of hollow dual-plasmonic nanoparticles (NPs) using Au@Cu2O core-shell NPs as templates and exploiting the nanoscale Kirkendall effect. In our synthesis, we used organic compounds as a source of chalcogenide ions for an anion exchange reaction at elevated temperatures using polyvinylpyrrolidone (PVP) as a capping reagent to transform the solid Cu2O shell into a hollow copper chalcogenide shell. The resulting structures possess different features depending on the chalcogenide precursor employed. TEM images confirm the complete transformation of Au@Cu2O templates when 1,1-dimethyl-2-selenourea was added and the formation of hollow Au@Cu2-x Se nanostructures. In contrast, residues of Cu2O attached to the Au core were present when thioacetamide was used for the synthesis of Au@Cu2-x S with all other conditions kept the same. The divergence of architectures caused distinct optical properties of Au@Cu2-x S and Au@Cu2-x Se NPs. This synthetic approach is an effective pathway for maneuvering the size of interior voids by varying the concentration of chalcogenide ions in the reaction mixture. The insights gained from this work will enrich the synthetic toolbox at the nanoscale and guide us on the rational design of multicomponent plasmonic nanoparticles with precisely controlled hollow interiors and sophisticated geometries, further enhancing our capabilities to fine-tune the electronic, optical, compositional, and physicochemical properties.
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