We report a robust synthesis of Ag@Au core-shell nanocubes by directly depositing Au atoms on the surfaces of Ag nanocubes as conformal, ultrathin shells. Our success relies on the introduction of a strong reducing agent to compete with and thereby block the galvanic replacement between Ag and HAuCl4. An ultrathin Au shell of 0.6 nm thick was able to protect the Ag in the core in an oxidative environment. Significantly, the core-shell nanocubes exhibited surface plasmonic properties essentially identical to those of the original Ag nanocubes, while the SERS activity showed a 5.4-fold further enhancement owing to an improvement in chemical enhancement. The combination of excellent SERS activity and chemical stability may enable a variety of new applications.

Heterogeneous copper sulfide based nanostructures have attracted intense attention based on their potential to combine the plasmonic properties of copper-deficient copper sulfides with properties of other semiconductors and metals. In general, copper sulfides are versatile platforms for production of other materials by cation incorporation and exchange processes. However, the outcomes of subsequent cation exchange (CE) or incorporation processes involving nanoheterostructure (NH) templates have not been explored. In this work, we incorporate indium and tin into CuS-ZnS NHs. We demonstrate that the outcomes of cation incorporation are strongly influenced by heterocation identity and valence and by the presence of a Cu-extracting agent. The selectivity of cation incorporation depends upon both the cation itself and the heterodomains in which CE reactions take place. The final nanocrystals (NCs) emerge in many forms including homogeneous NCs, heterodimers, core@shell NHs and NHs with three different domains. This selective cation incorporation not only facilitates the preparation of previously unavailable metal sulfide NHs but also provides insight into mechanisms of CE reactions.

Different shapes: Tetravalent, hexavalent, and dodecavalent silica particles were obtained by the growth of the silica core of binary tetrapods, hexapods, and dodecapods, respectively. The surface of the multivalent particles can be regioselectively functionalized, thereby leading to particles with anisotropic geometry and chemistry.