Cation Exchange Reactions in Colloidal Branched Nanocrystals

• Published in: ACS nano Vol. 5; no. 9; pp. 7176 - 7183
• Main Authors: Miszta, Karol, Dorfs, Dirk, Genovese, Alessandro, Kim, Mee Rahn, Manna, Liberato
• Format: Journal Article
• Language: English
• Published: United States American Chemical Society 27.09.2011
• Subjects: Cadmium selenides; Cation exchanging; Copper sulfides; Exchange; Intermetallics; Ion exchangers; Nanocrystals; Nanostructure; Wurtzite; copper selenide; branched nanostructures; nanocrystals; copper sulfide; cation exchange
• ISSN: 1936-0851; 1936-086X; 1936-086X
• DOI: 10.1021/nn201988w

Octapod-shaped colloidal nanocrystals composed of a central “core” region of cubic sphalerite CdSe and pods of hexagonal wurtzite CdS are subject to a cation exchange reaction in which Cd2+ ions are progressively exchanged by Cu+ ions. The reaction starts from the tip regions of the CdS pods and proceeds toward the center of the nanocrystals. It preserves both the shape and the anionic lattices of the heterostructures. During the exchange, the hexagonal wurtzite CdS pods are converted gradually into pods of hexagonal Cu2S chalcocite. Therefore, the partial cation exchange reactions lead to the formation of a ternary nanostructure, consisting of an octapod in which the central core is still CdSe, while the pods have a segmented CdS/Cu2S composition. When the cation exchange reaches the core, the cubic sphalerite CdSe core is converted into a core of cubic Cu2–x Se berzelianite phase. Therefore fully exchanged octapods are composed of a core of Cu2–x Se and eight pods of Cu2S. All these structures are stable, and the epitaxial interfaces between the various domains are characterized by low lattice mismatch. The Cu2–x Se(core)/Cu2S(pods) octapod represents another example of a nanostructure in which branching is achieved by proper organization of cubic and hexagonal domains in a single nanocrystal.