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Colloidal Cu2−x(SySe1−y) alloy nanocrystals with controllable crystal phase: synthesis, plasmonic properties, cation exchange and electrochemical lithiation†
Enrico Dilena,Chandramohan George,Karol Miszta,Mauro Povia,Alessandro Genovese,Alberto Casu,Mirko Prato,Liberato Manna
Journal of Materials Chemistry Pub Date : 05/16/2012 00:00:00 , DOI:10.1039/C2JM30788J
Abstract

We report synthetic routes to both cubic and hexagonal phase Cu2−x(SySe1−y) alloy nanocrystals exhibiting a well-defined near-infrared valence band plasmon resonance, the spectral position of which is dependent mainly on x, i.e. on Cu stoichiometry, and to a lesser extent on the crystal phase of the NCs. For cubic Cu2−x(SySe1−y) nanocrystals y could be varied in the 0.4–0.6 range, while for hexagonal nanocrystals y could be varied in the 0.3–0.7 range. Furthermore, the Cu2−x(SySe1−y) nanocrystals could be transformed into the corresponding Cd-based alloy nanocrystals with comparable SySe1−y stoichiometry, by cation exchange. The crystal phase of the resulting Cd(SySe1−y) nanocrystals was either cubic or hexagonal, depending on the phase of the starting nanocrystals. One sample of cubic Cu2−x(SySe1−y) nanocrystals, with S0.5Se0.5 chalcogenide stoichiometry, was then evaluated as the anode material in Li-ion batteries. The nanocrystals were capable of undergoing lithiation/delithiation via a displacement/conversion reaction (Cu to Li and vice versa) in a partially reversible manner.

Graphical abstract: Colloidal Cu2−x(SySe1−y) alloy nanocrystals with controllable crystal phase: synthesis, plasmonic properties, cation exchange and electrochemical lithiation
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