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Orthogonal reactivity and interface-driven selectivity during cation exchange of heterostructured metal sulfide nanorods†
Abigail M. Fagan,Benjamin C. Steimle
Chemical Communications Pub Date : 03/03/2022 00:00:00 , DOI:10.1039/D1CC07190D
Abstract

We report predictive guidelines for the substoichiometric cation exchange of model two-component metal sulfide nanorods containing divalent cations of similar hardness. Unit cell volume changes, cation radii, solubility constants, and solid state interfaces influence selectivity during substoichiometric exchange of Cu+ when multiple products are possible.

Graphical abstract: Orthogonal reactivity and interface-driven selectivity during cation exchange of heterostructured metal sulfide nanorods
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