Mechanisms for Adsorption of Methyl Viologen on CdS Quantum Dots

This paper describes the surface composition-dependent binding of the dichloride salt of methyl viologen (MV2+) to CdS quantum dots (QDs) enriched, to various degrees, with either Cd or S at the surface. The degree of enrichment is controlled synthetically and by postsynthetic dilution of the QDs in their solvent, THF. NMR shows the Cd-enriched Os to contain a relatively dense (2.8 ligands/nm(2)) surface layer of oleic acid, in the form of Cd-oleate, and 5-enriched QDs to contain relatively sparse (1.0 ligands/nm(2)) surface density of native ligands containing both oleic acid and octadecene. Electron transfer-mediated photoluminescence quenching of the QDs by MV2+ serves as a probe for the binding affinity of MV2+ for the surfaces of the QDs. Diluting Cd-enriched QDs removes Cd-oleate from the surface, exposing the stoichiometric CdS surface beneath and increasing the quenching efficiency of MV2+, whereas diluting S-enriched QD does not change their surface chemistry or the efficiency with which they are quenched by MV2+. The photoluminescence quenching data for all of the surface chemistries we studied fit well to a Langmuir model that accounts for binding of MV2+ through two reaction mechanisms: (i) direct adsorption of MV2+ to exposed stoichiometric CdS surfaces (with an equilibrium adsorption constant of 1.5 x 10(5) M-1), and (ii) adsorption of MV2+ to stoichiometric CdS surfaces upon displacement of weakly bound Cd-oleate complexes (with an equilibrium displacement constant of 3.5 x 10(3) M-1). Ab initio calculations of the binding energy for adsorption of the dichloride salt of MV2+ on Cd- and S-terminated surfaces reveal a substantial preference of MV2+ for 5-terminated lattices due to alignment of the positively charged nitrogens on MV2+ with the negatively charged sulfur. These findings suggest a strategy to maximize the adsorption of redox-active molecules in electron transfer-active geometries through synthetic and postsynthetic manipulation of the inorganic surface.