| Literature DB >> 31486120 |
Francesca Arcudi1, Dana Emily Westmoreland1, Emily Allyn Weiss1.
Abstract
Colloidal quantum dot (QD) photocatalysts have the electrochemical and optical properties to be highly effective for a range of redox reactions. QDs are proven photo-redox catalysts for a variety of reactions in organic solvents but are less prominent for aqueous reactions. Aqueous QD photocatalysts require hydrophilic ligand shells that provide long-term colloidal stability but are not so tight-binding as to prevent catalytic substrates from accessing the QD surface. Common thiolate ligands, which also poison many co-catalysts and undergo photo-oxidative desorption, are therefore often not an option. This paper describes a framework for the design of water-solubilizing ligands that are in dynamic exchange on and off the QD surface, but still provide long-term colloidal stability to CdS QDs. The binding affinity and inter-ligand electrostatic interactions of a bifunctional ligand, aminoethyl phosphonic acid (AEP), are tuned with the pH of the dispersion. The key to colloidal stability is electrostatic stabilization of the monolayer. This work demonstrates a means of mimicking the stabilizing power of a thiolate-bound ligand with a zwitterionic tail group, but without the thiolate binding group.Entities:
Keywords: catalysis; ligand design; nanotechnology; quantum dots; water chemistry
Year: 2019 PMID: 31486120 PMCID: PMC6854302 DOI: 10.1002/chem.201903908
Source DB: PubMed Journal: Chemistry ISSN: 0947-6539 Impact factor: 5.236