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RESEARCH PRODUCT

Size Reduction of CdSe/ZnS Core−Shell Quantum Dots Photosensitized by Benzophenone: Where Does the Cd(0) Go?

Raquel E. GalianMiguel De La GuardiaJulia Pérez-prieto

subject

Quenching (fluorescence)ChemistryAnalytical chemistryNanoparticleSurfaces and InterfacesCondensed Matter PhysicsPhotochemistrychemistry.chemical_compoundElectron transferKetylX-ray photoelectron spectroscopyQuantum dotElectrochemistryBenzophenoneGeneral Materials ScienceSpectroscopySpectroscopy

description

The size of core-shell CdSe/ZnS quantum dots can be decreased by using the combined action of an n,π* aromatic ketone and UVA light. Energy-dispersive X-ray spectroscopy as well as X-ray photoelectron spectroscopy techniques gave information on the photosensitization mechanism and the eventual destiny of Cd(2+) and Se(2-) core ions. Our data support the electron transfer from the BP ketyl radical to Cd(2+), leading to Cd(0) and H(+), as well as to the recovery of benzophenone. Elemental Cd remains on the core and, eventually, can be oxidized to CdO. In addition, Se(2-) counterions disperse inside the solution mainly attached to protonated amine ligands. The Se(2-) combines with H(+), leading to SeH(2), which is finally oxidized to Se(0) by oxygen. Therefore, quantum dots illumination in the presence of benzophenones brings about a profound nanoparticle reconstruction which takes place after dark storage; this agrees with the drastic quenching of the quantum dot emission detected immediately after illumination as well as the slow recovery in the dark.

https://doi.org/10.1021/la104037y