Nanoassemblies designed from semiconductor quantum dots and molecular arrays

E Zenkevich; F Cichos; A Shulga; E P Petrov; T Blaudeck; C von Borczyskowski

doi:10.1021/jp040595a

Nanoassemblies designed from semiconductor quantum dots and molecular arrays

J Phys Chem B. 2005 May 12;109(18):8679-92. doi: 10.1021/jp040595a.

Authors

E Zenkevich¹, F Cichos, A Shulga, E P Petrov, T Blaudeck, C von Borczyskowski

Affiliation

¹ Institute of Physics, Chemnitz University of Technology, 09107 Chemnitz, Germany.

PMID: 16852028
DOI: 10.1021/jp040595a

Abstract

The formation of nanoassemblies of CdSe/ZnS quantum dots (QD) and pyridyl-substituted free-base porphyrin (H(2)P) molecules has been spectroscopically identified by static and time-resolved techniques. The formation of nanoassemblies has been engineered by controlling the type and geometry of the H(2)P molecules. Pyridyl functionalization gives rise to a strong complex formation accompanied by QD photoluminescence (PL) quenching. For some of the systems, this quenching is partly related to fluorescence resonance energy transfer (FRET) from the QD to H(2)P and can be explained according to the Förster model. The quantitative interpretation of PL quenching due to complexation reveals that (i) on average only about (1)/(5) of the H(2)P molecules at a given H(2)P/QD molar ratio are assembled on the QD and (ii) only a limited number of "vacancies" accessible for H(2)P attachment exist on the QD surface.