Communication via Electron and Energy Transfer between Zinc Oxide Nanoparticles and Organic Adsorbates

• Published in: Journal of physical chemistry. C Vol. 113; no. 11; pp. 4669 - 4678
• Main Authors: Marczak, Renata, Werner, Fabian, Gnichwitz, Jan-Frederik, Hirsch, Andreas, Guldi, Dirk M, Peukert, Wolfgang
• Format: Journal Article
• Language: English
• Published: American Chemical Society 19.03.2009
• Subjects: C: Electron Transport, Optical and Electronic Devices, Hard Matter
• ISSN: 1932-7447; 1932-7455
• DOI: 10.1021/jp810696h

Stable ZnO nanoparticles suitable for further surface functionalization were synthesized in the liquid phase from homogeneous ethanolic solutions of the precursors lithium hydroxide and zinc acetate. It was found that the growth of the particles was governed by temperature as well as the presence of the reaction byproduct lithium acetate during the aging process. In particular, the reaction could be almost completely arrested by removal of this byproduct. The “washing” consisted of repeated precipitation of the ZnO particles by addition of alkanes such as heptane, removal of the supernatant, and redispersion in ethanol. Furthermore, the surface of the colloidal ZnO nanoparticles was successfully modified by catechol-anchoring group containing dye molecules, i.e., 5-(N-(3,4-dihydroxyphenethyl)-2-phenoxyacetamide)-10,15,20-(p-tert-butyltriphenyl)porphyrinatozinc (DOPAZ) and 5-(3,4-dihydroxy-N-phenylbenzamide)-10,15,20-tris(4-tert-butylphenyl)porphyrinatozinc (CAMIZ), for the study of photochemical properties. Thermogravimetric analysis proved the stability of the catechol anchor groups. Steady-state absorption spectroscopy as well as steady-state and time-resolved emission studies confirmed the electronic communication between the ZnO nanoparticles in their excited state and both of the porphyrins. More than 96% emission quenching of ZnO can be achieved by addition of the porphyrins, proving that the visible emission of the ZnO is caused by surface states, since only the surface of the particles was altered by the grafting experiments. Moreover, with increasing porphyrin concentrations the lifetimes changed from 46.0 to 15.3 ns. The shortened lifetimes prompt a new deactivation pathway, namely, through the electronic coupling of the porphyrins to the ZnO nanoparticle. Assuming that the decrease in lifetime is entirely due to electron transfer to the porphyrins, a rate constant of 0.35 × 108 s−1 could be determined for this process. When testing the excited state of the porphyrin in comparative assays between ZnO and Al2O3, we conclude a similar electron transfer deactivation.