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Updated: Apr 13, 2026

Synthesis, Characterization, and Functionalization of Hybrid Au/CdS and Au/ZnS Core/Shell Nanoparticles
Published on: March 2, 2016
Investigation of the Degree of Functionalization and Colloidal Stability of Shell-by-Shell Functionalized TiO2
Lisa M S Stiegler1,2, Vincent Wedler3, İdil Büküşoğlu1,2
1Institute of Interfaces and Particle Technology (IPT), Friedrich-Alexander-Universität Erlangen-Nürnberg (FAU), Cauerstraße 4, 91058, Erlangen, Germany.
Abstract:
In this work, a series of Shell-by-Shell (SbS)-functionalized colloidal systems consisting of 6 nm TiO2 anatase nanoparticles (NPs), one of the phosphonic acids (PAs) propylphosphonic acid (PAC3), hexylphosphonic acid (PAC6), dodecylphosphonic acid (PAC12), tetradecylphosphonic acid (PAC14), hexadecylphosphonic acid (PAC16), octadecylphosphonic acid (PAC18) and the amphiphile sodium dodecylbenzenesulfonate (SDBS) were prepared, resulting in TiO2-PACX@SDBS (X = 3, 6, 12, 14, 16, or 18) NPs dispersed in deionized water (DIW). During the whole functionalization process, the NPs were subjected to thermogravimetric analysis (TGA) to gain insights into their degree of functionalization and respective thermal stability. In addition, the colloidal stability of the NPs as a function of PA chain length was analyzed by analytical ultracentrifugation (AUC). By combining both TGA and AUC, it was found that the resulting hierarchical NP architectures form agglomerates, with the degree of agglomeration depending on the length of the PA used for the first-shell functionalization. This allows conclusions to be drawn about the efficiency of the overlap between the PA and the SDBS carbon chains.

