Colloidal Stability of TiO₂ Nanoparticles: The Roles of Phosphonate Ligand Length and Solution Temperature

Abstract

Abstract Surface ligands are essential tools for the stabilization of colloidal nanoparticles (NPs) in solvents. However, knowledge regarding the effects of the ligand shell, especially the ligand length, is insufficient and controversial. Here we demonstrate solution‐based experiments on n‐ alkylphosphonate‐capped TiO 2 NPs to investigate the effects of ligand length and solution temperature on colloidal stability. A robust ligand‐exchange process is achieved that draws free ligands and impurities away from the colloidal solution. In the case of 8 nm anatase NPs in toluene, the dodecylphosphonate ligand provided better colloidal stability than all the other n‐ alkylphosphonate ligands. In addition, relaxation studies suggested there is kinetic hysteresis in the dispersion/agglomeration transition. The proposed method is applicable to a wide range of surface ligands designed to maximize the colloidal stability of NPs.