Source abstract
Abstract
Understanding how nanoparticles form stable colloids is fundamental to their practical applications. Nonlinear ligands are known to increase the stability of nanoparticles in apolar solvents compared to shells of linear alkyl chains. Here, we reveal the molecular origin of this colloidal stability. We observe that even a single methyl side chain can suppress disorder-order transitions in the ligand shell, with double bonds or branches leading to drastic decreases in agglomeration temperature in such dispersions. Through a combination of temperature-dependent X-ray scattering and molecular dynamics simulations, we show that these simple structural modifications prevent ligand molecules from forming ordered bundles, maintaining shell disorder even at temperatures approaching solvent freezing. The absence of ligand order enhances colloidal stability by weakening attraction between the ligand shells via a combination of energetic and entropic factors. This mechanism extends dispersion stability by more than 100 K compared to linear ligands of equivalent length. Our findings provide a molecular-level explanation for the enhanced stability previously observed with branched and unsaturated ligands, offering an effective strategy for engineering nanoparticle dispersions that remain stable across broad temperature ranges.
Source: openalex_inverted_index · Quality: baseline
Affiliations
INM─Leibniz Institute for New Materials, Campus D2 2, Saarbrücken 66123, Germany
ARC Centre of Excellence in Exciton Science, School of Chemistry
University of Sydney
Polymer Chemistry, Saarland University, Campus C4 2, Saarbrücken 66123, Germany
Saarene, Saarland Center for Energy Materials and Sustainability
Colloid and Interface Chemistry, Saarland University, Campus D2 2, Saarbrücken 66123, Germany
The University of Sydney Nano Institute
The University of Sydney
Funding
Deutsche Forschungsgemeinschaft · Centre of Excellence in Exciton Science · Division of Physics