One
of the major challenges in controlling the colloidal stability
in nonpolar solvents concerns their surface charging strength. By
tuning surface chemical structures in nonpolar solvents, the surface
charge can be modulated with nonionic surfactants used as charge additives.
In this study, various self-assembled monolayers (SAMs) were coated
onto specific surfaces and nanoparticles to obtain different chemical
structures. X-ray photoelectron spectroscopy (XPS) and atomic force
microscope (AFM) measurements were used to quantify surface chemical
structures, whereas dynamic adsorption experiments and molecular dynamics
(MD) simulation were utilized to study the influence of these structures
on surfactant adsorption behavior. Surface charging optimization was
achieved by mediating the concentration of electron acceptors and
donors, which is reflected as matching the alkyl length of SAMs with
an appropriate concentration of hydroxyl group on the surfaces. The
charging strength of particles decreased above a certain surfactant
concentration, which is attributed to the competition between surfactant
adsorption stability and charge neutralization effect generated via
the disproportionation process.