Polyacrylamide
(PAM) is one of the most important water-soluble
polymers that has been extensively applied in water treatment, drug
delivery, and flexible electronic devices. The basic properties, e.g.,
microstructure, nanomechanics, and solubility, are deeply involved
in the performance of PAM materials. Current research has paid more
attention to the development and expansion of the macroscopic properties
of PAM materials, and the study of the mechanism involved with the
roles of water and ions on the properties of PAM is insufficient,
especially for the behaviors of neutral amide side groups. In this
study, single molecule force spectroscopy was combined with molecular
dynamic (MD) simulations, atomic force microscope imaging, and dynamic
light scattering to investigate the effects of monovalent ions on
the nanomechanics and molecular conformations of neutral PAM (NPAM).
These results show that the single-molecule elasticity and conformation
of NPAM exhibit huge variation in different monovalent salt solutions.
NPAM adopts an extended conformation in aqueous solutions of strong
hydrated ion (acetate), while transforms into a collapse globule in
the existence of weakly hydrated ion (SCN–). It
is believed that the competition between intramolecular and intermolecular
weak interactions plays a key role to adjust the molecular conformation
and elasticity of NPAM. The competition can be largely influenced
by the type of monovalent ions through hydration or a chaotropic
effect. Methods utilized in this study provide a means to better understand
the Hofmeister effect of ions on other macromolecules containing amide
groups at the single-molecule level.