Surfactant-laden
sessile droplet evaporation plays a crucial role
in a variety of omnipresent natural and technological applications,
such as drying, coating, spray, and inkjet printing. Surfactant molecules
can adsorb easily on interfaces and, hence, destructively ruin the
useful gas-trapping wetting state (i.e., Cassie–Baxter, CB)
of a drop on superhydrophobic (SH) surfaces. However, the influence
of surfactant adsorption or concentration on evaporation modes has
been rarely investigated so far. Here, we investigate the evaporation
dynamics of aqueous didodecyldimethylammonium bromide (DDAB)
sessile droplet on SH surfaces made of regular hydrophobic micropillars,
with various dimensionless surfactant concentrations (C
S), primarily using experiments. We find that all drops
initially form a CB state with a pinned base radius and evaporate
in a mode of constant contact radius (CCR). Water and low-C
S (=0.02) drop subsequently evaporate with a
constant contact angle (CCA) mode, followed by a CCR mode and, eventually,
a mixed-mode. By contrast, high-C
S (of
0.25–1) droplets undergo a complex mixed mode, with rapidly
increasing base radius, and finally a mixed mode, with slowly decreasing
base radius and contact angle. The experimental data reveal that contact-angle-dependent
evaporative mass flux, ṁ, collapses onto a
nearly universal curve depending on C
S. For the low-C
S (of 0–0.25) drops, ṁ is lower and consistent with an evaporative cooling
model, whereas high-C
S (of 0.5–1)
droplets are consistent with a pure vapor-diffusive model. We further
show that the critical C
S delineating
these two evaporative models correlates with saturated surfactant
adsorption on both liquid–solid and liquid–vapor interfaces.