This paper reports
the fabrication of photothermal cryogels for
freshwater production
via
the solar-driven evaporation
of seawater. Photothermal cryogels were prepared
via
in situ
oxidative polymerization of pyrrole with
ammonium persulfate on preformed poly(sodium acrylate) (PSA) cryogels.
We found that the pyrrole concentration used in the fabrication process
has a significant effect on the final PSA/PPy cryogels (PPCs), causing
the as-formed polypyrrole (PPy) layer on the PPC to evolve from nanoparticles
to lamellar sheets and to consolidated thin films. PPC fabricated
using the lowest pyrrole concentration (i.e., PPC10) displays the
best solar-evaporation efficiency compared to the other samples, which
is further improved by switching the operative mode from floating
to standing. Specifically, in the latter case, the apparent solar
evaporation rate and solar-to-vapor conversion efficiency reach 1.41
kg m
–2
h
–1
and 96.9%, respectively,
due to the contribution of evaporation from the exposed lateral surfaces.
The distillate obtained from the condensed vapor, generated
via
solar evaporation of a synthetic seawater through PPC10,
shows an at least 99.99% reduction of Na while all the other elements
are reduced to a subppm level. We attribute the superior solar evaporation
and desalination performance of PPC10 to its (i) higher photoabsorption
efficiency, (ii) higher heat localization effect, (iii) open porous
structure that facilitates vapor removal, (iv) rough pore surface
that increases the surface area for light absorption and water evaporation,
and (v) higher water-absorption capacity to ensure efficient water
replenishment to the evaporative sites. It is anticipated that the
gained know-how from this study would offer insightful guidelines
to better designs of polymer-based 3D photothermal materials for solar
evaporation as well as for other emerging solar-related applications.