Salinity gradient energy (SGE) is
an increasingly important form
of renewable energy occurring in nature when river water streams flow
into the sea. Charged polymeric gels have been recently proposed to
convert SGE into mechanical energy by utilizing their volumetric response
to solution salinity difference. However, most of these materials
have drawbacks such as mechanical weakness, manufacturing challenges,
and poor durability caused by various kinds of fouling, hampering
the new promise of SGE harvest. This study develops a facile, yet
versatile radiation cross-linking method to fabricate robust and antifouling
poly(acrylic acid-co-acrylamide) hydrogels that can
overcome the above-mentioned shortcomings. These cost-effective hydrogels
exhibit the superior capacity for the external load due to the hydrogen
bonds between the carboxyl and amide groups, and desirable antifouling
effect, i.e., high resistance to multivalent cations, bovine serum
albumin, and inorganic particles. The hydrogel-based osmotic engine
obtains a power density of 1.72 mW/g and energy efficiency (EE) of
2.84%, exceeding the values achieved by existing hydrogels under model
3.5% NaCl–0.035% NaCl cycling solution. Moreover, in a subsequent
test to extract SGE in the natural matrix of seawater and river water
mixing, we showed for the first time the copolymer hydrogels, unlike
common single-charged hydrogels that fail to swell by severe absorption
of Ca2+ and Mg2+ ions, enable the multiply cycling
and achieve a power density of 1.12 mW/g and EE of 1.17% under optimal
ionic density. Therefore, the facileness and versatility of the present
radiation method make P(AA-co-AAm) hydrogels suitable
for large-scale manufacturing and potential incorporation into SGE
harnessing.