Salt hydrate phase change materials are important in
advancing
thermal energy storage technologies for the development of renewable
energies. At present, their widespread use is limited by undesired
undercooling and phase separation, as well as their tendency to corrode
container materials. Herein, we report a direct ink writing (DIW)
additive manufacturing technique to print noncorrosive salt hydrate
composites with thoroughly integrated nucleating agents and thermally
conductive additives. First, salt hydrate particles are prepared from
nonaqueous Pickering emulsions and then employed as rheological modifiers
to formulate thixotropic inks with polymer dispersions in toluene
serving as the matrix. These inks are successfully printed at room
temperature and cured by solvent evaporation under ambient conditions.
The resulting printed and cured composites, containing up to 70 wt
% of the salt hydrate, exhibit reliable thermal cyclability for 10
cycles and suppressed undercooling compared to the bulk salt hydrate.
Remarkably, the composites consistently maintain their structural
integrity and thermal performance throughout the entirety of both
the melting and solidification processes. We demonstrate the versatility
of this approach by utilizing two salt hydrates, magnesium nitrate
hexahydrate (MNH, T
m = 89 °C) and
zinc nitrate hexahydrate (ZNH, T
m = 36
°C), to achieve desired thermal characteristics across a wide
range of temperatures. Further, we establish that the incorporation
of carbon black in these inks enhances the thermal conductivity by
at least 33%. This approach consolidates the strengths of additive
manufacturing and salt hydrate phase change materials to harness customizable
thermal properties, well suited for targeted thermal energy management
applications.