3D printing, or additive manufacturing, is one of the most impactful technologies in recent decades. It relies on the layer-by-layer fabrication of three-dimensional objects from digital models, unlike traditional subtractive techniques that shape parts by material removal. This approach enables high precision, design flexibility, reduced material waste, rapid prototyping, and the realization of complex geometries difficult to obtain with conventional manufacturing.
Despite these advantages, the most widely adopted and cost-effective 3D printing technologies, such as Fused Deposition Modeling (FDM) and Digital Light Projection (DLP), are largely limited to polymeric materials. This aspect drives the development of efficient and cost-effective metallization strategies able to impart metallic properties to 3D printed polymer components. Among available solutions, wet metallization techniques based on liquid electrolytes are particularly attractive in terms of cost and scalability.
A particularly promising way to carry out wet metallization on 3D printed parts is represented by the use of self-activating materials. These materials can be directly 3D printed and incorporate either a catalytic metal or a precursor of a catalytic species, such as a metal salt. When a precursor is used, it can be converted into the active catalyst through chemical reduction. Embedding the catalytic species within the printed part removes the need for the etching and surface activation steps typical of standard electroless plating, providing improved adhesion, coating uniformity and the possibility of selective metallization.
In the present work, self-activating composites containing non-precious transition metal salts are developed, 3D printed, and metallized. Nickel and copper salt microparticles are dispersed in a DLP resin to obtain printable composites. After printing, surface-exposed precursors are chemically reduced to form metallic nuclei, which initiate the electroless deposition of NiP and Cu. The resulting coatings are characterized in terms of adhesion, uniformity, and morphology. The possibility of achieving selective metallization is demonstrated as well.
