Search for: All records

Functional thin coatings are crucial in modern and emerging technologies, providing specified surface properties and protection, thereby influencing the performance and lifetime of materials and devices. The electrodeposition of polymer networks (EPoN) has recently been reported as a facile and potentially broadly applicable method to fabricate conformal polymeric ultrathin films on conductive substrates with arbitrary shapes and surface topography under mild solution conditions. In this work, a new generation of EPoN is introduced that utilizes a chemically reactive polymer appended by a small fraction of a electrochemical crosslinker as side groups. This EPoN iteration eliminates the need for precise end-group functionalization, enables the tuning of crosslink density and film thickness independent of polymer size, and the resulting reactive ultrathin films are amenable to post-deposition modification with desired functionalities using facile click-chemistry. To demonstrate this concept, we electrodeposit polyisoprene with small side-group fractions of the oxidative crosslinker phenol (<5%) as a thiol–ene-reactive polymer-network coating. The EPoN-derived ultrathin films are tunable and uniform with a thickness in the 100s of nanometers depending on phenol fraction and electrodeposition potential, and show a conformal morphology on complex porous electrode architectures. We further demonstrate post-EPoN functionalization of the ultrathin polyisoprene coatings with thiol–ene chemistry. 

This work elucidates a route to mesoporous magnetic materials with co-continuous morphologies from block copolymer self-assembly. The co-continuous structure impacts the magnetic behavior compared to non-structured chemically-identical materials.