Electrophoretic
deposition (EPD) has been recognized as a promising
large-scale film preparation technology for industrial application.
Inspired by the conventional EPD method and the crystal diffusion
growth strategy, we propose a modified electrophoretic-induced self-assembly
deposition (EPAD) technique to control the morphologies of organic
functional materials. Here, an ionic-type dye with a conjugated skeleton
and strong noncovalent interactions, celestine blue (CB), is chosen
as a module molecule for EPAD investigation. As expected, CB molecules
can assemble into different nanostructures, dominated by applied voltage,
concentration effect, and duration. Compared to a nanopillar layered
packing structure formed by the traditional spin-coating method, the
EPAD approach can produce a nanofiber structure under a fixed condition
of 10 V/10 min. Intriguingly, a memristor device based on a pillar-like
nanostructure exhibits WORM-type behavior, while a device based on
nanofibers presents Flash memory performance. The assemble process
and the memory mechanism are uncovered by molecular dynamics simulations
and density-functional theory (DFT) calculations. This work endows
the typical EPD technique with a fresh application scenario, where
an in-depth study on the growth mechanism of nanofibers and the positive
effect of unique morphologies on memristor performance are offered.