Artificial nanofluidic channels that achieve light-driven
ion transport
in biological systems based on photoelectric effect have attracted
significant attention for signal transduction and light energy conversion.
However, the light-responsive performance is limited by the charge
separation efficiency on the surface of the channels. Herein, we introduce
semiconductor p–n junctions into nanofluidic channels to enhance
their light-driven ion transport. The p–n junction is formed
by an n-type titanium dioxide (TiO2) nanoparticles layer
on an electrochemically fabricated p-type polypyrrole (PPy) membrane.
The light-induced charge separation at p–n junctions increases
the surface charge density of the positively charged PPy membrane.
Consequently, the light-driven ion current through the nanofluidic
channels is enhanced from 79.6 to 111.9 nA by 40.6% when compared
with a single-component p-type PPy membrane. The proof-of-concept
demonstration of enhanced light-driven ion transport by semiconductor
p–n junctions provides a route toward high-performance light-responsive
nanofluidic channels, which demonstrates potential applications for
light-controlled mass transport, signal transduction, and energy conversion.