Because of inefficient charge utilization
caused by localized π-electron
conjugation and large exciton binding energy, the photoelectrochemical
water-splitting efficiency of organic polymers is seriously limited.
Taking the graphitic carbon nitride (g-CN) polymer as an example,
we report a novel photoanode based on a vertically aligned g-CN porous
nanorod (PNR) array prepared in situ, using a thermal polycondensation
approach, with anodic aluminum oxide as the template. The g-CN PNR
array exhibits an excellent photocurrent density of 120.5 μA
cm–2 at 1.23 VRHE under
one sun illumination, the highest reported incident photon-to-current
efficiency of ∼15% at 360 nm, and an outstanding oxygen evolution
reaction stability in 0.1 M Na2SO4 aqueous solution,
which constitutes a benchmark performance among the reported g-CN-based
polymer photoanodes without any sacrificial reagents. When compared
with its planar counterpart, the enhanced performance of the PNR array
results principally from its unique structure that enables a high
degree of aromatic ring π-electron conjugation for higher mobility
of charge carriers, provides a direct pathway for the electron transport
to the substrate, produces a large portion of hole-accepting defect
sites and space charge region to promote exciton dissociation, and
also withstands more strain at the interface to ensure intimate contact
with the substrate. This work opens a new avenue to develop nanostructured
organic semiconductors for large-scale application of solar energy
conversion devices.