In
this study, we demonstrate a facile in situ synthetic strategy
to fabricate self-assembled organic/inorganic hybrid nanowires, wherein
a “pre-crystallization” approach was first utilized
to co-organize P3HT molecules and zinc precursors into highly elongated
nanowires, followed by a thermal oxidation treatment to directly grow
ZnO nanocrystals on the existing nanofibrillar template. By further
thermal annealing the ZnO embossed hybrid nanowires, a unique superhighway-like
architecture which composed of alternating parallel channels of P3HT
nanofibrils and ZnO nanocrystals could be further obtained. This donor/acceptor
(D/A) parallel-channel structure gave access to the improvements in
the exciton dissociation and charge transport, thereby enhancing photoluminescence
quenching, charge transport, and device performance. The photovoltaic
devices with the D/A parallel-lane structure gave a high PCE of 0.61%
as compared to only 0.07% from a conventional P3HT/ZnO bulk heterojuction
solar cell. Our approach offers a versatile route to coassemble inorganic
nanocrystals with π-conjugated polymer hosts, forming uniform
one-dimensional hybrid nanochannels potentially useful in optoelectronic
applications.