The defect tolerance
of halide perovskite materials has led to
efficient optoelectronic devices based on thin-film geometries with
unprecedented speed. Moreover, it has motivated research on perovskite
nanowires because surface recombination continues to be a major obstacle
in realizing efficient nanowire devices. Recently, ordered vertical
arrays of perovskite nanowires have been realized, which can benefit
from nanophotonic design strategies allowing precise control over
light propagation, absorption, and emission. An anodized aluminum
oxide template is used to confine the crystallization process, either
in the solution or in the vapor phase. This approach, however, results
in an unavoidable drawback: only nanowires embedded inside the AAO
are obtainable, since the AAO cannot be etched selectively. The requirement
for a support matrix originates from the intrinsic difficulty of controlling
precise placement, sizes, and shapes of free-standing nanostructures
during crystallization, especially in solution. Here we introduce
a method to fabricate free-standing solution-based vertical nanowires
with arbitrary dimensions. Our scheme also utilizes AAO; however,
in contrast to embedding the perovskite inside the matrix, we apply
a pressure gradient to extrude the solution from the free-standing
templates. The exit profile of the template is subsequently translated
into the final semiconductor geometry. The free-standing nanowires
are single crystalline and show a PLQY up to ∼29%. In principle,
this rapid method is not limited to nanowires but can be extended
to uniform and ordered high PLQY single crystalline perovskite nanostructures
of different shapes and sizes by fabricating additional masking layers
or using specifically shaped nanopore endings.