Two-dimensional (2D) Ruddlesden–Popper (RP) halide
perovskite
has attracted significant attention as a promising candidate for high-efficiency
light sources. RP perovskites, when synthesized into well-defined
nanowires (NWs), have the potential to serve as nanoscale coherent
light sources by incorporating optical cavity effects with their light
emission behaviors. However, RP perovskites tend to grow in macroscopic
thin sheets as opposed to relevant NW structures due to the layered
nature of the crystal lattice, which necessitates a new way of controlling
nanoscale morphologies. Here, we achieve NWs of RP BA2PbBr4 (BA = butylammonium), for the first time, using chemical
vapor deposition (CVD) by systematically navigating a wide range of
growth conditions and constructing growth regimes of distinct morphologies.
Of the two particular regimes that produce well-formed nanostructures,
we find that RP BA2PbBr4 grows into energetically
favored thin nanoplatelets (NPLs) at high temperatures, whereas intermediate
temperatures allow it to first grow into three-dimensional (3D) pyramidal
nuclei and then get elongated into NWs upon continued growth. We propose
temperature-dependent diffusion of surface species as a deciding factor
of our morphological control. We present crystallographic and elemental
analyses to confirm that our NWs have the appropriate lattice structures
and chemical stoichiometry of BA2PbBr4. Static
and time-resolved optical measurements show quantized absorption and
emission features at 400 and 406 nm, respectively, with a radiative
decay time of 1.7 ns that is much quicker than the 8.7 ns decay time
of a prototypical 3D CsPbBr3 perovskite. The RP NWs exhibit
a strong exciton binding energy of 279 meV, which can be understood
by the reduced dimensionality of BA2PbBr4. The
strong absorption and radiative emission characteristics suggest that
the RP BA2PbBr4 NWs are good candidates as bright,
ultrasmall light sources for nanophotonic and optical communication
applications.