Lead-based halide perovskites (APbX3, where A = organic
or inorganic cation, X = Cl, Br, I) are suitable materials for many
optoelectronic devices due to their many attractive properties. However,
the concern of lead toxicity and the poor ambient and operational
stability of the organic cation group greatly limit their practical
utilization. Therefore, there has recently been great interest in
lead-free, environment-friendly all-inorganic halide perovskites (IHPs).
Sb and Sn are common species suggested to replace Pb for Pb-free IHPs.
However, the large difference in the melting points of the precursor
materials (e.g., CsBr and SbBr3 precursors for Cs3Sb2Br9) makes the chemical vapor deposition
(CVD) growth of high-quality Pb-free IHPs a very challenging task.
In this work, we developed a two-step CVD method to overcome this
challenge and successfully synthesized Pb-free Cs3Sb2Br9 perovskite microplates. Cs3Sb2Br9 microplates ∼25 μm in size with
the exciton absorption peak at ∼2.8 eV and a band gap of ∼2.85
eV were obtained. The microplates have a smooth hexagonal morphology
and show a large Stokes shift of ∼450 meV and exciton binding
energy of ∼200 meV. To demonstrate the applications of these
microplates in optoelectronics, simple photoconductive devices were
fabricated. These photodetectors exhibit a current on/off ratio of
2.36 × 102, a responsivity of 36.9 mA/W, and a detectivity
of 1.0 × 1010 Jones with a fast response of rise and
decay time of 61.5 and 24 ms, respectively, upon 450 nm photon irradiation.
Finally, the Cs3Sb2Br9 microplates
also show good stability in ambient air without encapsulation. These
results demonstrate that the 2-step CVD process is an effective approach
to synthesize high-quality all-inorganic lead-free Cs3Sb2Br9 perovskite microplates that have the potential
for future high-performance optoelectronic device applications.