Unraveling the charge transfer across a heterointerface
is crucial
for cutting-edge optoelectronic applications, including photodetectors,
solar photovoltaics, light-emitting diodes, and so on. The incorporation
of perovskite nanocrystals (NCs) into optoelectronics is limited primarily
because of the presence of grain boundaries, carrier trapping, and
ion migration, which restricts charge/energy transfer. Combining perovskite
NCs with two-dimensional (2D) materials is a powerful approach to
enhance energy harvesting and transport at the 0D-2D heterointerface.
A simple sonication method was adopted to integrate zero-dimensional
(0D) mixed halide perovskite CsPbBr2I NCs and topological
2D Bi2Se3 nanosheets (NSs) to realize a nanohybrid
system. A series of optical signatures such as Raman shift, quenching
of photoluminescence (PL), and shortened fluorescence lifetime in
the nanohybrid clearly substantiate the interfacial charge transfer
dynamics. Cyclic voltammetry and Kelvin probe force microscopy analysis
and the optical studies established the type-I band alignment between
perovskite NCs and Bi2Se3 NSs. The charge transfer
dynamics of the nanohybrid was confirmed from the dramatic quenching
of the PL intensity of CsPbBr2I NCs and an associated increase
in the NIR PL as well as visible PL intensities of the Bi2Se3 NSs owing to increased carrier density caused by charge
transfer. Furthermore, improved photoresponse performance of the hybrid
system demonstrates the role of interfacial carrier transfer in 2D-0D
nanohybrids, suppressing the radiative recombination in the light-harvesting
perovskite NCs. The nanohybrid-based photodetector exhibits a high
spectral responsivity of 14.4 A/W, a spectral detectivity of 0.4 ×
1012 Jones, and a fast growth/decay time of 82 μs/24
μs. These results will stimulate further exploration of topological
2D materials/halide perovskite-based novel hybrid functional devices
for photodetection, light-harvesting, and light-emitting applications.