Plasmonic metal–semiconductor heterostructures
with well-defined
morphologies and spatial architectures have emerged as promising materials
for wide applications in photocatalysis and optoelectronics. However,
the synthesis of such structures with high quality and high yield
remains a great challenge due to the incompatibility between the two
materials. Herein, we report an optimized approach for the controlled
preparation of branched Ag-CdS icosapods, which possess 20 CdS arms
with an ordered spatial arrangement on the Ag cores. Moreover, the
length, diameter, and thickness of the CdS arms on the Ag nanoparticles
can be precisely tuned by the synthetic conditions, leading to Ag-CdS
icosapods with tunable absorption properties. Furthermore, more complex
hierarchical nanostructures can be achieved by the secondary growth
of nanoplate arrays on the CdS arms. As a proof of concept, a phototransistor
based on the self-assembled monolayer film of Ag-CdS icosapods shows
a stable photoresponse and quite a fast switching performance under
optical illumination of 540 nm without excitation of the CdS, which
originates from the generation and transfer of plasmon-induced hot
carriers in the Ag-CdS icosapods under an applied bias. This work
offers a reproducible approach to finely tuning metal–semiconductor
heterostructures with desirable architectures and paves the way for
more deeply understanding their structure–property correlation.