Cadmium
chalcogenides–metal hybrid nanostructures play an
important role in a wide range of applications and are key components
in photocatalysis. Hence, great efforts have been devoted to the exploration
of a variety of metal components, each offering different functionalities.
Silver is a vital catalyst used in the production of major industrial
chemicals, found in virtually every electronic device, widely exploited
as an antibacterial agent, used in fuel cells, and has been extensively
investigated for CO2 reduction. Yet, silver nanoparticles
were not utilized in conjunction with cadmium chalcogenide colloidal
nanostructures due to the tendency of Ag+ to undergo cation
exchange. We present here a new strategy that opens up a pathway for
avoiding cation exchange and obtaining metallic silver tipping on
cadmium chalcogenide nanorods. The formation of Ag trioctylphosphine
complex, as an intermediate in the course of Ag deposition on nanorods,
was identified to be a critical step, which prevents undesirable cation
exchange. Metallic Ag was confirmed by several advanced techniques
and its growth location on the tip of nanorods was carefully studied.
Moderate control over the crystalline Ag tip size was demonstrated
in the range of 1.5–5.4 nm.