Ag(I)-doped CdSe nanotetrapods (NTPs)
have been prepared using
the post-synthesis cation exchange method. The shape and crystal structure
of NTPs are found to be conserved after doping. The photoluminescence
(PL) spectrum is Stokes shifted by 110 nm (0.33 eV) in doped NTPs
at the highest dopant content (0.6%). The PL quantum yield increases
to 11% from a value of 1.6% in undoped NTPs, with the emergence of
a new, significantly longer component with a lifetime of 143 ns, at
the cost of the fastest, nanosecond or lower component in the undoped
NTPs. The dynamics of hole capture, which is the primary photoprocess
that brings about the PL enhancement, has been elucidated by ultrafast
transient absorption spectroscopy. Hence, Ag-doped colloidal three-dimensional
NTPs are shown to be promising photoluminescent materials, which are
less likely to suffer from the issue of the reabsorption of emitted
photons due to the large Stokes shift emission. There are immense
possibilities for their application in colloidal nanocrystal-based
optoelectronic and photonic devices like light-emitting diodes and
luminescent solar concentrators.