Cd
x
Hg1–x
Se
alloy nanocrystals are obtained from CdSe semiconductor
nanocrystals via cation exchange. By varying the composition during
the exchange process, the Cd
x
Hg1–x
Se alloy nanocrystals offer a widely tunable electronic
transition from visible to NIR and even to mid-IR range. The visible
bandgap transition of the CdSe colloidal quantum dot gradually red-shifts
to the near-IR with the addition of the Hg precursor, and then the
steady-state intraband (or intersub-band) transition of the Cd
x
Hg1–x
Se
alloy nanocrystals appears. Finally, as the electron density is increased
by successive addition of metal precursor, localized surface plasmon
resonances (LSPRs) appear as a major electronic transition in the
mid-IR regime. The shift of the major electronic transition from the
bandgap to LSPRs infers that the exciton spatially moves to the surface
from the inside of the nanocrystal through the cation change and further
crystal growth. The corresponding variance of the nanocrystals’
structural, compositional, optical, electrical, and magnetic properties
was carefully monitored by using X-ray diffraction (XRD), X-ray photoelectron
spectroscopy (XPS), electron-dispersive X-ray (EDS) spectroscopy,
time-resolved photoluminescence, photocurrent measurement, and electron
paramagnetic resonance (EPR) spectroscopy, respectively. While a shift
in only the bandgap has been observed in conventional quantum dots
when cation-exchanged, the major oscillating transition transfers
from the bandgap to the higher quantum states in Cd
x
Hg1–x
Se alloy nanocrystal
formed by the cation-exchange in this report. The compositional change
expanding the optical range of nanocrystals from visible to mid-IR
regime will provide a useful means of optimally tuning the electronic
transition of nanocrystal-based applications along with improved optical
selectivity demonstrated by a single intraband or LSPR peak.