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and heated, followed by injection of a chalcogen precursor solution into the
reagents. The
rst organometallic synthesis of capped Pb chalcogenide QDs
was actually achieved by the thermolysis of single-source precursors.
21,22
In
these cases, lead dithio- and diselenocarbamates were thermolysed in
trioctylphosphine oxide (TOPO) at relatively low temperatures (<200
C),
giving lead sul
de and lead selenide particles of varying sizes and shapes.
The electronic spectra clearly showed absorption in the red/near infrared
region, although no excitonic peak or emission was observed. Similar work,
reported later, also described the synthesis of PbS using Pb(S
2
CNEt
2
)
2
, with
nanoparticles exhibiting a wide range of morphologies.
23
The
d
n
1
y
4
n
g
|
7
rst hot injection method using two precursors was reported by
Murray
et al.
,
24
who importantly showed the
rst absorption spectra with
clear features (Figure 3.1), highlighting the
rst excitonic transition which
.
Figure 3.1
Absorption spectra of PbSe QDs of various diameters: (a) 3.0 nm, (b) 3.5
nm, (c) 4.5 nm, (d) 5.0 nm, (e) 5.5 nm, (f) 7.0 nm, (g) 8.0 nm, (h) 9.0 nm.
Reprinted with permission from C. B. Murray, S. Sun, W. Gaschler, H.
Doyle, T. A. Betley and C. R. Kagan,
IBM J. Res. Dev.
, 2001,
45
, 47.
Copyright 2001 IBM.
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