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Fig. 10.12 RHEED patterns of GaSb nanodots formed by codeposition ( a )of15MLGaSbat
300 Cand( b ) of 30ML GaSb at 450 C. ( c )and( d ) STM images corresponding to ( a )and
( b ), respectively. ( e ) Temperature dependence of densities of the formed nanodots ( solid circles )
and nanodot density estimated from Ga diffusion length on ultrathin SiO 2 surface ( open circles ).
( f ) Raman spectrum from the nanodots in ( d )
With a decrease in the codeposition temperature, the spot patterns in RHEED
became obscure as shown in Fig. 10.12 a, b, indicating degradation in nanodot crys-
tallinity. On the other hand, when the codeposition temperature was reduced, the
nanodot density continuously increased to 3
10 11 cm 2 at 300 C and the ultra-
×
10 12 cm 2 ) at 200 C as shown in Fig. 10.12 e. Figure 10.12 fis
Raman spectra for GaSb nanodots corresponding to Fig. 10.12 b, d. The sharp peak
related to Si crystal phonons near 520 cm 1 and the broad peak around 400 cm 1
also appeared for the Si substrates without GaSb nanodots, indicating that the sharp
peak at 223 cm 1 is related to GaSb nanodots. This peak at 223 cm 1 was assigned
to the transverse optical (TO) mode in GaSb nanodots from the TO mode in the
GaSb bulk (223.6 cm 1 )[ 51 ]. The peak positions were independent of the amount
of GaSb nanodots deposited in our experiment. The close peak positions of the nan-
odots and the bulk indicate that the lattice mismatch strains with Si almost relaxed
in the nanodots. This was also confirmed by comparing RHEED spot spacings in
Fig. 10.12 b with those of homoepitaxial Si nanodots [ 14 ].
high density (
1
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