P. Prete et al., Functional validation of novel Se and S alkyl precursors for the low temperature pyrolytic MOVPE growth of ZnSe, ZnS and ZnSSe, MATER CH PH, 66(2-3), 2000, pp. 253-258
We report on the pyrolytic metalorganic vapour phase epitaxy of ZnSe, ZnS a
nd ZnSSe by using diethyldisulphide [(C2H5)(2)S-2] and dimethyldiselenide [
(CH3)(2)Se-2], these dialkyls being suitable for the low (<400 degrees C) t
emperature growth of S- and Se-based compounds. (C2H5)(2)S-2 and (CH3)(2)Se
-2 allow a substantial reduction of ZnSe and ZnS growth temperatures with r
espect to diethylsulphide and dimethylselenide. Mass spectrometry (MS) frag
mentation products of (C2H5)(2)S-2 and (CH3)(2)Se-2 molecular ions are stud
ied to investigate the relative strengths of specific bonds in the molecule
s and to identify their decomposition paths. The decomposition of (C2H5)(2)
S-2 occurs mainly via the loss of ethylene molecules through beta-hydrogen
elimination reactions. On the contrary, the sequential loss of methyl radic
als seems the dominant path of (CH3)(2)Se-2, beta-like hydrogen elimination
reactions being still possible, although less likely than for (C2H5)(2)S-2
. The occurrence of a peculiar CH3. transposition reaction is also suggeste
d for (CH3)(2)Se-2. Weak or negligible [for (C2H5)(2)S-2] contributions to
the alkyl mass spectra are observed from Se-Se or S-S bond cleavage. This i
s ascribed to the strength of the Se-Se (or S-S) bond in the (CH3)(2)Se-2 [
(C2H5)(2)S-2] molecule, which would destabilise the Se-C (S-C) bonds, leadi
ng to the alkyl low thermal stability. Low H concentrations, i.e. (1-3) x 1
0(17) cm(-3), are found by secondary ion MS in ZnSe samples and attributed
to the low proclivity of (CH3)(2)Se-2 to decompose through beta-like hydrog
en reactions. (C) 2000 Elsevier Science S.A. All rights reserved.