The mechanisms of atomic diffusion in the cation sublattice of CdTe have be
en studied. For the present study two types of CdTe layers have been grown
by molecular beam epitaxy (MBE) at different Cd/Te flux ratio resulting in
different stoichiometry of the matrix material. Each of the samples contain
ed three build-in delta-like markers of MnTe, MgTe and ZnTe. From the sprea
d of the cations out of the markers, caused by a thermal annealing, the dif
fusivities of Mn, Mg, and Zn were determined by means of secondary ion beam
spectrometry (SIMS). We found that the stoichiometry of the CdTe matrix st
rongly influences on the diffusion activation energy but for a given matrix
the activation energy does not depend on the diffusing species. For CdTe l
ayer rich in Cd, the activation energies of cation diffusion for the three
investigated cations are found to be around 1.3 eV, while in Te-rich matrix
around 1.9 eV. This difference indicates that different diffusion mechanis
ms operate in these two cases. Assuming the interstitial mechanism in the f
ormer case and the vacancy mechanism in the latter, energies of the cation
migration in CdTe and of Cd vacancy formation are estimated to be equal to
1.3 and 0.6 eV, respectively. (C) 2000 Elsevier Science S.A. All rights res
erved.