AbstractThe metalorganic vapour phase epitaxy of ZnTe on single crystal (100)ZnTe:P wafers is reported. The technological steps to prepare a substrate surface suitable for the high quality homoepitaxy of ZnTe are identified and optimised in terms of structural and morphological properties of overgrown epilayers. Removal of ∼7 µm of material from the ZnTe:P wafers by chemical etching in 1% Br2‐methanol solution proved necessary to achieve a sufficiently smooth and homogeneous surface; in‐situ H2 heat treatment of the wafers at 350°C immediately before growth ensures optimal desorption of residual oxides, allowing epilayer crystalline quality comparable to the substrate. However, the structure of epilayers degrades for growth temperatures (TG) above 350 °C due to the occurrence of stacking faults (SFs) within ∼200‐300 nm from the epilayer‐substrate interface. Accordingly, the epilayer band‐edge luminescence vanishes below 350 nm, indicating a worsening of the material radiative efficiency in very thin epilayers. The epilayer surface morphology is the result of a complex interplay between SF nucleation and Te:Zn ad‐atom stoichiometry during growth. Almost featureless morphologies are obtained for growth at 350 °C, i.e. under nearly stoichiometric surface conditions. Pyramid‐like hillocks develop instead for TG ≥ 360 °C, corresponding to Te‐rich surface conditions, their density rapidly increasing up to around 9 × 106 cm–2 at TG = 400 °C. Hillocks occur in close pairs on the epilayer surface, their nucleation being strongly reduced if a thin ZnTe buffer layer is grown at low (325 °C) temperature, i.e. if SFs do not occur at the epilayer‐substrate interface. This demonstrates that hillocks form as a result of three‐dimensional growth around partial dislocations pairs bounding SFs, the phenomenon being driven by Te ad‐atoms experiencing a Schwoebel potential barrier at the surface step edges around the dislocations. (© 2005 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim)
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