Abstract
The development of 3C-SiC crystals from oriented hexagonal seed has always suffered from systematic twinning that appears during the nucleation step of the layer. To investigate the possibility to reduce or eliminate the incoherent twin boundaries at high temperature (for conditions close to bulk growth ones), we conducted an experimental study on 3C-SiC nucleation. A mechanism for the selection of one 3C-SiC orientation among the two possible is proposed. It is based on a strong interaction between the α-SiC substrate steps and the anisotropic lateral expansion of the β-SiC domains. This model is confirmed by cross-sectional high resolution transmission microscopy observations of the α−β interface. The mechanism is discussed with respect to the surface polarity (Si or C faces), the miscut angle, and the substrate polytype.
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