The chemistry and kinetics of the nitridation of GaAs (100) surfaces by N₂, N₂-H₂, and N₂-NH₃ radio-frequency plasmas, in a remote configuration, are investigated in situ and in real time using spectroscopic ellipsometry. The effects of the surface temperature in the range 70--700 ^∘{}C and of the gas-phase chemistry on both the nitridation kinetics and the composition of the resulting GaN layer are highlighted. Pure N₂ plasmas yield stoichiometric and smooth GaN layers with As segregation at the GaN/GaAs interface. The As segregation inhibits GaAs nitridation, because the N atoms scavenge the free As, and thereby limits the GaN thickness to a few angstroms. Thicker GaN layers (>100 {}) are obtained by N₂-H₂ and N₂-NH₃ plasmas, since hydrogen reduces the As segregation by the formation and desorption of AsHₓ species. For the three plasma mixtures, the self-limiting nature of the GaAs nitridation process is revealed and explained using simple kinetic and chemical models based on the fact that the GaAs nitridation can be considered to be a topochemical reaction. Also demonstrated is the ineffectiveness of the nitridation at T>~600^∘C, which is accompanied by the GaAs substrate decomposition and yields both a rough and Ga-rich GaN layer.
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Losurdo et al. (1998) studied this question.
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