It is shown by electron diffraction and microscopy that the first stage in the crystallization of chemically and electrolytically deposited amorphous Ni–P alloys on heating to 250°C is an f.c.c. metastable phase α with a=0·55 nm. In the second stage of crystallization, at 270–400°C, metastable hexagonal phases α1, α2 and α3 are formed. These phases have the same a=0·672 nm but different c parameters, the latter being in the ratio 2:3:8 with c(α1)=0·952 nm. They originate from the f.c.c. α phase with (001)hex parallel to {111}α and ⟨210⟩hex parallel to ⟨110⟩α. The growth habit of α1 exhibits a dendrite-like morphology consisting of 90° rotation twins about [001]α. Above 400°C, these hexagonal metastable phases transform into stable phases Ni3P, Ni12P5 and the nickel solid solution. The three ‘new’ metastable Ni3P phases reported by Vafaei-Makhsoos (1980) have not been confirmed; on the contrary, all the electron diffraction patterns of these phases can be indexed quite easily as those of Ni12P5.
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Kuo et al. (1985) studied this question.
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