The metallic interstitial nitride Ni3N was prepared from Ni(NH3)(6)Cl-2 and
NaNH2 in supercritical ammonia (p(NH3) approximate to 2 kbar) at 523 K. It
s previously reported crystal structure, as determined from X-ray powder da
ta, was confirmed by neutron powder diffraction: Ni3N crystallizes in the h
exagonal epsilon -Fe3N-type structure (P6(3)22, Z = 2, a = 4.6224 Angstrom
and c = 4.3059 Angstrom at room temperature). The N atoms on the octahedral
sites of an hcp arrangement of Ni show virtually complete occupational ord
er at ambient temperatures, which is preserved up to its thermal decomposit
ion at T approximate to 600 K. This behavior is in marked contrast to that
of the isotypic iron nitride, epsilon -Fe3N, which shows reversible partial
disordering within the same range of temperatures. Possible reasons for th
e different behaviors of the two nitrides epsilon -Fe3N and Ni3N are discus
sed.