Hafnium nitrides

The hafnium nitrides are the various salts produced from combining hafnium and nitrogen. The two most important such are hafnium(III) nitride, HfN; and hafnium(IV) nitride, Hf₃N₄. None can be prepared from hafnium oxide, but must instead be prepared from the elemental metal or a different hafnium nitride salt; attempted nitridation of the oxide gives an oxynitride instead.^[1]

HfN is refractory and generally produced as a thin film coating,^[2] although zone annealing gives the bulk material.^[3] HfN adopts the rock-salt crystal structure.^[2] The surplus hafnium electron delocalizes, so that HfN is a metal, conducting at room temperature and superconducting below 8.8 K (−443.83 °F). Its bright gold color is a cheaper alternative to gilding.^[4]

The dark red semiconductor Hf₃N₄ does not form at room temperature, but requires high pressure, high temperature synthesis in a diamond anvil cell. At 18 GPa (180,000 atm) and 2,800 K (4,580 °F), it adopts the cubic crystal structure and repeats according to space group I{{{1}}}3d.^[2] At lower pressures, the cubic structure is believed metastable, decaying to the orthorhombic structure of zirconium(IV) nitride.^[4]^[5] That structure forms outright at 19 GPa and 2,000 K (3,140 °F), and another metastable tetragonal structure forms at 12 GPa and 1,500 K (2,240 °F). Computational studies suggest that it may catalyze polymerization of nitrogen at very high temperatures, through a catenary anion in HfN₁₀.^[5]

In systems with limited nitrogen, hafnium also forms Hf₃N₂, as well as a solid solution hafnium alloy.^[6]

References

^ Bazhanov, D. I.; Knizhnik, A. A.; Safonov, A. A.; Bagatur’yants, A. A.; Stoker, M. W.; Korkin, A. A. (2005-02-15). "Structure and electronic properties of zirconium and hafnium nitrides and oxynitrides". Journal of Applied Physics. 97 (4). doi:10.1063/1.1851000. ISSN 0021-8979.
^ ^a ^b ^c Zerr, Andreas; Miehe, Gerhard; Riedel, Ralf (2003-03-01). "Synthesis of cubic zirconium and hafnium nitride having Th3P4 structure". Nature Materials. 2 (3): 185–189. doi:10.1038/nmat836. ISSN 1476-1122.
^ Christensen, A. Nørlund; Kress, W.; Miura, M.; Lehner, N. (1983-07-15). "Phonon anomalies in transition-metal nitrides: HfN". Physical Review B. 28 (2): 977–981. doi:10.1103/PhysRevB.28.977. ISSN 0163-1829.
^ ^a ^b Kroll, Peter (2003-03-25). "Hafnium Nitride with Thorium Phosphide Structure: Physical Properties and an Assessment of the Hf-N, Zr-N, and Ti-N Phase Diagrams at High Pressures and Temperatures". Physical Review Letters. 90 (12). doi:10.1103/PhysRevLett.90.125501. ISSN 0031-9007.
^ ^a ^b Zhang, Jin; Oganov, Artem R.; Li, Xinfeng; Niu, Haiyang (2017-01-18). "Pressure-stabilized hafnium nitrides and their properties". Physical Review B. 95 (2). doi:10.1103/PhysRevB.95.020103. ISSN 2469-9950.
^ Ushakov, Sergey V.; Navrotsky, Alexandra; Hong, Qi-Jun; van de Walle, Axel (26 Aug 2019) [6 Aug 2019]. "Carbides and nitrides of zirconium and hafnium". Materials. 2019 (12). Basel: MDPI. doi:10.3390/ma12172728.

Salts and covalent derivatives of the nitride ion

NH₃
N₂H₄
+H
HN²⁻
H₂N⁻

Be₃N₂
Be(N₃)₂

C₂N₂
β-C₃N₄
g-C₃N₄
C_$x$N_$y$

N₂

N_$x$O_$y$
+O

N₃F
N₂F₂
N₂F₄
NF₃
+F

Ne

Mg₃N₂
Mg(N₃)₂

S_$x$N_$y$
SN
S₂N₂
S₄N₄
SN₂H₂

NCl₃
ClN₃
+Cl

Ar

K₃N
KN₃

Ca₃N₂
Ca(N₃)₂

Mn_$x$N_$y$

Fe_$x$N_$y$

Zn₃N₂

Se₄N₄

Br₃N
BrN₃
+Br

Kr

Sr₃N₂
Sr(N₃)₂

Tc

Ru

Rh

Cd₃N₂

Sn

Te₄N₄?

Xe

Ba₃N₂
Ba(N₃)₂

*

Re_$x$N_$y$

Os

Ir

Pt

Au

Hg₃N₂

(PbNH)

Po

At

Rn

Fr

Ra₃N₂

**

Lr

Rf

Db

Sg

Bh

Hs

Mt

Ds

Rg

Cn

Nh

Fl

Mc

Lv

Ts

Og

*

**

Ac

Th_$x$N_$y$

U_$x$N_$y$

Cf

Es

Fm

Md

No

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