On the behavior of the LixNiO2 system: an electrochemical and structural overview

Lithium nickel oxide exhibits a departure from stoichiometry (Li1 − zNi1 + zO2) consisting in the presence of extra-nickel ions within the lithium sites. Using optimized experimental synthesis conditions, compositions very close to the ideal stoichiometry (z = 0.02) can be obtained. By using the sensitivity of the lithium site isotropic temperature factor to the stoichiometry, the amount of extra-nickel ions can be determined in a very precise way. The loss of reversibility at the first cycle is mainly related to the change in the oxidation state of the extra-nickel ions, which induces a local collapse of the structure and makes difficult the lithium re-intercalation. A systematic structural study of LixNiO2 phases has been performed by extended X-ray absorption fine structure (EXAFS) as well as X-ray and electron diffraction. In the case of the starting Li0.98Ni1.02O2 phase, a local distortion of the NiO6 octahedra, resulting from a dynamic Jahn-Teller effect of low spin trivalent nickel ions has been evidenced from the EXAFS study. For the partially de-intercalated materials (0.50 < x < 0.75) which crystallize in the monoclinic system, the EXAFS study shows that the NiO6 octahedra are only slightly distorted due to the occurrence of a hopping phenomenon between NiIV and NiIII. Electron diffraction experiments show the existence of a superstructure due to a peculiar lithium-ion ordering. Systematic electrochemical studies have shown that this ordering is strongly sensititve to the presence of extra-nickel ions.