Analysis of the NiCo 2O 4 spinel surface with Auger and X-ray photoelectron spectroscopy

Abstract

Nickel cobaltite, NiCo 2O 4, has been synthesized by sol–gel and thermal decomposition techniques and the surface composition studied with Auger (AES) and X-ray photoelectron spectroscopies (XPS). The as-introduced samples are near-stoichiometric, although samples fabricated by thermal decomposition tend to be oxygen-deficient by approximately 25% of the predicted spinel concentration. Nickel 2p XPS indicates the predominant form of the metal to be Ni 2+, with the cations located in octahedral sites. The cobalt cations are equally divided between tetrahedral and octahedral sites as Co 3+. The oxygen XP 1s spectrum is composed of two peaks, the main lattice peak at 529.6 eV and a component at 531.2 eV with about 40% of the total O 1s intensity in stoichiometric samples. While the possibility of hydroxyl contaminants cannot be discounted, most of the intensity in the 531.2 eV peak is believed to be intrinsic to the NiCo 2O 4 surface. Heating the cobaltite in ultrahigh vacuum (UHV) results in surface reduction, with the largest changes apparent in the Co 2p XP spectrum, which shows clear signs of reduction to octahedral Co 2+. Changes brought about by the reduction are not reversible, and although it is possible to reoxidize the material, the surface undergoes phase separation to Co 3O 4 and Ni x Co 1− x O.