An interpretation for the components of 2p <sub>3/2</sub> core level x-ray photoelectron spectra of the cations in some inverse spinel oxides
Arjun Subedi, Detian Yang, Wai Kiat Chin, Binny Tamang, Sushrisangita Sahoo, Paul Yancey, Rifat Mahbub, Jeffrey E. Shield, Rebecca Y. Lai, Xiaoshan Xu, P. A. Dowben, Vijaya Rangari
Abstract
Abstract In an effort to reconcile the various interpretations for the cation components of the 2 p 3/2 observed in x-ray photoelectron spectroscopy (XPS) of several spinel oxide materials, the XPS spectra of both spinel alloy nanoparticles and crystalline thin films are compared. We observed that different components of the 2 p 3/2 core level XPS spectra, of these inverse spinel thin films, are distinctly surface and bulk weighted, indicating surface-to-bulk core level shifts in the binding energies. Surface-to-bulk core level shifts in binding energies of Ni and Fe 2 p 3/2 core levels of NiFe 2 O 4 thin film are observed in angle-resolved XPS. The ratio between surface-weighted components and bulk-weighted components of the Ni and Fe core levels shows appreciable dependency on photoemission angle, with respect to surface normal. XPS showed that the ferrite nanoparticles Ni x Co 1− x Fe 2 O 4 ( x = 0.2, 0.5, 0.8, 1) resemble the surface of the NiFe 2 O 4 thin film. Surface-to-bulk core level shifts are also observed in CoFe 2 O 4 and NiCo 2 O 4 thin films but not as significantly as in NiFe 2 O 4 thin film. Estimates of surface stoichiometry of some spinel oxide nanoparticles and thin films suggested that the apportionment between cationic species present could be farther from expectations for thin films as compared to what is seen with nanoparticles.