An interpretation for the components of 2p3/2 core level X-ray photoelectron spectra of the cations in some inverse spinel oxides

In an effort to reconcile the various interpretations for the cation components of the 2p3/2 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 co...

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Veröffentlicht in:Journal of physics. Condensed matter 2024-03
Hauptverfasser: Subedi, Arjun, Yang, Detian, Chin, Wai Kiat, Tamang, Binny, Sahoo, Sushrisangita, Yancey, Paul, Mahbub, Rifat, Shield, Jeffrey, Lai, Rebecca Y, Xu, Xiaoshan, Dowben, Peter A, Rangari, Vijaya
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Sprache:eng
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Zusammenfassung:In an effort to reconcile the various interpretations for the cation components of the 2p3/2 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 2p3/2 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 2p3/2 core levels of NiFe2O4 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 NixCo1-xFe2O4 (x=0.2, 0.5, 0.8, 1) resemble the surface of the NiFe2O4 thin film. Surface-to-bulk core level shifts are also observed in CoFe2O4 and NiCo2O4 thin films but not as significantly as in NiFe2O4 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. &#xD.
ISSN:1361-648X