Please use this identifier to cite or link to this item: https://dspace.iiti.ac.in/handle/123456789/8132
Title: Effect of self-doping on the charge state of Fe ions and crystal field transitions in YFeO3: Experiments and theory
Authors: Warshi, M. Kamal
Kumar, Anil
Sati, Aanchal
Kumar, Rajesh
Sagdeo, Pankaj R.
Keywords: Density functional theory;Doping (additives);Hydrothermal synthesis;Ions;Iron;Light absorption;Sol-gels;Solid state reactions;X ray absorption;X rays;Yttrium oxide;Annealing temperatures;Crystal field transitions;Diffuse reflectance spectrum;Mixed valence state;Non-stoichiometry;Prominent features;Soft-X-ray absorption;Solid state reaction route;Iron compounds
Issue Date: 2019
Publisher: American Institute of Physics Inc.
Citation: Warshi, M. K., Kumar, A., Mishra, V., Sati, A., Sagdeo, A., Kumar, R., & Sagdeo, P. R. (2019). Effect of self-doping on the charge state of fe ions and crystal field transitions in YFeO3: Experiments and theory. Journal of Applied Physics, 125(20) doi:10.1063/1.5092736
Abstract: Detailed investigations on the appearance of d-d transitions in optical absorption spectra of YFeO3 samples have been done. For this purpose, pure and self-doped (vacancy at Y, Fe, and O sites) YFeO3 samples have been synthesized using sol-gel, the solid-state reaction route, and hydrothermal synthesis methods. It has been observed that the annealing of prepared samples at different temperatures leads to mixed oxidation states of Fe ions (i.e., the coexistence of Fe ions in mixed valence states such as Fe2+/Fe3+ or Fe3+/Fe4+). Furthermore, soft x-ray absorption (at the Fe L2,3 edge) and diffuse reflectance spectra analysis revealed that the intensity due to d-d transition is a prominent feature and is strongly associated with the annealing temperatures and the defects present in the samples. Experimental results followed by theoretical analysis carried out using density functional theory suggest that nonstoichiometry of the samples leads to the mixed valency (charge states) of Fe ions and hence to d-d transition in the YFeO3 (d5) system. © 2019 Author(s).
URI: https://doi.org/10.1063/1.5092736
https://dspace.iiti.ac.in/handle/123456789/8132
ISSN: 0021-8979
Type of Material: Journal Article
Appears in Collections:Department of Physics

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