Please use this identifier to cite or link to this item: https://dspace.iiti.ac.in/handle/123456789/10890
Title: Methodology to Probe Disorder Contribution in Raman Linewidth via Optical Absorption Spectroscopy in Orthoferrite EuFeO3
Authors: Rambadey, Omkar V.;Kumar, Anil;Kumar, Kailash V.T.S.Pavan;Mishra, Vikash N.;Sagdeo, Pankaj R.;
Keywords: Absorption spectroscopy; Electron-phonon interactions; Europium; Europium compounds; Light absorption; Large temperature variations; Linear relationships; Optical absorption spectroscopy; Orthoferrites; Phonon mode; Raman line width; Raman modes; Temperature-dependent raman; Urbach energy; Urbach tail; Iron compounds
Issue Date: 2022
Publisher: American Chemical Society
Citation: Rambadey, O. V., Kumar, A., Kumar, K., Mishra, V., & Sagdeo, P. R. (2022). Methodology to probe disorder contribution in raman linewidth via optical absorption spectroscopy in orthoferrite EuFeO3. Journal of Physical Chemistry C, 126(32), 13946-13956. doi:10.1021/acs.jpcc.2c03347
Abstract: The individual impact of disorder on different phonon modes has been investigated for orthoferrite EuFeO3 by perceiving a correlation between temperature-dependent Raman linewidth (Δ) and Urbach energy (EU). It has been found that the plot of Δ versus EU exhibits a linear relationship, whose slope (ζ) differs for each Raman mode. Interestingly, the Raman mode exhibiting larger temperature variation in width is found to acquire a larger slope. This has been understood as eclectic contribution of disorder toward altering the mode-widths. Furthermore, a careful analysis hints that parameter ζ may contain information of overlap between discrete (phonon) and electronic continuum (∼Urbach tail) states. This may be seen as a selective impact of disorder on individual phonons in view of the electron-phonon interaction. Hence, the slope of the linear plot between Δ and EU has been realized as a parameter that may represent the individual disorder contribution to modify Raman width of each mode, and thereby ζ has been interpreted to be the disorder-coupling parameter. © 2022 American Chemical Society.
URI: https://doi.org/10.1021/acs.jpcc.2c03347
https://dspace.iiti.ac.in/handle/123456789/10890
ISSN: 1932-7447
Type of Material: Journal Article
Appears in Collections:Department of Physics

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