2019
DOI: 10.1103/physrevb.99.064433
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Low-temperature Raman, high magnetic field Fe57 Mössbauer, and x-ray diffraction study of magnetodielectric coupling in polycrystalline GdFeO3

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Cited by 17 publications
(7 citation statements)
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“…The different intensity of the modes relates to the symmetries and the most intense ones have usually A g symmetry. The broadened band at about 1280 cm -1 can be endorsed as a two-phonon process related to the signal at about 630 cm -1 [28,31]. This scenario appropriately describes that observed for GFO-MW and GFO-P samples.…”
Section: Raman Spectroscopysupporting
confidence: 72%
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“…The different intensity of the modes relates to the symmetries and the most intense ones have usually A g symmetry. The broadened band at about 1280 cm -1 can be endorsed as a two-phonon process related to the signal at about 630 cm -1 [28,31]. This scenario appropriately describes that observed for GFO-MW and GFO-P samples.…”
Section: Raman Spectroscopysupporting
confidence: 72%
“…The experimental pattern (blue) is compared with the calculated one (red); in the bottom, the difference curve (grey) and the bars of the expected peak positions for GdFeO 3 are also shown. In the inset, as an example, an enlargement of the 20-35°angular region is shown for GCFO-P sample the literature [27][28][29][30], the room temperature firstorder Raman activity in polycrystalline GdFeO 3 is mainly expected in the region between 100 and 650 cm -1 . In particular, it is possible to discriminate (i) below 200 cm -1 the Raman features related to lattice modes involving Gd vibrations, (ii) between 200 and 400 cm -1 the contribution of different modes, reasonably ascribable to in-phase and out-ofphase FeO 6 rotations, (iii) between 400 cm -1 and 500 cm -1 the bending activity of O(1)-Fe-O(2) and stretching of Fe-O(1) and/or Fe-O(2) and (iv) above 600 cm -1 in-plane stretching modes.…”
Section: Raman Spectroscopymentioning
confidence: 88%
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“… where 8 N A and J 1 denote the number of bonds per mole and exchange constant for the Er-Fe pairs, respectively, and 3 N A and J 2 do the number of bonds per mole by considering the double counting and exchange constant for the Er-Er pairs, respectively 37 . Recent experiment of low- T Raman spectroscopy for the GdFeO 3 reveals that Raman shift for the mode relevant to the motion of Gd 3+ ions occurs below the T Gd and is found to be ∆ω ≈ 1 cm −1 38 . In a theoretical work on the GdFeO 3 , J 1 = 0.03 meV and J 2 = 0.05 meV were also calculated 41 .…”
Section: Resultsmentioning
confidence: 99%
“…For example FE distortion is reported in DyFeO 3 below T N,Dy with applied magnetic field [8] and also in the weak ferromagnetic (WFM) state between T SRT,Fe and T N,Fe in zero magnetic field [9]. In GdFeO 3 FE distortion is reported below T N,Gd [10].…”
Section: Introductionmentioning
confidence: 94%