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Evidence of mixed valence Cr $$^{+3}$$ + 3 /Cr $$^{+4}$$ + 4 in Y $$_{1-x}$$ 1 - x Ca $$_x$$ x CrO $$_3$$ 3 polycrystalline ceramics by X-ray photoelectron spectroscopy

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TLDR
In this paper, a high-resolution XRD and X-ray photoelectron spectroscopy (XPS) study was conducted on 100 compositions of polycrystalline ceramics and the results revealed that the average bond length decreases with increasing Ca content.
Abstract
Y $$_{{1-x}}$$ Ca $$_{x}$$ CrO $$_{3}$$ polycrystalline ceramics with 0.000 $$\le $$ x $$\le $$ 0.100 compositions were studied by X-ray diffraction (XRD) and X-ray photoelectron spectroscopy (XPS). The results revealed that the $$\langle $$ Cr–O $$\rangle $$ average bond length decreases with increasing Ca content. This fact infers that the charge compensation is through the change from Cr $$^{+3}$$ to Cr $$^{+4}$$ instead of oxygen vacancies. To confirm this supposition, the high-resolution XPS study revealed that as the Ca is introduced in the YCrO $$_{3}$$ matrix, the Cr 2p $$_{{3/2}}$$ core-level is well fitted at 576.22 and 577.57 eV belonging at Cr $$^{+3}$$ and Cr $$^{+4}$$ core-level, respectively. Furthermore, we found an increase of the valence band XPS spectra at the Fermi energy as the Ca replaces the Y site. This fact suggests an increase of the Cr 3d-state at the Fermi energy, which is confirmed by the XPS valence band spectra and the electrical conductivity measurements.

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Effect of Al-doped YCrO 3 on structural, electronic and magnetic properties

TL;DR: In this article, structural, dielectric and magnetic properties of the YCr1−xAlxO3 with 0 were investigated in the case of YCr 1−xO 3 with 0.
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Effects of Oxygen Vacancies and Cation Valence States on the Triboelectric Property of Substoichiometric Oxide Films.

TL;DR: In this paper, the polarity on the TiO2-x surface changes from negative to positive with the increase of the sample annealing temperature in an air atmosphere, which is attributed to the fact that the decrease of oxygen vacancies eases the films at capturing positive charges.
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Negative magnetization in the zero field-cooled and exchange-bias effect in Cu-doped PrCrO3

TL;DR: In this paper, structural, chemical state, morphology, and magnetic properties were investigated in the PrCr1−xCuxO3 orthochromite with 0 ≤ x ≤ 0.1 composition, and XRD patterns showed a complete solubility of the Cu ion, as well as an increase of the orthorhombic cell volume.
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A comprehensive review on the ferroelectric orthochromates: Synthesis, property, and application

TL;DR: In this paper , the parent and doped ferroelectric YCrO3 compounds are comprehensively reviewed based on scientific and patent literatures from 1954 to 2022, including poly-, nano-, and single-crystalline samples and thin films.
References
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Journal ArticleDOI

Revised effective ionic radii and systematic studies of interatomic distances in halides and chalcogenides

TL;DR: The effective ionic radii of Shannon & Prewitt [Acta Cryst. (1969), B25, 925-945] are revised to include more unusual oxidation states and coordinations as mentioned in this paper.
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Multiferroics: progress and prospects in thin films.

TL;DR: Novel device paradigms based on magnetoelectric coupling are discussed, the key scientific challenges in the field are outlined, and high-quality thin-film multiferroics are reviewed.
Journal ArticleDOI

Multiferroics: Towards a magnetoelectric memory

TL;DR: The room-temperature manipulation of magnetization by an electric field using the multiferroic BiFeO3 represents an essential step towards the magnetoelectric control of spintronics devices.
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Field-induced polar order at the Néel temperature of chromium in rare-earth orthochromites: Interplay of rare-earth and Cr magnetism

TL;DR: In this article, the authors reported field-induced switchable polar order in rare-earth orthochromites, showing that the polar order occurs in weakly ferromagnetic (FeO)-orthochromite orthochrome, but only when the rare earth ion is magnetic.
Journal ArticleDOI

Biferroic Y Cr O 3

TL;DR: In this article, the authors determined the structure and energy properties of the noncentrosymmetric monoclinic structure of the plane-wave basis of pseudopotentials and a plane wave basis.
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