Insights into the structural symmetry of single-crystal YCrO${}_3$ from synchrotron X-ray diffraction

Abstract

We report on the crystallographic information such as lattice parameters, atomic positions, bond lengths and angles, and local crystalline distortion size and mode of single-crystal YCrO${}_3$ compound by a high-resolution synchrotron X-ray diffraction study. The data was collected at 120 K (below $T_{\text{N}}\sim$ 141.5 K), 300 K (within [$T_{\text{N}}$, $T_{\text{C}}$]), and 500 K (above $T_{\text{C}}\sim$ 473 K). Taking advantages of high intensity and brilliance of synchrotron X-rays, we are able to refine collected patterns with the noncentrosymmetric monoclinic structural model ($P12_{1}1$, No. 4) that was proposed previously but detailed structural parameters have not determined yet. Meanwhile, we calculated patterns with the centrosymmetric orthorhombic space group (\emph{Pmnb}, No. 62) for a controlled study. Lattice constants \emph{a}, \emph{b}, and \emph{c} as well as unit-cell volume almost increase linearly upon warming. We observed more dispersive distributions of bond length and angle and local distortion strength with the $P12_{1}1$ space group. This indicates that (i) The local distortion mode of Cr2O${}_6$ at 120 K correlates the formation of the canted antiferromagnetic order by Cr1-Cr2 spin interactions mainly through intermediate of O3 and O4 ions. (ii) The strain-balanced Cr1-O3(O4) and Cr2-O5(O5) bonds as well as the local distortion modes of Cr1O${}_6$ and Cr2O${}_6$ octohedra at 300 K may be a microscopic origin of the previously-reported dielectric anomaly. Our study demonstrates that local crystalline distortion is a key factor for the formation of ferroelectric order and provides a complete set of crystallography for a full understanding of the interesting magnetic and quasi-ferroelectric properties of YCrO${}_3$ compound.

10 pages, 7 figures, 2 tables

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