First principles electric field gradients at A and B site cations across the NaRTiO4 Ruddlesden Popper series
L. F. Almeida, A. N. Ces\'ario, P. A. Sousa, P. Rocha-Rodrigues, L. V. C. Assali, H. M. Petrilli, J. P. Ara\'ujo, A. M. L. Lopes

TL;DR
This study uses ab-initio calculations to analyze electric field gradients and structural properties across the NaRTiO4 Ruddlesden-Popper series, revealing how ionic radius influences phase stability and hyperfine interactions.
Contribution
It provides detailed EFG signatures for different symmetries, aiding experimental identification of ground states in NaRTiO4 titanates.
Findings
EFG tensors vary systematically with ionic radius and symmetry.
High-temperature phases become more similar to ground states as ionic radius increases.
EFG signatures can distinguish between different structural symmetries.
Abstract
The Ruddlesden-Popper titanates, NaRTiO (R = rare-earth), exhibit a structural behaviour where non-centrosymmetry is driven by cooperative oxygen octahedral rotations (OORs) rather than conventional second-order Jahn-Teller distortions. In this work, we present an \textit{ab-initio} investigation of the structural, electronic and hyperfine properties of the entire NaRTiO series across the two disputed ground states, and , and the high temperature symmetries. Our results reveal an ionic-radius-dependent evolution from a tilt-dominated regime for small rare-earth ions to a distortion-dominated regime for larger cations, leading to an asymptotic regime in which the high-temperature phase becomes increasingly competitive with the ground-state structures as the ionic radius increases. In parallel, the electronic band gap follows a systematic…
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