Unveiling rare earth dopant configurations and crystal field analysis in tetragonal BaTiO3via machine learning and superposition modeling
Abstract
Barium titanate (BaTiO3) is a model ferroelectric perovskite with enduring technological relevance in electronics, catalysis, and energy storage. Rare-earth (RE) doping provides a powerful strategy to engineer its structural, electronic, and dielectric properties, yet a comprehensive understanding of dopant site selectivity and its consequences remains elusive. Here, we present the first systematic exploration of the entire RE series (4f0–4f14) in tetragonal BaTiO3 using an integrated workflow that couples machine-learning-driven structural optimization (CHGNet) with semi-empirical crystal-field analysis via the Superposition Model. This DFT-free approach enables efficient, large-scale mapping of doping trends, revealing clear correlations between ionic size, electronic configuration, site preference, lattice distortions, and stability. Our results show that Ba-site substitution is preferentially stabilized by intrinsic electronic charge redistribution, whereas Ti-site substitution exhibits opposite electronic polarization tendencies, indicating the predominance of intrinsic electronic compensation under equilibrium-like conditions, while oxygen-vacancy-assisted configurations remain metastable. The study further identifies the tetragonality ratio (c/a) as a sensitive descriptor of RE substitution, with Ba-site dopants generally enhancing and Ti-site dopants suppressing local ferroelectric distortion. In parallel, the derived crystal-field parameters provide a trend-based reference dataset for interpreting XRD, EPR, and luminescence spectra in RE-doped perovskites. By linking atomic-scale structure, local electronic redistribution, and lattice strain to ferroelectric distortion, this work establishes a predictive framework for tailoring RE-doped BaTiO3 and demonstrates a scalable computational paradigm for accelerating the discovery and design of functional oxide materials.

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