Ab initio prediction of fast non-equilibrium transport of nascent polarons in SrI₂: a key to high-performance scintillation
Journal article, 2016

The excellent light yield proportionality of europium-doped strontium iodide (SrI2:Eu) has resulted in state-of-the-art γ-ray detectors with remarkably high-energy resolution, far exceeding that of most halide compounds. In this class of materials, the formation of self-trapped hole polarons is very common. However, polaron formation is usually expected to limit carrier mobilities and has been associated with poor scintillator light-yield proportionality and resolution. Here using a recently developed first-principles method, we perform an unprecedented study of polaron transport in SrI2, both for equilibrium polarons, as well as nascent polarons immediately following a self-trapping event. We propose a rationale for the unexpected high-energy resolution of SrI2. We identify nine stable hole polaron configurations, which consist of dimerised iodine pairs with polaron-binding energies of up to 0.5 eV. They are connected by a complex potential energy landscape that comprises 66 unique nearest-neighbour migration paths. Ab initio molecular dynamics simulations reveal that a large fraction of polarons is born into configurations that migrate practically barrier free at room temperature. Consequently, carriers created during γ-irradiation can quickly diffuse away reducing the chance for non-linear recombination, the primary culprit for non-proportionality and resolution reduction. We conclude that the flat, albeit complex, landscape for polaron migration in SrI2 is a key for understanding its outstanding performance. This insight provides important guidance not only for the future development of high-performance scintillators but also of other materials, for which large polaron mobilities are crucial such as batteries and solid-state ionic conductors.

Author

Fei Zhou

Lawrence Livermore National Laboratory

B. Sadigh

Lawrence Livermore National Laboratory

Paul Erhart

Chalmers, Physics, Materials and Surface Theory

Daniel Åberg

Lawrence Livermore National Laboratory

npj Computational Materials

20573960 (eISSN)

Vol. 2 16022

Subject Categories

Inorganic Chemistry

Theoretical Chemistry

Condensed Matter Physics

DOI

10.1038/npjcompumats.2016.22

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1/3/2024 9