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Published on: January 22, 2019
First-principles study of rare-earth-free Cs4SrI6:Tl, a zero-dimensional halide perovskite for scintillation
Md Helal Miah1,2, Mayeen Uddin Khandaker1,3,4, Yahaya Saadu Itas1,5
1Applied Physics and Radiation Technologies Group, CCDCU, Faculty of Engineering and Technology, Sunway University Bandar Sunway Selangor 47500 Malaysia mu_khandaker@yahoo.com mayeenk@diu.edu.
Abstract:
In recent years, rare-earth-activated perovskite scintillators have drawn significant research attention owing to their characteristic and efficient 4f n ↔ 4f n-15d electronic transitions. However, the high cost and limited readiness of rare-earth elements motivate the search for alternative activators. In this context, thallium ions (Tl+) can offer a promising activator that can act as a two-level luminescent center, yielding characteristic emissions through 6s16p1 → 6s2 electronic transitions, similar to the well-known NaI:Tl scintillator while remaining cost-effective. In this investigation, density functional theory (DFT) calculations were performed to explore the opto-electronic and scintillation-relevant properties of the undoped and Tl+-doped Cs4SrI6 halide perovskites. The computed band structures demonstrated the reduction of band gap with the increasing Tl+ concentrations. The observed relatively flat bands near the band edges suggested large carrier effective masses, which may suppress carrier mobility and promote carrier localization. In halide systems with strong electron-phonon coupling, such localization can lead to the formation of self-trapped excitons that may recombine radiatively through Tl+ activator centers, enhancing the emission efficiency. More specifically, Tl+ introduces localized Tl+-6s* and Tl+-6p* states above valence band maximum (VBM) and below conduction band minimum (CBM) of the host Cs4SrI6, respectively. As the Tl+ concentration increases, these states (especially Tl+-6s*) become more prominent and enhance the probability of efficient and characteristic radiative emission from Tl+-6p*(6s16p1) → Tl+-6s* (6s2). urthermore, the estimated values of radiant quantum efficiency were 39.52%, 41.41%, and 43.70% for Cs4SrI6 doped with 1.52% Tl+, 3.03% Tl+, and 4.55% Tl+, respectively, which showed enhanced energy conversion efficiency. Additionally, the reduction in band gap with the increasing Tl+ concentration led to an increase in the theoretical upper limit of light yield (LY), exceeding 108 401 photons/MeV for the 4.55% Tl+ dopant under ideal conditions. Moreover, this investigation revealed an Auger-free luminescence process in Tl+-doped compounds, which reduced self-absorption losses. These results demonstrated that Tl+ in Cs4SrI6 offers a cost-effective and rare-earth-free alternative activator for perovskite-based scintillators, with the favorable characteristics of light emission and promising scintillation performance.
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