4.1 Article

Tuning Exciton Recombination Pathways in Inorganic Bismuth-Based Perovskite for Broadband Emission

Journal

ENERGY MATERIAL ADVANCES
Volume 2022, Issue -, Pages -

Publisher

AMER ASSOC ADVANCEMENT SCIENCE
DOI: 10.34133/2022/9845942

Keywords

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Funding

  1. National Key Research and Development Program of China [2021YFA1502300]
  2. National Natural Science Foundation of China [22090033]
  3. Youth Innovation Promotion Association of Chinese Academy of Sciences

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In this study, stable lead-free broadband emission under ambient conditions was achieved by introducing antimony (Sb) doping. The doping of Sb regulated the transfer of free excitons to extrinsic self-trapped excitons (STEs) and reduced nonradiative recombination, which are responsible for the significantly enhanced broad emission. Femtosecond transient absorption results elucidated the exciton dynamics and confirmed this mechanism.
Single-component emitters with broadband emission are attractive but challenging for illumination and display applications. The two-dimensional organic-inorganic hybrid perovskites have exhibited outstanding broad emission property due to low electronic dimensionality and strong exciton-phonon coupling. However, few layered all-inorganic lead-free perovskites with broadband emission have been explored, and the explicit mechanism of exciton recombination in them also needs in-depth understanding. Herein, the inorganic bismuth-based perovskite Cs3Bi2Br9 achieves the stable broadband emission under ambient temperature and pressure by tuning the exciton recombination pathways via antimony (Sb) doping, and the photoluminescence quantum yield (PLQY) realizes an enhancement from 2.9% to 15.9%. The photoluminescence excitation (PLE) spectra indicate that the doped Sb introduces newly extrinsic self-trapped states. The incorporation of Sb promotes the transfer of free excitons (FEs) to extrinsic self-trapped excitons (STEs) observed from Sb content-dependent steady-state PL spectra and, meanwhile, reduces the nonradiative recombination of the generated extrinsic STEs, which are primarily responsible for the remarkably enhanced broad emission. Furthermore, femtosecond transient absorption results elucidate a clear exciton dynamics, in which the transition from FEs to STEs might arise through the gradient energy levels, and finally extrinsic STEs at various energy states contribute to the broadband emission.

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