4.8 Article

Ultrafast Excited-State Localization in Cs2AgBiBr6 Double Perovskite

Journal

JOURNAL OF PHYSICAL CHEMISTRY LETTERS
Volume 12, Issue 13, Pages 3352-3360

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.jpclett.1c00653

Keywords

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Funding

  1. Engineering and Physical Sciences Research Council (EPSRC), UK
  2. Oxford-Radcliffe Scholarship
  3. Rhodes Trust through a Rhodes Scholarship
  4. Institute for Advanced Study at the Technical University of Munich
  5. Centre for Doctoral Training in New and Sustainable Photovoltaics
  6. EPSRC [EP/P033229/1, EP/V010840/1] Funding Source: UKRI
  7. Engineering and Physical Sciences Research Council [EP/S004947/1] Funding Source: researchfish

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The study investigates the evolution of photoexcited charge carriers in Cs2AgBiBr6 and reveals rapid localization of free carriers in an intrinsic small polaronic state, induced by strong electron-phonon coupling. Additionally, temperature-activated mobilities and broad emission from color centers were observed, suggesting a complex charge carrier dynamics in the material.
Cs2AgBiBr6 is a promising metal halide double perovskite offering the possibility of efficient photovoltaic devices based on lead-free materials. Here, we report on the evolution of photoexcited charge carriers in Cs2AgBiBr6 using a combination of temperature-dependent photoluminescence, absorption and optical pump-terahertz probe spectroscopy. We observe rapid decays in terahertz photoconductivity transients that reveal an ultrafast, barrier-free localization of free carriers on the time scale of 1.0 ps to an intrinsic small polaronic state. While the initially photogenerated delocalized charge carriers show bandlike transport, the self-trapped, small polaronic state exhibits temperature-activated mobilities, allowing the mobilities of both to still exceed 1 cm(2) V-1 s(-1) at room temperature. Self-trapped charge carriers subsequently diffuse to color centers, causing broad emission that is strongly red-shifted from a direct band edge whose band gap and associated exciton binding energy shrink with increasing temperature in a correlated manner. Overall, our observations suggest that strong electron-phonon coupling in this material induces rapid charge-carrier localization.

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