4.2 Article

Localized holes and delocalized electrons in photoexcited inorganic perovskites: Watching each atomic actor by picosecond X-ray absorption spectroscopy

Journal

STRUCTURAL DYNAMICS-US
Volume 4, Issue 4, Pages -

Publisher

AMER INST PHYSICS
DOI: 10.1063/1.4971999

Keywords

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Funding

  1. NCCR:Molecular Ultrafast Science and Technology (MUST)
  2. NRP70 Energy Turnaround of the Swiss SNF [407040_154056, 200020_155893, 200020_169914, 200021_135009, 200021_143638]
  3. Energy System Integration (ESI) platform at the PSI
  4. SEFRI via the COST Project [C13.0062/CM1202]
  5. European Union via FP7 European Research Council Starting Grant [306733]
  6. European Union's Horizon program through the Marie-Sklodowska Curie ITN network PHONSI [H2020-MSCA-ITN-642656]
  7. Scientific Centre for Optical and Electron Microscopy (ETH Zurich)
  8. Swiss Light Source
  9. Swiss National Science Foundation (SNF) [200020_155893] Funding Source: Swiss National Science Foundation (SNF)

Ask authors/readers for more resources

We report on an element-selective study of the fate of charge carriers in photoexcited inorganic CsPbBr3 and CsPb(ClBr)(3) perovskite nanocrystals in toluene solutions using time-resolved X-ray absorption spectroscopy with 80 ps time resolution. Probing the Br K-edge, the Pb L-3-edge, and the Cs L-2-edge, we find that holes in the valence band are localized at Br atoms, forming small polarons, while electrons appear as delocalized in the conduction band. No signature of either electronic or structural changes is observed at the Cs L-2-edge. The results at the Br and Pb edges suggest the existence of a weakly localized exciton, while the absence of signatures at the Cs edge indicates that the Cs+ cation plays no role in the charge transport, at least beyond 80 ps. This first, time-resolved element-specific study of perovskites helps understand the rather modest charge carrier mobilities in these materials. (C) 2016 Author(s).

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