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NIR Luminescence from Deep-Level Traps in CsPbBr3 Microcrystals

  • Jonathan Vandenwijngaerden
  • , Bapi Pradhan
  • , Bob Van Hout
  • , Eduard Fron
  • , Yasuyuki Araki
  • , Xianjun Zhang
  • , Yutaka Shibata
  • , Dario Santantonio
  • , Roger Bresoli-Obach
  • , Santi Nonell
  • , Haifeng Yuan
  • , Jialiang Xu
  • , Mark Van der Auweraer
  • , Maarten Roeffaers
  • , Johan Hofkens*
  • , Hiroshi Fukumura
  • , Elke Debroye*
  • *Corresponding author for this work

Research output: Indexed journal article Articlepeer-review

2 Citations (Scopus)

Abstract

In this study, we report the first observation of a near-infrared (NIR) emission band from all-inorganic CsPbBr3 and CsPb(Br/Cl)3 perovskite microcrystals. By means of temperature- and power-dependent NIR and visible luminescence spectroscopy, we demonstrate that a fraction of the excited states in these materials relax through radiative transitions involving traps located deep within the band gap, leading to broadband NIR emission. The quantum yield of this deep trap emission is quantitatively determined for the first time and amounts to approximately 0.3% at room temperature. Furthermore, by examining the picosecond-to-nanosecond dynamics of the excited states, using time-resolved luminescence spectroscopy, we observe that the population of NIR initial states occurs on a 660 ps time scale, consistent with the capture of free carriers by deep trap sites. Hence, this work deepens our fundamental understanding of previously unexplored recombination channels in metal halide perovskite microcrystals.

Original languageEnglish
Pages (from-to)3491-3500
Number of pages10
JournalJournal of Physical Chemistry Letters
Volume16
Issue number14
DOIs
Publication statusPublished - 10 Apr 2025

Keywords

  • Perovskite
  • Spectroscopy
  • Stability
  • Energy
  • Quantum dots
  • Photoluminescence
  • Hybrid
  • Photosystem-ii
  • Kinetics
  • Lead bromide

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