4.8 Article

Universal Size-Dependent Stokes Shifts in Lead Halide Perovskite Nanocrystals

期刊

JOURNAL OF PHYSICAL CHEMISTRY LETTERS
卷 11, 期 13, 页码 4937-4944

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acs.jpclett.0c01407

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资金

  1. Patrick and Jana Eilers Graduate Student Fellowship
  2. Division of Materials Sciences and Engineering, Office of Basic Energy Sciences, U.S. Department of Energy [DE-SC0014334]
  3. U.S. Department of Energy Office of Science, Office of Basic Energy Sciences [DE-FC02-04ER15533]
  4. University of Notre Dame Integrated Imaging Facility
  5. Air Force Office of Scientific Research, USA [FA9550-16-1-0362]
  6. DOE BES NERSC facility [91202]
  7. Office of Science of the DOE [DE-AC02-05CH11231]
  8. National Science Foundation [CHE-2004197]

向作者/读者索取更多资源

Size-dependent photoluminescence Stokes shifts (Delta E-s) universally exist in CsPbX3 (X = Cl-, Br-, or I-) perovskite nanocrystals (NCs). Delta E-s values, which range from similar to 15 to 100 meV for NCs with average edge lengths (l) from approximately 13 to 3 nm, are halide-dependent such that Delta E-s(CsPbI3) > Delta E-s(CsPbBr3) greater than or similar to Delta E-s(CsPbCl3). Observed size-dependent Stokes shifts are not artifacts of ensemble size distributions as demonstrated through measurements of single CsPbBr3 NC Stokes shifts ( = 42 +/- 5 meV), which are in near quantitative agreement with associated ensemble (l= 6.8 +/- 0.8 nm) AE, values (Delta E-s approximate to( )50 meV). Transient differential absorption measurements additionally illustrate no significant spectral dynamics on the picosecond time scale that would contribute to Delta E-s. This excludes polaron formation as being responsible for Delta E-s. Altogether, the results point to an origin for Delta E-s, intrinsic to the size-dependent electronic properties of individual perovskite NCs.

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