4.8 Article

Shape Evolution and Single Particle Luminescence of Organometal Halide Perovskite Nanocrystals

Journal

ACS NANO
Volume 9, Issue 3, Pages 2948-2959

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/nn507020s

Keywords

organometal halide perovskites; nanocrystals; preferred orientation; morphology control; size control; single particle photoluminescence

Funding

  1. U.S. Department of Energy, Office of Basic Energy Sciences, Division of Chemical Sciences, Geosciences, and Biosciences through the Ames Laboratory
  2. U.S. Department of Energy [DE-AC02-07CH11358]
  3. National Nuclear Security Administration of the U.S. Department of Energy [DE-AC52-06NA25396]

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Organometallic halide perovskites CH3NH3PbX3 (X = I, Br, Cl) have quickly become one of the most prOmising semiconductors for solar cells, with photovoltaics made of these materials reaching power conversion efficiencies of near 20%. Improving our ability to harness the full potential of organometal halide perovskites will require more cOntrollable syntheses that permit a detailed understanding oftheirfundamental chemiStry and photophysics. In this manuscript, we systematically synthesize CH3NH3PbX3 (X = I, Br) nanocrystals with different morphologies (dots, rods, plates or sheets)-by using different solvents and capping ligands.,CH3NH3PbX3 nanowires and nanorods capped with octylammonium halides.show relatively higher photoluminescence (PL) quantum yields and long PL lifetimes. CH(3)NH(3)Pbl(3) nanowires Monitored at the single particle level show shape-correlated PL emissiOn across whole particles, with little photobleaching'Observed and very few off periods; This work highlights the potential of low-dimensional organonrietal halide perovskite semiconductors in constructing new porous and nanostructured solar cell architectures, as well as in applying these materials to-other fields such as light-emitting devices and single particle imaging and tracking.

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