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Dismantling the “Red Wall” of Colloidal Perovskites: Highly Luminescent Formamidinium and Formamidinium–Cesium Lead Iodide Nanocrystals

[Image: see text] Colloidal nanocrystals (NCs) of APbX(3)-type lead halide perovskites [A = Cs(+), CH(3)NH(3)(+) (methylammonium or MA(+)) or CH(NH(2))(2)(+) (formamidinium or FA(+)); X = Cl(–), Br(–), I(–)] have recently emerged as highly versatile photonic sources for applications ranging from sim...

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Detalles Bibliográficos
Autores principales: Protesescu, Loredana, Yakunin, Sergii, Kumar, Sudhir, Bär, Janine, Bertolotti, Federica, Masciocchi, Norberto, Guagliardi, Antonietta, Grotevent, Matthias, Shorubalko, Ivan, Bodnarchuk, Maryna I., Shih, Chih-Jen, Kovalenko, Maksym V.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2017
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5800405/
https://www.ncbi.nlm.nih.gov/pubmed/28231432
http://dx.doi.org/10.1021/acsnano.7b00116
Descripción
Sumario:[Image: see text] Colloidal nanocrystals (NCs) of APbX(3)-type lead halide perovskites [A = Cs(+), CH(3)NH(3)(+) (methylammonium or MA(+)) or CH(NH(2))(2)(+) (formamidinium or FA(+)); X = Cl(–), Br(–), I(–)] have recently emerged as highly versatile photonic sources for applications ranging from simple photoluminescence down-conversion (e.g., for display backlighting) to light-emitting diodes. From the perspective of spectral coverage, a formidable challenge facing the use of these materials is how to obtain stable emissions in the red and infrared spectral regions covered by the iodide-based compositions. So far, red-emissive CsPbI(3) NCs have been shown to suffer from a delayed phase transformation into a nonluminescent, wide-band-gap 1D polymorph, and MAPbI(3) exhibits very limited chemical durability. In this work, we report a facile colloidal synthesis method for obtaining FAPbI(3) and FA-doped CsPbI(3) NCs that are uniform in size (10–15 nm) and nearly cubic in shape and exhibit drastically higher robustness than their MA- or Cs-only cousins with similar sizes and morphologies. Detailed structural analysis indicated that the FAPbI(3) NCs had a cubic crystal structure, while the FA(0.1)Cs(0.9)PbI(3) NCs had a 3D orthorhombic structure that was isostructural to the structure of CsPbBr(3) NCs. Bright photoluminescence (PL) with high quantum yield (QY > 70%) spanning red (690 nm, FA(0.1)Cs(0.9)PbI(3) NCs) and near-infrared (near-IR, ca. 780 nm, FAPbI(3) NCs) regions was sustained for several months or more in both the colloidal state and in films. The peak PL wavelengths can be fine-tuned by using postsynthetic cation- and anion-exchange reactions. Amplified spontaneous emissions with low thresholds of 28 and 7.5 μJ cm(–2) were obtained from the films deposited from FA(0.1)Cs(0.9)PbI(3) and FAPbI(3) NCs, respectively. Furthermore, light-emitting diodes with a high external quantum efficiency of 2.3% were obtained by using FAPbI(3) NCs.