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Stable Hexylphosphonate-Capped Blue-Emitting Quantum-Confined CsPbBr(3) Nanoplatelets

[Image: see text] Quantum-confined CsPbBr(3) nanoplatelets (NPLs) are extremely promising for use in low-cost blue light-emitting diodes, but their tendency to coalesce in both solution and film form, particularly under operating device conditions with injected charge-carriers, is hindering their ad...

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Detalles Bibliográficos
Autores principales: Shamsi, Javad, Kubicki, Dominik, Anaya, Miguel, Liu, Yun, Ji, Kangyu, Frohna, Kyle, Grey, Clare P., Friend, Richard H., Stranks, Samuel D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2020
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7296617/
https://www.ncbi.nlm.nih.gov/pubmed/32566752
http://dx.doi.org/10.1021/acsenergylett.0c00935
Descripción
Sumario:[Image: see text] Quantum-confined CsPbBr(3) nanoplatelets (NPLs) are extremely promising for use in low-cost blue light-emitting diodes, but their tendency to coalesce in both solution and film form, particularly under operating device conditions with injected charge-carriers, is hindering their adoption. We show that employing a short hexyl-phosphonate ligand (C(6)H(15)O(3)P) in a heat-up colloidal approach for pure, blue-emitting quantum-confined CsPbBr(3) NPLs significantly suppresses these coalescence phenomena compared to particles capped with the typical oleyammonium ligands. The phosphonate-passivated NPL thin films exhibit photoluminescence quantum yields of ∼40% at 450 nm with exceptional ambient and thermal stability. The color purity is preserved even under continuous photoexcitation of carriers equivalent to LED current densities of ∼3.5 A/cm(2). (13)C, (133)Cs, and (31)P solid-state MAS NMR reveal the presence of phosphonate on the surface. Density functional theory calculations suggest that the enhanced stability is due to the stronger binding affinity of the phosphonate ligand compared to the ammonium ligand.