| Literature DB >> 32566752 |
Javad Shamsi1, Dominik Kubicki1,2, Miguel Anaya1, Yun Liu1, Kangyu Ji1, Kyle Frohna1, Clare P Grey2, Richard H Friend1, Samuel D Stranks1,3.
Abstract
Quantum-confined CsPbBr3 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 (C6H15O3P) in a heat-up colloidal approach for pure, blue-emitting quantum-confined CsPbBr3 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/cm2. 13C, 133Cs, and 31P 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.Entities:
Year: 2020 PMID: 32566752 PMCID: PMC7296617 DOI: 10.1021/acsenergylett.0c00935
Source DB: PubMed Journal: ACS Energy Lett Impact factor: 23.101