| Literature DB >> 35748492 |
Clara Otero-Martínez1,2, Muhammad Imran3, Nadine J Schrenker4, Junzhi Ye5, Kangyu Ji5, Akshay Rao5, Samuel D Stranks5,6, Robert L Z Hoye7, Sara Bals4, Liberato Manna3, Jorge Pérez-Juste2, Lakshminarayana Polavarapu1.
Abstract
We report here fast A-site cation cross-exchange between APbX3 perovskite nanocrystals (NCs) made of different A-cations (Cs (cesium), FA (formamidinium), and MA (methylammonium)) at room temperature. Surprisingly, the A-cation cross-exchange proceeds as fast as the halide (X=Cl, Br, or I) exchange with the help of free A-oleate complexes present in the freshly prepared colloidal perovskite NC solutions. This enabled the preparation of double (MACs, MAFA, CsFA)- and triple (MACsFA)-cation perovskite NCs with an optical band gap that is finely tunable by their A-site composition. The optical spectroscopy together with structural analysis using XRD and atomically resolved high-angle annular dark-field scanning transmission electron microscopy (HAADF-STEM) and integrated differential phase contrast (iDPC) STEM indicates the homogeneous distribution of different cations in the mixed perovskite NC lattice. Unlike halide ions, the A-cations do not phase-segregate under light illumination.Entities:
Keywords: Cation Exchange; Mixed A-Cation Perovskites; Perovskite Nanocrystals; Phase Segregation; Triple-Cation Perovskites
Year: 2022 PMID: 35748492 PMCID: PMC9540746 DOI: 10.1002/anie.202205617
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 16.823