Growth and Self-Assembly of CsPbBr3 Nanocrystals in the TOPO/PbBr2 Synthesis as Seen with X‑ray Scattering

• Published in: Nano letters Vol. 23; no. 2; pp. 667 - 676
• Main Authors: Montanarella, Federico, Akkerman, Quinten A., Bonatz, Dennis, van der Sluijs, Maaike M., van der Bok, Johanna C., Prins, P. Tim, Aebli, Marcel, Mews, Alf, Vanmaekelbergh, Daniel, Kovalenko, Maksym V.
• Format: Journal Article
• Language: English
• Published: American Chemical Society 25.01.2023
• Subjects: Letter; perovskites; quantum dots; self-assembly; X-ray scattering; nanocrystals; lead halides; growth; in situ
• ISSN: 1530-6984; 1530-6992
• DOI: 10.1021/acs.nanolett.2c04532

Despite broad interest in colloidal lead halide perovskite nanocrystals (LHP NCs), their intrinsic fast growth has prevented controlled synthesis of small, monodisperse crystals and insights into the reaction mechanism. Recently, a much slower synthesis of LHP NCs with extreme size control has been reported, based on diluted TOPO/PbBr2 precursors and a diisooctylphosphinate capping ligand. We report new insights into the nucleation, growth, and self-assembly in this reaction, obtained by in situ synchrotron-based small-angle X-ray scattering and optical absorption spectroscopy. We show that dispersed 3 nm Cs­[PbBr3] agglomerates are the key intermediate species: first, they slowly nucleate into crystals, and then they release Cs­[PbBr3] monomers for further growth of the crystals. We show the merits of a low Cs­[PbBr3] monomer concentration for the reaction based on oleate ligands. We also examine the spontaneous superlattice formation mechanism occurring when the growing nanocrystals in the solvent reach a critical size of 11.6 nm.