Mixed Ligand Passivation as the Origin of Near-Unity Emission Quantum Yields in CsPbBr3 Nanocrystals

• Published in: Journal of the American Chemical Society Vol. 145; no. 11; pp. 6362 - 6370
• Main Authors: Ding, Yang, Zhang, Zhuoming, Toso, Stefano, Gushchina, Irina, Trepalin, Vadim, Shi, Kejia, Peng, Jeffrey W., Kuno, Masaru
• Format: Journal Article
• Language: English
• Published: United States American Chemical Society 22.03.2023; American Chemical Society (ACS)
• Subjects: Cations; INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CHEMISTRY; Ligands; Nuclear magnetic resonance spectroscopy; Passivation; Surface passivation
• ISSN: 0002-7863; 1520-5126
• DOI: 10.1021/jacs.2c13527

Key features of syntheses, involving the quaternary ammonium passivation of CsPbBr3 nanocrystals (NCs), include stable, reproducible, and large (often near-unity) emission quantum yields (QYs). The archetypical example involves didodecyl dimethyl ammonium (DDDMA+)-passivated CsPbBr3 NCs where robust QYs stem from interactions between DDDMA+ and NC surfaces. Despite widespread adoption of this synthesis, specific ligand–NC surface interactions responsible for large DDDMA+-passivated NC QYs have not been fully established. Multidimensional nuclear magnetic resonance experiments now reveal a new DDDMA+-NC surface interaction, beyond established “tightly bound” DDDMA+ interactions, which strongly affects observed emission QYs. Depending upon the existence of this new DDDMA+ coordination, NC QYs vary broadly between 60 and 85%. More importantly, these measurements reveal surface passivation through unexpected didodecyl ammonium (DDA+) that works in concert with DDDMA+ to produce near-unity (i.e., >90%) QYs.