Exogenous Metal Cations in the Synthesis of CsPbBr3 Nanocrystals and their Interplay with Tertiary Amines

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Hauptverfasser: Li, Zhanzhao, Goldoni, Luca, Wu, Ye, Imran, Muhammad, Ivanov, Yurii P., Divitini, Giorgio, Zito, Juliette, Panneerselvam, Iyyappa Rajan, Baranov, Dmitry, Infante, Ivan, De Trizio, Luca, Manna, Liberato
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Veröffentlicht: 2025
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author Li, Zhanzhao
Goldoni, Luca
Wu, Ye
Imran, Muhammad
Ivanov, Yurii P.
Divitini, Giorgio
Zito, Juliette
Panneerselvam, Iyyappa Rajan
Baranov, Dmitry
Infante, Ivan
De Trizio, Luca
Manna, Liberato
author_facet Li, Zhanzhao
Goldoni, Luca
Wu, Ye
Imran, Muhammad
Ivanov, Yurii P.
Divitini, Giorgio
Zito, Juliette
Panneerselvam, Iyyappa Rajan
Baranov, Dmitry
Infante, Ivan
De Trizio, Luca
Manna, Liberato
contents Current syntheses of CsPbBr3 halide perovskite nanocrystals (NCs) rely on over-stoichiometric amounts of Pb2+ precursors, resulting in unreacted lead ions at the end of the process. In our synthesis scheme of CsPbBr3 NCs we replaced excess Pb2+ with different exogenous metal cations (M) and investigated their effect on the synthesis products. These cations can be divided into two groups: group 1 delivers monodisperse CsPbBr3 cubes capped with oleate species (as for the case when Pb2+ is used in excess) and with photoluminescence quantum yield (PLQY) as high as 90% with some cations (for example with M= In3+); group 2 yields irregularly shaped CsPbBr3 NCs with broad size distributions. In both cases, the addition of a tertiary ammonium cation (didodecylmethyl ammonium, DDMA+) during the synthesis, after the nucleation of the NCs, reshapes the NCs to monodisperse truncated cubes. Such NCs feature a mixed oleate/DDMA+ surface termination with PLQY values up to 90%. For group 1 cations, this happens only if the ammonium cation is directly added as a salt (DDMA-Br) while for group 2 cations this happens even if the corresponding tertiary amine (DDMA) is added, instead of DDMA-Br. This is attributed to the fact that only group 2 cations can facilitate the protonation of DDMA by the excess oleic acid present in the reaction environment. In all cases studied, the incorporation of M cations is marginal and the reshaping of the NCs is only transient: if the reactions are run for a long time the truncated cubes evolve to cubes.
format Preprint
id arxiv_https___arxiv_org_abs_2512_08482
institution arXiv
publishDate 2025
record_format arxiv
spellingShingle Exogenous Metal Cations in the Synthesis of CsPbBr3 Nanocrystals and their Interplay with Tertiary Amines
Li, Zhanzhao
Goldoni, Luca
Wu, Ye
Imran, Muhammad
Ivanov, Yurii P.
Divitini, Giorgio
Zito, Juliette
Panneerselvam, Iyyappa Rajan
Baranov, Dmitry
Infante, Ivan
De Trizio, Luca
Manna, Liberato
Materials Science
Current syntheses of CsPbBr3 halide perovskite nanocrystals (NCs) rely on over-stoichiometric amounts of Pb2+ precursors, resulting in unreacted lead ions at the end of the process. In our synthesis scheme of CsPbBr3 NCs we replaced excess Pb2+ with different exogenous metal cations (M) and investigated their effect on the synthesis products. These cations can be divided into two groups: group 1 delivers monodisperse CsPbBr3 cubes capped with oleate species (as for the case when Pb2+ is used in excess) and with photoluminescence quantum yield (PLQY) as high as 90% with some cations (for example with M= In3+); group 2 yields irregularly shaped CsPbBr3 NCs with broad size distributions. In both cases, the addition of a tertiary ammonium cation (didodecylmethyl ammonium, DDMA+) during the synthesis, after the nucleation of the NCs, reshapes the NCs to monodisperse truncated cubes. Such NCs feature a mixed oleate/DDMA+ surface termination with PLQY values up to 90%. For group 1 cations, this happens only if the ammonium cation is directly added as a salt (DDMA-Br) while for group 2 cations this happens even if the corresponding tertiary amine (DDMA) is added, instead of DDMA-Br. This is attributed to the fact that only group 2 cations can facilitate the protonation of DDMA by the excess oleic acid present in the reaction environment. In all cases studied, the incorporation of M cations is marginal and the reshaping of the NCs is only transient: if the reactions are run for a long time the truncated cubes evolve to cubes.
title Exogenous Metal Cations in the Synthesis of CsPbBr3 Nanocrystals and their Interplay with Tertiary Amines
topic Materials Science
url https://arxiv.org/abs/2512.08482