Literature DB >> 29376343

Mesophase Formation Stabilizes High-Purity Magic-Sized Clusters.

Douglas R Nevers1, Curtis B Williamson1, Benjamin H Savitzky2, Ido Hadar3, Uri Banin3, Lena F Kourkoutis4,5, Tobias Hanrath1, Richard D Robinson6.   

Abstract

Magic-sized clusters (MSCs) are renowned for their identical size and closed-shell stability that inhibit conventional nanoparticle (NP) growth processes. Though MSCs have been of increasing interest, understanding the reaction pathways toward their nucleation and stabilization is an outstanding issue. In this work, we demonstrate that high concentration synthesis (1000 mM) promotes a well-defined reaction pathway to form high-purity MSCs (>99.9%). The MSCs are resistant to typical growth and dissolution processes. On the basis of insights from in situ X-ray scattering analysis, we attribute this stability to the accompanying production of a large (>100 nm grain size), hexagonal organic-inorganic mesophase that arrests growth of the MSCs and prevents NP growth. At intermediate concentrations (500 mM), the MSC mesophase forms, but is unstable, resulting in NP growth at the expense of the assemblies. These results provide an alternate explanation for the high stability of MSCs. Whereas the conventional mantra has been that the stability of MSCs derives from the precise arrangement of the inorganic structures (i.e., closed-shell atomic packing), we demonstrate that anisotropic clusters can also be stabilized by self-forming fibrous mesophase assemblies. At lower concentration (<200 mM or >16 acid-to-metal), MSCs are further destabilized and NPs formation dominates that of MSCs. Overall, the high concentration approach intensifies and showcases inherent concentration-dependent surfactant phase behavior that is not accessible in conventional (i.e., dilute) conditions. This work provides not only a robust method to synthesize, stabilize, and study identical MSC products but also uncovers an underappreciated stabilizing interaction between surfactants and clusters.

Entities:  

Year:  2018        PMID: 29376343     DOI: 10.1021/jacs.7b12175

Source DB:  PubMed          Journal:  J Am Chem Soc        ISSN: 0002-7863            Impact factor:   15.419


  6 in total

Review 1.  Magic-Size Semiconductor Nanostructures: Where Does the Magic Come from?

Authors:  Serena Busatto; Celso de Mello Donega
Journal:  ACS Mater Au       Date:  2022-01-28

2.  Size matters: Steric hindrance of precursor molecules controlling the evolution of CdSe magic-size clusters and quantum dots.

Authors:  Juan Shen; Chaoran Luan; Nelson Rowell; Yang Li; Meng Zhang; Xiaoqin Chen; Kui Yu
Journal:  Nano Res       Date:  2022-05-31       Impact factor: 10.269

3.  Formation of colloidal alloy semiconductor CdTeSe magic-size clusters at room temperature.

Authors:  Dong Gao; Xiaoyu Hao; Nelson Rowell; Theo Kreouzis; David J Lockwood; Shuo Han; Hongsong Fan; Hai Zhang; Chunchun Zhang; Yingnan Jiang; Jianrong Zeng; Meng Zhang; Kui Yu
Journal:  Nat Commun       Date:  2019-04-11       Impact factor: 14.919

4.  Stable CsPbBr3 Nanoclusters Feature a Disk-like Shape and a Distorted Orthorhombic Structure.

Authors:  Baowei Zhang; Davide Altamura; Rocco Caliandro; Cinzia Giannini; Lucheng Peng; Luca De Trizio; Liberato Manna
Journal:  J Am Chem Soc       Date:  2022-03-08       Impact factor: 15.419

5.  Room-Temperature Interconversion Between Ultrathin CdTe Magic-Size Nanowires Induced by Ligand Shell Dynamics.

Authors:  Serena Busatto; Claudia Spallacci; Johannes D Meeldijk; Stuart Howes; Celso de Mello Donega
Journal:  J Phys Chem C Nanomater Interfaces       Date:  2022-08-31       Impact factor: 4.177

6.  Interplay between Perovskite Magic-Sized Clusters and Amino Lead Halide Molecular Clusters.

Authors:  Evan T Vickers; Ziyi Chen; Vivien Cherrette; Tyler Smart; Peng Zhang; Yuan Ping; Jin Z Zhang
Journal:  Research (Wash D C)       Date:  2021-01-07
  6 in total

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