Published February 7, 2022 | Version v1
Journal article

Transformation pathways in colloidal CdTeSe magic-size clusters

  • 1. Engineering Research Center in Biomaterials, Sichuan University, Chengdu, Sichuan, 610065 (China)
  • 2. Laboratory of Ethnopharmacology, West China School of Medicine, West China Hospital, Sichuan University, Chengdu, Sichuan, 610065 (China)
  • 3. Metrology Research Centre, National Research Council Canada, Ontario, K1A 0R6 (Canada)
  • 4. Analytical & Testing Center, Sichuan University, Chengdu, Sichuan, 610065 (China)
  • 5. Institute of Atomic and Molecular Physics, Sichuan University, Chengdu, Sichuan, 610065 (China)

Description

A rarely studied transformation in colloidal ternary magic-size clusters (MSCs) is addressed. We report the first observation of the transformation from ternary CdTeSe MSC-399 to MSC-422, which occurs at room temperature. These two MSC types display sharp optical absorption resonances at 399 and 422 nm, respectively, and are related in that they are quasi isomers, together with their counterpart precursor compounds (PCs). Binary CdTe and CdSe samples were prepared in the prenucleation stage also called the induction period (IP). After they were mixed and placed in a mixture of toluene and octylamine, the transformation was found to take place and to be assisted by the addition of the CdSe IP sample. A binary IP sample contains corresponding binary PCs and monomers (Mo) and fragments (Fr). We argue that the transformation pathway is enabled by the corresponding ternary PCs, involving the substitution reaction, namely CdTeSe PC-399 + CdSe (Mo/Fr)-1 CdTeSe PC-422 + CdSe (Mo/Fr)-2. The present study provides an in-depth understanding of the formation characteristics of the MSCs. (© 2021 Wiley‐VCH GmbH)

Availability note (English)

Available from: http://dx.doi.org/10.1002/anie.202114551

Additional details

Identifiers

Publishing Information

Journal Title
Angewandte Chemie (International Edition)
Journal Volume
61
Journal Issue
7
Journal Page Range
p. 1-8
ISSN
1433-7851
CODEN
ACIEF5

Optional Information

Notes
AID: e202114551