Spontaneous chiral self-assembly of CdSe@CdS nanorods

  • Tianwei Duan
  • , Jing Ai
  • , Xiaoyan Cui
  • , Xiaowei Feng
  • , Yingying Duan*
  • , Lu Han*
  • , Jingang Jiang*
  • , Shunai Che*
  • *Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

32 Scopus citations

Abstract

The enantiomeric excess phenomenon in spontaneous chiral symmetry breaking (SCSB) is a crucial issue in the origin of homochirality in nature, whereas chiral inorganic compounds have long been reckoned as racemates. Here, we report the SCSB in the self-assembly of cadmium chalcogenide nanorods, leading to chiral biases away from the racemate. In the presence of achiral organics, helical CdSe@CdS nanorods (HCCNs) with unidirectionally rotated crystal lattices along the rod axis were stochastically formed on the epitaxial interface of the {111}cub/{0001}hex planes. The stability of helical dislocation structures, as supported by a theoretical analysis of their binding energies, suggested the possibility of the emergence of helical structures in an achiral environment. Hierarchical chiral films induced by simple solvent evaporation self-assembly of HCCNs exhibited spontaneous enantiomeric excess between batches, which was speculated to be originated from the enantiomeric excess seed assembly that induce one-handedness dominated system based on the majority rules.

Original languageEnglish
Pages (from-to)2695-2707
Number of pages13
JournalChem
Volume7
Issue number10
DOIs
StatePublished - 14 Oct 2021

Keywords

  • CdSe@CdS nanorods
  • UN SDG9: Industry, innovation, and infrastructure
  • chiral self-assembly
  • enantiomeric excess
  • optical activity
  • spontaneous chiral symmetry breaking

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