Issue 35, 2024

Ligand exchange induced crystal structure and morphology evolution of copper–tin–sulfur binary and ternary compounds

Abstract

In this manuscript, a simple one-pot heat-up method has been used to prepare multi-component copper–tin–sulfur nanomaterials, including binary Cu1.94S, ternary Cu4SnS4, and Cu1.94S/Cu4SnS4 nanocrystals by varying the reaction temperature, reaction time, and the type of copper source. Post-synthetic ligand exchange (LE) has further been introduced to replace the long-chain ligands originating from 1-dodecanethiol. It has been found that the LE process not only changes the surface ligands but also significantly affects the crystal structure and optical properties of nanocrystals. After LE, the crystal structures of Cu1.94S and Cu4SnS4 transformed to Cu7S4 and Cu3SnS4, respectively, with the Cu1.94S/Cu4SnS4 nanocrystals showing the same trend. This phenomenon could be ascribed to the loss of Cu+ originating from the strong complexation of Cu+ and ammonia with the formation of [Cu(NH3)n]2+ ions under aerobic conditions. Proton nuclear magnetic resonance (1H NMR) has been used to characterize the ligands on the surface before and after LE, which further demonstrated that the –SH was replaced during LE. Meanwhile, the band gaps of the obtained nanocrystals after LE show an obvious shift in the near-infrared region due to the evolution of crystal structures. This study will provide useful guidance for the LE of nanocrystals and the application of copper-based sulfide nanomaterials in optoelectronics and other fields.

Graphical abstract: Ligand exchange induced crystal structure and morphology evolution of copper–tin–sulfur binary and ternary compounds

Supplementary files

Article information

Article type
Paper
Submitted
01 fev 2024
Accepted
26 mar 2024
First published
03 iyl 2024

Dalton Trans., 2024,53, 14602-14609

Ligand exchange induced crystal structure and morphology evolution of copper–tin–sulfur binary and ternary compounds

S. Chen, Y. Xu, Y. Weng, P. Lou, X. Zhang and N. Bao, Dalton Trans., 2024, 53, 14602 DOI: 10.1039/D4DT00309H

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