Issue 48, 2012

Facile preparation of metal telluride nanocrystals using di-n-octylphosphine oxide (DOPO) as an air-stable and less toxic alternative to the common tri-alkylphosphines

Abstract

In this paper, we have developed a “green” method for the synthesis of metal telluride nanocrystals. In this method, di-n-octylphosphine oxide (DOPO) has been used to disperse Te and form Te–DOPO precursor. This new Te precursor was found to be highly reactive and suitable for the synthesis of metal telluride nanocrystals in various monodispersity, size, and shape. Dot-/tetrapod-shaped CdTe, dot-shaped ZnTe, dot-/cubic-shaped PbTe, dot-/rod-shaped Ag2Te, cubic-shaped Cu2−xTe, ternary alloyed CuInTe2, and quaternary alloyed Cu2ZnSnTe4 semiconductor nanocrystals all have been well-controlled synthesized. The photoluminescence emission of as-synthesized CdTe nanocrystals covered a wide range (570–735 nm) and the quality of as-synthesized metal telluride nanocrystals were reached or exceed the level compared with the traditional method using phosphine–Te precursor. The possible dissolving molecular mechanism of Te in DOPO in this synthesis was specially studied and illustrated that intramolecular proton transfer from the phosphorus (formation of DOPO–Te complex) was essential in the synthesis of metal telluride nanocrystals. This method provided a greener and less expensive route to large-scale synthesis of all kinds of high quality metal telluride nanocrystals.

Graphical abstract: Facile preparation of metal telluride nanocrystals using di-n-octylphosphine oxide (DOPO) as an air-stable and less toxic alternative to the common tri-alkylphosphines

Supplementary files

Article information

Article type
Paper
Submitted
17 Aug 2012
Accepted
09 Oct 2012
First published
11 Oct 2012

J. Mater. Chem., 2012,22, 25050-25056

Facile preparation of metal telluride nanocrystals using di-n-octylphosphine oxide (DOPO) as an air-stable and less toxic alternative to the common tri-alkylphosphines

H. Shen, X. Jiang, S. Wang, Y. Fu, C. Zhou and L. S. Li, J. Mater. Chem., 2012, 22, 25050 DOI: 10.1039/C2JM35598A

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