TY - JOUR
T1 - Synthesis of ternary CuInS2 nanocrystals; phase determination by complex ligand species
AU - Nose, Katsuhiro
AU - Soma, Yuki
AU - Omata, Takahisa
AU - Otsuka-Yao-Matsuo, Shinya
N1 - Copyright:
Copyright 2009 Elsevier B.V., All rights reserved.
PY - 2009/7/14
Y1 - 2009/7/14
N2 - Colloidal CuInS2 nanocrystals were synthesized in a hot organic solvent containing surfactant molecules. The CuInS2 phase was controlled by the ligand species of the metallic monomers. When the metallic monomers were coordinated with trioctylphosphite, the resulting CuInS 2 had a chalcopyrite or zincblende phase. When the metallic monomers were coordinated with hexadecyla-mine or oleylamine, the thermodynamically metastable wurtzite phase appeared. The experimental results indicated that the obtained phase was predominantly determined by the growth rate of the nanocrystals. The bond strength between the metallic monomers and ligand molecules and steric size of the ligand molecules influenced the growth rate. The CuInS2 nanocrystals showed photolumines-cence in the near-infrared region. Its energy was far from the optical energy band gap; the luminescence was attributable to the electron-hole recombination via deep defect levels. In the photoluminescence spectrum of the CuInS2/ZnS core/shell nanocrystals, a band near the optical energy band gap, whose Stokes' shift was ∼50 meV, appeared. The band was suggested to be attributable to the defect-related emission from CuInS2-ZnS alloy formed at the interfaces between the core CuInS2 and shell ZnS.
AB - Colloidal CuInS2 nanocrystals were synthesized in a hot organic solvent containing surfactant molecules. The CuInS2 phase was controlled by the ligand species of the metallic monomers. When the metallic monomers were coordinated with trioctylphosphite, the resulting CuInS 2 had a chalcopyrite or zincblende phase. When the metallic monomers were coordinated with hexadecyla-mine or oleylamine, the thermodynamically metastable wurtzite phase appeared. The experimental results indicated that the obtained phase was predominantly determined by the growth rate of the nanocrystals. The bond strength between the metallic monomers and ligand molecules and steric size of the ligand molecules influenced the growth rate. The CuInS2 nanocrystals showed photolumines-cence in the near-infrared region. Its energy was far from the optical energy band gap; the luminescence was attributable to the electron-hole recombination via deep defect levels. In the photoluminescence spectrum of the CuInS2/ZnS core/shell nanocrystals, a band near the optical energy band gap, whose Stokes' shift was ∼50 meV, appeared. The band was suggested to be attributable to the defect-related emission from CuInS2-ZnS alloy formed at the interfaces between the core CuInS2 and shell ZnS.
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U2 - 10.1021/cm802022p
DO - 10.1021/cm802022p
M3 - Article
AN - SCOPUS:67650693761
SN - 0897-4756
VL - 21
SP - 2607
EP - 2613
JO - Chemistry of Materials
JF - Chemistry of Materials
IS - 13
ER -