Ligand-controlling synthesis and ordered assembly of ZnS nanorods and nanodots

被引:156
作者
Li, YC [1 ]
Li, XH [1 ]
Yang, CH [1 ]
Li, YF [1 ]
机构
[1] Chinese Acad Sci, Inst Chem, Ctr Mol Sci, Key Lab Organ Solids, Beijing 100080, Peoples R China
关键词
D O I
10.1021/jp0489018
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The shape- and phase-controlled synthesis of ZnS nanocrystals (nanorods and nanodots) was realized by the selection of ligand molecules with a simple method of thermolysing single-source precursor-zinc ethylxanthate (Zn(exan)(2)) with octylamine (OA) or trioctylphosphine (TOP) as precursor solvent. The as-prepared nanocrystals were characterized by transmission electron microscopy (TEM), high-resolution transmission electron microscopy (HRTEM), selected area electron diffraction (SAED), and X-ray diffraction (XRD). In hexadecylamine (HDA) + OA system, diameter- and aspect-ratio-tunable hexagonal wurtzite ZnS nanorods were attained in the temperature range of 150-250 degreesC, and the nanorods self-assembled into two-dimensional (2-D) aligned arrays. While in the HDA + TOP system, a shape change from rod to spherical particle and a phase transition from wurtzite to sphalerite simultaneously occurred with the increase of TOP content in the solution, and sphalerite nanodots were prepared in high TOP content or in TOP (or trioctylamine (TOA)) solution without HDA. The mechanism of the shape- and phase-controlled growth of ZnS nanocrystals by selecting ligand molecules was analyzed. The absorption and photoluminescence spectra of the wurtzite ZnS nanorods and the sphalerite ZnS nanodots were also measured and contrasted. In addition, the mechanism and the strategies of assembling I-D ZnS nanorods on 2-D scale were discussed, and the ordered arrays of the nanorods and nanodots were obtained on a relatively large scale.
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收藏
页码:16002 / 16011
页数:10
相关论文
共 81 条
[1]  
ADAM Z, 2001, J AM CHEM SOC, V123, P1389
[2]  
ADAM Z, 2002, J AM CHEM SOC, V124, P3343
[3]   Perspectives on the physical chemistry of semiconductor nanocrystals [J].
Alivisatos, AP .
JOURNAL OF PHYSICAL CHEMISTRY, 1996, 100 (31) :13226-13239
[4]  
ALY AAM, 1988, CROAT CHEM ACTA, V61, P155
[5]   Synthesis and characterization of ethylxanthato complexes of zinc(II) with P-donor ligands [J].
Ara, I ;
El Bahij, F ;
Lachkar, M ;
Ben Larbi, N .
TRANSITION METAL CHEMISTRY, 2003, 28 (08) :908-912
[6]   Phase behavior of two-dimensional hard rod fluids [J].
Bates, MA ;
Frenkel, D .
JOURNAL OF CHEMICAL PHYSICS, 2000, 112 (22) :10034-10041
[7]   PHOTO-LUMINESCENCE AND PHOTOINDUCED OXYGEN-ADSORPTION OF COLLOIDAL ZINC-SULFIDE DISPERSIONS [J].
BECKER, WG ;
BARD, AJ .
JOURNAL OF PHYSICAL CHEMISTRY, 1983, 87 (24) :4888-4893
[8]   Monte Carlo study of electron initiated impact ionization in bulk zincblende and wurtzite phase ZnS [J].
Bellotti, E ;
Brennan, KF ;
Wang, R ;
Ruden, PP .
JOURNAL OF APPLIED PHYSICS, 1998, 83 (09) :4765-4772
[9]   Dielectric dispersion measurements of CdSe nanocrystal colloids: Observation of a permanent dipole moment [J].
Blanton, SA ;
Leheny, RL ;
Hines, MA ;
GuyotSionnest, P .
PHYSICAL REVIEW LETTERS, 1997, 79 (05) :865-868
[10]   Kinetically controlled synthesis of wurtzite ZnS nanorods through mild thermolysis of a covalent organic-inorganic network [J].
Chen, XJ ;
Xu, HF ;
Xu, NS ;
Zhao, FH ;
Lin, WJ ;
Lin, G ;
Fu, YL ;
Huang, ZL ;
Wang, HZ ;
Wu, MM .
INORGANIC CHEMISTRY, 2003, 42 (09) :3100-3106